Get started
Author

Ekaterina Marnat

Observed names: E. G. Marnat, E. Marnat, Е. Г. Марнат, Е.Г. Марнат
ORCID: 0000-0001-9284-4486
Observed ORCID: 0000-0001-9284-4486
OpenAlex ID: A5073748130
Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome
2023 · Vyacheslav Chernykh, Stanislav Krasovsky, et al. · International Journal of Molecular Sciences · 6
PDF
L138ins Variant of the CFTR Gene in Russian Infertile Men
2023 · Vyacheslav Chernykh, Tatyana Sorokina, et al. · Genes · 4
PDF
CFTR Gene Variants and Genotypes in Russian Patients with CBAVD Syndrome
2020 · E. G. Marnat, T. A. Adyan, et al. · Russian Journal of Genetics · 4
Comparative analysis of the results semen examination in patients with azoospermia caused by cystic fibrosis and congenital bilateral aplasia of vas deferens syndrome
2019 · M. I. Shtaut, T. M. Sorokina, et al. · Andrology and Genital Surgery · 4
PDF
Comparison of the CFTR gene variants and genotypes in Russian patients with various forms of pathozoospermia and CBAVD syndrome
2020 · Е.Г. Марнат, Т.А. Адян, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika» · 1
Молекулярно-генетические аспекты прогнозирования ранних репродуктивных потерь
2026 · О. В. Юсеф, Б. Р. Ибрагимов, et al. · Вестник Российского государственного медицинского университета
Genotypes with two CFTR gene variants and undiagnosed cystic fibrosis in Russian infertile men with CBAVD
2026 · V. Chernykh, E. Marnat, et al. · Journal of Cystic Fibrosis
P008 L138ins is a common CFTR gene mutation in infertile Russian men
2022 · E. Marnat, A. Sedova, et al. · Journal of Cystic Fibrosis
P007 CFTR genotypes and spermatology in cystic fibrosis patients without CBAVD
2022 · A. Sedova, E. Marnat, et al. · Journal of Cystic Fibrosis
An influence of the CFTR genotype on semen parameters in CBAVD syndrome patients
2021 · Е.Г. Марнат, Т.М. Сорокина, et al. · Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
PDF
P004 CFTR genotype in Russian patients with CBAVD syndrome
2021 · E. Marnat, T. Sorokina, et al. · Journal of Cystic Fibrosis
Варианты гена CFTR у российских пациентов с синдромом CBAVD
2020 · Е. Г. Марнат, Т. А. Адян, et al. · Генетика
P018 CFTR mutations and genotypes in Russian CBAVD patients
2019 · V. Chernykh, E. Marnat, et al. · Journal of Cystic Fibrosis
Сравнительный анализ результатов спермиологического исследования у пациентов с азооспермией, вызванной муковисцидозом и синдромом врожденной двусторонней аплазии семявыносящих протоков
2019 · М. И. Штаут, Т. М. Сорокина, et al.
Works count: 14
Citation count: 19
H-index: 4
I10-index:
Year
Topic
Type