A citation-based method for searching scientific literature

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



Claudia Giambartolomei, Damjan Vukcevic, Eric E Schadt, Lude Franke, Aroon D Hingorani, Chris Wallace, Vincent Plagnol. PLoS Genet 2014
Times Cited: 747




List of shared articles



Times cited


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
2


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
0

Partitioning gene-mediated disease heritability without eQTLs.
Daniel J Weiner, Steven Gazal, Elise B Robinson, Luke J O'Connor. Am J Hum Genet 2022
0

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
1

Beyond GWAS: from simple associations to functional insights.
Kazuyoshi Ishigaki. Semin Immunopathol 2022
1

Multi-omic insights into Parkinson's Disease: From genetic associations to functional mechanisms.
Brian M Schilder, Elisa Navarro, Towfique Raj. Neurobiol Dis 2022
3

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
5

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
0

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
0


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
0