A citation-based method for searching scientific literature

Frederick E Dewey, Michael F Murray, John D Overton, Lukas Habegger, Joseph B Leader, Samantha N Fetterolf, Colm O'Dushlaine, Cristopher V Van Hout, Jeffrey Staples, Claudia Gonzaga-Jauregui, Raghu Metpally, Sarah A Pendergrass, Monica A Giovanni, H Lester Kirchner, Suganthi Balasubramanian, Noura S Abul-Husn, Dustin N Hartzel, Daniel R Lavage, Korey A Kost, Jonathan S Packer, Alexander E Lopez, John Penn, Semanti Mukherjee, Nehal Gosalia, Manoj Kanagaraj, Alexander H Li, Lyndon J Mitnaul, Lance J Adams, Thomas N Person, Kavita Praveen, Anthony Marcketta, Matthew S Lebo, Christina A Austin-Tse, Heather M Mason-Suares, Shannon Bruse, Scott Mellis, Robert Phillips, Neil Stahl, Andrew Murphy, Aris Economides, Kimberly A Skelding, Christopher D Still, James R Elmore, Ingrid B Borecki, George D Yancopoulos, F Daniel Davis, William A Faucett, Omri Gottesman, Marylyn D Ritchie, Alan R Shuldiner, Jeffrey G Reid, David H Ledbetter, Aris Baras, David J Carey. Science 2016
Times Cited: 310



Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
Times Cited: 4858




List of shared articles



Times cited

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study.
Mahmoud Koko, Joshua E Motelow, Kate E Stanley, Dheeraj R Bobbili, Ryan S Dhindsa, Patrick May. Epilepsia 2022
0

Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients.
Yasue Horiuchi, Hiroyuki Matsubayashi, Yoshimi Kiyozumi, Seiichiro Nishimura, Satomi Higashigawa, Nobuhiro Kado, Takeshi Nagashima, Maki Mizuguchi, Sumiko Ohnami, Makoto Arai,[...]. Hum Genet 2021
4

A catalog of associations between rare coding variants and COVID-19 outcomes.
J A Kosmicki, J E Horowitz, N Banerjee, R Lanche, A Marcketta, E Maxwell, X Bai, D Sun, J D Backman, D Sharma,[...]. medRxiv 2021
10

ATAV: a comprehensive platform for population-scale genomic analyses.
Zhong Ren, Gundula Povysil, Joseph A Hostyk, Hongzhu Cui, Nitin Bhardwaj, David B Goldstein. BMC Bioinformatics 2021
6

Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia.
Xiaojun Chen, Fatao Liu, Zin Mar Aung, Yan Zhang, Gang Chai. Front Genet 2021
0

Distinct gene-set burden patterns underlie common generalized and focal epilepsies.
Mahmoud Koko, Roland Krause, Thomas Sander, Dheeraj Reddy Bobbili, Michael Nothnagel, Patrick May, Holger Lerche. EBioMedicine 2021
0