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 · 142 citations

Life Sciences, Genetics, Molecular Genetics +8

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 · 141 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 71 citations · Full text

Medicine, Dermatology, Bone Metabolism +16

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 · 46 citations

Public Health, Biostatistics, Genetics +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 · 44 citations · Full text

Medicine, Biostatistics, Genetics +17