211 results on '"Bowes L"'
Search Results
2. Anaesthesia for paediatric neurosurgery. Part 1: general considerations
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Stendall, C., Bowes, L., and Carver, E.
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- 2024
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3. Prognostic gene expression signature for high-grade serous ovarian cancer
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Millstein, J, Budden, T, Goode, EL, Anglesio, MS, Talhouk, A, Intermaggio, MP, Leong, HS, Chen, S, Elatre, W, Gilks, B, Nazeran, T, Volchek, M, Bentley, RC, Wang, C, Chiu, DS, Kommoss, S, Leung, SCY, Senz, J, Lum, A, Chow, V, Sudderuddin, H, Mackenzie, R, George, J, Group, AOCS, Bowtell, D, Chenevix-Trench, G, Green, A, Webb, P, DeFazio, A, Gertig, D, Traficante, N, Fereday, S, Moore, S, Hung, J, Harrap, K, Sadkowsky, T, Pandeya, N, Malt, M, Mellon, A, Robertson, R, Bergh, T Vanden, Jones, M, Mackenzie, P, Maidens, J, Nattress, K, Chiew, YE, Stenlake, A, Sullivan, H, Alexander, B, Ashover, P, Brown, S, Corrish, T, Green, L, Jackman, L, Ferguson, K, Martin, K, Martyn, A, Ranieri, B, White, J, Jayde, V, Mamers, P, Bowes, L, Galletta, L, Giles, D, Hendley, J, Alsop, K, Schmidt, T, Shirley, H, Ball, C, Young, C, Viduka, S, Tran, Hoa, Bilic, Sanela, Glavinas, Lydia, Brooks, Julia, Stuart-Harris, R, Kirsten, F, Rutovitz, J, Clingan, P, Glasgow, A, Proietto, A, Braye, S, Otton, G, Shannon, J, Bonaventura, T, Stewart, J, Begbie, S, Friedlander, M, Bell, D, Baron-Hay, S, Ferrier, AA, Gard, G, Nevell, D, Pavlakis, N, Valmadre, S, Young, B, Camaris, C, Crouch, R, Edwards, L, and Hacker, N
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Genetic Testing ,Genetics ,Cancer ,Ovarian Cancer ,Rare Diseases ,4.2 Evaluation of markers and technologies ,4.4 Population screening ,Detection ,screening and diagnosis ,Cystadenocarcinoma ,Serous ,Female ,Humans ,Ovarian Neoplasms ,Prognosis ,Proportional Hazards Models ,Survival Analysis ,Transcriptome ,formalin-fixed paraffin-embedded ,gene expression ,high-grade serous ovarian cancer ,overall survival ,prognosis ,AOCS Group ,Oncology & Carcinogenesis ,Clinical sciences ,Oncology and carcinogenesis - Abstract
BackgroundMedian overall survival (OS) for women with high-grade serous ovarian cancer (HGSOC) is ∼4 years, yet survival varies widely between patients. There are no well-established, gene expression signatures associated with prognosis. The aim of this study was to develop a robust prognostic signature for OS in patients with HGSOC.Patients and methodsExpression of 513 genes, selected from a meta-analysis of 1455 tumours and other candidates, was measured using NanoString technology from formalin-fixed paraffin-embedded tumour tissue collected from 3769 women with HGSOC from multiple studies. Elastic net regularization for survival analysis was applied to develop a prognostic model for 5-year OS, trained on 2702 tumours from 15 studies and evaluated on an independent set of 1067 tumours from six studies.ResultsExpression levels of 276 genes were associated with OS (false discovery rate < 0.05) in covariate-adjusted single-gene analyses. The top five genes were TAP1, ZFHX4, CXCL9, FBN1 and PTGER3 (P < 0.001). The best performing prognostic signature included 101 genes enriched in pathways with treatment implications. Each gain of one standard deviation in the gene expression score conferred a greater than twofold increase in risk of death [hazard ratio (HR) 2.35, 95% confidence interval (CI) 2.02-2.71; P < 0.001]. Median survival [HR (95% CI)] by gene expression score quintile was 9.5 (8.3 to -), 5.4 (4.6-7.0), 3.8 (3.3-4.6), 3.2 (2.9-3.7) and 2.3 (2.1-2.6) years.ConclusionThe OTTA-SPOT (Ovarian Tumor Tissue Analysis consortium - Stratified Prognosis of Ovarian Tumours) gene expression signature may improve risk stratification in clinical trials by identifying patients who are least likely to achieve 5-year survival. The identified novel genes associated with the outcome may also yield opportunities for the development of targeted therapeutic approaches.
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- 2020
4. Timing of whole genome duplication is associated with tumor-specific MHC-II depletion in serous ovarian cancer.
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Burdett, Nikki L., Willis, Madelynne O., Pandey, Ahwan, Twomey, Laura, Alaei, Sara, Bowtell, D., Chenevix-Trench, G., Green, A., Webb, P., DeFazio, A., Gertig, D., Traficante, N., Fereday, S., Moore, S., Hung, J., Harrap, K., Sadkowsky, T., Pandeya, N., Bowes, L., and Galletta, L.
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MAJOR histocompatibility complex ,OVARIAN cancer ,HOMOLOGOUS recombination ,GENOMES ,TREATMENT effectiveness ,OVERALL survival ,OVARIAN follicle ,WNT signal transduction - Abstract
Whole genome duplication is frequently observed in cancer, and its prevalence in our prior analysis of end-stage, homologous recombination deficient high grade serous ovarian cancer (almost 80% of samples) supports the notion that whole genome duplication provides a fitness advantage under the selection pressure of therapy. Here, we therefore aim to identify potential therapeutic vulnerabilities in primary high grade serous ovarian cancer with whole genome duplication by assessing differentially expressed genes and pathways in 79 samples. We observe that MHC-II expression is lowest in tumors which have acquired whole genome duplication early in tumor evolution, and further demonstrate that reduced MHC-II expression occurs in subsets of tumor cells rather than in canonical antigen-presenting cells. Early whole genome duplication is also associated with worse patient survival outcomes. Our results suggest an association between the timing of whole genome duplication, MHC-II expression and clinical outcome in high grade serous ovarian cancer that warrants further investigation for therapeutic targeting. There is high prevalence of whole genome duplication (WGD) in high grade serous ovarian cancer. Here, the authors compare tumours with and without WGD and find that those that acquired WGD early during tumour evolution are associated with worse survival and have the lowest expression of MHC-II. [ABSTRACT FROM AUTHOR]
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- 2024
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5. MyD88 and TLR4 Expression in Epithelial Ovarian Cancer
