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3,618 results on '"Murphy, Declan"'

355. How Does Age Affect Urinary Continence following Robot-Assisted Radical Prostatectomy? A Prospective Multi-Institutional Study Using Independently Collected, Validated Questionnaires

Author

Gondoputro, William, primary, Thompson, James, additional, Evans, Melanie, additional, Bolton, Damien, additional, Frydenberg, Mark, additional, Murphy, Declan G., additional, Haynes, Anne-Maree, additional, Agrawal, Shikha, additional, Stricker, Phillip, additional, and Papa, Nathan, additional

Published
2022
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358. Differences in social brain function in autism spectrum disorder are linked to the serotonin transporter: A randomised placebo-controlled single-dose crossover trial

Author

Wong, Nichol ML, primary, Dipasquale, Ottavia, additional, Turkheimer, Federico, additional, Findon, James L, additional, Wichers, Robert H, additional, Dimitrov, Mihail, additional, Murphy, Clodagh M, additional, Stoencheva, Vladimira, additional, Robertson, Dene M, additional, Murphy, Declan G, additional, Daly, Eileen, additional, and McAlonan, Grainne M, additional

Published
2022
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359. Nanotechnology

Author

Murphy, Declan G., Costello, Anthony J., Dasgupta, Prokar, editor, Fitzpatrick, John, editor, Kirby, Roger, editor, and Gill, Inderbir S., editor

Published
2010
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362. Unsupervised data-driven stratification of mentalizing heterogeneity in autism

Author

Lombardo, Michael V., Lai, Meng-Chuan, Auyeung, Bonnie, Holt, Rosemary J., Allison, Carrie, Smith, Paula, Chakrabarti, Bhismadev, Ruigrok, Amber N. V., Suckling, John, Bullmore, Edward T., Bailey, Anthony J., Baron-Cohen, Simon, Bolton, Patrick F., Bullmore, Edward T., Carrington, Sarah, Catani, Marco, Chakrabarti, Bhismadev, Craig, Michael C., Daly, Eileen M., Deoni, Sean C. L., Ecker, Christine, Happé, Francesca, Henty, Julian, Jezzard, Peter, Johnston, Patrick, Jones, Derek K., Lai, Meng-Chuan, Lombardo, Michael V., Madden, Anya, Mullins, Diane, Murphy, Clodagh M., Murphy, Declan G. M., Pasco, Greg, Ruigrok, Amber N. V., Sadek, Susan A., Spain, Debbie, Stewart, Rose, Suckling, John, Wheelwright, Sally J., Williams, Steven C., Ellie Wilson, C., Ecker, Christine, Craig, Michael C., Murphy, Declan G. M., Happé, Francesca, and Baron-Cohen, Simon

Published
2016
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372. Caregiver Burden as People with Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder Transition into Adolescence and Adulthood in the United Kingdom

Author

Cadman, Tim, Eklund, Hanna, Howley, Deirdre, Hayward, Hannah, Clarke, Hanna, Findon, James, Xenitidis, Kiriakos, Murphy, Declan, Asherson, Philip, and Glaser, Karen

Abstract

Objective: There is increasing recognition that autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) are associated with significant costs and burdens. However, research on their impact has focused mostly on the caregivers of young children; few studies have examined caregiver burden as children transition into adolescence and young adulthood, and no one has compared the impact of ASD to other neurodevelopmental disorders (e.g., ADHD). Method: We conducted an observational study of 192 families caring for a young person (aged 14 to 24 years) with a childhood diagnosis of ASD or ADHD (n = 101 and n = 91, respectively) in the United Kingdom. A modified stress-appraisal model was used to investigate the correlates of caregiver burden as a function of family background (parental education), primary stressors (symptoms), primary appraisal (need), and resources (use of services). Results: Both disorders were associated with a high level of caregiver burden, but it was significantly greater in ASD. In both groups, caregiver burden was mainly explained by the affected young person's unmet need. Domains of unmet need most associated with caregiver burden in both groups included depression/anxiety and inappropriate behavior. Specific to ASD were significant associations between burden and unmet needs in domains such as social relationships and major mental health problems. Conclusions: Adolescence and young adulthood are associated with high levels of caregiver burden in both disorders; in ASD, the level is comparable to that reported by persons caring for individuals with a brain injury. Interventions are required to reduce caregiver burden in this population. (Contains 5 tables.)

