Laurie H. Seaver

Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Jianming Fang, Susan L. Dagenais, Robert P. Erickson et al. · The American Journal of Human Genetics · 2000 · 609 citations · Full text

Mendelian Disorder, Genetic Disorder, Are Responsible +7

Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome

Claudia M.B. Carvalho, Melissa B. Ramocki, Davut Pehli̇van et al. · Nature Genetics · 2011 · 224 citations

Natural Sciences, Genetics, Genome Structure +11

Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

Margaret J. McMillin, Anita E. Beck, Jessica X. Chong et al. · The American Journal of Human Genetics · 2014 · 214 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

Decline in Prevalence of Neural Tube Defects in a High-Risk Region of the United States

Roger E. Stevenson, William Allen, G. Shashidhar Pai et al. · PEDIATRICS · 2000 · 211 citations

Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review

H. Eugene Hoyme, Laurie H. Seaver, W Crooks · American Journal of Medical Genetics · 1998 · 188 citations