Shixiong Tian

发表

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

P. Zhou, Yunxia Cao, Huan Wu, 2021, Reproductive biomedicine online.

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.

M. Ikawa, P. Ray, L. Jin, 2020, American journal of human genetics.

NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes

S. Baig, J. Rendu, J. Fauré, 2022, Molecular Genetics and Genomics.

Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice

P. Ray, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

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

J. Veltman, M. O’Bryan, P. Ray, 2021, American journal of human genetics.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Y. Li, Yong-Gang Yao, Zhixi Su, 2023, American journal of human genetics.

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility

L. Jin, Yunxia Cao, Huan Wu, 2022, Journal of Medical Genetics.

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA

L. Jin, Yunxia Cao, Huan Wu, 2023, Journal of Medical Genetics.

Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice.

L. Jin, Yunxia Cao, Huan Wu, 2019, American journal of human genetics.

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility

Yong Zhu, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice.

L. Jin, H. Saiyin, P. Zhou, 2020, American journal of human genetics.

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

Yunxia Cao, Huan Wu, Xiaojin He, 2021, American journal of human genetics.

Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility

L. Jin, Yunxia Cao, Huan Wu, 2021, Cells.

A homozygous frameshift mutation in ADAD2 cause male infertility with spermatogenic impairments.

F. Tao, Yue Lv, L. Jin, 2023, Journal of genetics and genomics = Yi chuan xue bao.

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

Mohan Liu, Xiaojin He, Chunyu Liu, 2022, Cell Discovery.

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice

Yunxia Cao, Caroline Cazin, Xiaojin He, 2021, Journal of Medical Genetics.