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X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

The New England journal of medicine, 2015-05, Vol.372 (22), p.2097-2107

2015

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Reproductive genetics and the aging male

Journal of assisted reproduction and genetics, 2018-06, Vol.35 (6), p.933-941

2018

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The impact of alicyclic substituents on the extraction ability of new family of 1,10-phenanthroline-2,9-diamides

RSC advances, 2020-07, Vol.1 (44), p.2622-2633

2020

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The influence of the volume concentration of hydrogen on the fine structure of the IR absorption spectra and conductivity features in congruent LiTaO3 crystals

Solid state ionics, 2024-05, Vol.408, p.116508, Article 116508

2024

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Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR): Molecular Cytogenetic Analysis

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4559

2020

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ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia

Scientific reports, 2023-10, Vol.13 (1), p.16563-16563, Article 16563

2023

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In vivo modeling of metastatic human high-grade serous ovarian cancer in mice

PLoS genetics, 2020-06, Vol.16 (6), p.e1008808-e1008808

2020

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Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas

PloS one, 2012-03, Vol.7 (3), p.e33251-e33251

2012

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X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

Scientific reports, 2018-11, Vol.8 (1), p.16280-7, Article 16280

2018

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Phase Composition and Properties of the Low-Temperature Structural Ceramics in the Clay-Calcium Containing Material System

Materials science forum, 2019-12, Vol.974, p.331-335, Article 331

2019

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In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes

Proceedings of the National Academy of Sciences - PNAS, 2023-07, Vol.120 (30), p.e2219925120-e2219925120

2023

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Whole‐genome sequencing identifies new candidate genes for nonobstructive azoospermia

Andrology (Oxford), 2022-11, Vol.10 (8), p.1605-1624

2022

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NMR Spectra Particularities in LiNbO3 Crystals with a Near-Stoichiometric Composition

Ceramics, 2023-03, Vol.6 (1), p.432-446

2023

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Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men

The Journal of urology, 2010-04, Vol.183 (4), p.1636

2010

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Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure

Frontiers in genetics, 2023-05, Vol.14, p.1134849-1134849

2023

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High quality RNA in semen and sperm: isolation, analysis and potential application in clinical testing

The Journal of urology, 2015-01, Vol.193 (1), p.352

2015

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Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient

Scientific reports, 2015-11, Vol.5 (1), p.17408-17408, Article 17408

2015

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ETV5 mutations: revisiting Sertoli cell only syndrome

Fertility and sterility, 2012-10, Vol.98 (4), p.821-821

Yatsenko, Alexander N., M.D., Ph.D

2012

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The Use of Pyrite Concentrate and Waste Formed at the Brown Coals Enlargement

Materials science forum, 2019-12, Vol.974, p.336-341

2019

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Mendelian genetics of male infertility

Annals of the New York Academy of Sciences, 2010-12, Vol.1214 (1), p.E1-E17

2010

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Effects of Tcte1 knockout on energy chain transportation and spermatogenesis: implications for male infertility

Human reproduction open, 2024, Vol.2024 (2), p.hoae020-hoae020

2024

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Familial deletion of the HOXA gene cluster associated with Hand–Foot–Genital syndrome and phenotypic variability

American journal of medical genetics. Part A, 2017-01, Vol.173 (1), p.221-224

2017

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Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men

Molecular human reproduction, 2012-01, Vol.18 (1), p.14-21

2012

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Non-invasive genetic diagnosis of male infertility using spermatozoal RNA : KLHL10 mutations in oligozoospermic patients impair homodimerization

Human molecular genetics, 2006-12, Vol.15 (23), p.3411-3419

2006

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FISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male

Reproductive biomedicine online, 2015-08, Vol.31 (2), p.217-224

2015

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X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

Reproductive genetics and the aging male

The impact of alicyclic substituents on the extraction ability of new family of 1,10-phenanthroline-2,9-diamides

The influence of the volume concentration of hydrogen on the fine structure of the IR absorption spectra and conductivity features in congruent LiTaO3 crystals

Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR): Molecular Cytogenetic Analysis

ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia

In vivo modeling of metastatic human high-grade serous ovarian cancer in mice

Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

Phase Composition and Properties of the Low-Temperature Structural Ceramics in the Clay-Calcium Containing Material System

In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes

Whole‐genome sequencing identifies new candidate genes for nonobstructive azoospermia

NMR Spectra Particularities in LiNbO3 Crystals with a Near-Stoichiometric Composition

Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men

Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure

High quality RNA in semen and sperm: isolation, analysis and potential application in clinical testing

Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient

ETV5 mutations: revisiting Sertoli cell only syndrome

The Use of Pyrite Concentrate and Waste Formed at the Brown Coals Enlargement

Mendelian genetics of male infertility

Effects of Tcte1 knockout on energy chain transportation and spermatogenesis: implications for male infertility

Familial deletion of the HOXA gene cluster associated with Hand–Foot–Genital syndrome and phenotypic variability

Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men

Non-invasive genetic diagnosis of male infertility using spermatozoal RNA : KLHL10 mutations in oligozoospermic patients impair homodimerization

FISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male

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