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Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.
Park J, Lucas AM, Zhang X, Chaudhary K, Cho JH, Nadkarni G, Dobbyn A, Chittoor G, Josyula NS, Katz N, Breeyear JH, Ahmadmehrabi S, Drivas TG, Chavali VRM, Fasolino M, Sawada H, Daugherty A, Li Y, Zhang C, Bradford Y, Weaver J, Verma A, Judy RL, Kember RL, Overton JD, Reid JG, Ferreira MAR, Li AH, Baras A, LeMaire SA, Shen YH, Naji A, Kaestner KH, Vahedi G, Edwards TL, Chen J, Damrauer SM, Justice AE, Do R, Ritchie MD, Rader DJ. Park J, et al. Among authors: ahmadmehrabi s. Nat Med. 2021 Jan;27(1):66-72. doi: 10.1038/s41591-020-1133-8. Epub 2021 Jan 11. Nat Med. 2021. PMID: 33432171 Free PMC article.
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.
Ahmadmehrabi S, Li B, Park J, Devkota B, Vujkovic M, Ko YA, Van Wagoner D, Tang WHW, Krantz I, Ritchie M; Regeneron Genetics Center; Brant J, Ruckenstein MJ, Epstein DJ, Rader DJ. Ahmadmehrabi S, et al. Hum Genet. 2021 Jun;140(6):957-967. doi: 10.1007/s00439-021-02263-6. Epub 2021 Mar 21. Hum Genet. 2021. PMID: 33745059
Genetics of Postlingual Sensorineural Hearing Loss.
Ahmadmehrabi S, Brant J, Epstein DJ, Ruckenstein MJ, Rader DJ. Ahmadmehrabi S, et al. Laryngoscope. 2021 Feb;131(2):401-409. doi: 10.1002/lary.28646. Epub 2020 Apr 3. Laryngoscope. 2021. PMID: 32243624 Review.
Hemodialysis-induced cardiovascular disease.
Ahmadmehrabi S, Tang WHW. Ahmadmehrabi S, et al. Semin Dial. 2018 May;31(3):258-267. doi: 10.1111/sdi.12694. Epub 2018 Apr 6. Semin Dial. 2018. PMID: 29624739 Free PMC article. Review.
Gut microbiome and its role in cardiovascular diseases.
Ahmadmehrabi S, Tang WHW. Ahmadmehrabi S, et al. Curr Opin Cardiol. 2017 Nov;32(6):761-766. doi: 10.1097/HCO.0000000000000445. Curr Opin Cardiol. 2017. PMID: 29023288 Free PMC article. Review.
11 results