A citation-based method for searching scientific literature

Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K C Yuen, Michael J Szego, Robin Z Hayeems, Randi Zlotnik Shaul, Michael Brudno, Marta Girdea, Brendan Frey, Babak Alipanahi, Sohnee Ahmed, Riyana Babul-Hirji, Ramses Badilla Porras, Melissa T Carter, Lauren Chad, Ayeshah Chaudhry, David Chitayat, Soghra Jougheh Doust, Cheryl Cytrynbaum, Lucie Dupuis, Resham Ejaz, Leona Fishman, Andrea Guerin, Bita Hashemi, Mayada Helal, Stacy Hewson, Michal Inbar-Feigenberg, Peter Kannu, Natalya Karp, Raymond Kim, Jonathan Kronick, Eriskay Liston, Heather MacDonald, Saadet Mercimek-Mahmutoglu, Roberto Mendoza-Londono, Enas Nasr, Graeme Nimmo, Nicole Parkinson, Nada Quercia, Julian Raiman, Maian Roifman, Andreas Schulze, Andrea Shugar, Cheryl Shuman, Pierre Sinajon, Komudi Siriwardena, Rosanna Weksberg, Grace Yoon, Chris Carew, Raith Erickson, Richard A Leach, Robert Klein, Peter N Ray, M Stephen Meyn, Stephen W Scherer, Ronald D Cohn, Christian R Marshall. NPJ Genom Med 2016
Times Cited: 165



Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
Times Cited: 526




List of shared articles



Times cited

Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders.
Yan Sun, Fengxia Liu, Chunna Fan, Yaoshen Wang, Lijie Song, Zhonghai Fang, Rui Han, Zhonghua Wang, Xiaodan Wang, Ziying Yang,[...]. BMC Med Genomics 2021
0

Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Catherine Rehder, Lora J H Bean, David Bick, Elizabeth Chao, Wendy Chung, Soma Das, Julianne O'Daniel, Heidi Rehm, Vandana Shashi, Lisa M Vincent. Genet Med 2021
4

Whole-genome sequencing of human remains to enable genealogy DNA database searches - A case report.
Andreas Tillmar, Peter Sjölund, Bo Lundqvist, Therese Klippmark, Cajsa Älgenäs, Henrik Green. Forensic Sci Int Genet 2020
7


Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease.
Christian R Marshall, Shimul Chowdhury, Ryan J Taft, Mathew S Lebo, Jillian G Buchan, Steven M Harrison, Ross Rowsey, Eric W Klee, Pengfei Liu, Elizabeth A Worthey,[...]. NPJ Genom Med 2020
7

Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias.
Roberta Russo, Roberta Marra, Barbara Eleni Rosato, Achille Iolascon, Immacolata Andolfo. Front Physiol 2020
5


Clinical sequencing: From raw data to diagnosis with lifetime value.
S M Caspar, N Dubacher, A M Kopps, J Meienberg, C Henggeler, G Matyas. Clin Genet 2018
39

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
46