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Block, Matthew S, Vierkant, Robert A, Rambau, Peter F, Winham, Stacey J, Wagner, Philipp, Traficante, Nadia, Tołoczko, Aleksandra, Tiezzi, Daniel G, Taran, Florin Andrei, Sinn, Peter, Sieh, Weiva, Sharma, Raghwa, Rothstein, Joseph H, Ramón y Cajal, Teresa, Paz-Ares, Luis, Oszurek, Oleg, Orsulic, Sandra, Ness, Roberta B, Nelson, Gregg, Modugno, Francesmary, Menkiszak, Janusz, McGuire, Valerie, McCauley, Bryan M, Mack, Marie, Lubiński, Jan, Longacre, Teri A, Li, Zheng, Lester, Jenny, Kennedy, Catherine J, Kalli, Kimberly R, Jung, Audrey Y, Johnatty, Sharon E, Jimenez-Linan, Mercedes, Jensen, Allan, Intermaggio, Maria P, Hung, Jillian, Herpel, Esther, Hernandez, Brenda Y, Hartkopf, Andreas D, Harnett, Paul R, Ghatage, Prafull, García-Bueno, José M, Gao, Bo, Fereday, Sian, Eilber, Ursula, Edwards, Robert P, de Sousa, Christiani B, de Andrade, Jurandyr M, Chudecka-Głaz, Anita, Chenevix-Trench, Georgia, Cazorla, Alicia, Brucker, Sara Y, Group, Australian Ovarian Cancer Study, Bowtell, D, Chenevix-Trench, G, Green, A, Webb, P, DeFazio, A, Gertig, D, Traficante, N, Fereday, S, Moore, S, Hung, J, Harrap, K, Sadkowsky, T, Pandeya, N, Malt, M, Mellon, A, Robertson, R, Bergh, T Vanden, Jones, M, Mackenzie, P, Maidens, J, Nattress, K, Chiew, YE, Stenlake, A, Sullivan, H, Alexander, B, Ashover, P, Brown, S, Corrish, T, Green, L, Jackman, L, Ferguson, K, Martin, K, Martyn, A, Ranieri, B, White, J, Jayde, V, Mamers, P, Bowes, L, Galletta, L, Giles, D, Hendley, J, Alsop, K, Schmidt, T, Shirley, H, Ball, C, Young, C, and Viduka, S
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Biomedical and Clinical Sciences ,Oncology and Carcinogenesis ,Clinical Research ,Cancer ,Rare Diseases ,Ovarian Cancer ,Adult ,Aged ,Biomarkers ,Tumor ,Carcinoma ,Ovarian Epithelial ,Female ,Humans ,Immunohistochemistry ,Middle Aged ,Myeloid Differentiation Factor 88 ,Ovarian Neoplasms ,Survival Analysis ,Tissue Array Analysis ,Toll-Like Receptor 4 ,Australian Ovarian Cancer Study Group ,Medical and Health Sciences ,Biomedical and clinical sciences - Abstract
ObjectiveTo evaluate myeloid differentiation primary response gene 88 (MyD88) and Toll-like receptor 4 (TLR4) expression in relation to clinical features of epithelial ovarian cancer, histologic subtypes, and overall survival.Patients and methodsWe conducted centralized immunohistochemical staining, semi-quantitative scoring, and survival analysis in 5263 patients participating in the Ovarian Tumor Tissue Analysis consortium. Patients were diagnosed between January 1, 1978, and December 31, 2014, including 2865 high-grade serous ovarian carcinomas (HGSOCs), with more than 12,000 person-years of follow-up time. Tissue microarrays were stained for MyD88 and TLR4, and staining intensity was classified using a 2-tiered system for each marker (weak vs strong).ResultsExpression of MyD88 and TLR4 was similar in all histotypes except clear cell ovarian cancer, which showed reduced expression compared with other histotypes (P
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- 2018
6. Refined cut-off for TP53 immunohistochemistry improves prediction of TP53 mutation status in ovarian mucinous tumors: implications for outcome analyses
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Kang, Eun Young, Cheasley, Dane, LePage, Cecile, Wakefield, Matthew J., da Cunha Torres, Michelle, Rowley, Simone, Salazar, Carolina, Xing, Zhongyue, Allan, Prue, Bowtell, David D.L., Mes-Masson, Anne-Marie, Provencher, Diane M., Rahimi, Kurosh, Kelemen, Linda E., Fasching, Peter A., Doherty, Jennifer A., Goodman, Marc T., Goode, Ellen L., Deen, Suha, Pharoah, Paul D.P., Brenton, James D., Sieh, Weiva, Mateoiu, Constantina, Sundfeldt, Karin, Cook, Linda S., Le, Nhu D., Anglesio, Michael S., Gilks, C. Blake, Huntsman, David G., Kennedy, Catherine J., Traficante, Nadia, Bowtell, D., Chenevix-Trench, G., Green, A., Webb, P., DeFazio, A., Gertig, D., Traficante, N., Fereday, S., Moore, S., Hung, J., Harrap, K., Sadkowsky, T., Pandeya, N., Malt, M., Mellon, A., Robertson, R., Bergh, T. Vanden, Jones, M., Mackenzie, P., Maidens, J., Nattress, K., Chiew, Y.E., Stenlake, A., Sullivan, H., Alexander, B., Ashover, P., Brown, S., Corrish, T., Green, L., Jackman, L., Ferguson, K., Martin, K., Martyn, A., Ranieri, B., White, J., Jayde, V., Mamers, P., Bowes, L., Galletta, L., Giles, D., Hendley, J., Alsop, K., Schmidt, T., Shirley, H., Ball, C., Young, C., Viduka, S., Tran, Hoa, Bilic, Sanela, Glavinas, Lydia, Brooks, Julia, Stuart-Harris, R., Kirsten, F., Rutovitz, J., Clingan, P., Glasgow, A., Proietto, A., Braye, S., Otton, G., Shannon, J., Bonaventura, T., Stewart, J., Begbie, S., Friedlander, M., Bell, D., Baron-Hay, S., Ferrier, A., Gard, G., Nevell, D., Pavlakis, N., Valmadre, S., Young, B., Camaris, C., Crouch, R., Edwards, L., Hacker, N., Marsden, D., Robertson, G., Beale, P., Beith, J., Carter, J., Dalrymple, C., Houghton, R., Russell, P., Links, M., Grygiel, J., Hill, J., Brand, A., Byth, K., Jaworski, R., Harnett, P., Sharma, R., Wain, G., Ward, B., Papadimos, D., Crandon, A., Cummings, M., Horwood, K., Obermair, A., Perrin, L., Wyld, D., Nicklin, J., Davy, M., Oehler, M.K., Hall, C., Dodd, T., Healy, T., Pittman, K., Henderson, D., Miller, J., Pierdes, J., Blomfield, P., Challis, D., McIntosh, R., Parker, A., Brown, B., Rome, R., Allen, D., Grant, P., Hyde, S., Laurie, R., Robbie, M., Healy, D., Jobling, T., Manolitsas, T., McNealage, J., Rogers, P., Susil, B., Sumithran, E., Simpson, I., Phillips, K., Rischin, D., Fox, S., Johnson, D., Lade, S., Loughrey, M., O'Callaghan, N., Murray, W., Waring, P., Billson, V., Pyman, J., Neesham, D., Quinn, M., Underhill, C., Bell, R., Ng, L.F., Blum, R., Ganju, V., Hammond, I., Leung, Y., McCartney, A., Buck, M., Haviv, I., Purdie, D., Whiteman, D., Zeps, N., DeFazio, Anna, Kaufmann, Scott, Churchman, Michael, Gourley, Charlie, Stephens, Andrew N., Meagher, Nicola S., Ramus, Susan J., Antill, Yoland C., Campbell, Ian, Scott, Clare L., Köbel, Martin, Gorringe, Kylie L., Ryland, Georgina L., Allan, Prue E., Alsop, Kathryn, Ananda, Sumitra, Au-Yeung, George, Böhm, Maret, Brand, Alison, Chenevix-Trench, Georgia, Christie, Michael, Chiew, Yoke-Eng, Dudley, Rhiannon, Fairweather, Nicole, Fereday, Sian, Fox, Stephen B., Hacker, Neville F., Hadley, Alison M., Hendley, Joy, Ho, Gwo-Yaw, Hunter, Sally M., Jobling, Tom W., Kalli, Kimberly R., Kaufmann, Scott H., Le Page, Cecile, McNally, Orla M., McAlpine, Jessica N., Mileshkin, Linda, Pyman, Jan, Samimi, Goli, Sharma, Ragwha, and Campbell, Ian G.
