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Using DNA sequencers as stethoscopes.
Gymrek M, Erlich Y. Gymrek M, et al. Genome Med. 2011 Nov 21;3(11):73. doi: 10.1186/gm289. Genome Med. 2011. PMID: 22103962 Free PMC article.
Identifying personal genomes by surname inference.
Gymrek M, McGuire AL, Golan D, Halperin E, Erlich Y. Gymrek M, et al. Science. 2013 Jan 18;339(6117):321-4. doi: 10.1126/science.1229566. Science. 2013. PMID: 23329047
OTX2 duplication is implicated in hemifacial microsomia.
Zielinski D, Markus B, Sheikh M, Gymrek M, Chu C, Zaks M, Srinivasan B, Hoffman JD, Aizenbud D, Erlich Y. Zielinski D, et al. Among authors: gymrek m. PLoS One. 2014 May 9;9(5):e96788. doi: 10.1371/journal.pone.0096788. eCollection 2014. PLoS One. 2014. PMID: 24816892 Free PMC article.
The landscape of human STR variation.
Willems T, Gymrek M, Highnam G; 1000 Genomes Project Consortium; Mittelman D, Erlich Y. Willems T, et al. Among authors: gymrek m. Genome Res. 2014 Nov;24(11):1894-904. doi: 10.1101/gr.177774.114. Epub 2014 Aug 18. Genome Res. 2014. PMID: 25135957 Free PMC article.
A global reference for human genetic variation.
1000 Genomes Project Consortium; Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR. 1000 Genomes Project Consortium, et al. Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393. Nature. 2015. PMID: 26432245 Free PMC article.
59 results