Chao-feng Tu

Changsha, 410078, China

Last Updated: 09/26/2026

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Found 10 publications

Biallelic variants in TBC1D8 are potentially associated with male infertility due to non-obstructive azoospermia or cryptozoospermia.

Biallelic variants in TBC1D8 are potentially associated with male infertility due to non-obstructive azoospermia or cryptozoospermia.

Journal: Asian journal of andrology

Published: February 20, 2025

Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans.

Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans.

Journal: Asian journal of andrology

Published: November 10, 2021

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans.

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans.

Journal: Asian journal of andrology

Published: October 10, 2020

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.

Journal: Human genetics

Published: August 19, 2020

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.

Journal: Human mutation

Published: April 06, 2020

Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?

Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?

Journal: Asian journal of andrology

Published: June 19, 2019

Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.

Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.

Journal: Asian journal of andrology

Published: May 23, 2018

Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China.

Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China.

Journal: Annals of hematology

Published: March 15, 2018

A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome.

A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome.

Journal: Asian journal of andrology

Published: September 01, 2017

DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing.

DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing.

Journal: Journal of medical genetics

Published: August 23, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026