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- 2021
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7. Prognostic gene expression signature for high-grade serous ovarian cancer
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Bowtell, D., Chenevix-Trench, G., Green, A., Webb, P., DeFazio, A., Gertig, D., Traficante, N., Fereday, S., Moore, S., Hung, J., Harrap, K., Sadkowsky, T., Pandeya, N., Malt, M., Mellon, A., Robertson, R., Vanden Bergh, T., Jones, M., Mackenzie, P., Maidens, J., Nattress, K., Chiew, Y.E., Stenlake, A., Sullivan, H., Alexander, B., Ashover, P., Brown, S., Corrish, T., Green, L., Jackman, L., Ferguson, K., Martin, K., Martyn, A., Ranieri, B., White, J., Jayde, V., Mamers, P., Bowes, L., Galletta, L., Giles, D., Hendley, J., Alsop, K., Schmidt, T., Shirley, H., Ball, C., Young, C., Viduka, S., Tran, Hoa, Bilic, Sanela, Glavinas, Lydia, Brooks, Julia, Stuart-Harris, R., Kirsten, F., Rutovitz, J., Clingan, P., Glasgow, A., Proietto, A., Braye, S., Otton, G., Shannon, J., Bonaventura, T., Stewart, J., Begbie, S., Friedlander, M., Bell, D., Baron-Hay, S., Ferrier,a, A., Gard, G., Nevell, D., Pavlakis, N., Valmadre, S., Young, B., Camaris, C., Crouch, R., Edwards, L., Hacker, N., Marsden, D., Robertson, G., Beale, P., Beith, J., Carter, J., Dalrymple, C., Houghton, R., Russell, P., Links, M., Grygiel, J., Hill, J., Brand, A., Byth, K., Jaworski, R., Harnett, P., Sharma, R., Wain, G., Ward, B., Papadimos, D., Crandon, A., Cummings, M., Horwood, K., Obermair, A., Perrin, L., Wyld, D., Nicklin, J., Davy, M., Oehler, M.K., Hall, C., Dodd, T., Healy, T., Pittman, K., Henderson, D., Miller, J., Pierdes, J., Blomfield, P., Challis, D., McIntosh, R., Parker, A., Brown, B., Rome, R., Allen, D., Grant, P., Hyde, S., Laurie, R., Robbie, M., Healy, D., Jobling, T., Manolitsas, T., McNealage, J., Rogers, P., Susil, B., Sumithran, E., Simpson, I., Phillips, K., Rischin, D., Fox, S., Johnson, D., Lade, S., Loughrey, M., O’Callaghan, N., Murray, W., Waring, P., Billson, V., Pyman, J., Neesham, D., Quinn, M., Underhill, C., Bell, R., Ng, L.F., Blum, R., Ganju, V., Hammond, I., Leung, Y., McCartney, A., Buck, M., Haviv, I., Purdie, D., Whiteman, D., Zeps, N., Millstein, J., Budden, T., Goode, E.L., Anglesio, M.S., Talhouk, A., Intermaggio, M.P., Leong, H.S., Chen, S., Elatre, W., Gilks, B., Nazeran, T., Volchek, M., Bentley, R.C., Wang, C., Chiu, D.S., Kommoss, S., Leung, S.C.Y., Senz, J., Lum, A., Chow, V., Sudderuddin, H., Mackenzie, R., George, J., Steed, H., Koziak, J.M., Köbel, M., McNeish, I.A., Goranova, T., Ennis, D., Macintyre, G., Silva De Silva, D., Ramón y Cajal, T., García-Donas, J., Hernando Polo, S., Rodriguez, G.C., Cushing-Haugen, K.L., Harris, H.R., Greene, C.S., Zelaya, R.A., Behrens, S., Fortner, R.T., Sinn, P., Herpel, E., Lester, J., Lubiński, J., Oszurek, O., Tołoczko, A., Cybulski, C., Menkiszak, J., Pearce, C.L., Pike, M.C., Tseng, C., Alsop, J., Rhenius, V., Song, H., Jimenez-Linan, M., Piskorz, A.M., Gentry-Maharaj, A., Karpinskyj, C., Widschwendter, M., Singh, N., Kennedy, C.J., Harnett, P.R., Gao, B., Johnatty, S.E., Sayer, R., Boros, J., Winham, S.J., Keeney, G.L., Kaufmann, S.H., Larson, M.C., Luk, H., Hernandez, B.Y., Thompson, P.J., Wilkens, L.R., Carney, M.E., Trabert, B., Lissowska, J., Brinton, L., Sherman, M.E., Bodelon, C., Hinsley, S., Lewsley, L.A., Glasspool, R., Banerjee, S.N., Stronach, E.A., Haluska, P., Ray-Coquard, I., Mahner, S., Winterhoff, B., Slamon, D., Levine, D.A., Kelemen, L.E., Benitez, J., Chang-Claude, J., Gronwald, J., Wu, A.H., Menon, U., Goodman, M.T., Schildkraut, J.M., Wentzensen, N., Brown, R., Berchuck, A., deFazio, A., Gayther, S.A., García, M.J., Henderson, M.J., Rossing, M.A., Beeghly-Fadiel, A., Fasching, P.A., Orsulic, S., Karlan, B.Y., Konecny, G.E., Huntsman, D.G., Bowtell, D.D., Brenton, J.D., Doherty, J.A., Pharoah, P.D.P., and Ramus, S.J.
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- 2020
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8. Anaesthesia for paediatric neurosurgery. Part 1: general considerations
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Stendall, C., primary, Bowes, L., additional, and Carver, E., additional
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- 2023
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9. Cognitive styles and future depressed mood in early adulthood: The importance of global attributions
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Pearson, R.M., Heron, J., Button, K., Bentall, R.P., Fernyhough, C., Mahedy, L., Bowes, L., and Lewis, G.
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- 2015
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10. Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci
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Devries, Amber A, Dennis, Joe, Tyrer, Jonathan P, Peng, Pei-chen, Coetzee, Simon G, Reyes, Alberto L, Plummer, Jasmine T, Davis, Brian D, Chen, Stephanie S, Dezem, Felipe Segato, Aben, Katja K H, Anton-culver, Hoda, Antonenkova, Natalia N, Beckmann, Matthias W, Beeghly-fadiel, Alicia, Berchuck, Andrew, Bogdanova, Natalia V, Bogdanova-markov, Nadja, Brenton, James D, Butzow, Ralf, Campbell, Ian, Chang-claude, Jenny, Chenevix-trench, G, Cook, Linda S, Defazio, A, Doherty, Jennifer A, Dörk, Thilo, Eccles, Diana M, Eliassen, A Heather, Fasching, Peter A, Fortner, Renée T, Giles, Graham G, Goode, Ellen L, Goodman, Marc T, Gronwald, Jacek, Webb, P, Friedlander, M, Obermair, A, Grant, P, Nagle, C, Beesley, V, Chevenix-trench, G, Bowtell, D, Blomfield, P, Brand, A, Davis, A, Leung, Y, Nicklin, J, Quinn, M, Livingstone, K, O'neill, H, Williams, M, Black, A, Hadley, A, Glasgow, A, Garrett, A, Rao, A, Shannon, C, Steer, C, Allen, D, Neesham, D, Otton, G, Au-yeung, G, Goss, G, Wain, G, Gard, G, Robertson, G, Lombard, J, Tan, J, Mcneilage, J, Power, J, Coward, J, Miller, J, Carter, J, Lamont, J, Wong, K M, Reid, K, Perrin, L, Milishkin, L, Nascimento, M, Buck, M, Bunting, M, Harrison, M, Chetty, N, Hacker, N, Mcnally, O, Harnett, P, Beale, P, Awad, R, Mohan, R, Farrell, R, Mcintosh, R, Rome, R, Sayer, R, Houghton, R, Hogg, R, Land, R, Baron-hay, S, Paramasivum, S, Pather, S, Hyde, S, Salfinger, S, Valmadre, S, Jobling, T, Manolitsas, T, Bonaventura, T, Arora, V, Green, A, Gertig, D, Traficante, N, Fereday, S, Moore, S, Hung, J, Harrap, K, Sadkowsky, T, Pandeya, N, Malt, M, Robertson, R, Bergh, T Vanden, Jones, M, Mckenzie, P, Maidens, J, Nattress, K, Chiew, Y E, Stenlake, A, Sullivan, H, Alexander, B, Ashover, P, Brown, S, Corrish, T, Green, L, Jackman, L, Ferguson, K, Martin, K, Martyn, A, Ranieri, B, White, J, Jayde, V, Bowes, L, Mamers, P, Galletta, L, Giles, D, Hendley, J, Alsop, K, Schmidt, T, Shirley, H, Ball, C, Young, C, Viduka, S, Tran, H, Bilic, S, Glavinas, L, Brooks, J, Stuart-harris, R, Kirsten, F, Rutovitz, J, Clingan, P, Proietto, A, Braye, S, Shannon, J, Stewart, J, Begbie, S, Håkansson, Niclas, Hildebrandt, Michelle A T, Huff, Chad, Huntsman, David G, Jensen, Allan, Kar, Siddhartha, Karlan, Beth Y, Khusnutdinova, Elza K, Kiemeney, Lambertus A, Kjaer, Susanne K, Kupryjanczyk, Jolanta, Labrie, Marilyne, Lambrechts, Diether, Le, Nhu D, Lubiński, Jan, May, Taymaa, Menon, Usha, Milne, Roger L, Modugno, Francesmary, Monteiro, Alvaro N, Moysich, Kirsten B, Odunsi, Kunle, Olsson, Håkan, Pearce, Celeste L, Pejovic, Tanja, Ramus, Susan J, Riboli, Elio, Riggan, Marjorie J, Romieu, Isabelle, Sandler, Dale P, Schildkraut, Joellen M, Setiawan, V Wendy, Sieh, Weiva, Song, Honglin, Sutphen, Rebecca, Terry, Kathryn L, Thompson, Pamela J, Titus, Linda, Tworoger, Shelley S, Van Nieuwenhuysen, Els, Edwards, Digna Velez, Webb, Penelope M, Wentzensen, Nicolas, Whittemore, Alice S, Wolk, Alicja, Wu, Anna H, Ziogas, Argyrios, Freedman, Matthew L, Lawrenson, Kate, Pharoah, Paul D P, Easton, Douglas F, Gayther, Simon A, Jones, Michelle R, Helsinki University Hospital Area, Clinicum, Department of Pathology, and HUSLAB
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Cancer Research ,GENES ,DNA Copy Number Variations ,SUSCEPTIBILITY LOCI ,3122 Cancers ,Carcinoma, Ovarian Epithelial ,Polymorphism, Single Nucleotide ,BREAST ,Humans ,Genetic Predisposition to Disease ,BRCA2 MUTATIONS ,GENOME-WIDE ASSOCIATION ,Alleles ,Ovarian Neoplasms ,Cancer och onkologi ,Science & Technology ,IDENTIFICATION ,REARRANGEMENTS ,COMMON VARIANTS ,GERMLINE MUTATIONS ,DELETIONS ,Oncology ,Urological cancers Radboud Institute for Health Sciences [Radboudumc 15] ,Cancer and Oncology ,Female ,Life Sciences & Biomedicine ,Genome-Wide Association Study - Abstract
Background Known risk alleles for epithelial ovarian cancer (EOC) account for approximately 40% of the heritability for EOC. Copy number variants (CNVs) have not been investigated as EOC risk alleles in a large population cohort. Methods Single nucleotide polymorphism array data from 13 071 EOC cases and 17 306 controls of White European ancestry were used to identify CNVs associated with EOC risk using a rare admixture maximum likelihood test for gene burden and a by-probe ratio test. We performed enrichment analysis of CNVs at known EOC risk loci and functional biofeatures in ovarian cancer–related cell types. Results We identified statistically significant risk associations with CNVs at known EOC risk genes; BRCA1 (PEOC = 1.60E-21; OREOC = 8.24), RAD51C (Phigh-grade serous ovarian cancer [HGSOC] = 5.5E-4; odds ratio [OR]HGSOC = 5.74 del), and BRCA2 (PHGSOC = 7.0E-4; ORHGSOC = 3.31 deletion). Four suggestive associations (P Conclusions CNVs in BRCA1 have been previously reported in smaller studies, but their observed frequency in this large population-based cohort, along with the CNVs observed at BRCA2 and RAD51C gene loci in EOC cases, suggests that these CNVs are potentially pathogenic and may contribute to the spectrum of disease-causing mutations in these genes. CNVs are likely to occur in a wider set of susceptibility regions, with potential implications for clinical genetic testing and disease prevention.
