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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 2
2008 1
2010 1
2011 2
2012 2
2013 2
2014 5
2015 3
2016 5
2017 2
2018 3
2024 0

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25 results

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Page 1
Characterizing genetic variants for clinical action.
Ramos EM, Din-Lovinescu C, Berg JS, Brooks LD, Duncanson A, Dunn M, Good P, Hubbard TJ, Jarvik GP, O'Donnell C, Sherry ST, Aronson N, Biesecker LG, Blumberg B, Calonge N, Colhoun HM, Epstein RS, Flicek P, Gordon ES, Green ED, Green RC, Hurles M, Kawamoto K, Knaus W, Ledbetter DH, Levy HP, Lyon E, Maglott D, McLeod HL, Rahman N, Randhawa G, Wicklund C, Manolio TA, Chisholm RL, Williams MS. Ramos EM, et al. Among authors: gordon es. Am J Med Genet C Semin Med Genet. 2014 Mar;166C(1):93-104. doi: 10.1002/ajmg.c.31386. Epub 2014 Mar 13. Am J Med Genet C Semin Med Genet. 2014. PMID: 24634402 Free PMC article.
Genetic and clinical heterogeneity in eIF2B-related disorder.
Maletkovic J, Schiffmann R, Gorospe JR, Gordon ES, Mintz M, Hoffman EP, Alper G, Lynch DR, Singhal BS, Harding C, Amartino H, Brown CM, Chan A, Renaud D, Geraghty M, Jensen L, Senbil N, Kadom N, Nazarian J, Yuanjian Feng, Zuyi Wang, Hartka T, Morizono H, Vanderver A. Maletkovic J, et al. Among authors: gordon es. J Child Neurol. 2008 Feb;23(2):205-15. doi: 10.1177/0883073807308705. J Child Neurol. 2008. PMID: 18263758
Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative.
Schmidlen TJ, Scheinfeldt L, Zhaoyang R, Kasper R, Sweet K, Gordon ES, Keller M, Stack C, Gharani N, Daly MB, Jarvis J, Christman MF. Schmidlen TJ, et al. Among authors: gordon es. J Genet Couns. 2016 Apr;25(2):385-94. doi: 10.1007/s10897-015-9883-z. Epub 2015 Aug 27. J Genet Couns. 2016. PMID: 26306685 Free PMC article.
Personalized genomic results: analysis of informational needs.
Schmidlen TJ, Wawak L, Kasper R, García-España JF, Christman MF, Gordon ES. Schmidlen TJ, et al. Among authors: gordon es. J Genet Couns. 2014 Aug;23(4):578-87. doi: 10.1007/s10897-014-9693-8. Epub 2014 Feb 3. J Genet Couns. 2014. PMID: 24488620
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.
Kay C, Collins JA, Wright GEB, Baine F, Miedzybrodzka Z, Aminkeng F, Semaka AJ, McDonald C, Davidson M, Madore SJ, Gordon ES, Gerry NP, Cornejo-Olivas M, Squitieri F, Tishkoff S, Greenberg JL, Krause A, Hayden MR. Kay C, et al. Among authors: gordon es. Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):346-357. doi: 10.1002/ajmg.b.32618. Epub 2018 Feb 20. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29460498
25 results