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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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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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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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Comprehensive 5-Year Study of Cytogenetic Aberrations in 668 Infertile Men

The Journal of urology, 2010-04, Vol.183 (4), p.1636-1642

2010

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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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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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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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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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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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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.352-359

2015

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The Genetics of Infertility: Current Status of the Field

Current genetic medicine reports, 2013-12, Vol.1 (4), p.247-260

2013

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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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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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ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies

Human molecular genetics, 2005-10, Vol.14 (19), p.2769-2778

2005

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UBE2B mRNA alterations are associated with severe oligozoospermia in infertile men

Molecular human reproduction, 2013-06, Vol.19 (6), p.388-394

2013

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Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10mutations in oligozoospermic patients impair homodimerization

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

2006

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Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male

Molecular cytogenetics, 2014-02, Vol.7 (1), p.14-14, Article 14

2014

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Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration

Human molecular genetics, 2001-11, Vol.10 (23), p.2671-2678

2001

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

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

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

Comprehensive 5-Year Study of Cytogenetic Aberrations in 668 Infertile Men

Reproductive genetics and the aging male

Mendelian genetics of male infertility

ETV5 mutations: revisiting Sertoli cell only syndrome

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

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

High Quality RNA in Semen and Sperm: Isolation, Analysis and Potential Application in Clinical Testing

The Genetics of Infertility: Current Status of the Field

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

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

ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies

UBE2B mRNA alterations are associated with severe oligozoospermia in infertile men

Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL10mutations in oligozoospermic patients impair homodimerization

Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male

Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration

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