Yuanwei G. Zhang

443 Huangshan Road
Hefei, 230027, China

Last Updated: 09/26/2026

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Found 58 publications

ProjectSVR: mapping single-cell RNA-seq data to reference atlases by supported vector regression.

ProjectSVR: mapping single-cell RNA-seq data to reference atlases by supported vector regression.

Journal: Briefings in bioinformatics
Published: June 15, 2025

A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.

A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.

Journal: Human molecular genetics
Published: January 30, 2025

Editorial: Predicting high-risk individuals for common diseases using multi-omics and epidemiological data, volume II.

Editorial: Predicting high-risk individuals for common diseases using multi-omics and epidemiological data, volume II.

Journal: Frontiers in genetics
Published: August 21, 2023

A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella.

A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella.

Journal: Journal of assisted reproduction and genetics
Published: May 29, 2023

A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns.

A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns.

Journal: Clinical genetics
Published: March 21, 2023

A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation.

A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation.

Journal: Cell discovery
Published: January 31, 2023

Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans.

Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans.

Journal: iScience
Published: December 20, 2022

Editorial: Complexity of tumor microenvironment: A major culprit in cancer development, volume II.

Editorial: Complexity of tumor microenvironment: A major culprit in cancer development, volume II.

Journal: Frontiers in endocrinology
Published: December 18, 2022

Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice.

Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice.

Journal: JCI insight
Published: November 02, 2022

Editorial: Complexity of tumor microenvironment: A major culprit in cancer development.

Editorial: Complexity of tumor microenvironment: A major culprit in cancer development.

Journal: Frontiers in endocrinology
Published: October 02, 2022

A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans.

A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans.

Journal: Frontiers in genetics
Published: August 11, 2022

Biallelic mutations in RNA-binding protein ADAD2 cause spermiogenic failure and non-obstructive azoospermia in humans.

Biallelic mutations in RNA-binding protein ADAD2 cause spermiogenic failure and non-obstructive azoospermia in humans.

Journal: Human reproduction open
Published: August 08, 2022
Showing 1-12 of 58

Last Updated: 09/26/2026