Qing Tan

No 81 Meishan Road
Hefei, 230032, China

Last Updated: 09/26/2026

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Found 23 publications

Geographical association of heavy metal exposure and semen quality: A national multi-center study.

Geographical association of heavy metal exposure and semen quality: A national multi-center study.

Journal: Ecotoxicology and environmental safety

Published: November 26, 2024

Broadening the ARMC2 mutational phenotype: linking multiple morphological abnormalities of the Flagella to Pulmonary Manifestations in Primary Ciliary Dyskinesia.

Broadening the ARMC2 mutational phenotype: linking multiple morphological abnormalities of the Flagella to Pulmonary Manifestations in Primary Ciliary Dyskinesia.

Journal: Reproductive biology and endocrinology : RB&E

Published: August 07, 2024

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility.

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility.

Journal: Human genomics

Published: June 21, 2024

LRRC23 deficiency causes male infertility with idiopathic asthenozoospermia by disrupting the assembly of radial spokes.

LRRC23 deficiency causes male infertility with idiopathic asthenozoospermia by disrupting the assembly of radial spokes.

Journal: Clinical genetics

Published: May 16, 2023

Novel HYDIN variants associated with male infertility in two Chinese families.

Novel HYDIN variants associated with male infertility in two Chinese families.

Journal: Frontiers in endocrinology

Published: December 08, 2022

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans.

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans.

Journal: International journal of biological sciences

Published: June 11, 2022

Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF.

Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF.

Journal: Reproductive biology and endocrinology : RB&E

Published: April 30, 2022

Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.

Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.

Journal: Human mutation

Published: November 09, 2021

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF.

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF.

Journal: Reproductive biology and endocrinology : RB&E

Published: October 18, 2021

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.

Journal: Reproductive biology and endocrinology : RB&E

Published: August 25, 2021

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.

Journal: Journal of assisted reproduction and genetics

Published: July 23, 2021

Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family.

Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family.

Journal: Frontiers in genetics

Published: June 02, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026