PRSice-2: Polygenic Risk Score software for biobank-scale data

por Choi, Shing Wan, O'Reilly, Paul F
Publicado 2019

EraSOR: a software tool to eliminate inflation caused by sample overlap in polygenic score analyses

por Choi, Shing Wan, Mak, Timothy Shin Heng, Hoggart, Clive J, O'Reilly, Paul F
Publicado 2023

Association of Polygenic Risk for Attention-Deficit/Hyperactivity Disorder With Co-occurring Traits and Disorders

por Du Rietz, Ebba, Coleman, Jonathan, Glanville, Kylie, Choi, Shing Wan, O’Reilly, Paul F., Kuntsi, Jonna
Publicado 2018

Genetic sensitivity analysis: Adjusting for genetic confounding in epidemiological associations

por Pingault, Jean-Baptiste, Rijsdijk, Frühling, Schoeler, Tabea, Choi, Shing Wan, Selzam, Saskia, Krapohl, Eva, O’Reilly, Paul F., Dudbridge, Frank
Publicado 2021

PRSet: Pathway-based polygenic risk score analyses and software

por Choi, Shing Wan, García-González, Judit, Ruan, Yunfeng, Wu, Hei Man, Porras, Christian, Johnson, Jessica, Hoggart, Clive J., O’Reilly, Paul F.
Publicado 2023

Disentangling Independent and Mediated Causal Relationships Between Blood Metabolites, Cognitive Factors, and Alzheimer’s Disease

por Lord, Jodie, Green, Rebecca, Choi, Shing Wan, Hübel, Christopher, Aarsland, Dag, Velayudhan, Latha, Sham, Pak, Legido-Quigley, Cristina, Richards, Marcus, Dobson, Richard, Proitsi, Petroula
Publicado 2021

Studying individual risk factors for self-harm in the UK Biobank: A polygenic scoring and Mendelian randomisation study

por Lim, Kai Xiang, Rijsdijk, Frühling, Hagenaars, Saskia P., Socrates, Adam, Choi, Shing Wan, Coleman, Jonathan R. I., Glanville, Kylie P., Lewis, Cathryn M., Pingault, Jean-Baptiste
Publicado 2020

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

por Saez-Atienzar, Sara, Bandres-Ciga, Sara, Langston, Rebekah G., Kim, Jonggeol J., Choi, Shing Wan, Reynolds, Regina H., Abramzon, Yevgeniya, Dewan, Ramita, Ahmed, Sarah, Landers, John E., Chia, Ruth, Ryten, Mina, Cookson, Mark R., Nalls, Michael A., Chiò, Adriano, Traynor, Bryan J.
Publicado 2021

Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease

por Hoggart, Clive, Shimizu, Chisato, Galassini, Rachel, Wright, Victoria J., Shailes, Hannah, Bellos, Evan, Herberg, Jethro A., Pollard, Andrew J., O’Connor, Daniel, Choi, Shing Wan, Seaby, Eleanor G., Menikou, Stephanie, Hibberd, Martin, Sallah, Neneh, Burgner, David, Brogan, Paul, Patel, Harsita, Kim, Jihoon, Tremoulet, Adriana H., Salo, Eeva, van Stijn, Diana, Kuijpers, Taco, Burns, Jane C., Levin, Michael
Publicado 2021

Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

por Coleman, Jonathan R.I., Peyrot, Wouter J., Purves, Kirstin L., Davis, Katrina A.S., Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A., Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M., Choi, Karmel W., Dunn, Erin C., Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J., Lewis, Cathryn M., O’Reilly, Paul F., McIntosh, Andrew M., Smith, Daniel J., Wray, Naomi R., Hotopf, Matthew, Eley, Thalia C., Breen, Gerome
Publicado 2020

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

por Wang, Zhe, Choi, Shing Wan, Chami, Nathalie, Boerwinkle, Eric, Fornage, Myriam, Redline, Susan, Bis, Joshua C., Brody, Jennifer A., Psaty, Bruce M., Kim, Wonji, McDonald, Merry-Lynn N., Regan, Elizabeth A., Silverman, Edwin K., Liu, Ching-Ti, Vasan, Ramachandran S., Kalyani, Rita R., Mathias, Rasika A., Yanek, Lisa R., Arnett, Donna K., Justice, Anne E., North, Kari E., Kaplan, Robert, Heckbert, Susan R., de Andrade, Mariza, Guo, Xiuqing, Lange, Leslie A., Rich, Stephen S., Rotter, Jerome I., Ellinor, Patrick T., Lubitz, Steven A., Blangero, John, Shoemaker, M. Benjamin, Darbar, Dawood, Gladwin, Mark T., Albert, Christine M., Chasman, Daniel I., Jackson, Rebecca D., Kooperberg, Charles, Reiner, Alexander P., O’Reilly, Paul F., Loos, Ruth J. F.
Publicado 2022

Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

por Glanville, Kylie P., Coleman, Jonathan R.I., Hanscombe, Ken B., Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L., Breen, Gerome, Air, Tracy M., Andlauer, Till F.M., Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H.R., Boomsma, Dorret I., Buttenschøn, Henriette N., Colodro-Conde, Lucía, Dannlowski, Udo, Direk, Nese, Dunn, Erin C., Forstner, Andreas J., de Geus, Eco J.C., Grabe, Hans J., Hamilton, Steven P., Jones, Ian, Jones, Lisa A., Knowles, James A., Kutalik, Zoltán, Levinson, Douglas F., Lewis, Glyn, Lind, Penelope A., Lucae, Susanne, Magnusson, Patrik K., McGuffin, Peter, McIntosh, Andrew M., Milaneschi, Yuri, Mors, Ole, Mostafavi, Sara, Müller-Myhsok, Bertram, Pedersen, Nancy L., Penninx, Brenda W.J.H., Potash, James B., Preisig, Martin, Ripke, Stephan, Shi, Jianxin, Shyn, Stanley I., Smoller, Jordan W., Streit, Fabian, Sullivan, Patrick F., Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Weissman, Myrna M., O'Reilly, Paul F., Lewis, Cathryn M.
Publicado 2020