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- 2022
11. Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression
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Culverhouse, R C, Saccone, N L, Horton, A C, Ma, Y, Anstey, K J, Banaschewski, T, Burmeister, M, Cohen-Woods, S, Etain, B, Fisher, H L, Goldman, N, Guillaume, S, Horwood, J, Juhasz, G, Lester, K J, Mandelli, L, Middeldorp, C M, Olié, E, Villafuerte, S, Air, T M, Araya, R, Bowes, L, Burns, R, Byrne, E M, Coffey, C, Coventry, W L, Gawronski, K AB, Glei, D, Hatzimanolis, A, Hottenga, J-J, Jaussent, I, Jawahar, C, Jennen-Steinmetz, C, Kramer, J R, Lajnef, M, Little, K, zu Schwabedissen, H M, Nauck, M, Nederhof, E, Petschner, P, Peyrot, W J, Schwahn, C, Sinnamon, G, Stacey, D, Tian, Y, Toben, C, Van der Auwera, S, Wainwright, N, Wang, J-C, Willemsen, G, Anderson, I M, Arolt, V, Åslund, C, Bagdy, G, Baune, B T, Bellivier, F, Boomsma, D I, Courtet, P, Dannlowski, U, de Geus, E JC, Deakin, J FW, Easteal, S, Eley, T, Fergusson, D M, Goate, A M, Gonda, X, Grabe, H J, Holzman, C, Johnson, E O, Kennedy, M, Laucht, M, Martin, N G, Munafò, M R, Nilsson, K W, Oldehinkel, A J, Olsson, C A, Ormel, J, Otte, C, Patton, G C, Penninx, B WJH, Ritchie, K, Sarchiapone, M, Scheid, J M, Serretti, A, Smit, J H, Stefanis, N C, Surtees, P G, Völzke, H, Weinstein, M, Whooley, M, Nurnberger, J I, Jr, Breslau, N, and Bierut, L J
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- 2018
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12. Trends in inpatient care for psychiatric disorders in NHS hospitals across England, 1998/99–2019/20: an observational time series analysis
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Degli Esposti, M, Ziauddeen, H, Bowes, L, Reeves, A, Chekroud, AM, Humphreys, DK, and Ford, T
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Psychiatry ,Adult ,Original Paper ,Inpatients ,Health (social science) ,Hospital episode statistics ,Time Factors ,Social Psychology ,Adolescent ,Epidemiology ,Mental Disorders ,Infant, Newborn ,Infant ,Time trends ,Hospitals ,State Medicine ,Psychiatry and Mental health ,Child, Preschool ,Humans ,Mental health ,Child ,Hospital admissions - Abstract
Purpose It is unclear how hospitals are responding to the mental health needs of the population in England, against a backdrop of diminishing resources. We aimed to document patterns in hospital activity by psychiatric disorder and how these have changed over the last 22 years. Methods In this observational time series analysis, we used routinely collected data on all NHS hospitals in England from 1998/99 to 2019/20. Trends in hospital admissions and bed days for psychiatric disorders were smoothed using negative binomial regression models with year as the exposure and rates (per 1000 person-years) as the outcome. When linear trends were not appropriate, we fitted segmented negative binomial regression models with one change-point. We stratified by gender and age group [children (0–14 years); adults (15 years +)]. Results Hospital admission rates and bed days for all psychiatric disorders decreased by 28.4 and 38.3%, respectively. Trends were not uniform across psychiatric disorders or age groups. Admission rates mainly decreased over time, except for anxiety and eating disorders which doubled over the 22-year period, significantly increasing by 2.9% (AAPC = 2.88; 95% CI: 2.61–3.16; p p Conclusion In the last 22 years, there have been overall reductions in hospital activity for psychiatric disorders. However, some disorders showed pronounced increases, pointing to areas of growing need for inpatient psychiatric care, especially among children.
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- 2022
13. 146 Virtual role-play: A useful tool for undergraduate obstetrics and gynaecology teaching during a pandemic
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Tuthill, E., primary, Bowes, L., additional, Kennelly, M., additional, and Turner, M., additional
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- 2022
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14. Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia
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Sung, L., Dix, D., Cellot, S., Gillmeister, B., Ethier, M.C., Roslin, N.M., Johnston, D.L., Feusner, J., Mitchell, D., Lewis, V., Aplenc, R., Yanofsky, R., Portwine, C., Price, V., Zelcer, S., Silva, M., Bowes, L., Michon, B., Stobart, K., Traubici, J., Allen, U., Beyene, J., den Hollander, N., and Paterson, A.D.
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- 2016
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15. Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case–control studies
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Munafò, M R, Bowes, L, Clark, T G, and Flint, J
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- 2005
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16. Invasive fungal infections in paediatric acute myeloid leukaemia
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Johnston, D. L., Lewis, V., Yanofsky, R., Gillmeister, B., Ethier, M. C., Mitchell, D., Cellot, S., Dix, D., Portwine, C., Price, V., Silva, M., Zelcer, S., Michon, B., Bowes, L., Stobart, K., Brossard, J., Beyene, J., and Sung, L.
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- 2013
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17. Bullying victimization in youths and mental health problems: ‘Much ado about nothing’?
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Arseneault, L., Bowes, L., and Shakoor, S.
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- 2010
18. Psychiatric disorders in adolescent cancer survivors: A systematic review of prevalence and predictors
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Kosir, U, Wiedemann, M, Wild, J, and Bowes, L
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Cancer Research ,medicine.medical_specialty ,business.industry ,Childhood cancer ,Adolescent cancer ,social sciences ,humanities ,Increased risk ,Oncology ,medicine ,population characteristics ,Systematic Review ,Psychiatry ,business ,human activities ,Psychosocial - Abstract
Background: Adolescent cancer survivors are a particularly vulnerable group of young patients. Compared with healthy peers, adolescent survivors face more psychosocial difficulties and are at increased risk of developing psychiatric disorders. Aims: We aimed to establish prevalence rates and predictors of psychiatric disorders in young cancer survivors and discuss areas for targeted interventions. Method: We systematically reviewed four major online databases: Embase, PsychINFO, Scopus, and Medline for quantitative studies evaluating mental health in adolescent cancer survivors. We used a narrative synthesis approach. Results: Nineteen studies met our inclusion criteria. Across the sample, up to 34% met criteria for post‐traumatic stress disorder (PTSD), 13% for clinical depression, and 8% for anxiety. Maladaptive coping, illness relapse, higher number of late effects, brain tumor diagnosis, and poor family functioning and parental distress were associated with higher psychological distress. Conclusions: A significant subset of adolescent survivors reports PTSD, anxiety, and depression symptoms. Individuals who present with more vulnerabilities and higher risk indices should be routinely assessed in order to reduce the psychological, social, and economic burden associated with poor mental health in this population. Early prevention strategies should target maladaptive coping mechanisms and promote healthy peer relationships and family functioning.
