2023 - Research.com Biology and Biochemistry in United Kingdom Leader Award
2019 - Fellow of the Royal Society, United Kingdom
Many of his studies on Gene apply to Fumarase as well. Ian Tomlinson conducts interdisciplinary study in the fields of Genetics and Molecular biology through his works. His multidisciplinary approach integrates Molecular biology and Gene in his work. Internal medicine and CDKN2A are commonly linked in his work. His study ties his expertise on Genetics together with the subject of CDKN2A. He integrates many fields, such as Oncology and Gynecology, in his works. In his works, he undertakes multidisciplinary study on Gynecology and Oncology. Ian Tomlinson combines Cancer and Lung in his research. In his work, Ian Tomlinson performs multidisciplinary research in Lung and Lung cancer.
His Genetics study frequently draws connections between related disciplines such as Gene expression. Ian Tomlinson incorporates Gene and Mutation in his studies. His study deals with a combination of Cancer and Body mass index. His Internal medicine study frequently involves adjacent topics like Odds ratio. He integrates many fields, such as Genotype and Allele, in his works. Ian Tomlinson incorporates Allele and Genotype in his research. Many of his studies on Single-nucleotide polymorphism involve topics that are commonly interrelated, such as SNP. Many of his studies on SNP apply to Single-nucleotide polymorphism as well. Ian Tomlinson merges many fields, such as Oncology and Gynecology, in his writings.
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)
Mutations in the SMAD4/DPC4 gene in juvenile polyposis.
James R. Howe;Stina Roth;John C. Ringold;Robert W. Summers.
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)
RAD51B in Familial Breast Cancer
Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski.
PLOS ONE (2016)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
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)
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)
The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis.
D I Swerdlow;M V Holmes;K B Kuchenbaecker.
The Lancet (2012)
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: