His primary scientific interests are in Breast cancer, Internal medicine, Genome-wide association study, Genetics and Genotype. His research integrates issues of Odds ratio, Single-nucleotide polymorphism and Genetic predisposition in his study of Breast cancer. The various areas that Arto Mannermaa examines in his Internal medicine study include Endocrinology and Oncology.
His Genome-wide association study research is multidisciplinary, incorporating elements of Mendelian randomization, Bioinformatics, Disease, Locus and 1000 Genomes Project. His work in Genetics addresses subjects such as Menarche, which are connected to disciplines such as Quantitative trait locus. His research in Genotype focuses on subjects like Allele, which are connected to Immunology and Surgery.
His primary areas of study are Breast cancer, Internal medicine, Oncology, Genetics and Genotype. His Breast cancer research includes elements of Odds ratio and Single-nucleotide polymorphism, Genome-wide association study. His Genome-wide association study research incorporates elements of Genotyping, TOX3 and Genetic association.
His study in Internal medicine is interdisciplinary in nature, drawing from both Endocrinology and Pathology. His studies deal with areas such as Genetic predisposition, Gynecology, Proportional hazards model, Ovarian cancer and Hazard ratio as well as Oncology. His work investigates the relationship between Genotype and topics such as Immunology that intersect with problems in Disease.
Arto Mannermaa mostly deals with Breast cancer, Oncology, Internal medicine, Genome-wide association study and Estrogen receptor. His Breast cancer research is multidisciplinary, incorporating perspectives in Single-nucleotide polymorphism, Genotype and Locus. His Oncology research includes themes of Odds ratio, Case-control study, Gynecology, Proportional hazards model and Tissue microarray.
His work in the fields of Ovarian cancer, Prostate, Prostate cancer and Colorectal cancer overlaps with other areas such as Risk assessment. His Genome-wide association study research focuses on subjects like Bioinformatics, which are linked to Disease and Menarche. His research in Estrogen receptor intersects with topics in Polygenic risk score, Cancer research, Predictive marker, Radiation therapy and Tumor Subtype.
Arto Mannermaa mainly focuses on Breast cancer, Internal medicine, Oncology, Genome-wide association study and Genetics. The study incorporates disciplines such as Single-nucleotide polymorphism, Genotype and Case-control study in addition to Breast cancer. His Single-nucleotide polymorphism study combines topics from a wide range of disciplines, such as Allele and Pathology.
In his study, Proportional hazards model and Ki-67 is strongly linked to Gynecology, which falls under the umbrella field of Internal medicine. Arto Mannermaa has included themes like Body mass index, Penetrance and PALB2 in his Oncology study. His Genome-wide association study study combines topics in areas such as Cancer, Genetic predisposition and Locus.
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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)
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.
Breast-Cancer Risk in Families with Mutations in PALB2
A. C. Antoniou;S. Casadei;T. Heikkinen;D. Barrowdale.
The New England Journal of Medicine (2014)
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)
Apolipoprotein E epsilon4 allele, elevated midlife total cholesterol level, and high midlife systolic blood pressure are independent risk factors for late-life Alzheimer disease.
Miia Kivipelto;Eeva-Liisa Helkala;Mikko P. Laakso;Tuomo Hänninen.
Annals of Internal Medicine (2002)
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)
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)
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