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1دورية أكاديمية
المؤلفون: Yongwen Zhuang, Na Yeon Kim, Lars G. Fritsche, Bhramar Mukherjee, Seunggeun Lee
المصدر: BMC Bioinformatics, Vol 25, Iss 1, Pp 1-19 (2024)
مصطلحات موضوعية: PRSbils, Polygenic risk score, Functional annotation, KEGG pathway, Biobank data, Continuous shrinkage, Computer applications to medicine. Medical informatics, R858-859.7, Biology (General), QH301-705.5
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1471-2105Test
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2دورية أكاديمية
المؤلفون: Yongwen Zhuang, Na Yeon Kim, Lars G. Fritsche, Bhramar Mukherjee, Seunggeun Lee
مصطلحات موضوعية: Genetics, PRSbils, Polygenic risk score, Functional annotation, KEGG pathway, Biobank data, Continuous shrinkage
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المؤلفون: Yongwen Zhuang, Brooke N Wolford, Kisung Nam, Wenjian Bi, Wei Zhou, Cristen J Willer, Bhramar Mukherjee, Seunggeun Lee
المصدر: Bioinformatics. 38:4337-4343
مصطلحات موضوعية: Statistics and Probability, Computational Mathematics, Phenotype, Computational Theory and Mathematics, Case-Control Studies, Computer Simulation, Polymorphism, Single Nucleotide, Molecular Biology, Biochemistry, Genome-Wide Association Study, Computer Science Applications
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c19e2c0bf9fca27a251efd5aaea9dc3Test
https://doi.org/10.1093/bioinformatics/btac459Test -
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المؤلفون: Arianna DiFlorio, Patrick F. Sullivan, Sebastian Zöllner, Margarita Rivera, Richard M. Myers, Stanley J. Watson, Jun Li, Anders Juréus, Sarah E. Bergen, Gonçalo R. Abecasis, Jordan W. Smoller, Michael Conlon O'Donovan, Neil Risch, Hoang T. Nguyen, Chen Jiang, Xiaoming Jia, Mehdi Pirooznia, Danielle Posthuma, Adam E. Locke, Peter P. Zandi, John B. Vincent, Niamh Mullins, Duncan Palmer, Shaun Purcell, Gerome Breen, Christina M. Hultman, Andreas Reif, Khanh K. Thai, Virginia L. Willour, Pui-Yan Kwok, Laura J. Scott, Anne U. Jackson, Michael John Owen, Fernando S. Goes, Steven A. McCarroll, James B. Potash, Mikael Landén, Jennifer L. Moran, Michele T. Pato, Hyun Min Kang, Marco P. Boks, Sinéad B. Chapman, W. Richard McCombie, Janet L. Sobell, Matthew Zawistowski, Rolf Adolfsson, Yongwen Zhuang, Michael Boehnke, René S. Kahn, Huda Akil, James T.R. Walters, Margit Burmeister, Douglas Blackwood, Cathryn M. Lewis, Eli A. Stahl, Mark N. Kvale, Melissa DelaBastide, Catherine Schaefer, Benjamin M. Neale, Giulio Genovese, Carlos N. Pato, Nicholas John Craddock, Andrew McQuillin, Shawn Levy, Aiden Corvin, Pamela Sklar, Weiqing Wang, Andrew M. McIntosh, Ling Shen, Eric T. Monson, Derek W. Morris, Douglas M. Ruderfer, Roel A. Ophoff, Peter McGuffin, Sarah Cohen-Woods, Willem H. Ouwehand
المساهمون: Complex Trait Genetics, Amsterdam Neuroscience - Complex Trait Genetics, Goes, Fernando S [0000-0001-6262-8264], Locke, Adam E [0000-0001-6227-198X], Palmer, Duncan [0000-0002-0824-0047], Wang, Weiqing [0000-0003-1565-0148], Genovese, Giulio [0000-0003-3066-5575], Jackson, Anne U [0000-0002-9672-2547], Nguyen, Hoang [0000-0001-6910-7269], Pirooznia, Mehdi [0000-0002-4210-6458], Zawistowski, Matthew [0000-0002-3005-083X], Abecasis, Gonçalo [0000-0003-1509-1825], Bergen, Sarah [0000-0002-5888-0034], Burmeister, Margit [0000-0002-1914-2434], Kwok, Pui-Yan [0000-0002-5087-3059], Li, Jun Z [0000-0001-6727-0812], Levy, Shawn E [0000-0002-1369-5740], Watson, Stanley [0000-0003-4980-5523], Blackwood, Douglas [0000-0002-4076-9346], Boehnke, Michael [0000-0002-6442-7754], Breen, Gerome [0000-0003-2053-1792], Landen, Mikael [0000-0002-4496-6451], Lewis, Cathryn [0000-0002-8249-8476], McCarroll, Steven A [0000-0002-6954-8184], McIntosh, Andrew [0000-0002-0198-4588], McQuillin, Andrew [0000-0003-1567-2240], Morris, Derek [0000-0002-3413-570X], O'Donovan, Michael [0000-0001-7073-2379], Boks, Marco [0000-0001-6163-7484], Kahn, Rene [0000-0001-5909-8004], Ouwehand, Willem [0000-0002-7744-1790], Owen, Michael [0000-0003-4798-0862], Potash, James B [0000-0002-5802-8079], Reif, Andreas [0000-0002-0992-634X], Vincent, John [0000-0003-0692-2519], Neale, Benjamin [0000-0003-1513-6077], Purcell, Shaun [0000-0002-7402-5812], Schaefer, Catherine [0000-0003-2644-055X], Stahl, Eli A [0000-0002-1192-0561], Zandi, Peter P [0000-0001-8423-2623], Scott, Laura J [0000-0002-4886-5084], Apollo - University of Cambridge Repository, Human genetics, Amsterdam Neuroscience - Compulsivity, Impulsivity & Attention, Amsterdam Reproduction & Development (AR&D), Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Digital Health
المصدر: Molecular Psychiatry, 26(9), 5239-5250. Nature Publishing Group
Molecular psychiatry, vol 26, iss 9
Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-Woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Chapman, S, DelaBastide, M, Juréus, A, Kang, H M, Kwok, P Y, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, DiFlorio, A, Hultman, C M, Landen, M, Lewis, C, McCarroll, S A, Richard McCombie, W, McGuffin, P, McIntosh, A, McQuillin, A, Morris, D, Myers, R M, O’Donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry, vol. 26, no. 9, pp. 5239-5250 . https://doi.org/10.1038/s41380-020-01006-9Test
Molecular Psychiatry
Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-Woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Champion, S, DelaBastide, M, Juréus, A, Kang, H M, Kwok, P-Y, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, DiFlorio, A, Hultman, C M, Landen, M, Lewis, C, McCarroll, S A, Richard McCombie, W, McGuffin, P, McIntosh, A, McQuillin, A, Morris, D, Myers, R M, O’Donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry, vol. 26, no. 9, pp. 5239-5250 . https://doi.org/10.1038/s41380-020-01006-9Test
Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Chapman, S, Delabastide, M, Juréus, A, Kang, H M, Kwok, P, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, Diflorio, A, Hultman, C M, Landen, M, Lewis, C, Mccarroll, S A, Richard Mccombie, W, Mcguffin, P, Mcintosh, A, Mcquillin, A, Morris, D, Myers, R M, O’donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry . https://doi.org/10.1038/s41380-020-01006-9Test
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Digibug: Repositorio Institucional de la Universidad de Granada
Universidad de Granada (UGR)مصطلحات موضوعية: Bipolar Disorder, Genome-wide association study, Biology, Medical and Health Sciences, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Clinical Research, Genetic variation, medicine, Genetics, 2.1 Biological and endogenous factors, Humans, Exome, Genetic Predisposition to Disease, Bipolar disorder, Polymorphism, Molecular Biology, Gene, 030304 developmental biology, Medicinsk genetik, Psychiatry, 0303 health sciences, Prevention, Human Genome, Psychology and Cognitive Sciences, Genetic Variation, Single Nucleotide, Heritability, Biological Sciences, medicine.disease, Serious Mental Illness, Phenotype, 3. Good health, Brain Disorders, Psychiatry and Mental health, Mental Health, Schizophrenia, Medical Genetics, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf; application/zip; text/xml
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2b28270dff0616afd7d691245b0f9b8Test
https://research.vu.nl/en/publications/5db60cd7-dd49-4271-b724-a8cb3ceb8d2cTest -
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المؤلفون: Wei Zhou, Kisung Nam, Seunggeun Lee, Wenjian Bi, Bhramar Mukherjee, Yongwen Zhuang, Cristen J. Willer, Brooke N. Wolford
مصطلحات موضوعية: Mixed model, education.field_of_study, medicine.medical_specialty, Calibration (statistics), Population, Biology, Biobank, Correlation, Statistics, Epidemiology, medicine, education, Genetic association, Type I and type II errors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::53360dcfeac4c139733ad28637dfe31cTest
https://doi.org/10.1101/2021.07.04.21259997Test