Zinchenko R - Search Results

1

A Rare Case of TP63-Associated Lymphopenia Revealed by Newborn Screening Using TREC.

Marakhonov A, Serebryakova E, Mukhina A, Vechkasova A, Prokhorov N, Efimova I, Balinova N, Lobenskaya A, Vasilyeva T, Zabnenkova V, Ryzhkova O, Rodina Y, Pershin D, Soloveva N, Fomenko A, Saydaeva D, Ibisheva A, Irbaieva T, Koroteev A, Zinchenko R, Voronin S, Shcherbina A, Kutsev S. Marakhonov A, et al. Among authors: zinchenko r. Int J Mol Sci. 2024 Oct 9;25(19):10844. doi: 10.3390/ijms251910844. Int J Mol Sci. 2024. PMID: 39409174 Free PMC article.

2

[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.

3

Evaluation of orphan diseases global burden.

Makarova EV, Krysanov IS, Valilyeva TP, Vasiliev MD, Zinchenko RA. Makarova EV, et al. Eur J Transl Myol. 2021 May 14;31(2):9610. doi: 10.4081/ejtm.2021.9610. Eur J Transl Myol. 2021. PMID: 33985324 Free PMC article.

4

[The intermediate outcomes of delegation of obligations of medicinal support of patients with rare diseases to the Federal level in 2019-2020].

Komarov IA, Krasilnikova EY, Aleksandrova OY, Zinchenko RA. Komarov IA, et al. Among authors: zinchenko ra. Probl Sotsialnoi Gig Zdravookhranenniiai Istor Med. 2022 Mar;30(2):207-210. doi: 10.32687/0869-866X-2022-30-2-207-210. Probl Sotsialnoi Gig Zdravookhranenniiai Istor Med. 2022. PMID: 35439376 Russian.

5

[Ethnic Marriage Assortativeness and Intensity of Metisation of Karachays].

El'chinova GI, Shakmanov MM, Revazova YA, Ivanov AV, Rusakova AV, Zinchenko RA. El'chinova GI, et al. Among authors: zinchenko ra. Genetika. 2015 Aug;51(8):941-5. Genetika. 2015. PMID: 26601494 Russian.

6

[Acceptability of using Karachay surnames as a quasigenetic marker in population and genetic studies].

El'chinova GI, Ivanov AV, El'kanova LA, Revazova YA, Zinchenko RA. El'chinova GI, et al. Among authors: zinchenko ra. Genetika. 2014 Jul;50(7):874-7. Genetika. 2014. PMID: 25720146 Russian.

7

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

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. 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

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

10

Clinical and morphological manifestations of aniridia-associated keratopathy on anterior segment optical coherence tomography and in vivo confocal microscopy.

Voskresenskaya A, Pozdeyeva N, Vasilyeva T, Batkov Y, Shipunov A, Gagloev B, Zinchenko R. Voskresenskaya A, et al. Among authors: zinchenko r. Ocul Surf. 2017 Oct;15(4):759-769. doi: 10.1016/j.jtos.2017.07.001. Epub 2017 Jul 8. Ocul Surf. 2017. PMID: 28698011

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