Kenneth Morgan

Overview

Best Publications

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

  A. Brooks-Wilson;M. Marcil;S. M. Clee;L.-H. Zhang

  2109
  Citations

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

  A Koufos;P Grundy;K Morgan;K A Aleck

  610
  Citations

• 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;J.C. Loredo-Osti

  591
  Citations

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

  Sara J. Brown;Sara J. Brown;Sara J. Brown;Yuka Asai;Heather J. Cordell;Linda E. Campbell

  552
  Citations

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

  F Rousseau;P Rouillard;M L Morel;E W Khandjian

  473
  Citations

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

  James C. Engert;Pierre Bérubé;Jocelyne Mercier;Carole Doré

  470
  Citations

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

  Jordan P Lerner-Ellis;Jamie C Tirone;Jamie C Tirone;Peter D Pawelek;Carole Doré

  450
  Citations

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

  Devendra K Amre;Savio D'Souza;Kenneth Morgan;Gillian Seidman

  434
  Citations

• Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

  J. Simard;P. Tonin;F. Durocher;K. Morgan

  411
  Citations

• Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.

  C. Dombrowski;S. Lévesque;M. L. Morel;P. Rouillard

  409
  Citations

• Allelic variation in TLR4 is linked to susceptibility to Salmonella enterica serovar Typhimurium infection in chickens.

  Gary Leveque;Vincenzo Forgetta;Shaun Morroll;Adrian L. Smith

  341
  Citations

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

  Patrick Frosk;Tracey Weiler;Edward Nylen;Thangirala Sudha

  337
  Citations

• Haplotype mapping and sequence analysis of the mouse Nramp gene predict susceptibility to infection with intracellular parasites.

  Danielle Malo;Kyle Vogan;Silvia Vidal;Jinxin Hu

  336
  Citations

• A survey of genetic and epigenetic variation affecting human gene expression.

  Tomi Pastinen;Robert Sladek;Scott Gurd;Alya’a Sammak

  325
  Citations

• Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11

  Paul Grundy;Alex Koufos;Kenneth Morgan;Frederick P. Li

  321
  Citations

• Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

  Celia M.T. Greenwood;T. Mary Fujiwara;T. Mary Fujiwara;Lucy J. Boothroyd;Mark A. Miller

  308
  Citations

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

  Laura Montermini;Andrea Richeter;Kenneth Morgan;Cristina M. Justice

  304
  Citations

• Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia

  Marie-Claude Vohl;Pierre Lepage;Daniel Gaudet;Carl G. Brewer

  253
  Citations

• Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene.

  Jing Liu;T.M. Fujiwara;N.T. Buu;F.O. Sanchez

  252
  Citations

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

  A Brooks-Wilson;Michel Marcil;Susanne M. Clee;Lin-Hua Zhang

  125
  Citations