1,049 results on '"van Os, J"'
Search Results
2. Monitoring en evaluatie van het Programma Stikstofreductie en Natuurverbetering : Syntheserapport
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van Zeijts, H., van Bussel, L.G.J., van Dijk, W.F.A., Trienekens, S.J., Poppeliers, S.W.M., Schmidt, A.M., Smits, N.A.C., Reinds, G.J., Marra, W.A., Boezeman, D., van Hinsberg, A., ‘t Hoen, M.J.J., Plantinga, R., Stammes, I.H., Stroeken, D.P., Vink, M.J., van der Werf, E.H., van Berkum, S., Cals, T.C.A., Mathijssen, P.J.H., van Os, J., Visser, J.B., Hazelhorst, S.B., Westerhoff, P.W., van Zeijts, H., van Bussel, L.G.J., van Dijk, W.F.A., Trienekens, S.J., Poppeliers, S.W.M., Schmidt, A.M., Smits, N.A.C., Reinds, G.J., Marra, W.A., Boezeman, D., van Hinsberg, A., ‘t Hoen, M.J.J., Plantinga, R., Stammes, I.H., Stroeken, D.P., Vink, M.J., van der Werf, E.H., van Berkum, S., Cals, T.C.A., Mathijssen, P.J.H., van Os, J., Visser, J.B., Hazelhorst, S.B., and Westerhoff, P.W.
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- 2024
3. Voortgang stikstofbronmaatregelen en verwachte effecten in 2030 : Monitoring en evaluatie van het Programma Stikstofreductie en Natuurverbetering
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Reinds, G.J., van Dijk, W.F.A., ’t Hoen, M.J.J., Stammes, I.H., Stroeken, D.P., Cals, T.C.A., van Os, J., Marra, W.A., Hazelhorst, S.B., Reinds, G.J., van Dijk, W.F.A., ’t Hoen, M.J.J., Stammes, I.H., Stroeken, D.P., Cals, T.C.A., van Os, J., Marra, W.A., and Hazelhorst, S.B.
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- 2024
4. Does pain hypervigilance further impact the lack of habituation to pain in individuals with chronic pain? A cross-sectional pain ERP study
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Vossen CJ, Luijcks R, van Os J, Joosten EA, and Lousberg R
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event-related fixed-interval area (ERFIA) ,multilevel analysis ,habituation ,pain hypervigilance ,chronic pain ,Medicine (General) ,R5-920 - Abstract
Catherine J Vossen,1 Rosan Luijcks,2 Jim van Os,2,3 Elbert A Joosten,1 Richel Lousberg2 1Department of Anaesthesiology and Pain Medicine, 2Department of Psychiatry & Psychology, Maastricht University Medical Centre, Maastricht, The Netherlands; 3King’s College London, King’s Health Partners, Department of Psychosis Studies, Institute of Psychiatry, London, UK Aim: In chronic pain, habituation is believed to be impaired, and pain hypervigilance can enhance the pain experience. The goal of this study was to determine whether pain hypervigilance further worsens habituation of event-related potentials, measured in a pain-rating protocol of 25 painful somatosensory electrical stimuli, in patients with chronic pain. Methods: Pain hypervigilance was assessed with the Pain Vigilance Awareness Questionnaire and analyzed using the event-related fixed interval areas multilevel technique, which enables one to study within-session habituation. In a cohort of 111 participants, 33 reported chronic pain. This chronic pain group was compared with 33 pain-free individuals, matched for age and sex. Results: The relationship between pain status and habituation was not moderated by pain hypervigilance. Chronic pain status affected linear habituation and dishabituation (quadratic function) from 220 to 260 ms for nearly all electrodes, and from 580 to 640 ms for frontal electrodes. The effect of pain hypervigilance on habituation was observed primarily from 480 to 820 ms poststimulus for right-sided and central electrodes.Conclusion: Pain hypervigilance and chronic pain independently influence habituation to painful stimuli – although not synergistically. To confirm that these effects are mediated by separate pathways, further research is required, in which electroencephalography is combined with other modalities with adequate spatial resolution, such as functional magnetic resonance imaging. Keywords: event-related fixed-interval area, ERFIA, multilevel analysis, habituation, pain hypervigilance, chronic pain
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- 2018
5. Nongenetic Factors Associated With Psychotic Experiences Among UK Biobank Participants: Exposome-Wide Analysis and Mendelian Randomization Analysis
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Lin, B.D., Pries, L.K., Sarac, H.S., van Os, J., Rutten, B.P.F., Luykx, J., Guloksuz, S., Psychiatry 1, RS: MHeNs - R3 - Neuroscience, Psychiatrie & Neuropsychologie, RS: MHeNs - R2 - Mental Health, and MUMC+: MA Psychiatrie (3)
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RISK ,Male ,ENVIRONMENT ,SYMPTOMS ,DISORDERS ,BEHAVIORS ,Mendelian Randomization Analysis ,Middle Aged ,PREVENTION ,Polymorphism, Single Nucleotide ,CANNABIS USE ,United Kingdom ,Cohort Studies ,Psychiatry and Mental health ,Exposome ,SCHIZOPHRENIA ,Humans ,Female ,MENTAL-HEALTH ,METAANALYSIS ,Biological Specimen Banks ,Genome-Wide Association Study - Abstract
IMPORTANCE Although hypothesis-driven research has identified several factors associated with psychosis, this one-exposure-to-one-outcome approach fails to embrace the multiplicity of exposures. Systematic approaches, similar to agnostic genome-wide analyses, are needed to identify genuine signals.OBJECTIVE To systematically investigate nongenetic correlates of psychotic experiences through data-driven agnostic analyses and genetically informed approaches to evaluate associations.DESIGN, SETTING, PARTICIPANTS This cohort study analyzed data from the UK Biobank Mental Health Survey from January 1 to June 1, 2021. An exposome-wide association study was performed in 2 equal-sized split discovery and replication data sets. Variables associated with psychotic experiences in the exposome-wide analysis were tested in a multivariable model. For the variables associated with psychotic experiences in the final multivariable model, the single-nucleotide variant-based heritability and genetic overlap with psychotic experiences using linkage disequilibrium score regression were estimated, and mendelian randomization (MR) approaches were applied to test potential causality. The significant associations observed in 1-sample MR analyses were further tested in multiple sensitivity tests, including collider-correction MR, 2-sample MR, and multivariable MR analyses.EXPOSURES After quality control based on a priori criteria, 247 environmental, lifestyle, behavioral, and economic variables.MAIN OUTCOMES AND MEASURES Psychotic experiences.RESULTS The study included 155 247 participants (87 896 [57%) female; mean [SD] age, 55.94 [7.74] years). In the discovery data set, 162 variables (66%) were associated with psychotic experiences. Of these, 148 (91%) were replicated. The multivariable analysis identified 36 variables that were associated with psychotic experiences. Of these, 28 had significant genetic overlap with psychotic experiences. One-sample MR analyses revealed forward associations with 3 variables and reverse associations with 3. Forward associations with ever having experienced sexual assault and pleiotropy of risk-taking behavior and reverse associations without pleiotropy of experiencing a physically violent crime as well as cannabis use and the reverse association with pleiotropy of worrying too long after embarrassment were confirmed in sensitivity tests. Thus, associations with psychotic experiences were found with both well-studied and unexplored multiple correlated variables. For several variables, the direction of the association was reversed in the final multivariable and MR analyses.CONCLUSIONS AND RELEVANCE The findings of this study underscore the need for systematic approaches and triangulation of evidence to build a knowledge base from ever-growing observational data to guide population-level prevention strategies for psychosis.
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- 2023
6. Evidence, and replication thereof, that molecular-genetic and environmental risks for psychosis impact through an affective pathway
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van Os, J., van Os, J., Pries, L.K., ten Have, M., de Graaf, R., van Dorsselaer, S., Delespaul, P., Bak, M., Kenis, G., Lin, B.D., Luykx, J.J., Richards, A.L., Akdede, B., Binbay, T., Altinyazar, V., Yalincetin, B., Gumus-Akay, G., Cihan, B., Soygur, H., Ulas, H., Cankurtaran, E.S., Kaymak, S.U., Mihaljevic, M.M., Petrovic, S.A., Mirjanic, T., Bernardo, M., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P.A., Garcia-Portilla, M.P., Sanjuan, J., Aguilar, E.J., Santos, J.L., Jimenez-Lopez, E., Arrojo, M., Carracedo, A., Lopez, G., Gonzalez-Penas, J., Parellada, M., Maric, N.P., Atbasoglu, C., Ucok, A., Alptekin, K., Saka, M.C., Arango, C., O'Donovan, M., Rutten, B.P.F., Guloksuz, S., van Os, J., van Os, J., Pries, L.K., ten Have, M., de Graaf, R., van Dorsselaer, S., Delespaul, P., Bak, M., Kenis, G., Lin, B.D., Luykx, J.J., Richards, A.L., Akdede, B., Binbay, T., Altinyazar, V., Yalincetin, B., Gumus-Akay, G., Cihan, B., Soygur, H., Ulas, H., Cankurtaran, E.S., Kaymak, S.U., Mihaljevic, M.M., Petrovic, S.A., Mirjanic, T., Bernardo, M., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P.A., Garcia-Portilla, M.P., Sanjuan, J., Aguilar, E.J., Santos, J.L., Jimenez-Lopez, E., Arrojo, M., Carracedo, A., Lopez, G., Gonzalez-Penas, J., Parellada, M., Maric, N.P., Atbasoglu, C., Ucok, A., Alptekin, K., Saka, M.C., Arango, C., O'Donovan, M., Rutten, B.P.F., and Guloksuz, S.
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Background There is evidence that environmental and genetic risk factors for schizophrenia spectrum disorders are transdiagnostic and mediated in part through a generic pathway of affective dysregulation. Methods We analysed to what degree the impact of schizophrenia polygenic risk (PRS-SZ) and childhood adversity (CA) on psychosis outcomes was contingent on co-presence of affective dysregulation, defined as significant depressive symptoms, in (i) NEMESIS-2 (n = 6646), a representative general population sample, interviewed four times over nine years and (ii) EUGEI (n = 4068) a sample of patients with schizophrenia spectrum disorder, the siblings of these patients and controls. Results The impact of PRS-SZ on psychosis showed significant dependence on co-presence of affective dysregulation in NEMESIS-2 [relative excess risk due to interaction (RERI): 1.01, p = 0.037] and in EUGEI (RERI = 3.39, p = 0.048). This was particularly evident for delusional ideation (NEMESIS-2: RERI = 1.74, p = 0.003; EUGEI: RERI = 4.16, p = 0.019) and not for hallucinatory experiences (NEMESIS-2: RERI = 0.65, p = 0.284; EUGEI: -0.37, p = 0.547). A similar and stronger pattern of results was evident for CA (RERI delusions and hallucinations: NEMESIS-2: 3.02, p < 0.001; EUGEI: 6.44, p < 0.001; RERI delusional ideation: NEMESIS-2: 3.79, p < 0.001; EUGEI: 5.43, p = 0.001; RERI hallucinatory experiences: NEMESIS-2: 2.46, p < 0.001; EUGEI: 0.54, p = 0.465). Conclusions The results, and internal replication, suggest that the effects of known genetic and non-genetic risk factors for psychosis are mediated in part through an affective pathway, from which early states of delusional meaning may arise.
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- 2022
7. First-Episode Psychosis Patients Who Deteriorated in the Premorbid Period Do Not Have Higher Polygenic Risk Scores Than Others: A Cluster Analysis of EU-GEI Data
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Ferraro, L, Quattrone, D, La Barbera, D, La Cascia, C, Morgan, C, Kirkbride, JB, Cardno, AG, Sham, P, Tripoli, G, Sideli, L, Seminerio, F, Sartorio, C, Szoke, A, Tarricone, I, Bernardo, M, Rodriguez, V, Stilo, SA, Gayer-Anderson, C, de Haan, L, Velthorst, E, Jongsma, H, Bart, RBP, Richards, A, Arango, C, Menezez, PR, Lasalvia, A, Tosato, S, Tortelli, A, Del Ben, CM, Selten, J-P, Jones, PB, van Os, J, The WP2 EU-GEI Group, Di Forti, M, Vassos, E, Murray, RM, Adult Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Ferraro, Laura, Quattrone, Diego, La Barbera, Daniele, La Cascia, Caterina, Morgan, Craig, Kirkbride, James B, Cardno, Alastair G, Sham, Pak, Tripoli, Giada, Sideli, Lucia, Seminerio, Fabio, Sartorio, Crocettarachele, Szoke, Andrei, Tarricone, Ilaria, Bernardo, Miquel, Rodriguez, Victoria, Stilo, Simona A, Gayer-Anderson, Charlotte, de Haan, Lieuwe, Velthorst, Eva, Jongsma, Hannah, Bart, Rutten B P, Richards, Alexander, Arango, Celso, Menezez, Paulo Rossi, Lasalvia, Antonio, Tosato, Sarah, Tortelli, Andrea, Del Ben, Cristina Marta, Selten, Jean-Paul, Jones, Peter B, van Os, Jim, Di Forti, Marta, Vassos, Evangelo, Murray, Robin M, Psychiatrie & Neuropsychologie, MUMC+: MA Psychiatrie (3), and RS: MHeNs - R3 - Neuroscience
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cannabis ,cannabi ,Adolescent ,BIPOLAR DISORDER ,ADJUSTMENT ,GENE-ENVIRONMENT INTERACTIONS ,CLASSIFICATION ,bipolar ,schizophrenia ,Psychiatry and Mental health ,Psychotic Disorders ,Risk Factors ,IQ ,ONSET ,premorbid ,Humans ,Cluster Analysis ,GENOME-WIDE ASSOCIATION ,TRAJECTORIES ,deterioration - Abstract
Cluster studies identified a subgroup of patients with psychosis whose premorbid adjustment deteriorates before the onset, which may reflect variation in genetic influence. However, other studies reported a complex relationship between distinctive patterns of cannabis use and cognitive and premorbid impairment that is worthy of consideration. We examined whether: (1) premorbid social functioning (PSF) and premorbid academic functioning (PAF) in childhood and adolescence and current intellectual quotient (IQ) define different clusters in 802 first-episode of psychosis (FEP) patients; resulting clusters vary in (2) polygenic risk scores (PRSs) for schizophrenia (SCZ_PRS), bipolar disorder (BD_PRS), major depression (MD_PRS), and IQ (IQ_PRS), and (3) patterns of cannabis use, compared to 1,263 population-based controls. Four transdiagnostic clusters emerged (BIC = 2268.5): (1) high-cognitive-functioning (n = 205), with the highest IQ (Mean = 106.1, 95% CI: 104.3, 107.9) and PAF, but low PSF. (2) Low-cognitive-functioning (n = 223), with the lowest IQ (Mean = 73.9, 95% CI: 72.2, 75.7) and PAF, but normal PSF. (3) Intermediate (n = 224) (Mean_IQ = 80.8, 95% CI: 79.1, 82.5) with low-improving PAF and PSF. 4) Deteriorating (n = 150) (Mean_IQ = 80.6, 95% CI: 78.5, 82.7), with normal-deteriorating PAF and PSF. The PRSs explained 7.9% of between-group membership. FEP had higher SCZ_PRS than controls [F(4,1319) = 20.4, P
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- 2022
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8. Affective wellbeing moderates the association between polygenic risk score for neuroticism and change in neuroticism
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Bahbouhová, J., primary, Cade, M. V., additional, De Sadeleer, A. T., additional, Dibbets, C., additional, Herrmann, L.-Q., additional, Hovens, P. O. F., additional, Jakson, B. M., additional, Reising, R. C., additional, Menne-Lothmann, C., additional, Decoster, J., additional, van Winkel, R., additional, Collip, D., additional, Delespaul, P., additional, De Hert, M., additional, Derom, C., additional, Thiery, E., additional, Jacobs, N., additional, Wichers, M., additional, van Os, J., additional, Rutten, B. P. F., additional, Gülöksüz, S., additional, and Klingenberg, B., additional
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- 2023
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9. Differential associations of childhood adversity subtypes and psychopathology in men and women
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Prachason, T., primary, Mutlu, I., additional, Fusar-Poli, L., additional, Menne-Lothmann, C., additional, Decoster, J., additional, van Winkel, R., additional, Collip, D., additional, Delespaul, P., additional, De Hert, M., additional, Derom, C., additional, Thiery, E., additional, Jacobs, N., additional, Wichers, M., additional, van Os, J., additional, Rutten, B. P. F., additional, Pries, L.-K., additional, and Gülöksüz, S., additional
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- 2023
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10. Impact of adverse childhood experiences on educational achievements in young people at clinical high risk of developing psychosis
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Tognin, S, Catalan, A, Kempton, MJ, Nelson, B, McGorry, P, Riecher-Rossler, A, Bressan, R, Barrantes-Vidal, N, Krebs, M-O, Nordentoft, M, Ruhrmann, S, Sachs, G, Rutten, BPF, van Os, J, de Haan, L, van der Gaag, M, McGuire, PR, Valmaggia, L, Tognin, S, Catalan, A, Kempton, MJ, Nelson, B, McGorry, P, Riecher-Rossler, A, Bressan, R, Barrantes-Vidal, N, Krebs, M-O, Nordentoft, M, Ruhrmann, S, Sachs, G, Rutten, BPF, van Os, J, de Haan, L, van der Gaag, M, McGuire, PR, and Valmaggia, L
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BACKGROUND: Adverse childhood experiences (ACE) can affect educational attainments, but little is known about their impact on educational achievements in people at clinical high risk of psychosis (CHR). METHODS: In total, 344 CHR individuals and 67 healthy controls (HC) were recruited as part of the European Community's Seventh Framework Programme-funded multicenter study the European Network of National Schizophrenia Networks Studying Gene-Environment Interactions (EU-GEI). The brief version of the Child Trauma Questionnaire was used to measure ACE, while educational attainments were assessed using a semi-structured interview. RESULTS: At baseline, compared with HC, the CHR group spent less time in education and had higher rates of ACE, lower rates of employment, and lower estimated intelligence quotient (IQ). Across both groups, the total number of ACE was associated with fewer days in education and lower level of education. Emotional abuse was associated with fewer days in education in HC. Emotional neglect was associated with a lower level of education in CHR, while sexual abuse was associated with a lower level of education in HC. In the CHR group, the total number of ACE, physical abuse, and neglect was significantly associated with unemployment, while emotional neglect was associated with employment. CONCLUSIONS: ACE are strongly associated with developmental outcomes such as educational achievement. Early intervention for psychosis programs should aim at integrating specific interventions to support young CHR people in their educational and vocational recovery. More generally, public health and social interventions focused on the prevention of ACE (or reduce their impact if ACE occur) are recommended.
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- 2023
11. Taalachterstand en psychose onder mensen met een migratieachtergrond
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Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, van Os, J, Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, and van Os, J
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BACKGROUND: Ethnic minorities in the Netherlands face an excess psychosis risk, and understanding of causality remains limited. Linguistic disadvantage and other indicators of societal exclusion might play a role, and offer potential targets for public health interventions.AIM: To establish the contribution of linguistic disadvantage, indicators of social distance and perceived discrimination to the increased risk of psychoses in migrants and ethnic minorities.METHODS: We used the Dutch data from an international case-control study into psychotic disorders (the EU-GEI study). A first episode of psychosis was our outcome variable, and we used well-defined data on established confounders (e.g. age and sex) and indicators of ethnicity, social distance, linguistic disadvantage and perceived discrimination as our predictor variables.RESULTS: Ethnic minorities face an increased psychosis risk. This appears to be the case for both first- and second- generation migrants and so-called ‘Western’ and non-Western migrants. Though confounders and social distance appear to contribute, linguistic disadvantage appears to play a role in the excess psychosis risk in first-generation migrants.CONCLUSION: Reducing the social consequences of linguistic disadvantage or social distance might be a starting point for concrete public health interventions aimed at preventing the increased psychosis risk faced by first-generation migrants.
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- 2023
12. Landbouwmilieumaatregelen voor akkerbouw en melkveebedrijven
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van Os, J., Agricola, H.J., de Vries, M., Fuchs, L.M., Sluijsmans, J.J.L., van Os, J., Agricola, H.J., de Vries, M., Fuchs, L.M., and Sluijsmans, J.J.L.
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Het Nationaal Programma Landelijk Gebied (NPLG) adresseert beleidsdoelen voor stikstof, klimaat, water en natuur, die integraal en gebiedsgericht zullen worden opgepakt en uitgewerkt. Daarbij is een overzicht gewenst van mogelijke maatregelen die op landbouwbedrijven genomen kunnen worden, tezamen met een beoordeling van effecten op de beoogde doelen en in hoeverre er bij afzonderlijke maatregelen sprake kan zijn van afwenteling naar andere thema’s of beleidsdoelen. Vanuit een dertigtal beschikbare onderzoeksrapporten zijn alle genoemde milieumaatregelen per bedrijfsonderdeel bij elkaar gezet voor akkerbouw- en melkveebedrijven. Vervolgens zijn voor groepen maatregelen de effecten op de milieudoelen beschreven en mogelijke interacties. Zowel voor akkerbouw- als melkveebedrijven komt een veelheid aan maatregelen naar voren, waaruit passende keuzes gemaakt kunnen worden, rekening houdend met verschillen in bedrijfsstructuur, fysieke omstandigheden en ligging ten opzichte van kwetsbare natuurgebieden.