Published
2012
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373. Detecting localised prostate cancer using radiomic features in PSMA PET and multiparametric MRI for biologically targeted radiation therapy.

Author

Chan, Tsz Him, Haworth, Annette, Wang, Alan, Osanlouy, Mahyar, Williams, Scott, Mitchell, Catherine, Hofman, Michael S., Hicks, Rodney J., Murphy, Declan G., and Reynolds, Hayley M.

Subjects
CONTRAST-enhanced magnetic resonance imaging, RADIOTHERAPY treatment planning, PROSTATE cancer, RADIOTHERAPY, PROSTATE cancer patients, MAGNETIC resonance imaging
Abstract

Background: Prostate-Specific Membrane Antigen (PSMA) PET/CT and multiparametric MRI (mpMRI) are well-established modalities for identifying intra-prostatic lesions (IPLs) in localised prostate cancer. This study aimed to investigate the use of PSMA PET/CT and mpMRI for biologically targeted radiation therapy treatment planning by: (1) analysing the relationship between imaging parameters at a voxel-wise level and (2) assessing the performance of radiomic-based machine learning models to predict tumour location and grade. Methods: PSMA PET/CT and mpMRI data from 19 prostate cancer patients were co-registered with whole-mount histopathology using an established registration framework. Apparent Diffusion Coefficient (ADC) maps were computed from DWI and semi-quantitative and quantitative parameters from DCE MRI. Voxel-wise correlation analysis was conducted between mpMRI parameters and PET Standardised Uptake Value (SUV) for all tumour voxels. Classification models were built using radiomic and clinical features to predict IPLs at a voxel level and then classified further into high-grade or low-grade voxels. Results: Perfusion parameters from DCE MRI were more highly correlated with PET SUV than ADC or T2w. IPLs were best detected with a Random Forest Classifier using radiomic features from PET and mpMRI rather than either modality alone (sensitivity, specificity and area under the curve of 0.842, 0.804 and 0.890, respectively). The tumour grading model had an overall accuracy ranging from 0.671 to 0.992. Conclusions: Machine learning classifiers using radiomic features from PSMA PET and mpMRI show promise for predicting IPLs and differentiating between high-grade and low-grade disease, which could be used to inform biologically targeted radiation therapy planning. [ABSTRACT FROM AUTHOR]

Published
2023
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374. Mapping myelin in white matter with T1-weighted/T2-weighted maps: discrepancy with histology and other myelin MRI measures.

Author

Sandrone, Stefano, Aiello, Marco, Cavaliere, Carlo, Thiebaut de Schotten, Michel, Reimann, Katja, Troakes, Claire, Bodi, Istvan, Lacerda, Luis, Monti, Serena, Murphy, Declan, Geyer, Stefan, Catani, Marco, and Dell'Acqua, Flavio

Subjects
WHITE matter (Nerve tissue), MYELIN, CORPUS callosum, MAGNETIC resonance imaging, HISTOLOGY
Abstract

The ratio of T1-weighted/T2-weighted magnetic resonance images (T1w/T2w MRI) has been successfully applied at the cortical level since 2011 and is now one of the most used myelin mapping methods. However, no reports have explored the histological validity of T1w/T2w myelin mapping in white matter. Here we compare T1w/T2w with ex vivo postmortem histology and in vivo MRI methods, namely quantitative susceptibility mapping (QSM) and multi-echo T2 myelin water fraction (MWF) mapping techniques. We report a discrepancy between T1w/T2w myelin maps of the human corpus callosum and the histology and analyse the putative causes behind such discrepancy. T1w/T2w does not positively correlate with Luxol Fast Blue (LFB)-Optical Density but shows a weak to moderate, yet significant, negative correlation. On the contrary, MWF is strongly and positively correlated with LFB, whereas T1w/T2w and MWF maps are weakly negatively correlated. The discrepancy between T1w/T2w MRI maps, MWF and histological myelin maps suggests caution in using T1w/T2w as a white matter mapping method at the callosal level. While T1w/T2w imaging may correlate with myelin content at the cortical level, it is not a specific method to map myelin density in white matter. [ABSTRACT FROM AUTHOR]

Published
2023
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375. Sensory salience processing moderates attenuated gazes on faces in autism spectrum disorder: a case–control study.