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- 2019
19. Collaborative meta-Analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression
- Author
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Culverhouse, R.C. Saccone, N.L. Horton, A.C. Ma, Y. Anstey, K.J. Banaschewski, T. Burmeister, M. Cohen-Woods, S. Etain, B. Fisher, H.L. Goldman, N. Guillaume, S. Horwood, J. Juhasz, G. Lester, K.J. Mandelli, L. Middeldorp, C.M. Olié, E. Villafuerte, S. Air, T.M. Araya, R. Bowes, L. Burns, R. Byrne, E.M. Coffey, C. Coventry, W.L. Gawronski, K.A.B. Glei, D. Hatzimanolis, A. Hottenga, J.-J. Jaussent, I. Jawahar, C. Jennen-Steinmetz, C. Kramer, J.R. Lajnef, M. Little, K. Zu Schwabedissen, H.M. Nauck, M. Nederhof, E. Petschner, P. Peyrot, W.J. Schwahn, C. Sinnamon, G. Stacey, D. Tian, Y. Toben, C. Van Der Auwera, S. Wainwright, N. Wang, J.-C. Willemsen, G. Anderson, I.M. Arolt, V. Aslund, C. Bagdy, G. Baune, B.T. Bellivier, F. Boomsma, D.I. Courtet, P. Dannlowski, U. De Geus, E.J.C. Deakin, J.F.W. Easteal, S. Eley, T. Fergusson, D.M. Goate, A.M. Gonda, X. Grabe, H.J. Holzman, C. Johnson, E.O. Kennedy, M. Laucht, M. Martin, N.G. Munafò, M.R. Nilsson, K.W. Oldehinkel, A.J. Olsson, C.A. Ormel, J. Otte, C. Patton, G.C. Penninx, B.W.J.H. Ritchie, K. Sarchiapone, M. Scheid, J.M. Serretti, A. Smit, J.H. Stefanis, N.C. Surtees, P.G. Völzke, H. Weinstein, M. Whooley, M. Nurnberger, J.I., Jr. Breslau, N. Bierut, L.J.
- Abstract
The hypothesis that the S allele of the 5-HTTLPR serotonin transporter promoter region is associated with increased risk of depression, but only in individuals exposed to stressful situations, has generated much interest, research and controversy since first proposed in 2003. Multiple meta-Analyses combining results from heterogeneous analyses have not settled the issue. To determine the magnitude of the interaction and the conditions under which it might be observed, we performed new analyses on 31 data sets containing 38 802 European ancestry subjects genotyped for 5-HTTLPR and assessed for depression and childhood maltreatment or other stressful life events, and meta-Analysed the results. Analyses targeted two stressors (narrow, broad) and two depression outcomes (current, lifetime). All groups that published on this topic prior to the initiation of our study and met the assessment and sample size criteria were invited to participate. Additional groups, identified by consortium members or self-identified in response to our protocol (published prior to the start of analysis) with qualifying unpublished data, were also invited to participate. A uniform data analysis script implementing the protocol was executed by each of the consortium members. Our findings do not support the interaction hypothesis. We found no subgroups or variable definitions for which an interaction between stress and 5-HTTLPR genotype was statistically significant. In contrast, our findings for the main effects of life stressors (strong risk factor) and 5-HTTLPR genotype (no impact on risk) are strikingly consistent across our contributing studies, the original study reporting the interaction and subsequent meta-Analyses. Our conclusion is that if an interaction exists in which the S allele of 5-HTTLPR increases risk of depression only in stressed individuals, then it is not broadly generalisable, but must be of modest effect size and only observable in limited situations. © 2018 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
- Published
- 2018
20. Repeat Irradiation for Children with Supratentorial High-Grade Glioma
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Oliveira, C., primary, Laperriere, N.J., additional, Bouffet, E., additional, Hawkins, C., additional, Ramaswamy, V., additional, Yee, R., additional, Bartels, U., additional, Tabori, U., additional, Huang, A., additional, Millar, B.A., additional, Crooks, B., additional, Bowes, L., additional, Zelcer, S., additional, and Derek, T., additional
- Published
- 2019
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21. Psychiatric disorders among adolescent cancer survivors: A systematic review
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Kosir, U, primary, Wiedemann, M, additional, Wild, J, additional, and Bowes, L, additional
- Published
- 2018
- Full Text
- View/download PDF
22. Refined cut-off for TP53 immunohistochemistry improves prediction of TP53mutation status in ovarian mucinous tumors: implications for outcome analyses
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Kang, Eun Young, Cheasley, Dane, LePage, Cecile, Wakefield, Matthew J., da Cunha Torres, Michelle, Rowley, Simone, Salazar, Carolina, Xing, Zhongyue, Allan, Prue, Bowtell, David D.L., Mes-Masson, Anne-Marie, Provencher, Diane M., Rahimi, Kurosh, Kelemen, Linda E., Fasching, Peter A., Doherty, Jennifer A., Goodman, Marc T., Goode, Ellen L., Deen, Suha, Pharoah, Paul D.P., Brenton, James D., Sieh, Weiva, Mateoiu, Constantina, Sundfeldt, Karin, Cook, Linda S., Le, Nhu D., Anglesio, Michael S., Gilks, C. Blake, Huntsman, David G., Kennedy, Catherine J., Traficante, Nadia, Bowtell, D., Chenevix-Trench, G., Green, A., Webb, P., DeFazio, A., Gertig, D., Traficante, N., Fereday, S., Moore, S., Hung, J., Harrap, K., Sadkowsky, T., Pandeya, N., Malt, M., Mellon, A., Robertson, R., Bergh, T. Vanden, Jones, M., Mackenzie, P., Maidens, J., Nattress, K., Chiew, Y.E., Stenlake, A., Sullivan, H., Alexander, B., Ashover, P., Brown, S., Corrish, T., Green, L., Jackman, L., Ferguson, K., Martin, K., Martyn, A., Ranieri, B., White, J., Jayde, V., Mamers, P., Bowes, L., Galletta, L., Giles, D., Hendley, J., Alsop, K., Schmidt, T., Shirley, H., Ball, C., Young, C., Viduka, S., Tran, Hoa, Bilic, Sanela, Glavinas, Lydia, Brooks, Julia, Stuart-Harris, R., Kirsten, F., Rutovitz, J., Clingan, P., Glasgow, A., Proietto, A., Braye, S., Otton, G., Shannon, J., Bonaventura, T., Stewart, J., Begbie, S., Friedlander, M., Bell, D., Baron-Hay, S., Ferrier, A., Gard, G., Nevell, D., Pavlakis, N., Valmadre, S., Young, B., Camaris, C., Crouch, R., Edwards, L., Hacker, N., Marsden, D., Robertson, G., Beale, P., Beith, J., Carter, J., Dalrymple, C., Houghton, R., Russell, P., Links, M., Grygiel, J., Hill, J., Brand, A., Byth, K., Jaworski, R., Harnett, P., Sharma, R., Wain, G., Ward, B., Papadimos, D., Crandon, A., Cummings, M., Horwood, K., Obermair, A., Perrin, L., Wyld, D., Nicklin, J., Davy, M., Oehler, M.K., Hall, C., Dodd, T., Healy, T., Pittman, K., Henderson, D., Miller, J., Pierdes, J., Blomfield, P., Challis, D., McIntosh, R., Parker, A., Brown, B., Rome, R., Allen, D., Grant, P., Hyde, S., Laurie, R., Robbie, M., Healy, D., Jobling, T., Manolitsas, T., McNealage, J., Rogers, P., Susil, B., Sumithran, E., Simpson, I., Phillips, K., Rischin, D., Fox, S., Johnson, D., Lade, S., Loughrey, M., O'Callaghan, N., Murray, W., Waring, P., Billson, V., Pyman, J., Neesham, D., Quinn, M., Underhill, C., Bell, R., Ng, L.F., Blum, R., Ganju, V., Hammond, I., Leung, Y., McCartney, A., Buck, M., Haviv, I., Purdie, D., Whiteman, D., Zeps, N., DeFazio, Anna, Kaufmann, Scott, Churchman, Michael, Gourley, Charlie, Stephens, Andrew N., Meagher, Nicola S., Ramus, Susan J., Antill, Yoland C., Campbell, Ian, Scott, Clare L., Köbel, Martin, Gorringe, Kylie L., Cheasley, Dane, Wakefield, Matthew J., Ryland, Georgina L., Allan, Prue E., Alsop, Kathryn, Ananda, Sumitra, Anglesio, Michael S., Au-Yeung, George, Böhm, Maret, Bowtell, David D.L., Brand, Alison, Chenevix-Trench, Georgia, Christie, Michael, Chiew, Yoke-Eng, Churchman, Michael, DeFazio, Anna, Dudley, Rhiannon, Fairweather, Nicole, Fereday, Sian, Fox, Stephen B., Gilks, C. Blake, Gourley, Charlie, Hacker, Neville F., Hadley, Alison M., Hendley, Joy, Ho, Gwo-Yaw, Huntsman, David G., Hunter, Sally M., Jobling, Tom W., Kalli, Kimberly R., Kaufmann, Scott H., Kennedy, Catherine J., Köbel, Martin, Le Page, Cecile, McNally, Orla M., McAlpine, Jessica N., Mes-Masson, Anne-Marie, Mileshkin, Linda, Provencher, Diane M., Pyman, Jan, Rahimi, Kurosh, Samimi, Goli, Sharma, Ragwha, Stephens, Andrew N., Traficante, Nadia, Antill, Yoland C., Scott, Clare L., Campbell, Ian G., and Gorringe, Kylie L.