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- 2023
13. Taalachterstand en psychose onder mensen met een migratieachtergrond
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Hersenen-Medisch 1, Brain, Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, van Os, J, Hersenen-Medisch 1, Brain, Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, and van Os, J
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- 2023
14. Methods for detecting heat stress in hutch-housed dairy calves in a continental climate
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Hersenen-Medisch 1, Brain, Dado-Senn, B, Ouellet, V, Lantigua, V, Van Os, J, Laporta, J, Hersenen-Medisch 1, Brain, Dado-Senn, B, Ouellet, V, Lantigua, V, Van Os, J, and Laporta, J
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- 2023
15. Assessing optimal frequency for image acquisition in computer vision systems developed to monitor feeding behavior of group-housed Holstein heifers
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Hersenen-Medisch 1, Brain, Bresolin, T, Ferreira, R, Reyes, F, Van Os, J, Dórea, J R R, Hersenen-Medisch 1, Brain, Bresolin, T, Ferreira, R, Reyes, F, Van Os, J, and Dórea, J R R
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- 2023
16. Longitudinal associations between alcohol use, smoking, genetic risk scoring and symptoms of depression in the general population: A prospective 6-year cohort study
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Psychiatrie_Medisch, Hersenen-Medisch 1, TN groep Adan, Brain, Diagnostiek & Vroege Psychose Medisch, Onderzoek, Neurogenetica, De Boer, N., Vermeulen, J., Lin, B., Van Os, J., Ten Have, M., De Graaf, R., Van Dorsselaer, S., Bak, M., Rutten, B., Batalla, A., Guloksuz, S., Luykx, J. J., Psychiatrie_Medisch, Hersenen-Medisch 1, TN groep Adan, Brain, Diagnostiek & Vroege Psychose Medisch, Onderzoek, Neurogenetica, De Boer, N., Vermeulen, J., Lin, B., Van Os, J., Ten Have, M., De Graaf, R., Van Dorsselaer, S., Bak, M., Rutten, B., Batalla, A., Guloksuz, S., and Luykx, J. J.
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- 2023
17. Associations between polygenic risk score loading, psychosis liability, and clozapine use among individuals with schizophrenia
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Lin, B.D., Pinzón-Espinosa, J., Blouzard, E., Van Der Horst, M.Z., Okhuijsen-pfeifer, C., Van Eijk, K.R., Guloksuz, S., Peyrot, W.J., Luykx, J.J., Hasan, A., Wagner, E., Pantelis, C., Everall, I.P., Ayhan, Y., Babaoğlu, M.O., Bak, M., Alink, W., Beld, E, Bouhuis, A., Edlinger, M., Erdoğan, I.M., Gutwinski, S., Hallikainen, T., Jeger-land, E., Lähteenvuo, M., De Koning, M.B., Morgenroth, C., Müderrisoğlu, A., Oviedo-salcedo, T., Schreiter, S., Repo-tiihonen, E., Tuppurainen, H., Veereschild, M., Veerman, S.R.T., Cohen, D., de Vos, M., Bogers, J.P.A.M., Anıl Yağcıoğlu, A.E., Tiihonen, J., Ripke, S., Bousman, C.A., Van Beek, H, van der Horst, M., Van Eijk, K., Ertuğrul, A., Yoca, G., Görlitz, T., Grootens, K., Leucht, S., Narang, A., Schneider-thoma, J., Kahn, R.S., Bekema, E., Kleymann, P., Alizadeh, B.Z., van Amelsvoort, T., Cahn, W., de Haan, L., Schirmbeck, F., Simons, C.J.P., van Os, J., Rutten, B., van Winkel, R., Lin, B.D., Pinzón-Espinosa, J., Blouzard, E., Van Der Horst, M.Z., Okhuijsen-pfeifer, C., Van Eijk, K.R., Guloksuz, S., Peyrot, W.J., Luykx, J.J., Hasan, A., Wagner, E., Pantelis, C., Everall, I.P., Ayhan, Y., Babaoğlu, M.O., Bak, M., Alink, W., Beld, E, Bouhuis, A., Edlinger, M., Erdoğan, I.M., Gutwinski, S., Hallikainen, T., Jeger-land, E., Lähteenvuo, M., De Koning, M.B., Morgenroth, C., Müderrisoğlu, A., Oviedo-salcedo, T., Schreiter, S., Repo-tiihonen, E., Tuppurainen, H., Veereschild, M., Veerman, S.R.T., Cohen, D., de Vos, M., Bogers, J.P.A.M., Anıl Yağcıoğlu, A.E., Tiihonen, J., Ripke, S., Bousman, C.A., Van Beek, H, van der Horst, M., Van Eijk, K., Ertuğrul, A., Yoca, G., Görlitz, T., Grootens, K., Leucht, S., Narang, A., Schneider-thoma, J., Kahn, R.S., Bekema, E., Kleymann, P., Alizadeh, B.Z., van Amelsvoort, T., Cahn, W., de Haan, L., Schirmbeck, F., Simons, C.J.P., van Os, J., Rutten, B., and van Winkel, R.
- Abstract
Importance: Predictors consistently associated with psychosis liability and course of illness in schizophrenia (SCZ) spectrum disorders (SSD), including the need for clozapine treatment, are lacking. Longitudinally ascertained medication use may empower studies examining associations between polygenic risk scores (PRSs) and pharmacotherapy choices. Objective: To examine associations between PRS-SCZ loading and groups with different liabilities to SSD (individuals with SSD taking clozapine, individuals with SSD taking other antipsychotics, their parents and siblings, and unrelated healthy controls) and between PRS-SCZ and the likelihood of receiving a prescription of clozapine relative to other antipsychotics. Design, Setting, and Participants: This genetic association study was a multicenter, observational cohort study with 6 years of follow-up. Included were individuals diagnosed with SSD who were taking clozapine or other antipsychotics, their parents and siblings, and unrelated healthy controls. Data were collected from 2004 until 2021 and analyzed between October 2021 and September 2022. Exposures: Polygenic risk scores for SCZ. Main Outcomes and Measures: Multinomial logistic regression was used to examine possible differences between groups by computing risk ratios (RRs), ie, ratios of the probability of pertaining to a particular group divided by the probability of healthy control status. We also computed PRS-informed odd ratios (ORs) for clozapine use relative to other antipsychotics. Results: Polygenic risk scores for SCZ were generated for 2344 participants (mean [SD] age, 36.95 years [14.38]; 994 female individuals [42.4%]) who remained after quality control screening (557 individuals with SSD taking clozapine, 350 individuals with SSD taking other antipsychotics during the 6-year follow-up, 542 parents and 574 siblings of individuals with SSD, and 321 unrelated healthy controls). All RR
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- 2023
18. Be(com)ing social: Daily-life social interactions and parental bonding
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Jeroen Decoster, de Hert M, Inez Myin-Germeys, Evert Thiery, Maude Schneider, Olivia J. Kirtley, Claudia Menne-Lothmann, Catherine Derom, Martien Wampers, Bart P. F. Rutten, Sinan Guloksuz, van Os J, Marieke Wichers, Robin Achterhof, Nele Jacobs, van Winkel R, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), RS: MHeNs - R2 - Mental Health, RS: MHeNs - R3 - Neuroscience, Psychiatrie & Neuropsychologie, MUMC+: MA Psychiatrie (3), and MUMC+: Hersen en Zenuw Centrum (3)
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Adult ,Male ,Parents ,PERCEPTIONS ,Adolescent ,PsyArXiv|Social and Behavioral Sciences|Developmental Psychology ,Social Interaction ,SUBSTANCE USE DISORDERS ,Developmental psychology ,Fathers ,Young Adult ,PSYCHOSIS ,PsyArXiv|Social and Behavioral Sciences|Developmental Psychology|Adolescence ,ADOLESCENTS ,Developmental and Educational Psychology ,Psychology ,Humans ,bepress|Social and Behavioral Sciences|Psychology|Child Psychology ,bepress|Social and Behavioral Sciences|Psychology|Developmental Psychology ,Child ,Life-span and Life-course Studies ,FUNCTIONING SCALE ,Demography ,INSTRUMENT ,PsyArXiv|Social and Behavioral Sciences|Developmental Psychology|Social Development ,Parenting ,experience sampling method ,ATTACHMENT STYLE ,socialization ,Parental bonding ,Object Attachment ,parenting style ,PsyArXiv|Social and Behavioral Sciences ,social functioning ,PERSPECTIVES ,MOOD ,bepress|Social and Behavioral Sciences ,Female ,adolescence - Abstract
Parents are known to provide a lasting basis for their children's social development. Understanding parent-driven socialization is particularly relevant in adolescence, as an increasing social independence is developed. However, the relationship between key parenting styles of care and control and the microlevel expression of daily-life social interactions has been insufficiently studied. Adolescent and young adult twins and their nontwin siblings (N = 635; mean age = 16.6; age range = 14.2-21.9; 58.6% female; 79.5% in or having completed higher secondary/tertiary education; 2.8% speaking language other than Dutch at home) completed the Parental Bonding Instrument (PBI) on parental care and control. Participants also completed a 6-day experience sampling period (10 daily beeps, mean compliance = 68.0%) to assess daily-life social interactions. Higher overall parental bonding quality (of both parents) related to more positive social experiences in daily life (e.g., belonging in company), but not to more social behaviors (e.g., being with others). Factor analysis indicated a three-factor structure of the PBI, with care, denial of psychological autonomy, and encouragement of behavioral freedom. Paternal care was uniquely predictive of better social experiences. These findings demonstrate how parenting styles may be uniquely associated with how adolescents experience their social world, with a potentially important role for fathers in particular. This complements the long-held idea of socialization through parenting by bringing it into the context of daily life and implies how both conceptualizations of social functioning and interventions aimed at alleviating social dysfunction might benefit from a stronger consideration of day-to-day social experiences. (PsycInfo Database Record (c) 2022 APA, all rights reserved). ispartof: DEVELOPMENTAL PSYCHOLOGY vol:58 issue:4 pages:792-805 ispartof: location:United States status: published
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- 2022
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19. Cognitive functioning throughout adulthood and illness stages in individuals with psychotic disorders and their unaffected siblings
