Peter Devilee mainly investigates Breast cancer, Genetics, Cancer, Internal medicine and Genome-wide association study. His study in Breast cancer is interdisciplinary in nature, drawing from both Cancer research, Single-nucleotide polymorphism, Genotype and Genetic predisposition. His studies deal with areas such as Mutation, RNA and PALB2 as well as Cancer.
His Internal medicine research includes elements of Endocrinology and Oncology. He interconnects Mendelian randomization, Bioinformatics, Disease, Genetic association and 1000 Genomes Project in the investigation of issues within Genome-wide association study. His Allele research is multidisciplinary, relying on both Genetic marker, Molecular biology and DNA.
His primary areas of investigation include Breast cancer, Genetics, Internal medicine, Oncology and Cancer. His biological study spans a wide range of topics, including Cancer research, Genome-wide association study, Genotype, Single-nucleotide polymorphism and Ovarian cancer. His Genome-wide association study study combines topics in areas such as Genetic association and Bioinformatics.
Genetics is represented through his Allele, Gene, Locus, Germline mutation and Haplotype research. His Internal medicine study frequently draws connections between adjacent fields such as Pathology. He combines subjects such as Genetic predisposition, Case-control study, Gynecology, Prospective cohort study and Risk factor with his study of Oncology.
Peter Devilee spends much of his time researching Breast cancer, Genetics, Internal medicine, Oncology and Genome-wide association study. The Breast cancer study combines topics in areas such as Single-nucleotide polymorphism, Genetic association, Genotype and Bioinformatics. His Genetics research focuses on subjects like Paraganglioma, which are linked to SDHB and Pheochromocytoma.
Internal medicine is a component of his Hazard ratio, Ovarian cancer, Cancer, Proportional hazards model and Family history studies. His study on Oncology also encompasses disciplines like
Peter Devilee mainly focuses on Breast cancer, Genome-wide association study, Genetics, Internal medicine and Oncology. Breast cancer is a subfield of Cancer that Peter Devilee explores. His Genome-wide association study study incorporates themes from Mendelian randomization, Genetic predisposition, Locus and 1000 Genomes Project.
As a part of the same scientific study, Peter Devilee usually deals with the Genetics, concentrating on Menarche and frequently concerns with Genomic imprinting, Genetic architecture, Polymorphism, Population variance and Heritability. In his study, Methylation, Histone methylation, Epigenetics and Histone is inextricably linked to Pathology, which falls within the broad field of Internal medicine. His Oncology study integrates concerns from other disciplines, such as Relative risk, Gynecology, Ovarian cancer, Hazard ratio and Family history.
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Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
D Ford;D F Easton;M Stratton;S Narod.
American Journal of Human Genetics (1998)
Pathology and Genetics of Tumours of the Breast and Female Genital Organs
Fattaneh A. Tavassoli;Peter Devilee.
World Hhealth Organization Classification of Tumours (2003)
Mutations in the p53 gene occur in diverse human tumour types
Janice M. Nigro;Suzanne J. Baker;Antonette C. Preisinger;J. Milburn Jessup.
Nature (1989)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton;Karen A. Pooley;Alison M. Dunning;Paul D. P. Pharoah.
Nature (2007)
Mutations in SDHD, a Mitochondrial Complex II Gene, in Hereditary Paraganglioma
Bora E. Baysal;Robert E. Ferrell;Joan E. Willett-Brozick;Elizabeth C. Lawrence.
Science (2000)
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
Hanne Meijers-Heijboer;Ans van den Ouweland;Jan Klijn;Marijke Wasielewski.
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)
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)
Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype
Sunil R. Lakhani;Jorge S. Reis-Filho;Laura Fulford;Frederique Penault-Llorca.
Clinical Cancer Research (2005)
Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations
Sunil R. Lakhani;Jocelyne Jacquemier;John P Sloane;Barry A. Gusterson.
Journal of the National Cancer Institute (1998)
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