Shixiong Tian

Shanghai MOST Key Laboratory Of Health And Disease Genomics, NHC Key Lab Of Reproduction Regulation
Shanghai, 200237, China

Last Updated: 09/26/2026

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Found 23 publications

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Journal: Science China. Life sciences

Published: August 15, 2024

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: April 18, 2024

Whole-exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization.

Whole-exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization.

Journal: Andrology

Published: September 13, 2023

A homozygous missense variant in YTHDC2 induces azoospermia in two siblings.

A homozygous missense variant in YTHDC2 induces azoospermia in two siblings.

Journal: Molecular genetics and genomics : MGG

Published: July 17, 2023

Deleterious variant in FAM71D cause male infertility with asthenoteratospermia.

Deleterious variant in FAM71D cause male infertility with asthenoteratospermia.

Journal: Molecular genetics and genomics : MGG

Published: December 18, 2022

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Journal: American journal of human genetics

Published: September 21, 2022

A homozygous frameshift mutation in ADAD2 causes male infertility with spermatogenic impairments.

A homozygous frameshift mutation in ADAD2 causes male infertility with spermatogenic impairments.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: August 26, 2022

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA.

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA.

Journal: Journal of medical genetics

Published: August 23, 2022

NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes.

NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes.

Journal: Molecular genetics and genomics : MGG

Published: April 14, 2022

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility.

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility.

Journal: Journal of medical genetics

Published: October 17, 2021

Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis.

Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis.

Journal: Cell discovery

Published: October 10, 2021

Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility.

Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility.

Journal: Cells

Published: April 16, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026