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Velthorst E., Mollon J., Murray R. M., de Haan L., Germeys I. M., Glahn D. C., Arango C., van der Ven E., Di Forti M., Bernardo M., Guloksuz S., Delespaul P., Mezquida G., Amoretti S., Bobes J., Saiz P. A., Garcia-Portilla M. P., Santos J. L., Jimenez-Lopez E., Sanjuan J., Aguilar E. J., Arrojo M., Carracedo A., Lopez G., Gonzalez-Penas J., Parellada M., Atbasoglu C., Saka M. C., Ucok A., Alptekin K., Akdede B., Binbay T., Altinyazar V., Ulas H., Yalincetin B., Gumus-Akay G., Beyaz B. C., Soygur H., Cankurtaran E. S., Kaymak S. U., Maric N. P., Mihaljevic M. M., Petrovic S. A., Mirjanic T., Del-Ben C. M., Ferraro L., Gayer-Anderson C., Jones P. B., Jongsma H. E., Kirkbride J. B., La Cascia C., Lasalvia A., Tosato S., Llorca P. -M., Menezes P. R., Morgan C., Quattrone D., Menchetti M., Selten J. -P., Szoke A., Tarricone I., Tortelli A., McGuire P., Valmaggia L., Kempton M. J., van der Gaag M., Riecher-Rossler A., Bressan R. A., Barrantes-Vidal N., Nelson B., McGorry P., Pantelis C., Krebs M. -O., Ruhrmann S., Sachs G., Rutten B. P. F., van Os J., Alizadeh B. Z., van Amelsvoort T., Bartels-Velthuis A. A., Bruggeman R., van Beveren N. J., Luykx J. J., Cahn W., Simons C. J. P., Kahn R. S., Schirmbeck F., van Winkel R., Calem M., Tognin S., Modinos G., Pisani S., Kraan T. C., van Dam D. S., Burger N., Amminger G. P., Politis A., Goodall J., Borgwardt S., Studerus E., Gadelha A., Brietzke E., Asevedo G., Asevedo E., Zugman A., Dominguez-Martinez T., Monsonet M., Cristobal-Narvaez P., Racioppi A., Kwapil T. R., Kazes M., Daban C., Bourgin J., Gay O., Mam-Lam-Fook C., Nordholm D., Rander L., Krakauer K., Glenthoj L. B., Glenthoj B., Gebhard D., Arnhold J., Klosterkotter J., Lasser I., Winklbaur B., Reichenberg A., Velthorst E., Mollon J., Murray R.M., de Haan L., Germeys I.M., Glahn D.C., Arango C., van der Ven E., Di Forti M., Bernardo M., Guloksuz S., Delespaul P., Mezquida G., Amoretti S., Bobes J., Saiz P.A., Garcia-Portilla M.P., Santos J.L., Jimenez-Lopez E., Sanjuan J., Aguilar E.J., Arrojo M., Carracedo A., Lopez G., Gonzalez-Penas J., Parellada M., Atbasoglu C., Saka M.C., Ucok A., Alptekin K., Akdede B., Binbay T., Altinyazar V., Ulas H., Yalincetin B., Gumus-Akay G., Beyaz B.C., Soygur H., Cankurtaran E.S., Kaymak S.U., Maric N.P., Mihaljevic M.M., Petrovic S.A., Mirjanic T., Del-Ben C.M., Ferraro L., Gayer-Anderson C., Jones P.B., Jongsma H.E., Kirkbride J.B., La Cascia C., Lasalvia A., Tosato S., Llorca P.-M., Menezes P.R., Morgan C., Quattrone D., Menchetti M., Selten J.-P., Szoke A., Tarricone I., Tortelli A., McGuire P., Valmaggia L., Kempton M.J., van der Gaag M., Riecher-Rossler A., Bressan R.A., Barrantes-Vidal N., Nelson B., McGorry P., Pantelis C., Krebs M.-O., Ruhrmann S., Sachs G., Rutten B.P.F., van Os J., Alizadeh B.Z., van Amelsvoort T., Bartels-Velthuis A.A., Bruggeman R., van Beveren N.J., Luykx J.J., Cahn W., Simons C.J.P., Kahn R.S., Schirmbeck F., van Winkel R., Calem M., Tognin S., Modinos G., Pisani S., Kraan T.C., van Dam D.S., Burger N., Amminger G.P., Politis A., Goodall J., Borgwardt S., Studerus E., Gadelha A., Brietzke E., Asevedo G., Asevedo E., Zugman A., Dominguez-Martinez T., Monsonet M., Cristobal-Narvaez P., Racioppi A., Kwapil T.R., Kazes M., Daban C., Bourgin J., Gay O., Mam-Lam-Fook C., Nordholm D., Rander L., Krakauer K., Glenthoj L.B., Glenthoj B., Gebhard D., Arnhold J., Klosterkotter J., Lasser I., Winklbaur B., Reichenberg A., RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience, Neurosciences, Psychiatry, Clinical Developmental Psychology, World Health Organization (WHO) Collaborating Center, Life Course Epidemiology (LCE), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), Adult Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Complex Trait Genetics, and Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep
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0301 basic medicine ,validity ,medicine.medical_treatment ,CHILDHOOD ,Neuropsychological Tests ,FAMÍLIA ,episode ,Cognition ,0302 clinical medicine ,DEFICITS ,Settore MED/48 -Scienze Infermierist. e Tecn. Neuro-Psichiatriche e Riabilitat ,Medicine ,Cognitive impairment ,Psychiatry ,Symptom severity ,Cannabis use ,IMPAIRMENT ,ABILITY ,Psychiatry and Mental health ,Schizophrenia ,RELIABILITY ,Neuropsychological Test ,Life Sciences & Biomedicine ,Human ,Clinical psychology ,Adult ,Biochemistry & Molecular Biology ,impairment ,schizophrenia-patients ,ability ,GENETIC RISK ,Psychotic Disorder ,SCHIZOPHRENIA-PATIENTS ,03 medical and health sciences ,Cellular and Molecular Neuroscience ,SDG 3 - Good Health and Well-being ,Settore M-PSI/08 - Psicologia Clinica ,Humans ,In patient ,Cognitive skill ,VALIDITY ,Antipsychotic ,Molecular Biology ,Settore MED/25 - Psichiatria ,Aged ,Cross-Sectional Studie ,DECLINE ,Science & Technology ,reliability ,business.industry ,Working memory ,Siblings ,Neurosciences ,Diagnostic markers ,medicine.disease ,Cross-Sectional Studies ,030104 developmental biology ,deficits ,Psychotic Disorders ,PSYCHOSIS, COGNITION, MULTICENTRIC STUDY ,Neurosciences & Neurology ,business ,EPISODE ,030217 neurology & neurosurgery - Abstract
The European Community’s Seventh Framework Programme under grant agreement No. HEALTH-F2-2010-241909 (EUGEI); The Spanish sample was supported by the Spanish Ministry of Science and Innovation, Instituto de Salud Carlos III (SAM16PE07CP1, PI16/02012, PI19/024) (...), Velthorst, E., Mollon, J., Murray, R.M., de Haan, L., Germeys, I.M., Glahn, D.C., Arango, C., van der Ven, E., Di Forti, M., Bernardo, M., Guloksuz, S., Delespaul, P., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P.A., García-Portilla, M.P., Santos, J.L., Jiménez-López, E., Sanjuan, J., Aguilar, E.J., Arrojo, M., Carracedo, A., López, G., González-Peñas, J., Parellada, M., Atbaşoğlu, C., Saka, M.C., Üçok, A., Alptekin, K., Akdede, B., Binbay, T., Altınyazar, V., Ulaş, H., Yalınçetin, B., Gümüş-Akay, G., Beyaz, B.C., Soygür, H., Cankurtaran, E.Ş., Kaymak, S.U., Maric, N.P., Mihaljevic, M.M., Petrovic, S.A., Mirjanic, T., Del-Ben, C.M., Ferraro, L., Gayer-Anderson, C., Jones, P.B., Jongsma, H.E., Kirkbride, J.B., La Cascia, C., Lasalvia, A., Tosato, S., Llorca, P.-M., Menezes, P.R., Morgan, C., Quattrone, D., Menchetti, M., Selten, J.-P., Szöke, A., Tarricone, I., Tortelli, A., McGuire, P., Valmaggia, L., Kempton, M.J., van der Gaag, M., Riecher-Rössler, A., Bressan, R.A., Barrantes-Vidal, N., Nelson, B., McGorry, P., Pantelis, C., Krebs, M.-O., Ruhrmann, S., Sachs, G., Rutten, B.P.F., van Os, J., Alizadeh, B.Z., van Amelsvoort, T., Bartels-Velthuis, A.A., Bruggeman, R., van Beveren, N.J., Luykx, J.J., Cahn, W., Simons, C.J.P., Kahn, R.S., Schirmbeck, F., van Winkel, R., Calem, M., Tognin, S., Modinos, G., Pisani, S., Kraan, T.C., van Dam, D.S., Burger, N., Amminger, G.P., Politis, A., Goodall, J., Borgwardt, S., Studerus, E., Gadelha, A., Brietzke, E., Asevedo, G., Asevedo, E., Zugman, A., Domínguez-Martínez, T., Monsonet, M., Cristóbal-Narváez, P., Racioppi, A., Kwapil, T.R., Kazes, M., Daban, C., Bourgin, J., Gay, O., Mam-Lam-Fook, C., Nordholm, D., Rander, L., Krakauer, K., Glenthøj, L.B., Glenthøj, B., Gebhard, D., Arnhold, J., Klosterkötter, J., Lasser, I., Winklbaur, B., Reichenberg, A., EU-GEI High Risk Study
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- 2021
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20. Methods for detecting heat stress in hutch-housed dairy calves in a continental climate
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Dado-Senn, B., primary, Ouellet, V., additional, Lantigua, V., additional, Van Os, J., additional, and Laporta, J., additional
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- 2023
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21. Longitudinal effects of genomic and exposomic vulnerability for schizophrenia on childhood psychosis expression: results from the ABCD Study
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Di Vincenzo, M., primary, Prachason, T., additional, Sampogna, G., additional, Arias-Magnasco, A., additional, Lin, B.D., additional, Pries, L.K., additional, Van Os, J., additional, Rutten, B.P., additional, and Guloksuz, S., additional
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- 2023
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22. The association between exposome score for schizophrenia and metabolic parameters in individuals with schizophrenia and healthy controls
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Erzin, G., primary, Atbaşoğlu, C., additional, Fusar-Poli, L., additional, Saka, M.C., additional, Üçok, A., additional, Alptekin, K., additional, Van Os, J., additional, Guloksuz, S., additional, and Gümüş-Akay, G., additional
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- 2023
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23. Assessing optimal frequency for image acquisition in computer vision systems developed to monitor feeding behavior of group-housed Holstein heifers
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Bresolin, T., primary, Ferreira, R., additional, Reyes, F., additional, Van Os, J., additional, and Dórea, J.R.R., additional
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- 2023
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24. Impact of adverse childhood experiences on educational achievements in young people at clinical high risk of developing psychosis
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Tognin, S., Catalan, A., Kempton, M.J., Nelson, B., McGorry, P., Riecher-Rossler, A., Bressan, R., Barrantes-Vidal, N., Krebs, M.O., Nordentoft, M., Ruhrmann, S., Sachs, G., Rutten, B.P.F., van Os, J., de Haan, L., van der Gaag, M., McGuire, P., Valmaggia, L.R., RS: MHeNs - R3 - Neuroscience, Psychiatrie & Neuropsychologie, and MUMC+: MA Psychiatrie (3)
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education ,EMOTION RECOGNITION ,ADULTS ,clinical high risk for psychosis ,Psychiatry and Mental health ,INDIVIDUALS ,ULTRA-HIGH RISK ,SCHOOL ,ACADEMIC-ACHIEVEMENT ,EMPLOYMENT ,Adverse childhood experiences ,PROTECTIVE FACTORS ,MENTAL-HEALTH ,TRAUMA - Abstract
Background Adverse childhood experiences (ACE) can affect educational attainments, but little is known about their impact on educational achievements in people at clinical high risk of psychosis (CHR). Methods In total, 344 CHR individuals and 67 healthy controls (HC) were recruited as part of the European Community’s Seventh Framework Programme-funded multicenter study the European Network of National Schizophrenia Networks Studying Gene–Environment Interactions (EU-GEI). The brief version of the Child Trauma Questionnaire was used to measure ACE, while educational attainments were assessed using a semi-structured interview. Results At baseline, compared with HC, the CHR group spent less time in education and had higher rates of ACE, lower rates of employment, and lower estimated intelligence quotient (IQ). Across both groups, the total number of ACE was associated with fewer days in education and lower level of education. Emotional abuse was associated with fewer days in education in HC. Emotional neglect was associated with a lower level of education in CHR, while sexual abuse was associated with a lower level of education in HC. In the CHR group, the total number of ACE, physical abuse, and neglect was significantly associated with unemployment, while emotional neglect was associated with employment. Conclusions ACE are strongly associated with developmental outcomes such as educational achievement. Early intervention for psychosis programs should aim at integrating specific interventions to support young CHR people in their educational and vocational recovery. More generally, public health and social interventions focused on the prevention of ACE (or reduce their impact if ACE occur) are recommended.
