Tonghang Guo

The CAS Key Laboratory Of Innate Immunity And Chronic Disease
Hefei, 230027, China

Last Updated: 09/26/2026

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Found 9 publications

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

Correction to: Sexually transmitted infections and semen quality from subfertile men with and without leukocytospermia.

Correction to: Sexually transmitted infections and semen quality from subfertile men with and without leukocytospermia.

Journal: Reproductive biology and endocrinology : RB&E
Published: April 20, 2022

Sexually transmitted infections and semen quality from subfertile men with and without leukocytospermia.

Sexually transmitted infections and semen quality from subfertile men with and without leukocytospermia.

Journal: Reproductive biology and endocrinology : RB&E
Published: February 07, 2021

Association of Alcohol Intake and Semen Parameters in Men With Primary and Secondary Infertility: A Cross-Sectional Study.

Association of Alcohol Intake and Semen Parameters in Men With Primary and Secondary Infertility: A Cross-Sectional Study.

Journal: Frontiers in physiology
Published: May 28, 2020

Compound heterozygosity for novel AURKC mutations in an infertile man with macrozoospermia.

Compound heterozygosity for novel AURKC mutations in an infertile man with macrozoospermia.

Journal: Andrologia
Published: January 21, 2020

Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.

Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.

Journal: Clinical genetics
Published: May 20, 2019

Meiotic defects and decreased expression of genes located around the chromosomal breakpoint in the testis of a patient with a novel 46,X,t(Y;1)(p11.3;p31) translocation.

Meiotic defects and decreased expression of genes located around the chromosomal breakpoint in the testis of a patient with a novel 46,X,t(Y;1)(p11.3;p31) translocation.

Journal: International journal of molecular medicine
Published: April 19, 2016

Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia.

Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia.

Journal: Molecular cytogenetics
Published: June 08, 2015

Meiotic chromosome behavior in a human male t(8;15) carrier.

Meiotic chromosome behavior in a human male t(8;15) carrier.

Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: November 22, 2013
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Last Updated: 09/26/2026