2019 - Fellow of the Royal Society, United Kingdom
His scientific interests lie mostly in Genetics, Genome-wide association study, Cancer, Internal medicine and Colorectal cancer. His study connects Cancer research and Genetics. Ian Tomlinson interconnects Breast cancer, Case-control study, Genetic association and Genetic variation in the investigation of issues within Genome-wide association study.
His study looks at the relationship between Cancer and fields such as Pathology, as well as how they intersect with chemical problems. His study in Internal medicine is interdisciplinary in nature, drawing from both Gastroenterology, Endocrinology and Oncology. The Colorectal cancer study combines topics in areas such as Rectum, Metastasis and Microsatellite instability.
The scientist’s investigation covers issues in Genetics, Internal medicine, Colorectal cancer, Oncology and Genome-wide association study. Cancer, Germline mutation, Locus, Mutation and Genotype are among the areas of Genetics where the researcher is concentrating his efforts. His Internal medicine research includes themes of Gastroenterology and Pathology.
His Colorectal cancer research is multidisciplinary, incorporating perspectives in Cancer research, Carcinoma, Microsatellite instability and Bioinformatics. His Oncology research includes elements of Ovarian cancer, Proportional hazards model, Risk factor and Hazard ratio. His research in Genome-wide association study intersects with topics in Allele, Case-control study, Genetic association and Genetic predisposition.
Ian Tomlinson mostly deals with Internal medicine, Oncology, Colorectal cancer, Cancer and Breast cancer. While the research belongs to areas of Internal medicine, Ian Tomlinson spends his time largely on the problem of Single-nucleotide polymorphism, intersecting his research to questions surrounding Genetic variation. His Oncology research includes themes of Genome-wide association study, Microsatellite instability, Proportional hazards model, Hazard ratio and Endometrial cancer.
His studies in Cancer integrate themes in fields like Computational biology and Gene, Germline. His Gene study is related to the wider topic of Genetics. Particularly relevant to Mutation is his body of work in Genetics.
His main research concerns Colorectal cancer, Internal medicine, Oncology, Genome-wide association study and Cancer. The study incorporates disciplines such as Carcinoma, Computational biology and Case-control study in addition to Colorectal cancer. His Oncology study combines topics in areas such as Odds ratio, Microsatellite instability, Hazard ratio, Biomarker and Prospective cohort study.
His research on Genetics and Single-nucleotide polymorphism is centered around Genome-wide association study. His study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Germline mutation, Epidemiology of cancer and Proportional hazards model. His Cancer research is multidisciplinary, incorporating elements of Mutation, Cancer research, Anticipation and Genetic predisposition.
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.
A serine/threonine kinase gene defective in Peutz–Jeghers syndrome
A Hemminki;D Markie;I Tomlinson;E Avizienyte.
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
Tomlinson Ip;Alam Na;Rowan Aj;Barclay E.
Nature Genetics (2002)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)
Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.
Oliver M Sieber;Lara Lipton;Michael Crabtree;Karl Heinimann.
The New England Journal of Medicine (2003)
Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis
James R. Howe;Stina Roth;John C. Ringold;Robert W. Summers.
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Ian Tomlinson;Ian Tomlinson;Emily Webb;Luis Carvajal-Carmona;Peter Broderick.
Nature Genetics (2007)
Genetic prognostic and predictive markers in colorectal cancer.
Axel Walther;Elaine Johnstone;Charles Swanton;Charles Swanton;Rachel Midgley.
Nature Reviews Cancer (2009)
Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies
Xiaohong R. Yang;Jenny Chang-Claude;Ellen L. Goode;Fergus J. Couch.
Journal of the National Cancer Institute (2011)
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
Claire Palles;Jean-Baptiste Cazier;Kimberley M Howarth;Enric Domingo.
Nature Genetics (2013)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Profile was last updated on December 6th, 2021.
Research.com Ranking is based on data retrieved from the Microsoft Academic Graph (MAG).
The ranking d-index is inferred from publications deemed to belong to the considered discipline.
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: