Ruyi Wang

Novel homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous marriage family

Binbin Wang, Xu Ma, Yunxia Cao, 2020 .

Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.

Binbin Wang, Xu Ma, Yunxia Cao, 2019, Fertility and sterility.

Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating family

Binbin Wang, Xu Ma, Yunxia Cao, 2020, Journal of Ovarian Research.

Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD

Binbin Wang, Chengquan Ma, Hongjun Li, 2020, Molecular genetics & genomic medicine.

A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens

Binbin Wang, Hongjun Li, Ming-Xin Zhang, 2019, Journal of Assisted Reproduction and Genetics.

Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort

Binbin Wang, Xu Ma, Yunxia Cao, 2021, Frontiers in Genetics.

Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies

Binbin Wang, Yunxia Cao, Ying Zhu, 2021, Orphanet Journal of Rare Diseases.

Novel association of SNP rs2297828 in PRDM16 gene with predisposition to type 2 diabetes.

Z. Su, Xiaoqian Yu, Qiuyue Guan, 2022, Gene.