Xueping Sun

State Key Laboratory Of Reproductive Medicine And Offspring Health
Nanjing, China

Last Updated: 09/26/2026

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Found 10 publications

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

Journal: Frontiers in genetics

Published: April 09, 2026

Reproductive outcomes of mosaic embryo transfers in preimplantation genetic testing for structural rearrangement cycles: a retrospective cohort study.

Reproductive outcomes of mosaic embryo transfers in preimplantation genetic testing for structural rearrangement cycles: a retrospective cohort study.

Journal: Journal of assisted reproduction and genetics

Published: July 25, 2025

Analysis of three Chinese pedigrees affected with recurrent hydatidiform mole due to variants of NLRP7 gene

Analysis of three Chinese pedigrees affected with recurrent hydatidiform mole due to variants of NLRP7 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: October 02, 2022

Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations.

Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations.

Journal: Frontiers in genetics

Published: September 02, 2022

Novel bi-allelic variants in ACTL7A are associated with male infertility and total fertilization failure.

Novel bi-allelic variants in ACTL7A are associated with male infertility and total fertilization failure.

Journal: Human reproduction (Oxford, England)

Published: July 17, 2021

De novo mutation in COL2A1 leads to lethal foetal skeletal dysplasia.

De novo mutation in COL2A1 leads to lethal foetal skeletal dysplasia.

Journal: Bone

Published: July 05, 2021

A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.

A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.

Journal: Journal of assisted reproduction and genetics

Published: December 01, 2020

Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing.

Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing.

Journal: Journal of assisted reproduction and genetics

Published: November 28, 2020

Homozygous missense mutation Arg207Cys in the WEE2 gene causes female infertility and fertilization failure.

Homozygous missense mutation Arg207Cys in the WEE2 gene causes female infertility and fertilization failure.

Journal: Journal of assisted reproduction and genetics

Published: November 04, 2018

Identification of a novel c.822 G>T mutation of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia

Identification of a novel c.822 G>T mutation of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 08, 2013

Showing 1-10 of 10

Last Updated: 09/26/2026