Lanlan Meng

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility

Chunyu Liu, Chaofeng Tu, Lingbo Wang et al. · The American Journal of Human Genetics · 2021 · 143 citations · Full text

Medicine, Genetics, Molecular Genetics +13

<i>DMC1</i> mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing

Wenbin He, Chaofeng Tu, Qiang Liu et al. · Journal of Medical Genetics · 2018 · 128 citations

Medicine, Genetics, Molecular Genetics +16

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice

Chaofeng Tu, Jiangshan Cong, Xiaojin He et al. · The American Journal of Human Genetics · 2021 · 115 citations · Full text

Medicine, Genetics, Molecular Genetics +7

Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

Yue‐Qiu Tan, Chaofeng Tu, Lanlan Meng et al. · Genetics in Medicine · 2017 · 113 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Biallelic mutations in <i>CFAP65</i> lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations

Weili Wang, Chaofeng Tu, Hongchuan Nie et al. · Journal of Medical Genetics · 2019 · 100 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16