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- 2023
25. Linguistic distance and psychosis in ethnic minorities
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Jongsma, H E, van der Ven, E M A, Velthorst, E, de Haan, L, Rutten, B P F, van Os, J, Clinical Developmental Psychology, APH - Mental Health, and World Health Organization (WHO) Collaborating Center
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SDG 16 - Peace ,SDG 16 - Peace, Justice and Strong Institutions ,SDG 10 - Reduced Inequalities ,Justice and Strong Institutions - Abstract
BACKGROUND: Ethnic minorities in the Netherlands face an excess psychosis risk, and understanding of causality remains limited. Linguistic disadvantage and other indicators of societal exclusion might play a role, and offer potential targets for public health interventions.AIM: To establish the contribution of linguistic disadvantage, indicators of social distance and perceived discrimination to the increased risk of psychoses in migrants and ethnic minorities.METHODS: We used the Dutch data from an international case-control study into psychotic disorders (the EU-GEI study). A first episode of psychosis was our outcome variable, and we used well-defined data on established confounders (e.g. age and sex) and indicators of ethnicity, social distance, linguistic disadvantage and perceived discrimination as our predictor variables.RESULTS: Ethnic minorities face an increased psychosis risk. This appears to be the case for both first- and second- generation migrants and so-called ‘Western’ and non-Western migrants. Though confounders and social distance appear to contribute, linguistic disadvantage appears to play a role in the excess psychosis risk in first-generation migrants.CONCLUSION: Reducing the social consequences of linguistic disadvantage or social distance might be a starting point for concrete public health interventions aimed at preventing the increased psychosis risk faced by first-generation migrants.
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- 2023
26. Cannabis use as a potential mediator between childhood adversity and first-episode psychosis: results from the EU-GEI case-control study
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Trotta, G, Rodriguez, V, Quattrone, D, Spinazzola, E, Tripoli, G, Gayer-Anderson, C, Freeman, Tp, Jongsma, He, Sideli, L, Aas, M, Stilo, Sa, La Cascia, C, Ferraro, L, La Barbera, D, Lasalvia, A, Tosato, S, Tarricone, I, D'Andrea, G, Tortelli, A, Schurhoff, F, Szoke, A, Pignon, B, Selten, Jp, Velthorst, E, de Haan, L, Llorca, Pm, Menezes, Pr, Del Ben, Cm, Santos, Jl, Arrojo, M, Bobes, J, Sanjuan, J, Bernardo, M, Arango, C, Kirkbride, Jb, Jones, Pb, Richards, A, Rutten, Bp, Van Os, J, Austin-Zimmerman, I, Zk, Li, Morgan, C, Sham, Pc, Vassos, E, Wong, C, Bentall, R, Fisher, Hl, Murray, Rm, Alameda, L, and Di Forti, M
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trauma ,psychotic disorders ,childhood experience ,mediation ,Cannabis use - Published
- 2023
27. Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders
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Okhuijsen-Pfeifer, C., van der Horst, M. Z., Bousman, C. A., Lin, B., van Eijk, K. R., Ripke, S., Ayhan, Y., Babaoglu, M. O., Bak, M., Alink, W., van Beek, H., Beld, E., Bouhuis, A., Edlinger, M., Erdogan, I. M., Ertuğrul, A., Yoca, G., Everall, I. P., Görlitz, T., van Amelsvoort, T., Bartels-Velthuis, A. A., Bruggeman, R., Cahn, W., Guloksuz, S., de Haan, L., Kahn, R. S., Schirmbeck, F., Simons, C. J. P., van Os, J., Alizadeh, B. Z., Luykx, J. J., Rutten, B. P. F., van Winkel, R., Grootens, K. P., Gutwinski, S., Hallikainen, T., Jeger-Land, E., de Koning, M., Lähteenvuo, M., Legge, S. E., Leucht, S., Morgenroth, C., Müderrisoğlu, A., Narang, A., Pantelis, C., Pardiñas, A. F., Oviedo-Salcedo, T., Schneider-Thoma, J., Schreiter, S., Repo-Tiihonen, E., Tuppurainen, H., Veereschild, M., Veerman, S., de Vos, M., Wagner, E., Cohen, D., Bogers, J. P. A. M., Walters, J. T. R., Yağcıoğlu, A. E. Anil, Tiihonen, J., Hasan, A., Clinical Cognitive Neuropsychiatry Research Program (CCNP), Life Course Epidemiology (LCE), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience, Adult Psychiatry, APH - Mental Health, ANS - Complex Trait Genetics, and ANS - Mood, Anxiety, Psychosis, Stress & Sleep
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POLYGENIC RISK SCORE ,GENETIC RISK ,N-DESMETHYLCLOZAPINE ,Schizophrenia/chemically induced ,Cytochrome P-450 CYP1A2/genetics ,Cellular and Molecular Neuroscience ,Cytochrome P-450 CYP1A2 ,Humans ,ddc:610 ,CYP2C19 ,BRAIN ,Clozapine ,POLYMORPHISMS ,Biological Psychiatry ,IDENTIFICATION ,PHARMACOGENETICS ,CYTOCHROME-P450 ,Clozapine/therapeutic use ,Cytochrome P-450 CYP2C19 ,Psychiatry and Mental health ,Cytochrome P-450 CYP2D6 ,Schizophrenia ,Cytochrome P-450 CYP2C19/genetics ,Antipsychotic Agents/therapeutic use ,Cytochrome P-450 CYP2D6/genetics ,PHARMACOLOGICAL-TREATMENT ,Antipsychotic Agents ,Genome-Wide Association Study - Abstract
Clozapine is the most effective antipsychotic for patients with treatment-resistant schizophrenia. However, response is highly variable and possible genetic underpinnings of this variability remain unknown. Here, we performed polygenic risk score (PRS) analyses to estimate the amount of variance in symptom severity among clozapine-treated patients explained by PRSs (R2) and examined the association between symptom severity and genotype-predicted CYP1A2, CYP2D6, and CYP2C19 enzyme activity. Genome-wide association (GWA) analyses were performed to explore loci associated with symptom severity. A multicenter cohort of 804 patients (after quality control N = 684) with schizophrenia spectrum disorder treated with clozapine were cross-sectionally assessed using the Positive and Negative Syndrome Scale and/or the Clinical Global Impression-Severity (CGI-S) scale. GWA and PRS regression analyses were conducted. Genotype-predicted CYP1A2, CYP2D6, and CYP2C19 enzyme activities were calculated. Schizophrenia-PRS was most significantly and positively associated with low symptom severity (p = 1.03 × 10−3; R2 = 1.85). Cross-disorder-PRS was also positively associated with lower CGI-S score (p = 0.01; R2 = 0.81). Compared to the lowest tertile, patients in the highest schizophrenia-PRS tertile had 1.94 times (p = 6.84×10−4) increased probability of low symptom severity. Higher genotype-predicted CYP2C19 enzyme activity was independently associated with lower symptom severity (p = 8.44×10−3). While no locus surpassed the genome-wide significance threshold, rs1923778 within NFIB showed a suggestive association (p = 3.78×10−7) with symptom severity. We show that high schizophrenia-PRS and genotype-predicted CYP2C19 enzyme activity are independently associated with lower symptom severity among individuals treated with clozapine. Our findings open avenues for future pharmacogenomic projects investigating the potential of PRS and genotype-predicted CYP-activity in schizophrenia.
