Martin Li

A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome

Lucy R. Osborne, Martin Li, Barbara R. Pober et al. · Nature Genetics · 2001 · 333 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +5

<i>BRAF</i> Mutation and <i>CDKN2A</i> Deletion Define a Clinically Distinct Subgroup of Childhood Secondary High-Grade Glioma

Matthew Mistry, Nataliya Zhukova, Daniele Merico et al. · Journal of Clinical Oncology · 2015 · 278 citations · Full text

Human Chromosome 7: DNA Sequence and Biology

Stephen W. Scherer, Joseph Cheung, Jeffrey R. MacDonald et al. · Science · 2003 · 214 citations · Full text

Dna, Cytogenetics, Genetics +24

Discovery of Human Inversion Polymorphisms by Comparative Analysis of Human and Chimpanzee DNA Sequence Assemblies

Lars Feuk, Jeffrey R. MacDonald, Terence Tang et al. · PLoS Genetics · 2005 · 202 citations · Full text

Genetics, Human Polymorphism, Genomics +19

Subclinical carotid atherosclerosis in patients with psoriatic arthritis

Lai‐Shan Tam, Qing Shang, Edmund K. Li et al. · Arthritis Care & Research · 2008 · 140 citations