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Page 1
Genetic etiology of hearing loss in Russia.
Posukh OL. Posukh OL. Hum Genet. 2022 Apr;141(3-4):649-663. doi: 10.1007/s00439-021-02327-7. Epub 2021 Aug 6. Hum Genet. 2022. PMID: 34363095 Review.
Global diversity, population stratification, and selection of human copy-number variation.
Sudmant PH, Mallick S, Nelson BJ, Hormozdiari F, Krumm N, Huddleston J, Coe BP, Baker C, Nordenfelt S, Bamshad M, Jorde LB, Posukh OL, Sahakyan H, Watkins WS, Yepiskoposyan L, Abdullah MS, Bravi CM, Capelli C, Hervig T, Wee JT, Tyler-Smith C, van Driem G, Romero IG, Jha AR, Karachanak-Yankova S, Toncheva D, Comas D, Henn B, Kivisild T, Ruiz-Linares A, Sajantila A, Metspalu E, Parik J, Villems R, Starikovskaya EB, Ayodo G, Beall CM, Di Rienzo A, Hammer MF, Khusainova R, Khusnutdinova E, Klitz W, Winkler C, Labuda D, Metspalu M, Tishkoff SA, Dryomov S, Sukernik R, Patterson N, Reich D, Eichler EE. Sudmant PH, et al. Among authors: posukh ol. Science. 2015 Sep 11;349(6253):aab3761. doi: 10.1126/science.aab3761. Epub 2015 Aug 6. Science. 2015. PMID: 26249230 Free PMC article.
Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population.
Romanov GP, Smirnova AA, Zamyatin VI, Mukhin AM, Kazantsev FV, Pshennikova VG, Teryutin FM, Solovyev AV, Fedorova SA, Posukh OL, Lashin SA, Barashkov NA. Romanov GP, et al. Among authors: posukh ol. Biology (Basel). 2022 Feb 7;11(2):257. doi: 10.3390/biology11020257. Biology (Basel). 2022. PMID: 35205123 Free PMC article.
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.
Solovyev AV, Kushniarevich A, Bliznetz E, Bady-Khoo M, Lalayants MR, Markova TG, Minárik G, Kádasi L, Metspalu E, Pshennikova VG, Teryutin FM, Khusnutdinova EK, Poliakov A, Metspalu M, Posukh OL, Barashkov NA, Fedorova SA. Solovyev AV, et al. Among authors: posukh ol. Hum Genet. 2022 Apr;141(3-4):697-707. doi: 10.1007/s00439-021-02405-w. Epub 2021 Nov 27. Hum Genet. 2022. PMID: 34839402
28 results