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







List of shared articles



Times cited

Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome.
Fikri Birey, Min-Yin Li, Aaron Gordon, Mayuri V Thete, Alfredo M Valencia, Omer Revah, Anca M Paşca, Daniel H Geschwind, Sergiu P Paşca. Cell Stem Cell 2022
3

Polygenic contribution to the relationship of loneliness and social isolation with schizophrenia.
Álvaro Andreu-Bernabeu, Covadonga M Díaz-Caneja, Javier Costas, Lucía De Hoyos, Carol Stella, Xaquín Gurriarán, Clara Alloza, Lourdes Fañanás, Julio Bobes, Ana González-Pinto,[...]. Nat Commun 2022
0

Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traits.
Biao Zeng, Jaroslav Bendl, Roman Kosoy, John F Fullard, Gabriel E Hoffman, Panos Roussos. Nat Genet 2022
0

Discovery of genomic loci of the human cerebral cortex using genetically informed brain atlases.
Carolina Makowski, Dennis van der Meer, Weixiu Dong, Hao Wang, Yan Wu, Jingjing Zou, Cin Liu, Sara B Rosenthal, Donald J Hagler, Chun Chieh Fan,[...]. Science 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


Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose.
Olivia Corradin, Richard Sallari, An T Hoang, Bibi S Kassim, Gabriella Ben Hutta, Lizette Cuoto, Bryan C Quach, Katreya Lovrenert, Cameron Hays, Berkley E Gryder,[...]. Mol Psychiatry 2022
1

Single nucleus multi-omics identifies human cortical cell regulatory genome diversity.
Chongyuan Luo, Hanqing Liu, Fangming Xie, Ethan J Armand, Kimberly Siletti, Trygve E Bakken, Rongxin Fang, Wayne I Doyle, Tim Stuart, Rebecca D Hodge,[...]. Cell Genom 2022
0

Reconstructing SNP allele and genotype frequencies from GWAS summary statistics.
Zhiyu Yang, Peristera Paschou, Petros Drineas. Sci Rep 2022
0

Cis-regulatory hubs: a new 3D model of complex disease genetics with an application to schizophrenia.
Loïc Mangnier, Charles Joly-Beauparlant, Arnaud Droit, Steve Bilodeau, Alexandre Bureau. Life Sci Alliance 2022
1


Common variants contribute to intrinsic human brain functional networks.
Bingxin Zhao, Tengfei Li, Stephen M Smith, Di Xiong, Xifeng Wang, Yue Yang, Tianyou Luo, Ziliang Zhu, Yue Shan, Nana Matoba,[...]. 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