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- 2022
28. Verbal memory performance predicts remission and functional outcome in people at clinical high-risk for psychosis
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Hedges, EP, Dickson, H, Tognin, S, Modinos, G, Antoniades, M, van der Gaag, M, de Haan, L, McGorry, P, Pantelis, C, Riecher-Rossler, A, Bressan, R, Barrantes-Vidal, N, Krebs, M-O, Nordentoft, M, Ruhrmann, S, Sachs, G, Rutten, BP, van Os, J, Valmaggia, LR, McGuire, P, Kempton, MJ, Hedges, EP, Dickson, H, Tognin, S, Modinos, G, Antoniades, M, van der Gaag, M, de Haan, L, McGorry, P, Pantelis, C, Riecher-Rossler, A, Bressan, R, Barrantes-Vidal, N, Krebs, M-O, Nordentoft, M, Ruhrmann, S, Sachs, G, Rutten, BP, van Os, J, Valmaggia, LR, McGuire, P, and Kempton, MJ
- Abstract
Robust deficits in cognitive functioning are present in people with psychosis and are evident in the early stages of the disorder. Impairments in verbal memory and verbal fluency are reliably seen in individuals at clinical high-risk for psychosis (CHR) compared to healthy populations. As previous studies have shown a relationship between cognition and longer-term outcomes in schizophrenia, the aim of this paper was to explore whether verbal memory and verbal fluency performance predicted outcomes in a large CHR sample recruited as part of the EU-GEI High Risk Study. Participants included 316 CHR individuals, 90.8% of whom were not currently on antipsychotic medication, and 60 healthy controls. Verbal memory and verbal fluency performance were measured at baseline. At two-year follow-up, CHR individuals were assessed by three different outcome measures, those who did and did not (1) transition to psychosis, (2) experience burdening impairment or disabilities, or (3) remit clinically from CHR status. Individuals with CHR displayed significant verbal memory and verbal fluency deficits at baseline compared to healthy controls (Hedges' g effect size = 0.24 to 0.66). There were no significant differences in cognitive performance of those who did and did not transition to psychosis. However, impaired immediate verbal recall predicted both functional disability and non-remission from the CHR state. Results remained significant when analyses were restricted to only include antipsychotic-free CHR participants. These findings may inform the development of early interventions designed to improve cognitive deficits in the early stages of psychosis.
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- 2022
29. Impact of Comorbid Affective Disorders on Longitudinal Clinical Outcomes in Individuals at Ultra-high Risk for Psychosis
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Schirmbeck, F, van der Burg, NC, Blankers, M, Vermeulen, JM, McGuire, P, Valmaggia, LR, Kempton, MJ, van der Gaag, M, Riecher-Rossler, A, Bressan, RA, Barrantes-Vidal, N, Nelson, B, Amminger, GP, McGorry, P, Pantelis, C, Krebs, M-O, Ruhrmann, S, Sachs, G, Rutten, BPF, van Os, J, Nordentoft, M, Glenthoj, B, Fusar-Poli, P, de Haan, L, Schirmbeck, F, van der Burg, NC, Blankers, M, Vermeulen, JM, McGuire, P, Valmaggia, LR, Kempton, MJ, van der Gaag, M, Riecher-Rossler, A, Bressan, RA, Barrantes-Vidal, N, Nelson, B, Amminger, GP, McGorry, P, Pantelis, C, Krebs, M-O, Ruhrmann, S, Sachs, G, Rutten, BPF, van Os, J, Nordentoft, M, Glenthoj, B, Fusar-Poli, P, and de Haan, L
- Abstract
INTRODUCTION: Diagnoses of anxiety and/or depression are common in subjects at Ultra-High Risk for Psychosis (UHR) and associated with extensive functional impairment. Less is known about the impact of affective comorbidities on the prospective course of attenuated psychotic symptoms (APS). METHOD: Latent class mixed modelling identified APS trajectories in 331 UHR subjects assessed at baseline, 6, 12, and 24 months follow-up. The prognostic value of past, baseline, and one-year DSM-IV depressive or anxiety disorders on trajectories was investigated using logistic regression, controlling for confounders. Cox proportional hazard analyses investigated associations with transition risk. RESULTS: 46.8% of participants fulfilled the criteria for a past depressive disorder, 33.2% at baseline, and 15.1% at one-year follow-up. Any past, baseline, or one-year anxiety disorder was diagnosed in 42.9%, 37.2%, and 27.0%, respectively. Participants were classified into one of three latent APS trajectory groups: (1) persistently low, (2) increasing, and (3) decreasing. Past depression was associated with a higher risk of belonging to the increasing trajectory group, compared to the persistently low (OR = 3.149, [95%CI: 1.298-7.642]) or decreasing group (OR = 3.137, [1.165-8.450]). In contrast, past (OR = .443, [.179-1.094]) or current (OR = .414, [.156-1.094]) anxiety disorders showed a trend-level association with a lower risk of belonging to the increasing group compared to the persistently low group. Past depression was significantly associated with a higher risk of transitioning to psychosis (HR = 2.123, [1.178-3.828]). CONCLUSION: A past depressive episode might be a particularly relevant risk factor for an unfavorable course of APS in UHR individuals. Early affective disturbances may be used to advance detection, prognostic, and clinical strategies.
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- 2022
30. Long-term treatment of antipsychotics and combined therapy with other psychotropic medications inducing weight gain in patients with non-affective psychotic disorder: Evidence from GROUP, a longitudinal study
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Burin, L.M., Hahn, M.K., da Rocha, N.S., van Amelsvoort, T., Bartels-Velthuis, A.A., Bruggeman, R., de Haan, L., Schirmbeck, F., Simons, C.J.P., van Os, J., Cahn, W., Burin, L.M., Hahn, M.K., da Rocha, N.S., van Amelsvoort, T., Bartels-Velthuis, A.A., Bruggeman, R., de Haan, L., Schirmbeck, F., Simons, C.J.P., van Os, J., and Cahn, W.
- Abstract
Introduction: Antipsychotics (APs) can cause weight gain. Little is known about changes in weight when APs are combined with other psychotropics. This study examines the weight change in patients undergoing long-term treatment with APs or with AP combined with other psychotropics. Methods: Patients with non-affective psychotic disorder from the GROUP study were divided into three groups: AP medication group (APm) (n = 100), AP in combination with other psychotropics (APc) (n = 73), and medication-free (Meds-free) (n = 100). Weight change was examined at inclusion and after three years using a paired-sample t-test. An Independent-sample t-test was performed to evaluate weight change among patients taking clozapine, olanzapine, and quetiapine and individuals not taking these medications. Linear regression was performed to evaluate the association between covariates and weight. Results: Patients in the APm group [mean = 1.800 kg, t(99)=2.849, 95% CI(0.546, 3.054), p = 0.005] and the APc group [mean = 1.877 kg, t(72)=2.688, 95% CI(0.485, 3.268), p = 0.009] showed significant weight gain. Patients taking clozapine, olanzapine or quetiapine showed significant weight gain compared to those not taking these medications [mean difference=1.707 kg, t(271)= 2.061, 95% CI(0.077, 3.337), p = 0.040)]. Conclusion: Patients receiving APs and APs with other psychotropics gain weight during long-term treatment. It is possible that weight gain is mainly driven by APs.
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- 2022
31. Lower Emotional Complexity as a Prospective Predictor of Psychopathology in Adolescents From the General Population
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Schreuder, Marieke J., Wichers, M., Hartman, C.A., Menne-Lothmann, C., Decoster, J., van Winkel, R., Delespaul, P., De Hert, M., Derom, C., Thiery, E., Rutten, B.P.F., Jacobs, N., van Os, J., Wigman, J.T.W., Schreuder, Marieke J., Wichers, M., Hartman, C.A., Menne-Lothmann, C., Decoster, J., van Winkel, R., Delespaul, P., De Hert, M., Derom, C., Thiery, E., Rutten, B.P.F., Jacobs, N., van Os, J., and Wigman, J.T.W.
- Abstract
Emotional complexity (EC) involves the ability to distinguish between distinct emotions (differentiation) and the experience of a large range of emotions (diversity). Lower EC has been related to psychopathology in cross-sectional studies. This study aimed to investigate (a) whether EC prospectively predicts psychopathology and (b) whether this effect is contingent on stressful life events. To further explore EC, we compared the effects of differentiation and diversity. Adolescents from the general population (N = 401) rated 8 negatively valenced emotions 10 times a day for 6 consecutive days. Further, they completed the Symptom Checklist-90 (baseline and 1-year follow-up) and a questionnaire on past year's life events at follow-up. Logistic regression analyses tested whether EC-reflected by emotion differentiation (intraclass correlation coefficient [ICC]) and diversity (diversity index [DI])-predicted prognosis (good: remitting or lacking symptoms vs. bad: worsening or persisting symptoms). EC predicted prognoses but only when based on the ICC (OREC.ICC = 1.42, p = .02). An ECICC 1 SD above average increased the probability of good prognosis from .67 to .74. This effect was not related to stressful life events (OREC x Life events = 1.03, p = .86) and disappeared when emotion intensity (mean level) was taken into account (OREC = 1.20, p = .20). Predicting future prognosis does not necessitate complex measures of emotional experience (ICC, DI) but rather might be achieved through simpler indices (mean). The discrepant effects of the ICC and DI on prognosis suggest that impaired emotion representation (ICC) plays a more important role in vulnerability to mental ill health than does low diversity of emotions (DI).
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- 2022
32. Actualisatie leegstand agrarisch vastgoed Noord-Brabant 2022 : Ontwikkeling aard en omvang agrarisch vastgoed tussen 2017 en 2020 in de provincie Noord-Brabant
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van Os, J., Smidt, R.A., van Os, J., and Smidt, R.A.
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Every year, many farms stop farming. In 2016, Wageningen Environmental Research (former called Alterra) made an analysis for the province of Noord-Brabant of the art, size and solution directions of the current and future vacancy of agricultur al real estate in the province of Noord-Brabant (Alterra report 2713), based onthe data from 2012. A new analysis was made in 2019, based on the data from 2017. This 2022 report is an analysis based on data from 2020 and concerns an update of vacant agricultural buildings, the expected vacancy and its forecast for the year 2035., Jaarlijks stoppen veel agrarische bedrijven. In 2016 heeft Wageningen Environmental Research (toen Alterra geheten) voor de provincie Noord-Brabant een analyse gemaakt van de aard, omvang en oplossingsrichtingen van de huidige en toekomstige leegstand van agrarisch vastgoed in de provincie Noord-Brabant (Alterra-rapport 2713), gebaseerd op de gegevens van 2012. In 2019 is een nieuwe analyse gemaakt, op basis van de gegevens van 2017. Dit rapport van 2022 betreft een analyse op basis van gegevens van 2020 en gaat over een actualisatie van vrijgekomen agrarische bebouwing, de verwachte leegstand en de prognose daarvan naar het jaar 2035.
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- 2022
33. Geografische Informatie Agrarische Bedrijven 2019 : documentatie van het GIAB 2019 bestand
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van Os, J., Kros, J., van Os, J., and Kros, J.
