His primary scientific interests are in Genetics, Haplotype, Allele, Locus and Candidate gene. Kenneth Morgan has included themes like Molecular biology and Endocrinology in his Genetics study. His studies in Haplotype integrate themes in fields like Nucleic acid sequence, Fragile X syndrome, Allele frequency and Fragile X-associated tremor/ataxia syndrome, FMR1.
Kenneth Morgan has researched Allele in several fields, including Regulation of gene expression, Epigenetics, Human genome and Gene expression profiling. He combines subjects such as Aniridia, Genetic linkage and Wilms' tumor with his study of Locus. His Candidate gene research includes themes of Odds ratio, Immunology, Atopic dermatitis and Atopy.
Kenneth Morgan focuses on Genetics, Allele, Locus, Haplotype and Genetic linkage. His study brings together the fields of Molecular biology and Genetics. His biological study spans a wide range of topics, including Imprinting, Genetic variation, X chromosome and Genotype.
His study looks at the relationship between Locus and topics such as Limb-girdle muscular dystrophy, which overlap with Muscular dystrophy. His Haplotype research is multidisciplinary, incorporating elements of Ataxia, Chromosome, Mutation and Allele frequency. His Genetic linkage study incorporates themes from Chromosome 13, Chromosomal region, Linkage and Identity by descent.
His scientific interests lie mostly in Genetics, Immunology, Crohn's disease, Allele and Locus. As a part of the same scientific family, Kenneth Morgan mostly works in the field of Genetics, focusing on Internal medicine and, on occasion, Endocrinology. His study on Interleukin 10 and Asthma is often connected to Peanut allergy and Cryptococcal Pneumonia as part of broader study in Immunology.
In general Allele study, his work on Haplotype often relates to the realm of Offspring, thereby connecting several areas of interest. Kenneth Morgan frequently studies issues relating to Genetic linkage and Locus. His research in Genetic linkage focuses on subjects like Gene mapping, which are connected to Candidate gene.
His main research concerns Genetics, Disease gene identification, Internal medicine, Locus and Crohn's disease. His research integrates issues of Mucopolysaccharidosis and Rickets in his study of Genetics. His Rickets study integrates concerns from other disciplines, such as Hypercalciuria and Hypophosphatemia.
His study in Internal medicine is interdisciplinary in nature, drawing from both Gastroenterology and Pediatrics. His research in Locus intersects with topics in Calcitriol receptor and Chromosome 12. His Crohn's disease study combines topics in areas such as Logistic regression, Incidence, Retrospective cohort study and Confidence interval.
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Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
A. Brooks-Wilson;M. Marcil;S. M. Clee;L.-H. Zhang.
Nature Genetics (1999)
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
A Koufos;P Grundy;K Morgan;K A Aleck.
American Journal of Human Genetics (1989)
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.
American Journal of Human Genetics (2006)
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.
American Journal of Human Genetics (1995)
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.
The Journal of Allergy and Clinical Immunology (2011)
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.
Nature Genetics (2000)
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families
J. Simard;P. Tonin;F. Durocher;K. Morgan.
Nature Genetics (1994)
Premutation and intermediate-size FMR1 alleles in 10 572 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.
Human Molecular Genetics (2002)
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Jordan P Lerner-Ellis;Jordan P Lerner-Ellis;Jamie C Tirone;Jamie C Tirone;Peter D Pawelek;Carole Doré.
Nature Genetics (2006)
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.
The American Journal of Gastroenterology (2007)
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