Varaico: Literature-Extracted Genetic Variants

Gene:DNAH1
Variant:p.P3909delFs
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DNAH1

NM_015512.5:p.P3909delFs

Associated Papers

The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility.

Gao Y et al.

Human Reproduction Update, 2026

An electronic medical record retrieval system can be used to identify missed diagnosis in patients with primary ciliary dyskinesia.

Zhou W et al.

Journal of Internal Medicine, 2025

Genetic etiological spectrum of sperm morphological abnormalities.

Arora M et al.

Journal of Assisted Reproduction and Genetics, 2024

The Molecular Basis of Multiple Morphological Abnormalities of Sperm Flagella and Its Impact on Clinical Practice.

Zhou Y et al.

Genes, 2024

Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.

Long S et al.

Andrology, 2024

Novel compound heterozygous mutations in DNAH1 cause primary infertility in Han Chinese males with multiple morphological abnormalities of the sperm flagella.

Wang M et al.

Asian Journal of Andrology, 2023

Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.

Malcher A et al.

Andrology, 2022

Novel DNAH1 Mutation Loci Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Literature Review.

Zhuang BJ et al.

The World Journal of Men's Health, 2022

Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.

Cong PK et al.

Nature Communications, 2022

35618720 (PubMed )
Supplement: 41467_2022_30526_MOESM5_ESM.xlsx › Data_2

Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.

Li Y et al.

Human Reproduction (oxford, England), 2021

Successful Live Birth Following Natural Cycle Oocyte Retrieval in a Woman with Primary Infertility and Atypical Primary Ovarian Insufficiency with a DNAH1 Gene Deletion Mutation.

Liu M et al.

Genetic Testing and Molecular Biomarkers, 2021

Mutational landscape of DNAH1 in Chinese patients with multiple morphological abnormalities of the sperm flagella: cohort study and literature review.

Yu W et al.

Journal of Assisted Reproduction and Genetics, 2021

Novel bi-allelic mutations in DNAH1 cause multiple morphological abnormalities of the sperm flagella resulting in male infertility.

Jiang C et al.

Translational Andrology and Urology, 2021

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.

Tu C et al.

Scientific Reports, 2019

Associations between DNAH1 gene polymorphisms and male infertility: A retrospective study.

Yang X et al.

Medicine, 2018

Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men.

Auguste Y et al.

American Journal of Human Genetics, 2018

A systematic review on the genetics of male infertility in the era of next-generation sequencing.

Robay A et al.

Arab Journal of Urology, 2018

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.

Sha Y et al.

Fertility and Sterility, 2017

Homozygous DNAH1 frameshift mutation causes multiple morphological anomalies of the sperm flagella in Chinese.

Wang X et al.

Clinical Genetics, 2017

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