feng zhang - Gynecology

Author Information

Feng Zhang is affiliated with the Obstetrics and Gynecology Hospital, NHC Key Laboratory of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), State Key Laboratory of Genetic Engineering at School of Life Sciences, Fudan University, Shanghai, China.

Research Contributions

Feng Zhang has made significant contributions to the field of reproductive health and genetics. His research primarily focuses on identifying genetic mutations and their impact on fertility and reproductive health. Notable studies include the identification of the VHL mutation in non-obstructive azoospermia-associated cystic renal cell carcinoma, and the discovery of the impact of X-linked TENT5D deficiency on male infertility. His work also extends to understanding the genetic basis of autism spectrum disorders and muscular dystrophy, showcasing a broad interest in genetic disorders beyond reproductive health.

Aliases

Feng Zhang

Publication and Citation Metrics

Publication Count	96
Citation Count	3202
h-index	31

Publications:

Whole-Exome Sequencing Identifies the VHL Mutation (c.262T > C, p.Try88Arg) in Non-Obstructive Azoospermia-Associated Cystic Renal Cell Carcinoma

DOI: 10.3390/curroncol29040192

Year: 2022

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

DOI: 10.1038/s41421-021-00369-9

Year: 2022

A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling

DOI: 10.1038/s41380-022-01539-1

Year: 2022

HSD17B12 dosage insufficiency induced premature ovarian insufficiency in humans and mice

DOI: 10.1002/ctm2.737

Year: 2022

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

DOI: 10.1186/s12958-021-00880-4

Year: 2022

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility

DOI: 10.1136/jmedgenet-2021-108271

Year: 2022

CEP128 is involved in spermatogenesis in humans and mice

DOI: 10.1038/s41467-022-29109-7

Year: 2022

Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient

DOI: 10.1002/mgg3.1820

Year: 2021

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

DOI: 10.1093/hmg/ddab185

Year: 2021

A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees

DOI: 10.1002/ajmg.a.62545

Year: 2021

Who Should Avoid Contraceptive Pills?

What is Pelvic Organ Prolapse?

What role do NSAIDs play in gynecological care?

How Can Providers Improve Their Non-Verbal Communication?

What Can Be Done to Address These Disparities?

Why is Prior Probability Important?

How Can Premenstrual Syndrome (PMS) Be Managed?

How Are RCTs Conducted in Gynecology?

What if You Feel Uncomfortable?

Why are Regular Ultrasounds Important?

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