Author

Bast, Nico, Mason, Luke, Ecker, Christine, Baumeister, Sarah, Banaschewski, Tobias, Jones, Emily J. H., Murphy, Declan G. M., Buitelaar, Jan K., Loth, Eva, Pandina, Gahan, the EU-AIMS LEAP Group, Ahmad, Jumana, Ambrosino, Sara, Auyeung, Bonnie, Baron-Cohen, Simon, Beckmann, Christian F., Bölte, Sven, Bourgeron, Thomas, Bours, Carsten, and Brammer, Michael

Subjects
AUTISM spectrum disorders, SENSORIMOTOR integration, PUPILLARY reflex, GAZE, CASE-control method, SPECIFIC language impairment in children, SENSORY disorders
Abstract

Background: Attenuated social attention is a key marker of autism spectrum disorder (ASD). Recent neuroimaging findings also emphasize an altered processing of sensory salience in ASD. The locus coeruleus–norepinephrine system (LC-NE) has been established as a modulator of this sensory salience processing (SSP). We tested the hypothesis that altered LC-NE functioning contributes to different SSP and results in diverging social attention in ASD. Methods: We analyzed the baseline eye-tracking data of the EU-AIMS Longitudinal European Autism Project (LEAP) for subgroups of autistic participants (n = 166, age = 6–30 years, IQ = 61–138, gender [female/male] = 41/125) or neurotypical development (TD; n = 166, age = 6–30 years, IQ = 63–138, gender [female/male] = 49/117) that were matched for demographic variables and data quality. Participants watched brief movie scenes (k = 85) depicting humans in social situations (human) or without humans (non-human). SSP was estimated by gazes on physical and motion salience and a corresponding pupillary response that indexes phasic activity of the LC-NE. Social attention is estimated by gazes on faces via manual areas of interest definition. SSP is compared between groups and related to social attention by linear mixed models that consider temporal dynamics within scenes. Models are controlled for comorbid psychopathology, gaze behavior, and luminance. Results: We found no group differences in gazes on salience, whereas pupillary responses were associated with altered gazes on physical and motion salience. In ASD compared to TD, we observed pupillary responses that were higher for non-human scenes and lower for human scenes. In ASD, we observed lower gazes on faces across the duration of the scenes. Crucially, this different social attention was influenced by gazes on physical salience and moderated by pupillary responses. Limitations: The naturalistic study design precluded experimental manipulations and stimulus control, while effect sizes were small to moderate. Covariate effects of age and IQ indicate that the findings differ between age and developmental subgroups. Conclusions: Pupillary responses as a proxy of LC-NE phasic activity during visual attention are suggested to modulate sensory salience processing and contribute to attenuated social attention in ASD. [ABSTRACT FROM AUTHOR]

Published
2023
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376. Modern Active Surveillance in Prostate Cancer: A Narrative Review.

Author

Pattenden, Trent A., Samaranayke, Dhanika, Morton, Andrew, Wee Loon Ong, Murphy, Declan G., Pritchard, Elizabeth, Evans, Susan, Millar, Jeremy, Chalasani, Venu, Rashid, Prem, Winter, Matthew, Vela, Ian, Pryor, David, Mark, Stephen, Lawrentschuk, Nathan, and Thangasamy, Isaac A.

Subjects
PROSTATE cancer treatment, WATCHFUL waiting, PROSTATE cancer risk factors, PATIENT selection, MEDICAL care
Abstract

The authors reviewed and sumarised the literature about active surveillance in prostate cancer. It provides a useful reference on patient selection criteria, surveillence investigations, barriers and enablers of active surveillence and evolving technologies that will be used in the future. The use of PSA screening has led to downstaging and downgrading of prostate cancer at diagnosis, increasing detection of indolent disease. Active surveillance aims to reduce over-treatment by delaying or avoiding radical treatment and its associated morbidity. However, there is not a consensus on the selection cr iter ia and monitoring schedules that should be used. This article aims to summarize the evidence supporting the safety of active surveillance, the current selection cr iter ia recommended and in use, the incidence of active surveillance, barriers existing to its uptake and future developments in patient selection. [ABSTRACT FROM AUTHOR]

