Yanwei Sha

Xiamen, China

Last Updated: 09/26/2026

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Found 57 publications

CEP131 Deficiency Leads to Multiple Morphological Abnormalities of the Sperm Flagellum-Associated Male Infertility via Impaired CEP290 Interaction.

CEP131 Deficiency Leads to Multiple Morphological Abnormalities of the Sperm Flagellum-Associated Male Infertility via Impaired CEP290 Interaction.

Journal: Andrology

Published: November 29, 2025

Identification of a Homozygous Nonsense Variant in KCTD19 Causing Meiotic Arrest and Non-Obstructive Azoospermia in Humans.

Identification of a Homozygous Nonsense Variant in KCTD19 Causing Meiotic Arrest and Non-Obstructive Azoospermia in Humans.

Journal: Clinical genetics

Published: September 24, 2025

Mutations in CFAP57 disrupt the localization of MYH10 and IFT88, leading to flagellogenesis failure in humans and mice.

Mutations in CFAP57 disrupt the localization of MYH10 and IFT88, leading to flagellogenesis failure in humans and mice.

Journal: Human genomics

Published: July 23, 2025

Mechanisms of non-obstructive azoospermia caused by TOP6BL variants.

Mechanisms of non-obstructive azoospermia caused by TOP6BL variants.

Journal: Reproduction (Cambridge, England)

Published: July 02, 2025

Genetic Underpinnings of Oligoasthenoteratozoospermia.

Genetic Underpinnings of Oligoasthenoteratozoospermia.

Journal: Clinical genetics

Published: July 22, 2024

Novel bi-allelic DNAH3 variants cause oligoasthenoteratozoospermia.

Novel bi-allelic DNAH3 variants cause oligoasthenoteratozoospermia.

Journal: Frontiers in endocrinology

Published: July 10, 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

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants.

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants.

Journal: iScience

Published: March 03, 2024

Corrigendum to "Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis" [EBioMedicine 96(2023) 104798].

Corrigendum to "Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis" [EBioMedicine 96(2023) 104798].

Journal: EBioMedicine

Published: January 03, 2024

A novel homozygous splice variant in DNAAF4 is associated with asthenozoospermia.

A novel homozygous splice variant in DNAAF4 is associated with asthenozoospermia.

Journal: Acta biochimica et biophysica Sinica

Published: September 07, 2023

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

Journal: Human reproduction open

Published: July 19, 2023

Eif4enif1 haploinsufficiency disrupts oocyte mitochondrial dynamics and leads to subfertility.

Eif4enif1 haploinsufficiency disrupts oocyte mitochondrial dynamics and leads to subfertility.

Journal: Development (Cambridge, England)

Published: July 03, 2023

Showing 1-12 of 57

Last Updated: 09/26/2026