Kenneth Morgan

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

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

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

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

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

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Imbalances in Dietary Consumption of Fatty Acids, Vegetables, and Fruits Are Associated With Risk for Crohn's Disease in Children

Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

A survey of genetic and epigenetic variation affecting human gene expression

An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.

Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene