Zinchenko RA - Search Results

1

Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population.

Petrova NV, Marakhonov AV, Balinova NV, Abrukova AV, Konovalov FA, Kutsev SI, Zinchenko RA. Petrova NV, et al. Among authors: zinchenko ra. Genes (Basel). 2021 May 27;12(6):820. doi: 10.3390/genes12060820. Genes (Basel). 2021. PMID: 34071867 Free PMC article.

2

Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.

Kazantseva A, Goltsov A, Zinchenko R, Grigorenko AP, Abrukova AV, Moliaka YK, Kirillov AG, Guo Z, Lyle S, Ginter EK, Rogaev EI. Kazantseva A, et al. Science. 2006 Nov 10;314(5801):982-5. doi: 10.1126/science.1133276. Science. 2006. PMID: 17095700

3

[Population study of the Udmurt population: analysis of ten polymorphic DNA loci of the nuclear genome].

Bermisheva MA, Petrova NV, Zinchenko RA, Timkovskaia EE, Malyshev PIu, Gavrilina SG, Ginter EK, Kusnutdinova EK. Bermisheva MA, et al. Among authors: zinchenko ra. Genetika. 2007 May;43(5):688-705. Genetika. 2007. PMID: 17633563 Russian.

4

Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.

Bliznetz EA, Tverskaya SM, Zinchenko RA, Abrukova AV, Savaskina EN, Nikulin MV, Kirillov AG, Ginter EK, Polyakov AV. Bliznetz EA, et al. Among authors: zinchenko ra. Eur J Hum Genet. 2009 May;17(5):664-72. doi: 10.1038/ejhg.2008.234. Epub 2009 Jan 28. Eur J Hum Genet. 2009. PMID: 19172990 Free PMC article.

5

[Epidemiology of monogenic hereditary diseases in Rostov oblast: population dynamic factors determining the differentiation of the load of hereditary diseases in eight districts].

Zinchenko RA, Amelina SS, Shokarev RA, Val'kov RA, Val'kova TI, Vetrova NV, Kriventsova NV, El'chinova GI, Petrova NV, Khlebnikova OV. Zinchenko RA, et al. Genetika. 2009 Apr;45(4):536-45. Genetika. 2009. PMID: 19507707 Russian.

6

A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A.

Meshcheryakova TI, Zinchenko RA, Vasilyeva TA, Marakhonov AV, Zhylina SS, Petrova NV, Kozhanova TV, Belenikin MS, Petrin AN, Mutovin GR. Meshcheryakova TI, et al. Among authors: zinchenko ra. Ann Hum Genet. 2015 Mar;79(2):148-52. doi: 10.1111/ahg.12098. Epub 2015 Jan 15. Ann Hum Genet. 2015. PMID: 25590586

7

[Results of the population and genetic study in the Republic of Tatarstan].

El'chinova GI, Vasil'eva TA, El'kanova LA, Revazova IuA, Petrova NV, Timkovskaia EE, Zinchenko RA. El'chinova GI, et al. Among authors: zinchenko ra. Genetika. 2014 May;50(5):619-24. Genetika. 2014. PMID: 25715478 Russian.

8

Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles.

Zernov NV, Skoblov MY, Marakhonov AV, Shimomura Y, Vasilyeva TA, Konovalov FA, Abrukova AV, Zinchenko RA. Zernov NV, et al. Among authors: zinchenko ra. J Invest Dermatol. 2016 Jun;136(6):1097-1105. doi: 10.1016/j.jid.2016.01.037. Epub 2016 Feb 20. J Invest Dermatol. 2016. PMID: 26902920 Free article.

9

High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia.

Petrova NV, Kashirskaya NY, Vasilyeva TA, Timkovskaya EE, Voronkova AY, Shabalova LA, Kondratyeva EI, Sherman VD, Novoselova OG, Kapranov NI, Zinchenko RA, Ginter EK, Makaov AKh, Kerem B. Petrova NV, et al. Among authors: zinchenko ra. J Cyst Fibros. 2016 May;15(3):e28-32. doi: 10.1016/j.jcf.2016.02.003. J Cyst Fibros. 2016. PMID: 26948992 Free article.

10

Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations.

Vasilyeva TA, Voskresenskaya AA, Käsmann-Kellner B, Khlebnikova OV, Pozdeyeva NA, Bayazutdinova GM, Kutsev SI, Ginter EK, Semina EV, Marakhonov AV, Zinchenko RA. Vasilyeva TA, et al. Among authors: zinchenko ra. Clin Genet. 2017 Dec;92(6):639-644. doi: 10.1111/cge.13019. Epub 2017 Aug 2. Clin Genet. 2017. PMID: 28321846

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