Genetics, Genome-wide association study, Single-nucleotide polymorphism, Locus and Genetic association are his primary areas of study. His study in Genetics is interdisciplinary in nature, drawing from both Bipolar disorder and Case-control study. Within one scientific family, Stuart MacGregor focuses on topics pertaining to Glaucoma under Genome-wide association study, and may sometimes address concerns connected to Macular degeneration and Genetic correlation.
His work deals with themes such as Meta-analysis, Alcohol dependence, Polymorphism and Bioinformatics, which intersect with Single-nucleotide polymorphism. His research in Locus intersects with topics in Endometriosis and Cutaneous melanoma. His Genetic association research is multidisciplinary, incorporating elements of Quantitative trait locus and Heritability.
His scientific interests lie mostly in Genome-wide association study, Genetics, Single-nucleotide polymorphism, Internal medicine and Stereochemistry. His Genome-wide association study research incorporates elements of SNP, Odds ratio, Genetic association, Locus and Glaucoma. His work carried out in the field of Genetic association brings together such families of science as Meta-analysis and Heritability.
The concepts of his Single-nucleotide polymorphism study are interwoven with issues in Bioinformatics and Candidate gene. Stuart MacGregor has included themes like Gastroenterology, Mendelian randomization and Oncology in his Internal medicine study. His Stereochemistry research incorporates themes from Crystallography, Ligand, Medicinal chemistry and Regioselectivity.
His primary scientific interests are in Genome-wide association study, Internal medicine, Single-nucleotide polymorphism, Oncology and Genetics. His Genome-wide association study research includes elements of Meta-analysis, Disease, Genetic association, Locus and Glaucoma. He has researched Genetic association in several fields, including Genetic architecture and Heritability.
His studies deal with areas such as Gastroenterology and Mendelian randomization as well as Internal medicine. His biological study spans a wide range of topics, including Case-control study, Polymorphism, Barrett's esophagus and Genetic predisposition. The Oncology study combines topics in areas such as Skin cancer, Relative risk, Ovarian cancer, Breast cancer and Risk factor.
Stuart MacGregor mostly deals with Genome-wide association study, Single-nucleotide polymorphism, Genetics, Internal medicine and Odds ratio. His Genome-wide association study research includes themes of SNP, Genetic association, Glaucoma and Genetic architecture. His Single-nucleotide polymorphism research is multidisciplinary, incorporating elements of Polymorphism, Cutaneous melanoma, Mental health, Physiology and TAS1R2.
Many of his studies on Genetics involve topics that are commonly interrelated, such as Case-control study. His studies in Internal medicine integrate themes in fields like Gastroenterology, Oncology and Open angle glaucoma. His Odds ratio research integrates issues from Body mass index, Cancer, Mendelian randomization, Intraocular pressure and Confidence interval.
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.
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Shaun M. Purcell;Shaun M. Purcell;Naomi R. Wray;Jennifer L. Stone;Jennifer L. Stone;Peter M. Visscher.
Rare chromosomal deletions and duplications increase risk of schizophrenia
Jennifer L. Stone;Jennifer L. Stone;Jennifer L. Stone;Michael C. O’Donovan;Hugh Gurling;George K. Kirov.
A versatile gene-based test for genome-wide association studies
Jimmy Z. Liu;Allan F. Mcrae;Dale R. Nyholt;Sarah E. Medland.
American Journal of Human Genetics (2010)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
Ricardo Segurado;Sevilla D. Detera-Wadleigh;Douglas F. Levinson;Cathryn M. Lewis.
American Journal of Human Genetics (2003)
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned
N. R. Wray;M. L. Pergadia;D. H.R. Blackwood;B. W.J.H. Penninx.
Molecular Psychiatry (2012)
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Satoru Yokoyama;Susan L. Woods;Glen M. Boyle;Lauren G. Aoude.
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J M Verhoeven;Pirro G Hysi;Robert Wojciechowski;Robert Wojciechowski;Qiao Fan.
Nature Genetics (2013)
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
Kathryn P Burdon;Stuart Macgregor;Alex W Hewitt;Alex W Hewitt;Shiwani Sharma.
Nature Genetics (2011)
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Gudmar Thorleifsson;G Bragi Walters;Alex W Hewitt;Alex W Hewitt;Gisli Masson.
Nature Genetics (2010)
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis
Jodie N Painter;Carl A Anderson;Carl A Anderson;Dale R Nyholt;Stuart Macgregor.
Nature Genetics (2011)
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