Ans M. W. van den Ouweland mainly focuses on Genetics, Breast cancer, Gene, Cancer and Genome-wide association study. Many of her studies involve connections with topics such as Tuberous sclerosis and Genetics. Her work deals with themes such as TOX3, Single-nucleotide polymorphism, Case-control study and Oncology, which intersect with Breast cancer.
As a part of the same scientific family, Ans M. W. van den Ouweland mostly works in the field of Gene, focusing on Molecular biology and, on occasion, PKD1, Chromosomal translocation, Polycystin 2, Polycystic kidney disease and Cosmid. Her Cancer study combines topics in areas such as CHEK2, Kinase activity and PALB2. Her Genome-wide association study study improves the overall literature in Genotype.
Ans M. W. van den Ouweland mostly deals with Genetics, Breast cancer, Internal medicine, Oncology and Gene. Her work focuses on many connections between Genetics and other disciplines, such as Tuberous sclerosis, that overlap with her field of interest in Genetic counseling. Her studies deal with areas such as Genome-wide association study, Single-nucleotide polymorphism, Case-control study and Bioinformatics as well as Breast cancer.
Her Internal medicine study incorporates themes from Germline mutation and Endocrinology. Her work in Oncology covers topics such as CHEK2 which are related to areas like PALB2. Her Gene study combines topics from a wide range of disciplines, such as Molecular biology and Mutation.
Her primary scientific interests are in Internal medicine, Genetics, Oncology, Breast cancer and Genome-wide association study. Ans M. W. van den Ouweland combines subjects such as Germline mutation and Gynecology with her study of Internal medicine. Ans M. W. van den Ouweland interconnects Odds ratio, Cancer, CHEK2, Estrogen receptor and Family history in the investigation of issues within Oncology.
Her Breast cancer research includes themes of Ovarian cancer and Case-control study. Ans M. W. van den Ouweland is researching Genome-wide association study as part of the investigation of Single-nucleotide polymorphism and Genotype. Her Molecular biology research incorporates themes from TSC2, Chromosome 22, TSC1 and Tuberous sclerosis.
Ans M. W. van den Ouweland focuses on Breast cancer, Internal medicine, Oncology, Genome-wide association study and Routine screening. Her Breast cancer study frequently links to related topics such as Relative risk. Her work carried out in the field of Oncology brings together such families of science as Odds ratio, Estrogen receptor, Family history and Disease.
Her Family history research is multidisciplinary, incorporating elements of Cancer, Ovarian cancer, Major gene, Allele and Cohort. The research on Single-nucleotide polymorphism and Genotype is part of her Genome-wide association study project. Her Single-nucleotide polymorphism research is multidisciplinary, relying on both Genotyping, Survival analysis and Bioinformatics.
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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.
Identification and characterization of the tuberous sclerosis gene on chromosome 16
Mark Nellist;Bart Janssen;Phillip T. Brook-Carter;Arjenne L. W. Hesseling-Janssen.
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34
Marjon van Slegtenhorst;Ronald de Hoogt;Caroline Hermans;Mark Nellist.
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)
THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16
Christopher Ward;Belén Peral;Jim Hughes;Siep Thomas.
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)
Identification of the familial cylindromatosis tumour-suppressor gene.
Graham R. Bignell;William Warren;Sheila Seal;Meiko Takahashi.
Nature Genetics (2000)
Interaction Between Hamartin and Tuberin, the TSC1 and TSC2 Gene Products
Marjon van Slegtenhorst;Mark Nellist;Bas Nagelkerken;Jeremy Cheadle.
Human Molecular Genetics (1998)
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
Shahana Ahmed;Gilles Thomas;Maya Ghoussaini;Catherine S. Healey.
Nature Genetics (2009)
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