Published
2023
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379. Tumor immune microenvironment of primary prostate cancer with and without germline mutations in homologous recombination repair genes

Author

Trigos, Anna Sofia, Pasam, Anupama, Banks, Patricia, Wallace, Roslyn, Guo, Christina, Keam, Simon, Thorne, Heather, kConFab, Mitchell, Catherine, Lade, Stephen, Clouston, David, Hakansson, Alexander, Liu, Yang, Blyth, Benjamin, Murphy, Declan, Lawrentschuk, Nathan, Bolton, Damien, Moon, Daniel, Darcy, Phil, Haupt, Ygal, Williams, Scott G, Castro, Elena, Olmos, David, Goode, David, Neeson, Paul, and Sandhu, Shahneen

Subjects
Pharmacology, Male, Cancer Research, Immunology, Prostatic Neoplasms, Recombinational DNA Repair, Oncology, gene expression profiling, genetic markers, Tumor Microenvironment, Molecular Medicine, Immunology and Allergy, Humans, Immune Checkpoint Inhibitors, Germ-Line Mutation
Abstract

BackgroundAberrations in homologous recombination repair (HRR) genes are emerging as important biomarkers for personalized treatment in prostate cancer (PCa). HRR deficiency (HRD) could affect the tumor immune microenvironment (TIME), potentially contributing to differential responses to poly ADP-ribose polymerase (PARP) inhibitors and immune checkpoint inhibitors. Spatial distribution of immune cells in a range of cancers identifies novel disease subtypes and is related to prognosis. In this study we aimed to determine the differences in the TIME of PCa with and without germline (g) HRR mutations.MethodsWe performed gene expression analysis, multiplex immunohistochemistry of T and B cells and quantitative spatial analysis of PCa samples from 36 patients withgHRD and 26 patients with sporadic PCa. Samples were archival tumor tissue from radical prostatectomies with the exception of one biopsy. Results were validated in several independent cohorts.ResultsAlthough the composition of the T cell and B cells was similar in the tumor areas ofgHRD-mutated and sporadic tumors, the spatial profiles differed between these cohorts. We describe two T-cell spatial profiles across primary PCa, a clustered immune spatial (CIS) profile characterized by dense clusters of CD4+T cells closely interacting with PD-L1+cells, and a free immune spatial (FIS) profile of CD8+cells in close proximity to tumor cells.gHRD tumors had a more T-cell inflamed microenvironment than sporadic tumors. The CIS profile was mainly observed in sporadic tumors, whereas a FIS profile was enriched ingHRD tumors. A FIS profile was associated with lower Gleason scores, smaller tumors and longer time to biochemical recurrence and metastasis.ConclusionsgHRD-mutated tumors have a distinct immune microenvironment compared with sporadic tumors. Spatial profiling of T-cells provides additional information beyond T-cell density and is associated with time to biochemical recurrence, time to metastasis, tumor size and Gleason scores.

Published
2022

380. Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism

Author

Pretzsch, Charlotte M., Floris, Dorothea L., Schäfer, Tim, Bletsch, Anke, Gurr, Caroline, Lombardo, Michael V., Chatham, Chris H., Tillmann, Julian, Charman, Tony, Arenella, Martina, Jones, Emily, Ambrosino, Sara, Bourgeron, Thomas, Dumas, Guillaume, Cliquet, Freddy, Leblond, Claire S., Loth, Eva, Oakley, Bethany, Buitelaar, Jan K., Baron-Cohen, Simon, Beckmann, Christian F., Persico, Antonio M., Banaschewski, Tobias, Durston, Sarah, Freitag, Christine M., Murphy, Declan G. M., and Ecker, Christine

