Juleen A. Cavanaugh

Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

Heng Fong Seow, Stefan Bröer, Angelika Bröer et al. · Nature Genetics · 2004 · 274 citations · Full text

Mendelian Disorder, Biochemistry, Genetic Disorder +9

Molecular Cloning of Mouse Amino Acid Transport System B0, a Neutral Amino Acid Transporter Related to Hartnup Disorder

Angelika Bröer, Karin Klingel, Sonja Kowalczuk et al. · Journal of Biological Chemistry · 2004 · 249 citations · Full text

Amino Acids, Molecular Biology, Cytoskeleton +18

Screening for Hemochromatosis in Asymptomatic Subjects With or Without a Family History

Lawrie W. Powell, Jeannette L. Dixon, Grant A. Ramm et al. · Archives of Internal Medicine · 2006 · 202 citations · Full text

International Collaboration Provides Convincing Linkage Replication in Complex Disease through Analysis of a Large Pooled Data Set: Crohn Disease and Chromosome 16

Juleen A. Cavanaugh · The American Journal of Human Genetics · 2001 · 197 citations · Full text

Genome-wide Association Study, Disease Susceptibility, Molecular Epidemiology +10

Prevalence of CARD15/NOD2 Mutations in Caucasian Healthy People

Jean‐Pierre Hugot, Isabelle Zaccaria, Juleen A. Cavanaugh et al. · The American Journal of Gastroenterology · 2007 · 191 citations