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Metabolic markers in male infertility: a pilot study

Journal of Men's Health, 2024-09, Vol.20 (9), p.138-145

2024

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Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome

Indian journal of medical research (New Delhi, India : 1994), 2023-10, Vol.158 (4), p.397-406

2023

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Transcriptome Analysis of Insulin Signaling-Associated Transcription Factors in C. elegans Reveal Their Genome-Wide Target Genes Specificity and Complexity

International journal of molecular sciences, 2021-11, Vol.22 (22), p.12462

2021

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An investigation of steroid biosynthesis pathway genes in women with polycystic ovary syndrome

Journal of human reproductive sciences, 2022-07, Vol.15 (3), p.240-249

2022

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Human reproductive genetics: Emerging technologies & clinical applications

Indian journal of medical research (New Delhi, India : 1994), 2022-09, Vol.156 (3), p.564

Halder, Ashutosh

2022

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22(R)-hydroxycholesterol for dopaminergic neuronal specification of MSCs and amelioration of Parkinsonian symptoms in rats

Cell death discovery, 2021-01, Vol.7 (1), p.13-13, Article 13

2021

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Amniotic band syndrome and/or limb body wall complex: split or lump

Application of clinical genetics, 2010-01, Vol.3 (default), p.7-15

Halder, Ashutosh

2010

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Dihydrotestosterone- A Potential Biomarker of Hyperandrogenaemia in Polycystic Ovary Syndrome: A Case-control Study from North India

Journal of clinical and diagnostic research, 2022-02, Vol.16 (2), p.QC09-QC14

2022

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Mosaicism in 22q11.2 Microdeletion Syndrome

Journal of clinical and diagnostic research, 2018-11, Vol.12 (11), p.GC01-GC06

2018

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Association of Cadmium, Chromium, Manganese and Lead with Hyperprolactinemia: A Pilot Study

Journal of clinical and diagnostic research, 2020, Vol.14 (1), p.QC04-QC07

2020

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Single Strand Conformation Polymorphism and Sequencing of HS6ST2 Gene in Patients of Idiopathic Premature Ovarian Failure

Journal of clinical and diagnostic research, 2020-02, Vol.14 (2), p.GC01-GC08

2020

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The therapeutic effect of bone marrow–derived liver cells in the phenotypic correction of murine hemophilia A

Blood, 2009-11, Vol.114 (20), p.4552-4561

2009

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Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size

Molecular cytogenetics, 2012-03, Vol.5 (1), p.13-13

2012

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CFTR gene variants in Indian congenital bilateral absence of vas deferens & its relevance in genetic counselling

Indian journal of medical research (New Delhi, India : 1994), 2020-12, Vol.152 (6), p.535-537

2020

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High Serum Estradiol and Heavy Metals Responsible for Human Spermiation Defect-A Pilot Study

Journal of clinical and diagnostic research, 2016-12, Vol.10 (12), p.RC09-RC13

2016

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SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome

Scientifica (Cairo), 2016-01, Vol.2016 (2016), p.1-18

2016

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Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India

BMC medical genetics, 2010-06, Vol.11 (1), p.101-101, Article 101

2010

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Cytokine profile in multiple myeloma

Cytokine (Philadelphia, Pa.), 2020-12, Vol.136, p.155271-155271, Article 155271

2020

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The Sertoli Cell Only Syndrome and Glaucoma in a Sex - Determining Region Y (SRY) Positive XX Infertile Male

Journal of clinical and diagnostic research, 2013-07, Vol.7 (7), p.1457-1459

2013

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LANDSCAPE OF PATHOGENIC MUTATIONS IN POLYCYSTIC OVARY SYNDROME: TOWARDS COMPREHENSIVE GENOMIC EVALUATIONS

Fertility and sterility, 2023-10, Vol.120 (4), p.e105-e105

2023

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Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray

Gene, 2021-10, Vol.801, p.145851-145851, Article 145851

2021

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Sertoli cell only syndrome: Status of sertoli cell maturation and function

Indian journal of endocrinology and metabolism, 2012-12, Vol.16 (Suppl 2), p.S512-S513

2012

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Music in medicine: An overview

Indian journal of clinical anaesthesia, 2023-03, Vol.10 (1), p.69-78

2023

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Comprehensive chromosomal screening for preimplantation genetic testing: A mini-review

Fertility Science and Research, 2023-10, Vol.10 (4), p.188-194

2023

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Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases

Molecular cytogenetics, 2008-08, Vol.1 (1), p.18-18

2008

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Metabolic markers in male infertility: a pilot study

Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome

Transcriptome Analysis of Insulin Signaling-Associated Transcription Factors in C. elegans Reveal Their Genome-Wide Target Genes Specificity and Complexity

An investigation of steroid biosynthesis pathway genes in women with polycystic ovary syndrome

Human reproductive genetics: Emerging technologies & clinical applications

22(R)-hydroxycholesterol for dopaminergic neuronal specification of MSCs and amelioration of Parkinsonian symptoms in rats

Amniotic band syndrome and/or limb body wall complex: split or lump

Dihydrotestosterone- A Potential Biomarker of Hyperandrogenaemia in Polycystic Ovary Syndrome: A Case-control Study from North India

Mosaicism in 22q11.2 Microdeletion Syndrome

Association of Cadmium, Chromium, Manganese and Lead with Hyperprolactinemia: A Pilot Study

Single Strand Conformation Polymorphism and Sequencing of HS6ST2 Gene in Patients of Idiopathic Premature Ovarian Failure

The therapeutic effect of bone marrow–derived liver cells in the phenotypic correction of murine hemophilia A

Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size

CFTR gene variants in Indian congenital bilateral absence of vas deferens & its relevance in genetic counselling

High Serum Estradiol and Heavy Metals Responsible for Human Spermiation Defect-A Pilot Study

SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome

Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India

Cytokine profile in multiple myeloma

The Sertoli Cell Only Syndrome and Glaucoma in a Sex - Determining Region Y (SRY) Positive XX Infertile Male

LANDSCAPE OF PATHOGENIC MUTATIONS IN POLYCYSTIC OVARY SYNDROME: TOWARDS COMPREHENSIVE GENOMIC EVALUATIONS

Identification of genomic imbalances (CNVs as well as LOH) in sertoli cell only syndrome cases through cytoscan microarray

Sertoli cell only syndrome: Status of sertoli cell maturation and function

Music in medicine: An overview

Comprehensive chromosomal screening for preimplantation genetic testing: A mini-review

Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases

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