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To compile the national emissions inventory, the National Institute for Public Health and the Environment (RIVM) has to have an accurate picture of the locations of all the livestock farms in the Netherlands. The GIAB-plus dataset (Geographical Information on Agricultural Businesses) was created for this purpose in 2009. In this dataset, animal numbers taken from the agricultural census are reallocated across the farm locations obtained from the animal registers and associated with the types of livestock housing recorded in the agricultural census. Since 2015 the livestock housing census have been made available as a supplement. These record for each location the average number of animals, divided into animal group, each agricultural business held and in which types of housing, per calendar year. Since emission year 2016 this additional information has been used as the basis for the GIAB dataset and the information from the agricultural census and animal registers is used as an aid to check these records and where necessary improve the data they contain. This report describes how the GIAB 2019 was compiled and what it can be used for. Besides localising emissions from livestock farming, the dataset can be used in regional studies of the agricultural structure and for research into the spread of animal diseases., Ten behoeve van de nationale emissieregistratie van het RIVM is het nodig om een goed beeld te hebben van de bedrijfslocaties van veehouderijbedrijven in Nederland. Vanaf 2009 is daarvoor het zogenaamde GIAB-plus-bestand gemaakt: Geografische Informatie Agrarische Bedrijven, waarbij de dieraantallen van de landbouwtelling zijn herverdeeld over veehouderijlocaties vanuit de dierregistraties en gekoppeld aan de staltypen die in de landbouwtelling bekend zijn. Vanaf 2015 is de opgave huisvesting als aanvulling beschikbaar gekomen, waarin bedrijven per locatie opgeven hoeveel dieren per diergroep gemiddeld over het kalender in een bepaald staltype gehuisvest zijn. Deze aanvullende informatie wordt vanaf emissiejaar 2016 gebruikt als basis voor het GIAB- bestand, waarbij de informatie vanuit landbouwtelling en dierregistraties gebruikt worden als hulpmiddel om deze opgave te checken en waar nodig te verbeteren. Dit rapport geeft aan hoe het GIAB2019 is samengesteld en wat de gebruiksmogelijkheden zijn. Behalve voor het lokaliseren van emissies uit de veehouderij is het bestand ook toepasbaar in regionale onderzoeken naar de landbouwstructuur en onderzoek naar verspreiding van dierziekten.
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- 2022
34. Nongenetic Factors Associated With Psychotic Experiences Among UK Biobank Participants Exposome-Wide Analysis and Mendelian Randomization Analysis
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Lin, B.D., Pries, L.K., Sarac, H.S., van Os, J., Rutten, B.P.F., Luykx, J., Guloksuz, S., Lin, B.D., Pries, L.K., Sarac, H.S., van Os, J., Rutten, B.P.F., Luykx, J., and Guloksuz, S.
- Abstract
IMPORTANCE Although hypothesis-driven research has identified several factors associated with psychosis, this one-exposure-to-one-outcome approach fails to embrace the multiplicity of exposures. Systematic approaches, similar to agnostic genome-wide analyses, are needed to identify genuine signals.OBJECTIVE To systematically investigate nongenetic correlates of psychotic experiences through data-driven agnostic analyses and genetically informed approaches to evaluate associations.DESIGN, SETTING, PARTICIPANTS This cohort study analyzed data from the UK Biobank Mental Health Survey from January 1 to June 1, 2021. An exposome-wide association study was performed in 2 equal-sized split discovery and replication data sets. Variables associated with psychotic experiences in the exposome-wide analysis were tested in a multivariable model. For the variables associated with psychotic experiences in the final multivariable model, the single-nucleotide variant-based heritability and genetic overlap with psychotic experiences using linkage disequilibrium score regression were estimated, and mendelian randomization (MR) approaches were applied to test potential causality. The significant associations observed in 1-sample MR analyses were further tested in multiple sensitivity tests, including collider-correction MR, 2-sample MR, and multivariable MR analyses.EXPOSURES After quality control based on a priori criteria, 247 environmental, lifestyle, behavioral, and economic variables.MAIN OUTCOMES AND MEASURES Psychotic experiences.RESULTS The study included 155 247 participants (87 896 [57%) female; mean [SD] age, 55.94 [7.74] years). In the discovery data set, 162 variables (66%) were associated with psychotic experiences. Of these, 148 (91%) were replicated. The multivariable analysis identified 36 variables that were associated with psychotic experiences. Of these, 28 had significant genetic overlap with psychotic experiences. One-sample MR analyses revealed forward associatio
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- 2022
35. Veehouderij structuur 2021
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van Os, J. and van Os, J.
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Op verzoek van Wakker Dier heeft Wageningen Environmental Research (WENR) opnieuw een overzicht gemaakt van de veehouderijstructuur in Nederland. Waar in voorgaande jaren regelmatig de focus lag op grootschalige veehouderijbedrijven, heeft WENR ervoor gekozen om de gehele sector in beeld te brengen, inclusief de kleinere locaties en bedrijven.
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- 2022
36. Genetic and psychosocial stressors have independent effects on the level of subclinical psychosis: findings from the multinational EU-GEI study
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Hersenen-Medisch 1, Brain, Pignon, B, Peyre, H, Ayrolles, A, Kirkbride, J B, Jamain, S, Ferchiou, A, Richard, J R, Baudin, G, Tosato, S, Jongsma, H, de Haan, L, Tarricone, I, Bernardo, M, Velthorst, E, Braca, M, Arango, C, Arrojo, M, Bobes, J, Del-Ben, C M, Di Forti, M, Gayer-Anderson, C, Jones, P B, La Cascia, C, Lasalvia, A, Menezes, P R, Quattrone, D, Sanjuán, J, Selten, J P, Tortelli, A, Llorca, P M, van Os, J, Rutten, B P F, Murray, R M, Morgan, C, Leboyer, M, Szöke, A, Schürhoff, F, Hersenen-Medisch 1, Brain, Pignon, B, Peyre, H, Ayrolles, A, Kirkbride, J B, Jamain, S, Ferchiou, A, Richard, J R, Baudin, G, Tosato, S, Jongsma, H, de Haan, L, Tarricone, I, Bernardo, M, Velthorst, E, Braca, M, Arango, C, Arrojo, M, Bobes, J, Del-Ben, C M, Di Forti, M, Gayer-Anderson, C, Jones, P B, La Cascia, C, Lasalvia, A, Menezes, P R, Quattrone, D, Sanjuán, J, Selten, J P, Tortelli, A, Llorca, P M, van Os, J, Rutten, B P F, Murray, R M, Morgan, C, Leboyer, M, Szöke, A, and Schürhoff, F
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- 2022
37. The validation of a serious game for teaching ultrasound skills
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Hersenen-Medisch 1, Brain, Olgers, T J, van Os, J M, Bouma, H R, Ter Maaten, J C, Hersenen-Medisch 1, Brain, Olgers, T J, van Os, J M, Bouma, H R, and Ter Maaten, J C
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- 2022
38. Samenspel tussen genetische achtergrond en omgevingsfactoren in de psychiatrie: stand van zaken en toekomstperspectief
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Onderzoeksgroep 2, Brain, Hersenen-Medisch 1, Onderzoek, Rutten, B P F, Guloksuz, S, Boks, M, van Os, J, Luykx, J J, van Winkel, R, Onderzoeksgroep 2, Brain, Hersenen-Medisch 1, Onderzoek, Rutten, B P F, Guloksuz, S, Boks, M, van Os, J, Luykx, J J, and van Winkel, R
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- 2022
39. Vertaalt de sterke sociale gradiënt van de ggz zich in een uniform sterke samenhang tussen ggz en sociale zorg?
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Hersenen-Medisch 1, Brain, van Os, J., Hersenen-Medisch 1, Brain, and van Os, J.
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- 2022
40. Preschool Social Participation, the Impact of Early Life Stress and Parental Health
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Hersenen-Medisch 1, Brain, Doove, B. M., Schiffelers, B. A.A.H., Lukkien, C., van Os, J., Feron, F. J.M., Drukker, M., Hersenen-Medisch 1, Brain, Doove, B. M., Schiffelers, B. A.A.H., Lukkien, C., van Os, J., Feron, F. J.M., and Drukker, M.
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- 2022
41. Additional file 1 of The validation of a serious game for teaching ultrasound skills
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Olgers, T. J., van Os, J. M., Bouma, H. R., and ter Maaten, J. C.
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Additional file 1. Questionnaire UnderWater.
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- 2022
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42. Differences in patterns of stimulant use and their impact on first-episode psychosis incidence – an analysis of the EUGEI study
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Rodríguez-Toscano, E., Alloza, C., Fraguas, D., Durán-Cutilla, M., Roldán, L., Gutiérrez, T. Sánchez, López-Montoya, G., Parellada, M., Moreno, C., Gayer-Anderson, C., Jongsma, H.E., Di Forti, M., Velthorst, E., de Haan, L., Selten, J., Szöke, A., Llorca, P., Tortelli, A., Bobes, J., Tarricone, I., Berardi, D., Ruggeri, M., Lasalvia, A., Ferraro, L., Menezes, P.R., Rutten, B.P., Van Os, J., Jones, P.B., Murray, R.M., Kirkbride, J.B., Morgan, C., Díaz-Caneja, C.M., and Arango, C.
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- 2022
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43. Dimensions of psychotic symptoms and experiences in firs-episode psychosis, unaffected siblings, and community controls – associations with state and trait cytokines
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Corsi-Zuelli, F., Quattrone, D., Ragazzi, T., Loureiro, C., Shuhama, R., Van Os, J., Menezes, P.R., Louzada-Junior, P., and Del-Ben, C.
