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High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men

Scientific reports, 2019-04, Vol.9 (1), p.6276, Article 6276

2019

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Mutations in the desert hedgehog (DHH) gene in the disorders of sexual differentiation and male infertility

Journal of assisted reproduction and genetics, 2021-07, Vol.38 (7), p.1871-1878

2021

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Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility

Human molecular genetics, 2023-01, Vol.32 (4), p.533-542

2023

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Repeated implantation failure versus repeated implantation success: discrimination at a metabolomic level

Human reproduction (Oxford), 2016-06, Vol.31 (6), p.1265-1274

2016

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Mutations in the prostate specific antigen (PSA/KLK3) correlate with male infertility

Scientific reports, 2017-09, Vol.7 (1), p.11225-9, Article 11225

2017

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Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding

Fertility and sterility, 2009-03, Vol.91 (3), p.933.e23-933.e28

2009

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Surgical correction of rare Müllerian anomalies and spontaneous pregnancies: a case report

Fertility and sterility, 2008-03, Vol.89 (3), p.723.e13-723.e16

2008

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Androgen insensitivity syndrome： do trinucleotide repeats in androgen receptor gene have any role

Asian journal of andrology, 2008-07, Vol.10 (4), p.616-624

2008

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L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function

Steroids, 2013-12, Vol.78 (12-13), p.1288-1292

2013

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A novel missense mutation C11994T in the mitochondrial ND4 gene as a cause of low sperm motility in the Indian subcontinent

Fertility and sterility, 2006-12, Vol.86 (6), p.1783-1785

2006

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SRY-negative 46,XX male with normal genitals, complete masculinization and infertility

Molecular human reproduction, 2006-05, Vol.12 (5), p.341-346

2006

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C601S mutation in the androgen receptor results in partial loss of androgen function

The Journal of steroid biochemistry and molecular biology, 2010-11, Vol.122 (5), p.359-363

2010

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Mitochondrial DNA variations associated with recurrent pregnancy loss among Indian women

Mitochondrion, 2011-05, Vol.11 (3), p.450-456

2011

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G708E Mutation in the Androgen Receptor Results in Complete Loss of Androgen Function

Journal of andrology, 2011-03, Vol.32 (2), p.193-198

2011

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CAG Repeat Expansion in the Androgen Receptor Gene Is Not Associated With Male Infertility in Indian Populations

Journal of andrology, 2002-11, Vol.23 (6), p.815-818

2002

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A Novel Human Sex-Determining Gene Linked to Xp11.21-11.23

The journal of clinical endocrinology and metabolism, 2006-10, Vol.91 (10), p.4028-4036

2006

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No Association of Androgen Receptor GGN Repeat Length Polymorphism With Infertility in Indian Men

Journal of andrology, 2006-11, Vol.27 (6), p.785-789

2006

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Novel Variants in UBE2B Gene and Idiopathic Male Infertility

Journal of andrology, 2008-09, Vol.29 (5), p.564-571

2008

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CAG repeat variation in the mtDNA polymerase γ is not associated with oligoasthenozoospermia

International journal of andrology, 2009-12, Vol.32 (6), p.647-655

2009

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APOB Gene Signal Peptide Deletion Polymorphism Is Not Associated With Infertility in Indian Men

Journal of andrology, 2009-11, Vol.30 (6), p.734-738

2009

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Y Chromosome Deletions in Azoospermic Men in India

Journal of andrology, 2003-07, Vol.24 (4), p.588-597

2003

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Male Infertility: No Evidence of Involvement of Androgen Receptor Gene Among Indian Men

Journal of andrology, 2006-01, Vol.27 (1), p.102-105

2006

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A 47, XXY female

The Lancet (British edition), 1998-10, Vol.352 (9134), p.1121-1121

1998

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C601 S mutation in the androgen receptor results in partial loss of androgen function

The Journal of steroid biochemistry and molecular biology, 2010, Vol.122 (5), p.359-363

2010

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A novel human sex-determining gene linked to Xpll.21-11.23

The journal of clinical endocrinology and metabolism, 2006, Vol.91 (10), p.4028-4036

2006

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High frequencies of Non Allelic Homologous Recombination (NAHR) events at the AZF loci and male infertility risk in Indian men

Mutations in the desert hedgehog (DHH) gene in the disorders of sexual differentiation and male infertility

Exome sequencing and functional analyses revealed CETN1 variants leads to impaired cell division and male fertility

Repeated implantation failure versus repeated implantation success: discrimination at a metabolomic level

Mutations in the prostate specific antigen (PSA/KLK3) correlate with male infertility

Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding

Surgical correction of rare Müllerian anomalies and spontaneous pregnancies: a case report

Androgen insensitivity syndrome： do trinucleotide repeats in androgen receptor gene have any role

L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function

A novel missense mutation C11994T in the mitochondrial ND4 gene as a cause of low sperm motility in the Indian subcontinent

SRY-negative 46,XX male with normal genitals, complete masculinization and infertility

C601S mutation in the androgen receptor results in partial loss of androgen function

Mitochondrial DNA variations associated with recurrent pregnancy loss among Indian women

G708E Mutation in the Androgen Receptor Results in Complete Loss of Androgen Function

CAG Repeat Expansion in the Androgen Receptor Gene Is Not Associated With Male Infertility in Indian Populations

A Novel Human Sex-Determining Gene Linked to Xp11.21-11.23

No Association of Androgen Receptor GGN Repeat Length Polymorphism With Infertility in Indian Men

Novel Variants in UBE2B Gene and Idiopathic Male Infertility

CAG repeat variation in the mtDNA polymerase γ is not associated with oligoasthenozoospermia

APOB Gene Signal Peptide Deletion Polymorphism Is Not Associated With Infertility in Indian Men

Y Chromosome Deletions in Azoospermic Men in India

Male Infertility: No Evidence of Involvement of Androgen Receptor Gene Among Indian Men

A 47, XXY female

C601 S mutation in the androgen receptor results in partial loss of androgen function

A novel human sex-determining gene linked to Xpll.21-11.23

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