Abstract

Individuals with autism spectrum disorder (henceforth referred to as autism) display significant variation in clinical outcome. For instance, across age, some individuals’ adaptive skills naturally improve or remain stable, while others’ decrease. To pave the way for ‘precision-medicine’ approaches, it is crucial to identify the cross-sectional and, given the developmental nature of autism, longitudinal neurobiological (including neuroanatomical and linked genetic) correlates of this variation. We conducted a longitudinal follow-up study of 333 individuals (161 autistic and 172 neurotypical individuals, aged 6–30 years), with two assessment time points separated by ~12–24 months. We collected behavioural (Vineland Adaptive Behaviour Scale-II, VABS-II) and neuroanatomical (structural magnetic resonance imaging) data. Autistic participants were grouped into clinically meaningful “Increasers”, “No-changers”, and “Decreasers” in adaptive behaviour (based on VABS-II scores). We compared each clinical subgroup’s neuroanatomy (surface area and cortical thickness at T1, ∆T (intra-individual change) and T2) to that of the neurotypicals. Next, we explored the neuroanatomical differences’ potential genomic associates using the Allen Human Brain Atlas. Clinical subgroups had distinct neuroanatomical profiles in surface area and cortical thickness at baseline, neuroanatomical development, and follow-up. These profiles were enriched for genes previously associated with autism and for genes previously linked to neurobiological pathways implicated in autism (e.g. excitation-inhibition systems). Our findings suggest that distinct clinical outcomes (i.e. intra-individual change in clinical profiles) linked to autism core symptoms are associated with atypical cross-sectional and longitudinal, i.e. developmental, neurobiological profiles. If validated, our findings may advance the development of interventions, e.g. targeting mechanisms linked to relatively poorer outcomes.

Published
2023
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383. High prostate‐specific membrane antigen ( PSMA) positron emission tomography (PET) maximum standardized uptake value in men with PI‐RADS score 4 or 5 confers a high probability of significant prostate cancer

Author

Ptasznik, Gideon, primary, Papa, Nathan, additional, Kelly, Brian D., additional, Thompson, James, additional, Stricker, Phillip, additional, Roberts, Matthew J., additional, Hofman, Michael S., additional, Buteau, James, additional, Murphy, Declan G., additional, Emmett, Louise, additional, and Moon, Daniel, additional

Published
2022
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384. Stereotactic Radiotherapy and Short-course Pembrolizumab for Oligometastatic Renal Cell Carcinoma—The RAPPORT Trial

Author

Siva, Shankar, primary, Bressel, Mathias, additional, Wood, Simon T., additional, Shaw, Mark G., additional, Loi, Sherene, additional, Sandhu, Shahneen K., additional, Tran, Ben, additional, A. Azad, Arun, additional, Lewin, Jeremy H., additional, Cuff, Katharine E., additional, Liu, Howard Y., additional, Moon, Daniel, additional, Goad, Jeremy, additional, Wong, Lih-Ming, additional, LimJoon, Michael, additional, Mooi, Jennifer, additional, Chander, Sarat, additional, Murphy, Declan G., additional, Lawrentschuk, Nathan, additional, and Pryor, David, additional

Published
2022
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385. Corrigendum to “What Experts Think About Prostate Cancer Management During the COVID-19 Pandemic: Report from the Advanced Prostate Cancer Consensus Conference 2021” [Eur Urol 2022]

