His main research concerns Genetics, Psychiatry, Internal medicine, Genome-wide association study and Psychosis. His study looks at the relationship between Psychiatry and fields such as Ethnic group, as well as how they intersect with chemical problems. Receptor is closely connected to Endocrinology in his research, which is encompassed under the umbrella topic of Internal medicine.
His Genome-wide association study research incorporates themes from Alzheimer's disease, Odds ratio and Genetic association. His research in Psychosis intersects with topics in Schizophrenia, Incidence, First episode, Mania and Etiology. As a part of the same scientific study, he usually deals with the Single-nucleotide polymorphism, concentrating on Apolipoprotein E and frequently concerns with Bioinformatics.
His scientific interests lie mostly in Psychiatry, Genetics, Psychosis, Internal medicine and Disease. His Psychiatry research is multidisciplinary, incorporating elements of Ethnic group and Clinical psychology. Genetics is closely attributed to Alzheimer's disease in his research.
His Psychosis study frequently draws parallels with other fields, such as Schizophrenia. As part of his studies on Internal medicine, Kevin Morgan frequently links adjacent subjects like Endocrinology. His Genome-wide association study study frequently draws connections between related disciplines such as PICALM.
Kevin Morgan mainly investigates Disease, Genetics, Genome-wide association study, Gene and Genetic association. The Disease study combines topics in areas such as Exome sequencing and Bioinformatics. To a larger extent, Kevin Morgan studies Single-nucleotide polymorphism with the aim of understanding Genome-wide association study.
His Single-nucleotide polymorphism study incorporates themes from Cohort and Genomics. The study incorporates disciplines such as Immunology, TREM2, Microglia and Amyloid beta in addition to Gene. His Genetic association study integrates concerns from other disciplines, such as Genetic risk and Computational biology.
Kevin Morgan mostly deals with Disease, Genetics, Genome-wide association study, Genetic association and Gene. His studies deal with areas such as Exome sequencing, Bioinformatics and Medical genetics as well as Disease. His Genetics research integrates issues from Alzheimer's disease and Dementia with Lewy bodies.
His biological study spans a wide range of topics, including Bipolar disorder, Nonsynonymous substitution, TREM2, Genotyping and Heritability. His study in Genetic association is interdisciplinary in nature, drawing from both Differential Methylation, DNA methylation, Epigenome, Transcriptome and Cortex. His biological study spans a wide range of topics, including Apolipoprotein E and Single-nucleotide polymorphism.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The Associational Economy: Firms, Regions, and Innovation
Philip Nicholas Cooke;Kevin John Morgan.
OUP Catalogue (1999)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))
D Harold;R Abraham;P Hollingworth;R Sims.
Nature Genetics (2013)
The Learning Region: Institutions, Innovation and Regional Renewal
Kevin Morgan.
Regional Studies (1997)
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)
The Associational Economy: Firms, Regions, and Innovation
Kevin Morgan;Philip Cooke.
Social Science Research Network (1998)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)
Falls by elderly people at home: prevalence and associated factors.
A. J. Blake;K. Morgan;M. J. Bendall;H. Dallosso.
Age and Ageing (1988)
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
Valentina Escott-Price;Céline Bellenguez;Li-San Wang;Seung-Hoan Choi.
PLOS ONE (2014)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
King's College London
King's College London
King's College London
University of Cambridge
Van Andel Institute
University College London
University of Pretoria
Van Andel Institute
Mayo Clinic
Mayo Clinic
University of Cagliari
University of Notre Dame
University of Malaga
Argonne National Laboratory
Cornell University
University of Illinois at Urbana-Champaign
Hainan Medical University
Jilin University
Otto-von-Guericke University Magdeburg
Max Planck Society
Pennsylvania State University
Université Libre de Bruxelles
Government of Canada
University of Melbourne
University of Queensland
African Institute for Mathematical Sciences