Partitioning heritability by functional annotation using genome-wide association summary statistics.
Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh, Stephan Ripke, Felix R Day, Shaun Purcell, Eli Stahl, Sara Lindstrom, John R B Perry, Yukinori Okada, Soumya Raychaudhuri, Mark J Daly, Nick Patterson, Benjamin M Neale, Alkes L Price. Nat Genet 2015
Times Cited: 865
Times Cited: 865
Claudia Giambartolomei, Damjan Vukcevic, Eric E Schadt, Lude Franke, Aroon D Hingorani, Chris Wallace, Vincent Plagnol. PLoS Genet 2014
Times Cited: 747
Times Cited: 747
List of shared articles
Times cited
Fine-mapping of Parkinson's disease susceptibility loci identifies putative causal variants.
Brian M Schilder, Towfique Raj. Hum Mol Genet 2022
Brian M Schilder, Towfique Raj. Hum Mol Genet 2022
Integrative Prioritization of Causal Genes for Coronary Artery Disease.
Ke Hao, Raili Ermel, Katyayani Sukhavasi, Haoxiang Cheng, Lijiang Ma, Ling Li, Letizia Amadori, Simon Koplev, Oscar FranzĂ©n, Valentina d'Escamard,[...]. Circ Genom Precis Med 2022
Ke Hao, Raili Ermel, Katyayani Sukhavasi, Haoxiang Cheng, Lijiang Ma, Ling Li, Letizia Amadori, Simon Koplev, Oscar FranzĂ©n, Valentina d'Escamard,[...]. Circ Genom Precis Med 2022
Methods for statistical fine-mapping and their applications to auto-immune diseases.
Qingbo S Wang, Hailiang Huang. Semin Immunopathol 2022
Qingbo S Wang, Hailiang Huang. Semin Immunopathol 2022
Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms.
Guanghao Qi, Diptavo Dutta, Andrew Leroux, Debashree Ray, John Muschelli, Ciprian Crainiceanu, Nilanjan Chatterjee. Genet Epidemiol 2022
Guanghao Qi, Diptavo Dutta, Andrew Leroux, Debashree Ray, John Muschelli, Ciprian Crainiceanu, Nilanjan Chatterjee. Genet Epidemiol 2022
Partitioning gene-mediated disease heritability without eQTLs.
Daniel J Weiner, Steven Gazal, Elise B Robinson, Luke J O'Connor. Am J Hum Genet 2022
Daniel J Weiner, Steven Gazal, Elise B Robinson, Luke J O'Connor. Am J Hum Genet 2022
Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity.
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, Kushal K Dey, Joseph Nasser, Karthik A Jagadeesh, Daniel J Weiner, Huwenbo Shi, Charles P Fulco, Luke J O'Connor,[...]. Nat Genet 2022
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, Kushal K Dey, Joseph Nasser, Karthik A Jagadeesh, Daniel J Weiner, Huwenbo Shi, Charles P Fulco, Luke J O'Connor,[...]. Nat Genet 2022
Beyond GWAS: from simple associations to functional insights.
Kazuyoshi Ishigaki. Semin Immunopathol 2022
Kazuyoshi Ishigaki. Semin Immunopathol 2022
Multi-omic insights into Parkinson's Disease: From genetic associations to functional mechanisms.
Brian M Schilder, Elisa Navarro, Towfique Raj. Neurobiol Dis 2022
Brian M Schilder, Elisa Navarro, Towfique Raj. Neurobiol Dis 2022
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.
Heidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, Gyda Bjornsdottir, Aster V E Harder, Lisette J A Kogelman, Laurent F Thomas, Raymond Noordam, Christian Benner, Padhraig Gormley,[...]. Nat Genet 2022
Heidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, Gyda Bjornsdottir, Aster V E Harder, Lisette J A Kogelman, Laurent F Thomas, Raymond Noordam, Christian Benner, Padhraig Gormley,[...]. Nat Genet 2022
Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge.
Michael Wainberg, Daniele Merico, Matthew C Keller, Eric B Fauman, Shreejoy J Tripathy. Mol Psychiatry 2022
Michael Wainberg, Daniele Merico, Matthew C Keller, Eric B Fauman, Shreejoy J Tripathy. Mol Psychiatry 2022
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
Marijana Vujkovic, Shweta Ramdas, Kim M Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J Cordell, Jing He, Yevgeniy Gindin, Chuhan Chung, Robert P Myers,[...]. Nat Genet 2022
Marijana Vujkovic, Shweta Ramdas, Kim M Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J Cordell, Jing He, Yevgeniy Gindin, Chuhan Chung, Robert P Myers,[...]. Nat Genet 2022
Shared genetic etiology and causality between COVID-19 and venous thromboembolism: evidence from genome-wide cross trait analysis and bi-directional Mendelian randomization study.
Xin Huang, Minhao Yao, Peixin Tian, Jason Y Y Wong, Zilin Li, Zhonghua Liu, Jie V Zhao. medRxiv 2022
Xin Huang, Minhao Yao, Peixin Tian, Jason Y Y Wong, Zilin Li, Zhonghua Liu, Jie V Zhao. medRxiv 2022
Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets.
Michael H Guo, Prashanth Sama, Brenna A LaBarre, Hrishikesh Lokhande, John Balibalos, Ci Chu, Xiaomi Du, Pouya Kheradpour, Charles C Kim, Taylor Oniskey,[...]. Genome Biol 2022
Michael H Guo, Prashanth Sama, Brenna A LaBarre, Hrishikesh Lokhande, John Balibalos, Ci Chu, Xiaomi Du, Pouya Kheradpour, Charles C Kim, Taylor Oniskey,[...]. Genome Biol 2022