2001 - Fellow of the Royal Society of Edinburgh
Member of the European Molecular Biology Organization (EMBO)
Fellow of The Academy of Medical Sciences, United Kingdom
His scientific interests lie mostly in Genetics, Genome-wide association study, Single-nucleotide polymorphism, Schizophrenia and DISC1. Heritability, Quantitative trait locus, Candidate gene, Linkage disequilibrium and Genetic variation are among the areas of Genetics where the researcher is concentrating his efforts. His Genome-wide association study research incorporates elements of Bioinformatics, Medical genetics, Disease, Genetic association and Genetic architecture.
David J. Porteous interconnects Alzheimer's disease and Cognition in the investigation of issues within Single-nucleotide polymorphism. His Schizophrenia research is multidisciplinary, incorporating elements of Bipolar disorder, Case-control study and Autism spectrum disorder. His DISC1 research is multidisciplinary, relying on both Psychosis, PDE4B, DISC2 and Scaffold protein.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Internal medicine, Gene and Genetic association. His research links Bipolar disorder with Genetics. His work deals with themes such as Schizophrenia and Psychosis, which intersect with Bipolar disorder.
His research in Genome-wide association study intersects with topics in Cognition, Disease, Heritability, Major depressive disorder and Genetic architecture. His studies deal with areas such as Neuroticism and Clinical psychology as well as Major depressive disorder. His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology and Oncology.
David J. Porteous mainly investigates Genome-wide association study, Genetics, Internal medicine, DNA methylation and Disease. His Genome-wide association study study integrates concerns from other disciplines, such as Evolutionary biology, Biobank, Mendelian randomization, Schizophrenia and Genetic association. His study focuses on the intersection of Schizophrenia and fields such as Clinical psychology with connections in the field of Depression, Socioeconomic status and Bipolar disorder.
His research in Gene, Genome, Quantitative trait locus, Single-nucleotide polymorphism and Allele are components of Genetics. As a member of one scientific family, David J. Porteous mostly works in the field of Internal medicine, focusing on Cardiology and, on occasion, PR interval. His Disease research integrates issues from Body mass index, Bioinformatics, Family history, Cohort and Comorbidity.
David J. Porteous spends much of his time researching Genome-wide association study, Genetics, Internal medicine, Genetic association and Disease. David J. Porteous has researched Genome-wide association study in several fields, including Biobank, Schizophrenia, Cohort study, COPD and Genetic architecture. His Schizophrenia study incorporates themes from Bipolar disorder, Depression and Autism spectrum disorder.
His Internal medicine research incorporates themes from Type 2 diabetes, Oncology and Cardiology. The study incorporates disciplines such as Genetic predisposition, DNA methylation, Mood, Meta-analysis and Major depressive disorder in addition to Genetic association. His studies in Disease integrate themes in fields like Body mass index, Intensive care, dNaM and Bioinformatics.
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.
Disruption of two novel genes by a translocation co-segregating with schizophrenia
J. Kirsty Millar;Julie C. Wilson-Annan;Susan Anderson;Sheila Christie.
Human Molecular Genetics (2000)
Schizophrenia and Affective Disorders—Cosegregation with a Translocation at Chromosome 1q42 That Directly Disrupts Brain-Expressed Genes: Clinical and P300 Findings in a Family
Douglas Blackwood;Douglas Blackwood;A. Fordyce;M. T. Walker;D. M. St Clair.
American Journal of Human Genetics (2001)
The candidate Wilms' tumour gene is involved in genitourinary development
Kathryn Pritchard-Jones;Stewart Fleming;Duncan Davidson;Wendy Bickmore.
Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis.
Natasha J. Caplen;Eric W.F.W. Alton;Peter G. Mddleton;Julia R. Dorin.
Nature Medicine (1995)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Naomi R. Wray;Stephan Ripke;Stephan Ripke;Stephan Ripke;Manuel Mattheisen;MacIej Trzaskowski.
Nature Genetics (2018)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
James J. Lee;Robbee Wedow;Aysu Okbay;Edward Kong.
Nature Genetics (2018)
Genome-wide association study identifies 74 loci associated with educational attainment
Aysu Okbay;Jonathan P. Beauchamp;Mark Alan Fontana;James J. Lee.
Genome-wide association studies establish that human intelligence is highly heritable and polygenic
G. Davies;A. Tenesa;A. Tenesa;A. Payton;J. Yang.
Molecular Psychiatry (2011)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F. Pardiñas;Peter Holmans;Andrew J. Pocklington;Valentina Escott-Price.
Nature Genetics (2018)
DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling.
J. Kirsty Millar;Benjamin S. Pickard;Shaun Mackie;Rachel James.
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