Lei Wang

CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

Bo Yuan, Lei Wang, Pengfei Liu et al. · Genetics in Medicine · 2020 · 68 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Mouse mutants in schizophrenia risk genes GRIN2A and AKAP11 show EEG abnormalities in common with schizophrenia patients

Linnea Herzog, Lei Wang, Eunah Yu et al. · Translational Psychiatry · 2023 · 62 citations · Full text

Life Sciences, Genetics, Psychiatry +17

Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease–associated loci for BAFopathies

Chun‐An Chen, John Lattier, Wenmiao Zhu et al. · Genetics in Medicine · 2021 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities

Fuad Chowdhury, Lei Wang, Mohammed Al‐Raqad et al. · Genetics in Medicine · 2021 · 25 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Contribution of uniparental disomy in a clinical trio exome cohort of 2675 patients

Lei Wang, Pengfei Liu, Weimin Bi et al. · Molecular Genetics & Genomic Medicine · 2021 · 11 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17