Stig E. Bojesen focuses on Internal medicine, Genome-wide association study, Breast cancer, Genetics and Single-nucleotide polymorphism. Stig E. Bojesen works mostly in the field of Internal medicine, limiting it down to topics relating to Oncology and, in certain cases, Prostate cancer, as a part of the same area of interest. His work carried out in the field of Genome-wide association study brings together such families of science as Mendelian randomization, Genetic predisposition, Bioinformatics, Genetic association and Lung cancer.
His Breast cancer research is multidisciplinary, relying on both TOX3 and Genotype. His Genetics research focuses on subjects like Menarche, which are linked to Genomic imprinting and Genetic architecture. The study incorporates disciplines such as Cancer screening and Genotyping in addition to Single-nucleotide polymorphism.
His scientific interests lie mostly in Internal medicine, Breast cancer, Oncology, Genome-wide association study and Genetics. His study in Internal medicine focuses on Odds ratio, Hazard ratio, Cancer, Prospective cohort study and Lung cancer. His Cancer study combines topics from a wide range of disciplines, such as Germline mutation, Cohort study and C-reactive protein.
His work deals with themes such as Case-control study, Genetic predisposition, Genotype and Bioinformatics, which intersect with Breast cancer. Stig E. Bojesen usually deals with Oncology and limits it to topics linked to Confidence interval and Confounding. His Genome-wide association study study is associated with Single-nucleotide polymorphism.
Stig E. Bojesen mostly deals with Internal medicine, Breast cancer, Oncology, Genome-wide association study and Odds ratio. His Internal medicine research integrates issues from Gastroenterology and Mendelian randomization. Stig E. Bojesen does research in Breast cancer, focusing on Estrogen receptor specifically.
He has included themes like Single-nucleotide polymorphism, Allele, Confounding and Medical genetics in his Oncology study. His biological study spans a wide range of topics, including Expression quantitative trait loci, Computational biology and Prostate cancer. His Cancer study contributes to a more complete understanding of Genetics.
His primary areas of study are Internal medicine, Breast cancer, Odds ratio, Cancer and Gastroenterology. His Internal medicine study combines topics in areas such as Mendelian randomization and Oncology. The various areas that Stig E. Bojesen examines in his Breast cancer study include Genome-wide association study, Disease and Confidence interval.
In Genome-wide association study, Stig E. Bojesen works on issues like Quantitative trait locus, which are connected to Lung cancer. The Odds ratio study which covers Risk factor that intersects with Logistic regression, Epidemiology, Genetic predisposition, Estrogen Receptor Status and Family history. His research on Cancer concerns the broader Genetics.
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Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton;Karen A. Pooley;Alison M. Dunning;Paul D. P. Pharoah.
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
Nature Genetics (2013)
Statin Use and Reduced Cancer-Related Mortality
Sune F. Nielsen;Børge G. Nordestgaard;Stig E. Bojesen.
The New England Journal of Medicine (2012)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
A common coding variant in CASP8 is associated with breast cancer risk
Angela Cox;Alison M. Dunning;Montserrat Garcia-Closas;Sabapathy Balasubramanian.
Nature Genetics (2007)
C-reactive Protein As a Predictor of Prognosis in Chronic Obstructive Pulmonary Disease
Morten Dahl;Jørgen Vestbo;Peter Lange;Stig E. Bojesen.
American Journal of Respiratory and Critical Care Medicine (2007)
RAD51B in Familial Breast Cancer
Liisa M. Pelttari;Sofia Khan;Mikko Vuorela;Johanna I. Kiiski.
PLOS ONE (2016)
MicroRNA related polymorphisms and breast cancer risk
Sofia Khan;Dario Greco;Dario Greco;Kyriaki Michailidou;Roger L. Milne;Roger L. Milne.
PLOS ONE (2014)
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Stig E. Bojesen;Stig E. Bojesen;Karen A. Pooley;Sharon E. Johnatty;Jonathan Beesley.
Nature Genetics (2013)
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
Shahana Ahmed;Gilles Thomas;Maya Ghoussaini;Catherine S. Healey.
Nature Genetics (2009)
Profile was last updated on December 6th, 2021.
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