A citation-based method for searching scientific literature

Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett, Jerry H Kim, Elisabeth A Rosenthal, Daniel S Kim, Holly K Tabor, Michael J Bamshad, Arno G Motulsky, C Ronald Scott, Colin C Pritchard, Tom Walsh, Wylie Burke, Wendy H Raskind, Peter Byers, Fuki M Hisama, Deborah A Nickerson, Gail P Jarvik. Am J Hum Genet 2013
Times Cited: 270



Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti, Dmitry Dukhovny, David W Bates, Calum A MacRae, Michael F Murray, Heidi L Rehm, Amy L McGuire, Robert C Green. Ann Intern Med 2017
Times Cited: 100




List of shared articles



Times cited

Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing.
Christopher Lee, Omar Elsekaily, David C Kochan, Lubna Alhalabi, Faizan Faizee, Richard Sharp, Noralane M Lindor, Iftikhar J Kullo. Genet Med 2021
0

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
54

The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Hila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, David A Fasel, Adele Mitrotti, Rik Westland, Louise Bier, Chunhua Weng, Zhong Ren, Brett Copeland,[...]. Ann Intern Med 2019
21

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17

Implementation of genomics in medical practice to deliver precision medicine for an Asian population.
Yasmin Bylstra, Sonia Davila, Weng Khong Lim, Ryanne Wu, Jing Xian Teo, Sylvia Kam, Tamra Lysaght, Steve Rozen, Bin Tean Teh, Khung Keong Yeo,[...]. NPJ Genom Med 2019
10

Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study.
Xin Niu, Laura M Amendola, Ragan Hart, Caroline S Bennette, Patrick Heagerty, Martha Horike-Pyne, Susan B Trinidad, Elisabeth A Rosenthal, Bryan Comstock, Chris Nefcy,[...]. Contemp Clin Trials 2019
4

Cost Analyses of Genomic Sequencing: Lessons Learned from the MedSeq Project.
Kurt D Christensen, Kathryn A Phillips, Robert C Green, Dmitry Dukhovny. Value Health 2018
6