Henian Cao

Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

Henian Cao · Human Molecular Genetics · 2000 · 655 citations · Full text

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

Christopher T. Johansen, Jian Wang, Matthew B. Lanktree et al. · Nature Genetics · 2010 · 441 citations

Genome-wide Association Study, Metabolic Syndrome, Allelic Variant +13

<i>PPARG</i> F388L, a Transactivation-Deficient Mutant, in Familial Partial Lipodystrophy

Robert A. Hegele, Henian Cao, Christy Frankowski et al. · Diabetes · 2002 · 261 citations · Full text

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)

Henian Cao, Robert A. Hegele · Journal of Human Genetics · 2003 · 221 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Severe hypertriglyceridemia is primarily polygenic

Jacqueline S. Dron, Jian Wang, Henian Cao et al. · Journal of clinical lipidology · 2018 · 205 citations · Full text