- Abstract
TP53mutations are implicated in the progression of mucinous borderline tumors (MBOT) to mucinous ovarian carcinomas (MOC). Optimized immunohistochemistry (IHC) for TP53 has been established as a proxy for the TP53mutation status in other ovarian tumor types. We aimed to confirm the ability of TP53 IHC to predict TP53mutation status in ovarian mucinous tumors and to evaluate the association of TP53mutation status with survival among patients with MBOT and MOC. Tumor tissue from an initial cohort of 113 women with MBOT/MOC was stained with optimized IHC for TP53 using tissue microarrays (75.2%) or full sections (24.8%) and interpreted using established criteria as normal or abnormal (overexpression, complete absence, or cytoplasmic). Cases were considered concordant if abnormal IHC staining predicted deleterious TP53mutations. Discordant tissue microarray cases were re-evaluated on full sections and interpretational criteria were refined. The initial cohort was expanded to a total of 165 MBOT and 424 MOC for the examination of the association of survival with TP53mutation status, assessed either by TP53 IHC and/or sequencing. Initially, 82/113 (72.6%) cases were concordant using the established criteria. Refined criteria for overexpression to account for intratumoral heterogeneity and terminal differentiation improved concordance to 93.8% (106/113). In the expanded cohort, 19.4% (32/165) of MBOT showed evidence for TP53mutation and this was associated with a higher risk of recurrence, disease-specific death, and all-cause mortality (overall survival: HR = 4.6, 95% CI 1.5–14.3, p= 0.0087). Within MOC, 61.1% (259/424) harbored a TP53mutation, but this was not associated with survival (overall survival, p= 0.77). TP53 IHC is an accurate proxy for TP53mutation status with refined interpretation criteria accounting for intratumoral heterogeneity and terminal differentiation in ovarian mucinous tumors. TP53mutation status is an important biomarker to identify MBOT with a higher risk of mortality.
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- 2021
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23. Self-help cancer group gives hope
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Fortune, Christopher J. and Bowes, L. Jane
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- 1986
24. Modifiable predictors of depression following childhood maltreatment: a systematic review and meta-analysis
- Author
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Braithwaite, E C, primary, O'Connor, R M, additional, Degli-Esposti, M, additional, Luke, N, additional, and Bowes, L, additional
- Published
- 2017
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25. Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression
- Author
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Culverhouse, R C, primary, Saccone, N L, additional, Horton, A C, additional, Ma, Y, additional, Anstey, K J, additional, Banaschewski, T, additional, Burmeister, M, additional, Cohen-Woods, S, additional, Etain, B, additional, Fisher, H L, additional, Goldman, N, additional, Guillaume, S, additional, Horwood, J, additional, Juhasz, G, additional, Lester, K J, additional, Mandelli, L, additional, Middeldorp, C M, additional, Olié, E, additional, Villafuerte, S, additional, Air, T M, additional, Araya, R, additional, Bowes, L, additional, Burns, R, additional, Byrne, E M, additional, Coffey, C, additional, Coventry, W L, additional, Gawronski, K A B, additional, Glei, D, additional, Hatzimanolis, A, additional, Hottenga, J-J, additional, Jaussent, I, additional, Jawahar, C, additional, Jennen-Steinmetz, C, additional, Kramer, J R, additional, Lajnef, M, additional, Little, K, additional, zu Schwabedissen, H M, additional, Nauck, M, additional, Nederhof, E, additional, Petschner, P, additional, Peyrot, W J, additional, Schwahn, C, additional, Sinnamon, G, additional, Stacey, D, additional, Tian, Y, additional, Toben, C, additional, Van der Auwera, S, additional, Wainwright, N, additional, Wang, J-C, additional, Willemsen, G, additional, Anderson, I M, additional, Arolt, V, additional, Åslund, C, additional, Bagdy, G, additional, Baune, B T, additional, Bellivier, F, additional, Boomsma, D I, additional, Courtet, P, additional, Dannlowski, U, additional, de Geus, E J C, additional, Deakin, J F W, additional, Easteal, S, additional, Eley, T, additional, Fergusson, D M, additional, Goate, A M, additional, Gonda, X, additional, Grabe, H J, additional, Holzman, C, additional, Johnson, E O, additional, Kennedy, M, additional, Laucht, M, additional, Martin, N G, additional, Munafò, M R, additional, Nilsson, K W, additional, Oldehinkel, A J, additional, Olsson, C A, additional, Ormel, J, additional, Otte, C, additional, Patton, G C, additional, Penninx, B W J H, additional, Ritchie, K, additional, Sarchiapone, M, additional, Scheid, J M, additional, Serretti, A, additional, Smit, J H, additional, Stefanis, N C, additional, Surtees, P G, additional, Völzke, H, additional, Weinstein, M, additional, Whooley, M, additional, Nurnberger Jr, J I, additional, Breslau, N, additional, and Bierut, L J, additional
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- 2017
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26. Peer victimisation during adolescence and its impact on depression in early adulthood: prospective cohort study in the United Kingdom
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Bowes, L., primary, Joinson, C., additional, Wolke, D., additional, and Lewis, G., additional
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- 2015
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27. Second Bacteremia During Antibiotic Treatment in Children With Acute Myeloid Leukemia: A Report From the Canadian Infections in Acute Myeloid Leukemia Research Group
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Tran, T. H., primary, Yanofsky, R., additional, Johnston, D. L., additional, Dix, D., additional, Gillmeister, B., additional, Ethier, M.-C., additional, Portwine, C., additional, Price, V., additional, Mitchell, D., additional, Cellot, S., additional, Lewis, V., additional, Zelcer, S., additional, Silva, M., additional, Michon, B., additional, Bowes, L., additional, Stobart, K., additional, Brossard, J., additional, Beyene, J., additional, and Sung, L., additional
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- 2014
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28. Situation sociale et consommation de produits psychoactifs (tabac, alcool, cannabis et autres drogues illégales) chez les jeunes adultes
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Melchior, M., primary, Chollet, A., additional, Fombonne, E., additional, Bowes, L., additional, and Redonnet, B., additional
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- 2013
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29. Consommations de tabac, d’alcool et de cannabis chez les jeunes adultes : le contexte socioéconomique
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Melchior, M., primary, Chollet, A., additional, Fombonne, E., additional, Bowes, L., additional, and Redonnet, B., additional
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- 2012
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30. Lifecourse SEP and tobacco and cannabis use
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Bowes, L., primary, Chollet, A., additional, Fombonne, E., additional, Galera, C., additional, and Melchior, M., additional
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- 2012
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31. Introducing care pathway commissioning to primary dental care: measuring performance
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Harris, R., primary, Bridgman, C., additional, Ahmad, M., additional, Bowes, L., additional, Haley, R., additional, Saleem, S., additional, Singh, R., additional, and Taylor, S., additional
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- 2011
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32. High rates of consistency in bullying reports from mothers and children
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Shakoor, S., primary, Jaffee, S. R., additional, Andreou, P., additional, Bowes, L., additional, Ambler, A. P., additional, Caspi, A., additional, and Arseneault, L., additional
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- 2011
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33. Bullying victimization in youths and mental health problems: ‘Much ado about nothing’?