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- 2022
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44. Genetic and psychosocial stressors have independent effects on the level of subclinical psychosis: findings from the multinational EU-GEI study
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Pignon, B., primary, Peyre, H., additional, Ayrolles, A., additional, Kirkbride, J. B., additional, Jamain, S., additional, Ferchiou, A., additional, Richard, J. R., additional, Baudin, G., additional, Tosato, S., additional, Jongsma, H., additional, de Haan, L., additional, Tarricone, I., additional, Bernardo, M., additional, Velthorst, E., additional, Braca, M., additional, Arango, C., additional, Arrojo, M., additional, Bobes, J., additional, Del-Ben, C. M., additional, Di Forti, M., additional, Gayer-Anderson, C., additional, Jones, P. B., additional, La Cascia, C., additional, Lasalvia, A., additional, Menezes, P. R., additional, Quattrone, D., additional, Sanjuán, J., additional, Selten, J. P., additional, Tortelli, A., additional, Llorca, P. M., additional, van Os, J., additional, Rutten, B. P. F., additional, Murray, R. M., additional, Morgan, C., additional, Leboyer, M., additional, Szöke, A., additional, and Schürhoff, F., additional
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- 2022
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45. Common variant at 16p11.2 conferring risk of psychosis
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Steinberg, S, de Jong, S, Mattheisen, M, Costas, J, Demontis, D, Jamain, S, Pietiläinen, O P H, Lin, K, Papiol, S, Huttenlocher, J, Sigurdsson, E, Vassos, E, Giegling, I, Breuer, R, Fraser, G, Walker, N, Melle, I, Djurovic, S, Agartz, I, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Olsen, L, Hansen, T, Ingason, A, Pirinen, M, Strengman, E, Hougaard, D M, Ørntoft, T, Didriksen, M, Hollegaard, M V, Nordentoft, M, Abramova, L, Kaleda, V, Arrojo, M, Sanjuán, J, Arango, C, Etain, B, Bellivier, F, Méary, A, Schürhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rossner, M, Christiansen, C, Kiemeney, L A, Franke, B, van den Berg, L H, Veldink, J, Curran, S, Bolton, P, Poot, M, Staal, W, Rehnstrom, K, Kilpinen, H, Freitag, C M, Meyer, J, Magnusson, P, Saemundsen, E, Martsenkovsky, I, Bikshaieva, I, Martsenkovska, I, Vashchenko, O, Raleva, M, Paketchieva, K, Stefanovski, B, Durmishi, N, Pejovic Milovancevic, M, Lecic Tosevski, D, Silagadze, T, Naneishvili, N, Mikeladze, N, Surguladze, S, Vincent, J B, Farmer, A, Mitchell, P B, Wright, A, Schofield, P R, Fullerton, J M, Montgomery, G W, Martin, N G, Rubino, I A, van Winkel, R, Kenis, G, De Hert, M, Réthelyi, J M, Bitter, I, Terenius, L, Jönsson, E G, Bakker, S, van Os, J, Jablensky, A, Leboyer, M, Bramon, E, Powell, J, Murray, R, Corvin, A, Gill, M, Morris, D, O'Neill, F A, Kendler, K, Riley, B, Craddock, N, Owen, M J, O'Donovan, M C, Thorsteinsdottir, U, Kong, A, Ehrenreich, H, Carracedo, A, Golimbet, V, Andreassen, O A, Børglum, A D, Mors, O, Mortensen, P B, Werge, T, Ophoff, R A, Nöthen, M M, Rietschel, M, Cichon, S, Ruggeri, M, Tosato, S, Palotie, A, St Clair, D, Rujescu, D, Collier, D A, Stefansson, H, and Stefansson, K
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- 2014
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46. Daily use of high-potency cannabis is associated with more positive symptoms in first-episode psychosis patients: The EU-GEI case-control study
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Quattrone, D, Ferraro, L, Tripoli, G, La Cascia, C, Quigley, H, Quattrone, A, Jongsma, HE, Del Peschio, S, Gatto, G, EU-GEI group, Gayer-Anderson, C, Jones, PB, Kirkbride, JB, La Barbera, D, Tarricone, I, Berardi, D, Tosato, S, Lasalvia, A, Szöke, A, Arango, C, Bernardo, M, Bobes, J, Del Ben, CM, Menezes, PR, Llorca, P-M, Santos, JL, Sanjuán, J, Tortelli, A, Velthorst, E, de Haan, L, Rutten, BPF, Lynskey, MT, Freeman, TP, Sham, PC, Cardno, AG, Vassos, E, van Os, J, Morgan, C, Reininghaus, U, Lewis, CM, Murray, RM, Di Forti, M, Adult Psychiatry, ANS - Complex Trait Genetics, ANS - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Mental Health, Quattrone, Diego [0000-0002-6051-8309], Apollo - University of Cambridge Repository, Quattrone D., Ferraro L., Tripoli G., La Cascia C., Quigley H., Quattrone A., Jongsma H.E., Del Peschio S., Gatto G., EU-GEI group, Gayer-Anderson C., Jones P.B., Kirkbride J.B., La Barbera D., Tarricone I., Berardi D., Tosato S., Lasalvia A., Szoke A., Arango C., Bernardo M., Bobes J., Del Ben C.M., Menezes P.R., Llorca P.-M., Santos J.L., Sanjuan J., Tortelli A., Velthorst E., De Haan L., Rutten B.P.F., Lynskey M.T., Freeman T.P., Sham P.C., Cardno A.G., Vassos E., Van Os J., Morgan C., Reininghaus U., Lewis C.M., Murray R.M., Di Forti M., RS: MHeNs - R3 - Neuroscience, Psychiatrie & Neuropsychologie, MUMC+: MA Psychiatrie (3), RS: MHeNs - R2 - Mental Health, and MUMC+: Hersen en Zenuw Centrum (3)
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Marijuana Abuse ,IMPACT ,Poison control ,Cannabis use ,cannabis-associated psychosis ,0302 clinical medicine ,SCHIZOPHRENIA ,Settore MED/48 -Scienze Infermierist. e Tecn. Neuro-Psichiatriche e Riabilitat ,health care economics and organizations ,Applied Psychology ,RISK ,OUTCOMES ,biology ,Human factors and ergonomics ,psychopathology ,first episode psychosis ,psychotic experiences ,symptom dimensions ,3. Good health ,Psychiatry and Mental health ,Schizophrenia ,HEALTH ,Psychopathology ,Psychosis ,medicine.medical_specialty ,DISORDERS ,education ,03 medical and health sciences ,Injury prevention ,medicine ,Humans ,Psychiatry ,ABUSE ,Settore MED/25 - Psichiatria ,SUBSTANCE USE ,METAANALYSIS ,Cannabis ,business.industry ,Case-control study ,Original Articles ,medicine.disease ,biology.organism_classification ,030227 psychiatry ,psychotic experience ,Psychotic Disorders ,first episode psychosi ,Case-Control Studies ,ONSET ,Gene-Environment Interaction ,business ,cannabis-associated psychosi ,030217 neurology & neurosurgery - Abstract
The work was supported by: Clinician Scientist Medical Research Council fellowship (project reference MR/M008436/1) to MDF; the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care South London at King’s College Hospital NHS Foundation Trust to DQ; DFG Heisenberg professorship (no. 389624707) to UR. National Institute for Health Research (NIHR) Biomedical Research Centre for Mental Health at South London and Maudsley NHS Foundation Trust and King’s College London. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care. The EU-GEI Project is funded by the European Community’s Seventh Framework Programme under grant agreement No. HEALTH-F2-2010-241909 (Project EU-GEI). The Brazilian study was funded by the São Paulo Research Foundation under grant number 2012/0417-0., Quattrone, D., Ferraro, L., Tripoli, G., La Cascia, C., Quigley, H., Quattrone, A., Jongsma, H.E., Del Peschio, S., Gatto, G., Gayer-Anderson, C., Jones, P.B., Kirkbride, J.B., La Barbera, D., Tarricone, I., Berardi, D., Tosato, S., Lasalvia, A., Szöke, A., Arango, C., Bernardo, M., Bobes, J., Del Ben, C.M., Menezes, P.R., Llorca, P.-M., Santos, J.L., Sanjuán, J., Tortelli, A., Velthorst, E., De Haan, L., Rutten, B.P.F., Lynskey, M.T., Freeman, T.P., Sham, P.C., Cardno, A.G., Vassos, E., Van Os, J., Morgan, C., Reininghaus, U., Lewis, C.M., Murray, R.M., Di Forti, M.
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- 2020
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47. Neighbourhood Socioeconomic Disadvantage and Behavioural Problems from Late Childhood into Early Adolescence
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Schneiders, J., Drukker, M., van der Ende, J., Verhulst, F. C., van Os, J., and Nicolson, N. A.
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- 2003
48. Social disadvantage, linguistic distance, ethnic minority status and first-episode psychosis: results from the EU-GEI case-control study
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Jongsma H, Gayer-Anderson C, Tarricone I, Velthorst E, van der Ven E, Quattrone D, di Forti M, Menezes P, Del-Ben C, Arango C, Lasalvia A, Berardi D, La Cascia C, Bobes J, Bernardo M, Sanjuan J, Santos J, Arrojo M, de Haan L, Tortelli A, Szoke A, Murray R, Rutten B, van Os J, Morgan C, Jones P, Kirkbride J, EU-GEI WP2 Group, Jongsma, Hannah E [0000-0001-6346-5903], and Apollo - University of Cambridge Repository
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Adult ,Male ,Adolescent ,Social Determinants of Health ,social disadvantage ,Communication Barriers ,Black People ,Health Status Disparities ,Middle Aged ,White People ,Europe ,Young Adult ,Psychotic Disorders ,Case-Control Studies ,Discrimination ,Ethnic and Racial Minorities ,Ethnicity ,Odds Ratio ,Schizophrenia ,Humans ,epidemiology ,Female ,Gene-Environment Interaction - Abstract
BACKGROUND: Ethnic minority groups in Western countries face an increased risk of psychotic disorders. Causes of this long-standing public health inequality remain poorly understood. We investigated whether social disadvantage, linguistic distance and discrimination contributed to these patterns.; METHODS: We used case-control data from the EUropean network of national schizophrenia networks studying Gene-Environment Interactions (EU-GEI) study, carried out in 16 centres in six countries. We recruited 1130 cases and 1497 population-based controls. Our main outcome measure was first-episode ICD-10 psychotic disorder (F20-F33), and exposures were ethnicity (white majority, black, mixed, Asian, North-African, white minority and other), generational status, social disadvantage, linguistic distance and discrimination. Age, sex, paternal age, cannabis use, childhood trauma and parental history of psychosis were included as a priori confounders. Exposures and confounders were added sequentially to multivariable logistic models, following multiple imputation for missing data.; RESULTS: Participants from any ethnic minority background had crude excess odds of psychosis [odds ratio (OR) 2.03, 95% confidence interval (CI) 1.69-2.43], which remained after adjustment for confounders (OR 1.61, 95% CI 1.31-1.98). This was progressively attenuated following further adjustment for social disadvantage (OR 1.52, 95% CI 1.22-1.89) and linguistic distance (OR 1.22, 95% CI 0.95-1.57), a pattern mirrored in several specific ethnic groups. Linguistic distance and social disadvantage had stronger effects for first- and later-generation groups, respectively.; CONCLUSION: Social disadvantage and linguistic distance, two potential markers of sociocultural exclusion, were associated with increased odds of psychotic disorder, and adjusting for these led to equivocal risk between several ethnic minority groups and the white majority.
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- 2021
49. Incidence Of Schizophrenia In Ethnic Minorities In London: Ecological Study Into Interactions With Environment
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Boydell, J., van Os, J., McKenzie, K., Allardyce, J., Goel, R., McCreadie, R. G., and Murray, R. M.
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- 2001
50. Neighbourhood Level and Individual Level SES Effects on Child Problem Behaviour: A Multilevel Analysis
- Author
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Kalff, A. C., Kroes, M., Vles, J. S. H., Hendriksen, J. G. M., Feron, F. J. M., Steyaert, J., van Zeben, T. M. C. B., Jolles, J., and van Os, J.
- Published
- 2001
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