Peikuan Cong

Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis

Pei-Wen Chiang, Juan Wang, Yang Chen et al. · Nature Genetics · 2012 · 140 citations

Identifies Nmnat1 Mutations, Developmental Biology, Mendelian Disorder +9

Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project

Peikuan Cong, Wei-Yang Bai, Jinchen Li et al. · Nature Communications · 2022 · 133 citations · Full text

Systemic evaluation of the relationship between psoriasis, psoriatic arthritis and osteoporosis: observational and Mendelian randomisation study

Jiangwei Xia, Shuyang Xie, Ke-Qi Liu et al. · Annals of the Rheumatic Diseases · 2020 · 65 citations · Full text

Genotype imputation and reference panel: a systematic evaluation on haplotype size and diversity

Wei-Yang Bai, Xiaowei Zhu, Peikuan Cong et al. · Briefings in Bioinformatics · 2019 · 45 citations

Genetics, Genomics, Reference Panel +17

Observational and genetic evidence highlight the association of human sleep behaviors with the incidence of fracture

Yu Qian, Jiangwei Xia, Ke-Qi Liu et al. · Communications Biology · 2021 · 40 citations · Full text