Feng Zhang

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Gao L, Zhang F, Hejtmancik JF, et al. (2024) Phenotypic and Genotypic Features of a Chinese Cohort with Retinal Hemangioblastoma. Genes. 15
Tian S, Faheem M, Satti HS, et al. (2024) A homozygous missense variant in YTHDC2 induces azoospermia in two siblings. Molecular Genetics and Genomics : Mgg. 299: 84
Zhou D, Wu H, Wang L, et al. (2024) Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice. Journal of Genetics and Genomics = Yi Chuan Xue Bao
Song C, Qin Y, Li Y, et al. (2024) Deleterious variants in RNF111 impair female fertility and induce premature ovarian insufficiency in humans and mice. Science China. Life Sciences
Mori T, Fujimaru T, Liu C, et al. (2024) CFAP47 is a novel causative gene implicated in X-linked polycystic kidney disease. Medrxiv : the Preprint Server For Health Sciences
Zhu X, Liu L, Tian S, et al. (2024) Deleterious variant in FAM71D cause male infertility with asthenoteratospermia. Molecular Genetics and Genomics : Mgg. 299: 35
Gao Y, Liu L, Tian S, et al. (2024) Whole-exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization. Andrology
Wang Y, Chen J, Huang X, et al. (2024) Gene-knockout by iSTOP enables rapid reproductive disease modeling and phenotyping in germ cells of the founder generation. Science China. Life Sciences
Chen S, Wang L, Chen L, et al. (2023) A novel preimplantation genetic testing strategy for a subtelomeric genetic disorder: A case study. Genes & Diseases. 11: 101014
Zhou Y, Wang Y, Chen J, et al. (2023) Dnali1 is required for sperm motility and male fertility in mice. Basic and Clinical Andrology. 33: 32