A citation-based method for searching scientific literature

Laura M Amendola, Michael O Dorschner, Peggy D Robertson, Joseph S Salama, Ragan Hart, Brian H Shirts, Mitzi L Murray, Mari J Tokita, Carlos J Gallego, Daniel Seung Kim, James T Bennett, David R Crosslin, Jane Ranchalis, Kelly L Jones, Elisabeth A Rosenthal, Ella R Jarvik, Andy Itsara, Emily H Turner, Daniel S Herman, Jennifer Schleit, Amber Burt, Seema M Jamal, Jenica L Abrudan, Andrew D Johnson, Laura K Conlin, Matthew C Dulik, Avni Santani, Danielle R Metterville, Melissa Kelly, Ann Katherine M Foreman, Kristy Lee, Kent D Taylor, Xiuqing Guo, Kristy Crooks, Lesli A Kiedrowski, Leslie J Raffel, Ora Gordon, Kalotina Machini, Robert J Desnick, Leslie G Biesecker, Steven A Lubitz, Surabhi Mulchandani, Greg M Cooper, Steven Joffe, C Sue Richards, Yaoping Yang, Jerome I Rotter, Stephen S Rich, Christopher J O'Donnell, Jonathan S Berg, Nancy B Spinner, James P Evans, Stephanie M Fullerton, Kathleen A Leppig, Robin L Bennett, Thomas Bird, Virginia P Sybert, William M Grady, Holly K Tabor, Jerry H Kim, Michael J Bamshad, Benjamin Wilfond, Arno G Motulsky, C Ronald Scott, Colin C Pritchard, Tom D Walsh, Wylie Burke, Wendy H Raskind, Peter Byers, Fuki M Hisama, Heidi Rehm, Debbie A Nickerson, Gail P Jarvik. Genome Res 2015
Times Cited: 224







List of shared articles



Times cited

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman,[...]. Genet Med 2021
11

A pediatric perspective on genomics and prevention in the twenty-first century.
Bimal P Chaudhari, Kandamurugu Manickam, Kim L McBride. Pediatr Res 2020
1

Management of Secondary Genomic Findings.
Alexander E Katz, Robert L Nussbaum, Benjamin D Solomon, Heidi L Rehm, Marc S Williams, Leslie G Biesecker. Am J Hum Genet 2020
6

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

Dissecting in silico Mutation Prediction of Variants in African Genomes: Challenges and Perspectives.
Christian Domilongo Bope, Emile R Chimusa, Victoria Nembaware, Gaston K Mazandu, Jantina de Vries, Ambroise Wonkam. Front Genet 2019
8