Xi Wang

12 Dahuisi Road
Haidian, 100081, China

Last Updated: 09/26/2026

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Found 12 publications

Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees.

Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees.

Journal: Molecular genetics & genomic medicine

Published: July 28, 2018

TMCO1 is essential for ovarian follicle development by regulating ER Ca2+ store of granulosa cells.

TMCO1 is essential for ovarian follicle development by regulating ER Ca2+ store of granulosa cells.

Journal: Cell death and differentiation

Published: July 19, 2017

Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.

Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.

Journal: Human reproduction (Oxford, England)

Published: April 27, 2017

A novel homozygous mutation of bone morphogenetic protein 15 identified in a consanguineous marriage family with primary ovarian insufficiency.

A novel homozygous mutation of bone morphogenetic protein 15 identified in a consanguineous marriage family with primary ovarian insufficiency.

Journal: Reproductive biomedicine online

Published: March 02, 2017

The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency.

The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency.

Journal: Menopause (New York, N.Y.)

Published: August 24, 2016

Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa.

Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa.

Journal: Oncotarget

Published: July 22, 2016

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina.

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina.

Journal: Oncotarget

Published: July 20, 2016

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

Journal: Journal of assisted reproduction and genetics

Published: April 03, 2016

CX3CR1 polymorphisms associated with an increased risk of developmental dysplasia of the hip in human.

CX3CR1 polymorphisms associated with an increased risk of developmental dysplasia of the hip in human.

Journal: Journal of orthopaedic research : official publication of the Orthopaedic Research Society

Published: March 11, 2016

A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency.

A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency.

Journal: Human reproduction (Oxford, England)

Published: February 25, 2016

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

Journal: Molecular human reproduction

Published: February 22, 2016

Genetic analysis of DACT1 in 100 Chinese Han women with Müllerian duct anomalies.

Genetic analysis of DACT1 in 100 Chinese Han women with Müllerian duct anomalies.

Journal: Reproductive biomedicine online

Published: August 18, 2015

Showing 1-12 of 12

Last Updated: 09/26/2026