Hongchuan Nie

Changsha, China

Last Updated: 09/26/2026

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Found 19 publications

A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics.

A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics.

Journal: Journal of assisted reproduction and genetics

Published: November 10, 2025

Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.

Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.

Journal: Journal of assisted reproduction and genetics

Published: November 20, 2023

Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella.

Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella.

Journal: Frontiers in cell and developmental biology

Published: March 11, 2023

Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.

Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.

Journal: Journal of assisted reproduction and genetics

Published: October 06, 2022

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Journal: Frontiers in genetics

Published: May 05, 2022

Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.

Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.

Journal: Molecular human reproduction

Published: December 24, 2021

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia.

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia.

Journal: Journal of medical genetics

Published: September 30, 2021

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

Journal: American journal of human genetics

Published: September 03, 2021

TCF3 Regulates the Proliferation and Apoptosis of Human Spermatogonial Stem Cells by Targeting PODXL.

TCF3 Regulates the Proliferation and Apoptosis of Human Spermatogonial Stem Cells by Targeting PODXL.

Journal: Frontiers in cell and developmental biology

Published: April 15, 2021

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Journal: Human molecular genetics

Published: March 23, 2021

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

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

Journal: American journal of human genetics

Published: March 08, 2021

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Journal: Journal of assisted reproduction and genetics

Published: January 29, 2020

Showing 1-12 of 19

Last Updated: 09/26/2026