Author

Turco, Fabio, primary, Armstrong, Andrew, additional, Attard, Gerhardt, additional, Beer, Tomasz M., additional, Beltran, Himisha, additional, Bjartell, Anders, additional, Bossi, Alberto, additional, Briganti, Alberto, additional, Bristow, Rob G., additional, Bulbul, Muhammad, additional, Caffo, Orazio, additional, Chi, Kim N., additional, Clarke, Caroline, additional, Clarke, Noel, additional, Davis, Ian D., additional, de Bono, Johann, additional, Duran, Ignacio, additional, Eeles, Ros, additional, Efstathiou, Eleni, additional, Efstathiou, Jason, additional, Evans, Christopher P., additional, Fanti, Stefano, additional, Feng, Felix Y., additional, Fizazi, Karim, additional, Frydenberg, Mark, additional, George, Dan, additional, Gleave, Martin, additional, Halabi, Susan, additional, Heinrich, Daniel, additional, Higano, Celestia, additional, Hofman, Michael S., additional, Hussain, Maha, additional, James, Nicholas, additional, Jones, Rob, additional, Kanesvaran, Ravindran, additional, Khauli, Raja B., additional, Klotz, Laurence, additional, Leibowitz, Raya, additional, Logothetis, Christopher, additional, Maluf, Fernando, additional, Millman, Robin, additional, Morgans, Alicia K., additional, Morris, Michael J., additional, Mottet, Nicolas, additional, Mrabti, Hind, additional, Murphy, Declan G., additional, Murthy, Vedang, additional, Oh, William K., additional, Ekeke, Onyeanunam Ngozi, additional, Ost, Piet, additional, O'Sullivan, Joe M., additional, Padhani, Anwar R., additional, Parker, Christopher, additional, Poon, Darren M.C., additional, Pritchard, Colin C., additional, Rabah, Danny M., additional, Rathkopf, Dana, additional, Reiter, Robert E., additional, Rubin, Mark, additional, Ryan, Charles J., additional, Saad, Fred, additional, Sade, Juan Pablo, additional, Sartor, Oliver, additional, Scher, Howard I., additional, Shore, Neal, additional, Skoneczna, Iwona, additional, Small, Eric, additional, Smith, Matthew, additional, Soule, Howard, additional, Spratt, Daniel, additional, Sternberg, Cora N., additional, Suzuki, Hiroyoshi, additional, Sweeney, Christopher, additional, Sydes, Matthew, additional, Taplin, Mary-Ellen, additional, Tilki, Derya, additional, Tombal, Bertrand, additional, Türkeri, Levent, additional, Uemura, Hiroji, additional, Uemura, Hirotsugu, additional, van Oort, Inge, additional, Yamoah, Kosj, additional, Ye, Dingwei, additional, Zapatero, Almudena, additional, Gillessen, Silke, additional, and Omlin, Aurelius, additional

Published
2022
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387. The PRIMARY Score: Using intra-prostatic PSMA PET/CT patterns to optimise prostate cancer diagnosis.

Author

Emmett, Louise M, primary, Papa, Nathan, additional, Buteau, James, additional, Ho, Bao, additional, Liu, Victor, additional, Roberts, Matthew, additional, Thompson, James, additional, Moon, Daniel, additional, Sheehan-Dare, Gemma, additional, Alghazo, Omar, additional, Agrawal, Shikha, additional, Murphy, Declan G., additional, Stricker, Phillip, additional, Hope, Thomas A., additional, and Hofman, Michael, additional

Published
2022
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388. Adults with autism spectrum disorder and the criminal justice system: An investigation of prevalence of contact with the criminal justice system, risk factors and sex differences in a specialist assessment service

Author

Blackmore, Charlotte E, primary, Woodhouse, Emma L, additional, Gillan, Nicola, additional, Wilson, Ellie, additional, Ashwood, Karen L, additional, Stoencheva, Vladimira, additional, Nolan, Alexandra, additional, McAlonan, Grainne M, additional, Robertson, Dene M, additional, Whitwell, Susannah, additional, Deeley, Quinton, additional, Craig, Michael C, additional, Zinkstok, Janneke, additional, Wichers, Rob, additional, Spain, Debbie, additional, Roberts, Ged, additional, Murphy, Declan GM, additional, Murphy, Clodagh M, additional, and Daly, Eileen, additional

Published
2022
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390. Pharmacological and dietary-supplement treatments for autism spectrum disorder: a systematic review and network meta-analysis

Author

Siafis, Spyridon, primary, Çıray, Oğulcan, additional, Wu, Hui, additional, Schneider-Thoma, Johannes, additional, Bighelli, Irene, additional, Krause, Marc, additional, Rodolico, Alessandro, additional, Ceraso, Anna, additional, Deste, Giacomo, additional, Huhn, Maximilian, additional, Fraguas, David, additional, San José Cáceres, Antonia, additional, Mavridis, Dimitris, additional, Charman, Tony, additional, Murphy, Declan G., additional, Parellada, Mara, additional, Arango, Celso, additional, and Leucht, Stefan, additional

Published
2022
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392. Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder

