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Editorial: Genetic factors in male infertility

Frontiers in genetics, 2023-04, Vol.14, p.1187445-1187445

2023

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Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice

American journal of human genetics, 2019-04, Vol.104 (4), p.738-748

2019

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Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice

American journal of human genetics, 2020-09, Vol.107 (3), p.514-526

2020

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Sperm DNA integrity status is associated with DNA methylation signatures of imprinted genes and non-imprinted genes

Journal of assisted reproduction and genetics, 2021-08, Vol.38 (8), p.2041-2048

2021

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DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath

Cell death & disease, 2023-02, Vol.14 (2), p.127-127, Article 127

2023

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Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility

Journal of human genetics, 2019-01, Vol.64 (1), p.49-54

2019

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A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

Journal of assisted reproduction and genetics, 2020-06, Vol.37 (6), p.1431-1439

2020

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Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Reproductive biology and endocrinology, 2022-03, Vol.20 (1), p.41-41, Article 41

2022

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Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Human genetics, 2021-09, Vol.140 (9), p.1367-1377

2021

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Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection

Journal of assisted reproduction and genetics, 2020-04, Vol.37 (4), p.829-840

2020

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Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

Reproductive biology and endocrinology, 2021-08, Vol.19 (1), p.129-129, Article 129

2021

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Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Reproductive biology and endocrinology, 2022-04, Vol.20 (1), p.63-63, Article 63

2022

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Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Journal of assisted reproduction and genetics, 2022-01, Vol.39 (1), p.251-259

2022

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Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

Reproductive biology and endocrinology, 2022-01, Vol.20 (1), p.5-5, Article 5

2022

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Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Reproductive biology and endocrinology, 2022-05, Vol.20 (1), p.79-79, Article 79

2022

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Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Reproductive biology and endocrinology, 2022-04, Vol.20 (1), p.74-74, Article 74

2022

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Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family

Frontiers in genetics, 2021-07, Vol.12

2021

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A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens

Journal of assisted reproduction and genetics, 2020-06, Vol.37 (6), p.1421-1429

2020

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Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality

Frontiers in genetics, 2021-06, Vol.12, p.666136-666136

2021

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Novel HYDIN variants associated with male infertility in two Chinese families

Frontiers in endocrinology (Lausanne), 2023-01, Vol.14, p.1118841-1118841

2023

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Altered mRNAs Profiles in the Testis of Patients With "Secondary Idiopathic Non-Obstructive Azoospermia"

Frontiers in cell and developmental biology, 2022-05, Vol.10, p.824596-824596

2022

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miR-323-3p regulates the steroidogenesis and cell apoptosis in polycystic ovary syndrome (PCOS) by targeting IGF-1

Gene, 2019-01, Vol.683, p.87-100

2019

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Melatonin alleviates deoxynivalenol-induced apoptosis of human granulosa cells by reducing mutually accentuated FOXO1 and ER stress

Biology of reproduction, 2021-08, Vol.105 (2), p.554-566

2021

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Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice

American journal of human genetics, 2021-08, Vol.108 (8), p.1466-1477

2021

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Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella

Journal of medical genetics, 2019-02, Vol.56 (2), p.96

2019

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Editorial: Genetic factors in male infertility

Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice

Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice

Sperm DNA integrity status is associated with DNA methylation signatures of imprinted genes and non-imprinted genes

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath

Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility

A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection

Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens

Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality

Novel HYDIN variants associated with male infertility in two Chinese families

Altered mRNAs Profiles in the Testis of Patients With "Secondary Idiopathic Non-Obstructive Azoospermia"

miR-323-3p regulates the steroidogenesis and cell apoptosis in polycystic ovary syndrome (PCOS) by targeting IGF-1

Melatonin alleviates deoxynivalenol-induced apoptosis of human granulosa cells by reducing mutually accentuated FOXO1 and ER stress

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice

Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella

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