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Yanwei Sha

xiamen university

H指数:24

被引数:1,615

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

CEP131 缺乏通过破坏 CEP290 相互作用导致精子鞭毛相关形态异常和男性不育

IF3.4

2026-06-160

PRE

Mechanisms of non-obstructive azoospermia caused by TOP6BL variants

由TOP6BL变异引起的非梗阻性无精子症的机制

IF3.7

2025-12-010

PRE

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

鉴定导致人类减数分裂停滞和非梗阻性无精子症的KCTD19纯合无义变异。

Clinical Genetics

IF2.3

2025-11-010

PRE

Novel bi-allelic DNAH3 variants cause oligoasthenoteratozoospermia

新型双等位基因DNAH3变体导致少弱畸形性精子症

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2024-10-281

OAAI

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

IF4.3

2024-09-111

OAAI

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

DNAH3中的双等位基因变体导致人类和小鼠的男性不育和弱畸形性精子症

HUMAN REPRODUCTION OPEN

IF11.1

2024-01-115

OAAI

Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis

IF10.8

2023-10-016

OAAI

Genetic mechanisms of fertilization failure and early embryonic arrest: a comprehensive review

受精失败和早期胚胎停滞的遗传机制: 综述

HUMAN REPRODUCTION UPDATE

IF16.1

2023-09-2715

PRE

Novel mutations of TEX11 are associated with non-obstructive azoospermia

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-04-144

OAAI

TENT5D disruption causes oligoasthenoteratozoospermia and male infertility

IF3.4

2023-02-2313

PRE

Homozygous mutation in DNALI1 leads to asthenoteratozoospermia by affecting the inner dynein arms

DNALI1的纯合突变通过影响内部动力蛋白臂而导致弱畸形性精子症

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-01-167

OAAI

Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced in vitro fertilization

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-01-117

OAAI

Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice

JOURNAL OF MEDICAL GENETICS

IF3.7

2022-05-097

PRE

TBC1D21 is an essential factor for sperm mitochondrial sheath assembly and male fertility‡

BIOLOGY OF REPRODUCTION

IF3

2022-04-099

PRE

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2022-01-0132

OAAI

Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure

ACTA BIOCHIMICA ET BIOPHYSICA SINICA

IF3.4

2021-09-0318

OA

Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella

REPRODUCTIVE BIOMEDICINE ONLINE

IF3.5

2021-05-0137

PREAI

Mutations in DNAH8 contribute to multiple morphological abnormalities of sperm flagella and male infertility

ACTA BIOCHIMICA ET BIOPHYSICA SINICA

IF3.4

2021-03-1117

PRE

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY

IF4.7

2021-02-2027

OAAI

Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention

JOURNAL OF OVARIAN RESEARCH

IF4.2

2020-09-2241

OAAI