A citation-based method for searching scientific literature

David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein, W Andrew Faucett, Lars Feuk, Jan M Friedman, Ada Hamosh, Laird Jackson, Erin B Kaminsky, Klaas Kok, Ian D Krantz, Robert M Kuhn, Charles Lee, James M Ostell, Carla Rosenberg, Stephen W Scherer, Nancy B Spinner, Dimitri J Stavropoulos, James H Tepperberg, Erik C Thorland, Joris R Vermeesch, Darrel J Waggoner, Michael S Watson, Christa Lese Martin, David H Ledbetter. Am J Hum Genet 2010
Times Cited: 1457



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: 160




List of shared articles



Times cited

Application of Next Generation Sequencing in Laboratory Medicine.
Yiming Zhong, Feng Xu, Jinhua Wu, Jeffrey Schubert, Marilyn M Li. Ann Lab Med 2021
5

Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, Ian Backstrom, Gregory Costain, Tracy Heung, Daniele Merico, Christian R Marshall, Anne S Bassett, Ryan K C Yuen. Transl Psychiatry 2021
0

Cost-effectiveness of genome-wide sequencing for unexplained developmental disabilities and multiple congenital anomalies.
Chunmei Li, Stacey Vandersluis, Corinne Holubowich, Wendy J Ungar, Elaine S Goh, Kym M Boycott, Nancy Sikich, Irfan Dhalla, Vivian Ng. Genet Med 2021
1

Clinical application of whole-exome sequencing: A retrospective, single-center study.
Qiang Zhang, Zailong Qin, Shang Yi, Hao Wei, Xun Zhao Zhou, Jiasun Su. Exp Ther Med 2021
0

Whole genome analysis identifies the association of TP53 genomic deletions with lower survival in Stage III colorectal cancer.
Li C Xia, Paul Van Hummelen, Matthew Kubit, HoJoon Lee, John M Bell, Susan M Grimes, Christina Wood-Bouwens, Stephanie U Greer, Tyler Barker, Derrick S Haslem,[...]. Sci Rep 2020
0