Author

Ecker, Christine, primary, Pretzsch, Charlotte M., additional, Bletsch, Anke, additional, Mann, Caroline, additional, Schaefer, Tim, additional, Ambrosino, Sara, additional, Tillmann, Julian, additional, Yousaf, Afsheen, additional, Chiocchetti, Andreas, additional, Lombardo, Michael V., additional, Warrier, Varun, additional, Bast, Nico, additional, Moessnang, Carolin, additional, Baumeister, Sarah, additional, Dell’Acqua, Flavio, additional, Floris, Dorothea L., additional, Zabihi, Mariam, additional, Marquand, Andre, additional, Cliquet, Freddy, additional, Leblond, Claire, additional, Moreau, Clara, additional, Puts, Nick, additional, Banaschewski, Tobias, additional, Jones, Emily J.H., additional, Mason, Luke, additional, Bölte, Sven, additional, Meyer-Lindenberg, Andreas, additional, Persico, Antonio M., additional, Durston, Sarah, additional, Baron-Cohen, Simon, additional, Spooren, Will, additional, Loth, Eva, additional, Freitag, Christine M., additional, Charman, Tony, additional, Dumas, Guillaume, additional, Bourgeron, Thomas, additional, Beckmann, Christian F., additional, Buitelaar, Jan K., additional, and Murphy, Declan G.M., additional

Published
2022
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395. Efficacy and safety of balovaptan for socialisation and communication difficulties in autistic adults in North America and Europe: a phase 3, randomised, placebo-controlled trial

Author

Jacob, Suma, primary, Veenstra-VanderWeele, Jeremy, additional, Murphy, Declan, additional, McCracken, James, additional, Smith, Janice, additional, Sanders, Kevin, additional, Meyenberg, Christoph, additional, Wiese, Thomas, additional, Deol-Bhullar, Gurpreet, additional, Wandel, Christoph, additional, Ashford, Elizabeth, additional, and Anagnostou, Evdokia, additional

Published
2022
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396. Large variation in conservative management of low‐risk prostate cancer in Australia and New Zealand

Author

Ong, Wee Loon, primary, Thangasamy, Isaac, additional, Murphy, Declan, additional, Pritchard, Elizabeth, additional, Evans, Susan, additional, Millar, Jeremy, additional, Chalasani, Venu, additional, Rashid, Prem, additional, Winter, Matthew, additional, Vela, Ian, additional, Pryor, David, additional, Mark, Stephen, additional, and Lawrentschuk, Nathan, additional

Published
2022
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398. Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium

Author

Sha, Zhiqiang, primary, van Rooij, Daan, additional, Anagnostou, Evdokia, additional, Arango, Celso, additional, Auzias, Guillaume, additional, Behrmann, Marlene, additional, Bernhardt, Boris, additional, Bolte, Sven, additional, Busatto, Geraldo F., additional, Calderoni, Sara, additional, Calvo, Rosa, additional, Daly, Eileen, additional, Deruelle, Christine, additional, Duan, Meiyu, additional, Duran, Fabio Luis Souza, additional, Durston, Sarah, additional, Ecker, Christine, additional, Ehrlich, Stefan, additional, Fair, Damien, additional, Fedor, Jennifer, additional, Fitzgerald, Jacqueline, additional, Floris, Dorothea L., additional, Franke, Barbara, additional, Freitag, Christine M., additional, Gallagher, Louise, additional, Glahn, David C., additional, Haar, Shlomi, additional, Hoekstra, Liesbeth, additional, Jahanshad, Neda, additional, Jalbrzikowski, Maria, additional, Janssen, Joost, additional, King, Joseph A., additional, Lazaro, Luisa, additional, Luna, Beatriz, additional, McGrath, Jane, additional, Medland, Sarah E., additional, Muratori, Filippo, additional, Murphy, Declan G. M., additional, Neufeld, Janina, additional, O’Hearn, Kirsten, additional, Oranje, Bob, additional, Parellada, Mara, additional, Pariente, Jose C., additional, Postema, Merel C., additional, Remnelius, Karl Lundin, additional, Retico, Alessandra, additional, Rosa, Pedro Gomes Penteado, additional, Rubia, Katya, additional, Shook, Devon, additional, Tammimies, Kristiina, additional, Taylor, Margot J., additional, Tosetti, Michela, additional, Wallace, Gregory L., additional, Zhou, Fengfeng, additional, Thompson, Paul M., additional, Fisher, Simon E., additional, Buitelaar, Jan K., additional, and Francks, Clyde, additional

Published
2022
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