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Arseneault, L., primary, Bowes, L., additional, and Shakoor, S., additional
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- 2009
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34. Culture of marmoset blastocysts on matrigel: A model of differentiation during the implantation period
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Lopata, Alex, primary, Kohlman, D. J., additional, Bowes, L. G., additional, and Watkins, W. B., additional
- Published
- 1995
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35. Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case–control studies.
- Author
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Munafò, M. R., Bowes, L., Clark, T. G., and Flint, J.
- Subjects
- *
GENETICS of schizophrenia , *GENES , *METHYLTRANSFERASES , *META-analysis , *REGRESSION analysis , *PSYCHOSES - Abstract
There is strong evidence for a genetic contribution to schizophrenia, but the contribution of individual candidate genes remains uncertain. We attempted to replicate a recent meta-analysis that reported an association of the catechol O-methyltransferase (COMT) Val allele with schizophrenia, and suggested that this effect may be moderated by ancestry. We included reports published subsequent to the original meta-analysis, and included a formal test of the moderating effect of ancestry in order to test whether the association operates differently in populations of European ancestry compared to populations of Asian ancestry. A corrected P-value for the 5% significance threshold was employed where appropriate, using Bonferroni's method, and studies that demonstrated departure from Hardy–Weinberg equilibrium among controls were excluded. When all studies were included in a meta-regression, there was evidence for a significant association of COMT Val allele frequency with schizophrenia case status and a significant main effect of ancestry. The interaction of COMT Val allele frequency and ancestry was also significant. However, when only studies that reported allele frequencies that did not depart significantly from Hardy–Weinberg equilibrium among controls were included, these effects were no longer significant. The results of our meta-analysis do not support an association between the COMT Val allele and schizophrenia case status, and do not support recent claims that this association may be moderated by ancestry.Molecular Psychiatry (2005) 10, 765–770. doi:10.1038/sj.mp.4001664; published online 12 April 2005 [ABSTRACT FROM AUTHOR]
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- 2005
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36. Improving teacher preparation and selection: lessons from the Pennsylvania experience
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Strauss, R. P., Bowes, L. R., Marks, M. S., and Plesko, M. R.
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- 2000
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37. Cognitive styles and future depressed mood in early adulthood: The importance of global attributions
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Pearson, R.M., Heron, J., Button, K., Bentall, R.P., Fernyhough, C., Mahedy, L., Bowes, L., and Lewis, G.
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Questionnaires ,Research Report ,Adult ,Male ,Adolescent ,Global attribution ,Cohort Studies ,Young Adult ,Cognition ,Predictive Value of Tests ,Surveys and Questionnaires ,Humans ,Longitudinal Studies ,Prospective Studies ,Cognitive styles ,Psychiatric Status Rating Scales ,Depressive Disorder ,Depression ,ALSPAC ,Self Concept ,Clinical Psychology ,Psychiatry and Mental health ,Affect ,England ,Female ,Latent traits ,Follow-Up Studies - Abstract
BACKGROUND: Cognitive theories of depression suggest that beliefs of low self-worth and the tendency to attribute negative events to causes that are global (widespread rather than specific) and stable (will persist rather than change in the future) are associated with the development of depressed mood. Such theories are supported by evidence from prospective studies and have guided the development of successful treatment and prevention strategies such as CBT. However, the relative importance of different psychological constructs within cognitive theories is unknown. This is important to refine cognitive theories and develop more efficient prevention strategies.METHOD: We used prospective data from over 3500 young adults from the Avon Longitudinal Study for Parents and Children (ALSPAC) cohort in the UK to investigate the association between cognitive style, measured by short forms of the Dysfunctional Attitudes Scale (DAS) and Cognitive Styles Questionnaire-Short Form (CSQ-SF) at age 18, and future depressed mood at age 19. Structural equation modelling techniques were used to separate cognitive style constructs.RESULTS: Cognitive styles were associated with future depressed mood, independently of baseline mood, both as measured by the DAS-SF and the CSQ-SF. Of the different CSQ-SF constructs, only global attributions were associated with both baseline and future mood independently of other constructs.LIMITATIONS: The study was subject to attrition and the follow-up was relatively short (10 months).CONCLUSION: The findings suggest that the tendency to attribute negative events specifically to global causes could be particularly important for depression. Reducing global attributions is potentially important in the prevention and treatment of depression.
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38. Discussion: “Relation of Efficiency to Capacity in the Boiler Room” (Phillips, Victor B., 1917, Trans. ASME, 39, pp. 67–87)
- Author
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Kent, William, Bowes, L. C., Goss, W. F. M., Spitzglass, J. M., Carpenter, R. C., Alpern, M., Barrus, George H., Bannister, Bryant, Reinicker, N. G., Hirshfeld, C. F., and Phillips, Victor B.
- Published
- 1917
- Full Text
- View/download PDF
39. Targeted training using a paediatric tracheostomy emergency algorithm improves performance in simulated scenarios
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Atkinson, D., Iain Bruce, Perkins, R., Neal, R., Bateman, N., Wyatt, M., Bowes, L., and Brendan McGrath
40. Do men and women differ in response to nicotine replacement therapy: A meta-analysis
- Author
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Marcus Munafo, Bradburn, M., Bowes, L., David, S., and Murphy, Mfg
41. PROLONGATION OF RABBIT SKIN ALLOGRAFT SURVIVAL BY DONOR BLOOD AND STEROID ADMINISTERED BEFORE TRANSPLANTATION
- Author
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KING, H. P., primary, CLUNIE, G. J. A., additional, BOWES, L. G., additional, and DUMBLE, L. J., additional
- Published
- 1982
- Full Text
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42. PERSISTENT HYALOID ARTERY
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BOWES, L. M., primary
- Published
- 1913
- Full Text
- View/download PDF
43. Researching Resilience.
- Author
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Bowes L
- Published
- 2010
- Full Text
- View/download PDF
44. The Way We Were: 1938.
- Author
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Bowes, L. M.
- Subjects
DOGS ,DOMESTIC animals ,PERIODICALS ,SERIAL publications ,ANIMALS - Abstract
Looks at the June 1938 issue of "Dog World" magazine. Tips on raising dogs.
- Published
- 2005
45. Social networks in transition: investigating relationship developments & their impact during the transition to university
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Kempnich, MEJ, Dunbar, R, Wölfer, R, Hewstone, M, and Bowes, L
- Abstract
Supportive relationships are key to a healthy, long, and fulfilled life (Umberson & Karas Montez, 2010). While much is known about the general structure of our personal relationships (i.e., ego networks; Sutcliffe et al., 2012) and self-bounded communities (i.e., complete or cohort networks; Zhou et al., 2005), we still know relatively little about how these social networks adapt to critical life events, such as the transition of entering university (Wrzus et al., 2013). This thesis investigates the effects of this first major transition on young adults’ personal relationships, social integration, and mental health. In Chapter 1, I introduce the theoretical and empirical background underlying my research and present my unique prospective, longitudinal social network design in which students of two consecutive cohorts at a College of Oxford University participated (five assessments, across 2.5 years in Study 1, N = 90; and seven, across 1.5 years in Study 2, N = 81). In Chapter 2, I examine how these students manage their personal relationships and find that ego networks are overall remarkably robust and grow uniformly within just the first two months at university. In Chapter 3, I investigate how students socially integrate into their new social environment and find that cohort networks driven by homophily factors form rapidly and stabilise just as quickly. In Chapter 4, I study the mental health trajectories of these young adults and find uncommonly high levels of anxiety and depression that temporarily or gradually worsen during the transition. Finally, in Chapter 5, I discuss the main findings and outline their theoretical, methodological, and practical implications. Overall, this thesis shows that the impact of the transition to university on students’ social relationships and mental health occurs rapidly. Future research might focus on the first few weeks of this transition in more detail and differentiate students’ individual experiences further.
