Kenneth Morgan

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee et al. · Nature Genetics · 1999 · 1.7K citations

Mendelian Disorder, Disease Mechanism, Genetic Disorder +13

SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis

Clemens Bergwitz, Nicole M. Roslin, Martin Tieder et al. · The American Journal of Human Genetics · 2006 · 479 citations · Full text

Slc34a3 Mutations, Urology, Molecular Physiology +10

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

Sara Brown, Yuka Asai, Heather J. Cordell et al. · Journal of Allergy and Clinical Immunology · 2011 · 466 citations · Full text

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

Alex Koufos, Paul E. Grundy, Kenneth Morgan et al. · PubMed · 1989 · 455 citations

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

James C. Engert, Pierre Bérubé, Jocelyne Mercier et al. · Nature Genetics · 2000 · 434 citations

Genetic Disorder, Genetics, New Gene +7