Xiang Li

Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR

David J. Vandenbergh, Antonio M. Persico, Anita L. Hawkins et al. · Genomics · 1992 · 709 citations · Full text

Molecular Neuroscience, Genetic Disorder, Genetics +9

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Ethylin Wang Jabs, Ulrich Müller, Xiang Li et al. · Cell · 1993 · 678 citations

Sclerostin, Developmental Biology, Genetic Disorder +6

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

Ethylin Wang Jabs, Xiang Li, Alan F. Scott et al. · Nature Genetics · 1994 · 471 citations

Fibrosis, Mendelian Disorder, Human Growth +9

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions

Kelly D. Farwell, Layla Shahmirzadi, Dima El‐Khechen et al. · Genetics in Medicine · 2014 · 462 citations · Full text

A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies <i>Taq</i>I RFLPs

Christopher K. Surratt, Antonio M. Persico, Xiaodong Yang et al. · FEBS Letters · 1993 · 82 citations · Full text