- Published
- 2023
46. Cognitive factors in adjustment after social trauma
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Graham, B, Ehlers, A, and Bowes, L
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Clinical psychology - Abstract
This project uses mixed methods to investigate cognitive and behavioural factors associated with social anxiety disorder (SAD) and posttraumatic stress disorder (PTSD) symptoms among young people who have been bullied. The aim is to explore the social trauma of bullying, investigate factors that increase vulnerability to ongoing emotional distress, and develop bespoke measures that are clinically useful and statistically robust. Following a general introduction in Chapter 1, this thesis is structured into two main sections. In the first section, I present four studies exploring and evaluating factors associated with adjustment after bullying. In Chapter 2, longitudinal analysis of a large prospective cohort study shows that children who were severely bullied and have an external locus of control are more likely to experience a steeper increase in social fear during early adolescence compared to those with an internal locus of control. The following chapters describe development and validation of measures of bullying-related cognitions and coping strategies associated with PTSD and social anxiety among young adults. Chapter 3 reports pilot data on cognitive themes related to bullying that are associated with SAD and PTSD symptoms and suggests the online survey format is acceptable. In Chapter 4, qualitative analyses of semi-structured interviews with young adults about their experiences of bullying and their past and ongoing reactions suggest additional themes that may be associated with higher ongoing symptoms. Chapter 5, the last in this section, draws these findings together and describes statistical evaluation of new measures of cognitions and behaviours related to bullying which were derived from the previous studies. Data is from an online survey study with over a thousand young people starting university or college in the UK. The newly developed measures were reliable and valid, defined as the Bullied Cognitions Inventory, Bullied Social Attitudes Inventory, and the Bullied Social Behaviours Scale. In the second section, associations of the new cognitive and behavioural measures with SAD and PTSD are tested. Chapter 6 reports the extent to which these measures distinguish between SAD, PTSD, or no likely clinical diagnosis in the online survey data. Participants in this study were invited to complete three additional surveys during their first year of university and, in Chapter 7, longitudinal analyses are reported that explore changes in PTSD and SAD symptoms and the extent to which the new measures can predict differing outcomes. Together, these studies highlight the social trauma of bullying and identify cognitive and behavioural factors associated with SAD and PTSD symptoms among young adults who have been bullied. Psychometrically validated scales suggest themes that distinguish between symptoms as well as transdiagnostic features. Results and limitations are discussed, as well as suggestions for clinical application and future research.
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- 2023
47. The role of ingroup contact in intergroup contact theory
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Bracegirdle, CA, Hewstone, M, Wölfer, R, Reimer, N, Fell, B, and Bowes, L
- Subjects
psychology - Abstract
A wealth of research examining intergroup contact theory (Allport, 1954; Brown & Hewstone, 2005) has shown that outgroup contact improves outgroup attitudes. Few studies have examined the corresponding role of ingroup contact, despite its prevalence and evidence suggesting it may detrimentally affect intergroup relations (e.g., Levin et al., 2003; Wilder & Thompson, 1980), or the corresponding effects on ingroup attitudes. This thesis addresses these lacunae by investigating the ways in which ingroup contact, in addition to outgroup contact, shapes both ingroup and outgroup attitudes. In so doing, this thesis aims to achieve a more comprehensive understanding of how contact influences intergroup relations through the incorporation of ingroup contact in intergroup contact theory. Chapter 1 details the theoretical and empirical rationale that underpins this thesis, introduces the 10 studies (total N = 34,944) comprising this thesis, and outlines the analysis techniques used to test the proposed hypotheses (i.e., latent growth modelling, meta-analysis, random-intercept cross lagged panel modelling, and longitudinal social network analysis). Chapter 2 examines the relationship between ingroup and outgroup contact and finds that, at least for friendships, more ingroup contact is associated with less outgroup contact, and vice versa. Chapter 3 investigates the effects of contact on attitudes and identifies positive between-person associations for ingroup contact and ingroup attitudes, and for outgroup contact and outgroup attitudes, yet obtains little evidence for the corresponding within-person effects. Chapter 4 explores the socialisation of ingroup and outgroup attitudes and reports that individuals’ attitudes are influenced by the attitudes held by their ingroup, but not their outgroup, friends. Finally, Chapter 5 discusses the research presented in this thesis and outlines its theoretical, methodological and practical implications. Overall, this thesis shows that ingroup contact has an important role in shaping both ingroup and outgroup attitudes, which highlights the imperative need for further research in this nascent area of study.
- Published
- 2022
48. Adolescent social anxiety: testing aspects of the cognitive model and developing an internet version of cognitive therapy
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Leigh, E, Clark, D, and Bowes, L
- Subjects
Clinical child psychology - Abstract
Social anxiety disorder is a common anxiety disorder that can markedly interfere with life and is particularly persistent in the absence of treatment. Outcomes for the treatment of adults with social anxiety disorder have improved considerably in the last twenty years, particularly due to the development of psychological therapies designed to target specific cognitive and behavioural processes that maintain the disorder. Internet versions of the therapies that have been developed also hold the promise of being able to greatly increase the availability of effective therapy in adults. The overarching aim of the thesis is to improve our understanding of the cognitive and behavioural maintenance mechanisms of adolescent social anxiety and to develop an effective and scalable intervention for the disorder in youth. My first study is a systematic review of empirical research examining the Clark & Wells (1995) cognitive model of social anxiety in adolescents. My second and third studies adopt experimental methods to test key hypotheses of the model in adolescents. The fourth and fifth studies are concerned with improving measurement of social anxiety symptoms and related cognitions to aid research and clinical activities. The sixth and final study is a randomised waitlist-controlled trial of internet-delivered cognitive therapy for social anxiety disorder in adolescents. Adopting a strategy of closely interweaving clinical and experimental studies, the thesis provides support for: (1) the applicability of the cognitive model of Clark & Wells (1995) to adolescents; (2) self-report measures of social anxiety symptoms and related cognitions; and (3) internet-delivered cognitive therapy for the treatment of adolescent social anxiety disorder.
- Published
- 2022
49. Drivers of student satisfaction and student outcomes in K-12 online learning environments
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Beaton, J, Bowes, L, and Kemp, P
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Education - Abstract
My thesis examines what drives student outcomes and student satisfaction in online schooling. Specifically, I examine whether psychometric matching between students and tutors can be used to enhance outcomes or satisfaction and in light of this, the key considerations for governments seeking to regulate the online schooling landscape. Two systematic literature reviews are conducted: firstly, what drives student outcomes and student satisfaction in online schooling and secondly (Chapter Two), the use of algorithmic matching between students and educators in schooling to improve student outcomes and/or student satisfaction (Chapter Three). I perform a qualitative analysis of leading virtual high schools, interviewing 21 students using NVivo qualitative analysis software (Chapter Four). I conduct cross-sectional analysis on a data-set from Crimson Education, an online education company, to evaluate the impact of psychometric characteristics on student satisfaction (Chapter Five). I run a randomized control trial to test the causality of a psychometric matching algorithm on student outcomes and student satisfaction (Chapter Six). My randomized control trial analysis finds that psychometric matching can lead to significant impact on writing scores and on student satisfaction within Western Europe and Latin America. My cross-sectional analysis also finds that student satisfaction scores can be impacted by the psychometric characteristics of students. Finally, I provide a set of recommendations for public policy makers looking to adapt legislation to the emerging online high schooling sector in light of my findings from earlier chapters, in particular my qualitative analysis and systematic reviews (Chapter Seven).
- Published
- 2022
50. Exploring art as a means for communication and connection: From technology-enhanced art experiences to the Paradox of Sad Art
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Venkatesan, T, Dunbar, R, Cross, I, Knobe, J, Wang, QJ, Bowes, L, and Hadi, R
- Subjects
Psychology and art ,Psychology of technology - Abstract
Art is a powerful form of communication between artists and audiences. In this thesis, I will explore two questions that emerge from the literature on art as a means of communication and connection between artist and audience: 1) how can technology be used to augment the sense of psychological connection between the audience and artist? and 2) why do we like sad art? To answer the first question, Chapters 2 and 3 present experimental data showing that listening to music while wearing haptic devices (versus no haptics) and headphones (versus speakers) increases empathy, parasocial bond, and loyalty towards the artist and also decreases feelings of loneliness in the listener. Results indicate that feelings of social presence mediate the relationship between these immersive technologies and these measures of psychological connection to the artist. To answer the second question, Chapter 4 presents data from five experiments. Studies 1 and 2 show that framing a text as art versus not-art increases liking for the negative emotions expressed in it. Study 3 showed that there was an effect of art/not-art on liking even after controlling for differences in perceived fictionality between art/not-art. Study 4 found that appropriation mediates the effect of art/not-art on liking and, thus, explains liking for sad art. Study 5 controlled for a possible confound in the study design and found that the results replicated. Together, this thesis explores art as a means of communication and connection by providing new insights on the use of technology to enhance connection with artists and by finding empirical evidence to support the philosophical debate on the enjoyment of sad art. These studies shed light on the ways in which art can be used to connect with others and also connect with ourselves and our own emotions.
- Published
- 2021
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