Hao Geng

Multigenerational paternal obesity enhances the susceptibility to male subfertility in offspring via Wt1 N6-methyladenosine modification

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

Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

Cigarette Smoke-Induced Gastric Cancer Cell Exosomes Affected the Fate of Surrounding Normal Cells via the Circ0000670/Wnt/β-Catenin Axis

Novel <scp> <i>MEIOB</i> </scp> pathogenic variants including a homozygous non‐canonical splicing variant, cause meiotic arrest and human non‐obstructive azoospermia

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Loss of function mutation in <i>DNAH7</i> induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Novel <i>FSIP2</i> Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans

Biallelic loss‐of‐function mutations in <i>SEPTIN4</i> ( <i>C17ORF47</i> ), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

A novel homozygous mutation in the meiotic gene <i>MSH4</i> leading to male infertility due to non-obstructive azoospermia.

Cigarette smoke extract induces epithelial–mesenchymal transition of human bladder cancer T24 cells through activation of ERK1/2 pathway