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Margreet G.E.M. Ausems

Medical Genetics Center · NL
Area of research
Genetics · Pathology and Forensic Medicine
Research interest
Research interests include BRCA gene mutations in cancer, Genetic factors in colorectal cancer, Nutrition, Genetics, and Disease, and Global Cancer Incidence and Screening.
h-index
56
citations
10,791
works
295
NIH funding
primary concept
Medicine
email

Recent publications

Cancer risks for other sites in addition to breast in CHEK2 c.1100delC families
Genetics in Medicine 2024cited by 12position: middledoi
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
Breast Cancer Research 2023cited by 13position: middledoi
Patients’ experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study
The Breast 2023cited by 11position: lastdoi
Mainstream germline genetic testing in men with metastatic prostate cancer: design and protocol for a multicenter observational study
BMC Cancer 2022cited by 14position: lastdoi
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
Cancers 2022cited by 5position: middledoi
European experts consensus: BRCA/homologous recombination deficiency testing in first-line ovarian cancer
Annals of Oncology 2021cited by 163position: middledoi
Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer
Familial Cancer 2021cited by 30position: lastdoi
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers
Breast Cancer Research 2020cited by 74position: middledoi
Lessons Learned from Setting Up a Prospective, Longitudinal, Multicenter Study with Women at High Risk for Breast Cancer
Cancer Epidemiology Biomarkers & Prevention 2020cited by 20position: middledoi
Systematic development of a training program for healthcare professionals to improve communication about breast cancer genetic counseling with low health literate patients
Familial Cancer 2020cited by 19position: middledoi
Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers
Breast Cancer Research 2020cited by 3position: middledoi
Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers
European Urology 2019cited by 235position: middledoi
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort
Familial Cancer 2019cited by 24position: lastdoi
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers
British Journal of Cancer 2019cited by 23position: middledoi
‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
Familial Cancer 2019cited by 16position: middledoi
Height and Body Mass Index as Modifiers of Breast Cancer Risk in <i>BRCA1</i>/<i>2</i> Mutation Carriers: A Mendelian Randomization Study
JNCI Journal of the National Cancer Institute 2018cited by 74position: middledoi
The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations
JNCI Cancer Spectrum 2018cited by 33position: middledoi
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition
British Journal of Cancer 2018cited by 19position: middledoi
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Nature Genetics 2017cited by 469position: middledoi
BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD
Journal of Assisted Reproduction and Genetics 2017cited by 50position: middledoi
Serum AMH levels in healthy women from<i>BRCA1/2</i>mutated families: are they reduced?
Human Reproduction 2016cited by 37position: middledoi
Am I My Family's Keeper? Disclosure Dilemmas in Next-Generation Sequencing
Human Mutation 2016cited by 27position: middledoi
Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline <i>CDH1</i> mutation carriers
Journal of Medical Genetics 2015cited by 561position: middledoi
Does rapid genetic counseling and testing in newly diagnosed breast cancer patients cause additional psychosocial distress? results from a randomized clinical trial
Genetics in Medicine 2015cited by 32position: middledoi
Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study
European Urology 2014cited by 248position: middledoi
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
PLoS Genetics 2013cited by 115position: middledoi
Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations
Journal of Medical Genetics 2013cited by 88position: middledoi
Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)
BMJ 2012cited by 232position: middledoi
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
Journal of Medical Genetics 2012cited by 119position: middledoi
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers
Breast Cancer Research 2012cited by 96position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Eveline M. A. Bleiker · Cancer Institute (WIA)4 papers (2015–2023)Mary E. Velthuizen · University Hospital Heidelberg3 papers (2019–2023)Frans B.L. Hogervorst · Amgen (United States)3 papers (2013–2019)Senno Verhoef · Friedrich-Alexander-Universität Erlangen-Nürnberg3 papers (2013–2019)Cora M. Aalfs · Utrecht University2 papers (2019–2023) · 2 papers (2013–2019)Frank J. Broekmans · University Medical Center Utrecht2 papers (2016–2017)Margriet Collée · Erasmus MC Cancer Institute2 papers (2019–2024)Matti A. Rookus · University Hospital Heidelberg2 papers (2012–2013) · 2 papers (2015–2019)Jan C. Oosterwijk · Sunnybrook Health Science Centre2 papers (2013–2016)Maria E. Velthuizen · Utrecht University2 papers (2013–2016)Lizet E. van der Kolk · Lund University2 papers (2016–2019)Theodora C van Tilborg · Utrecht University2 papers (2016–2017) · 2 papers (2016–2017)Kyra Bokkers · University Hospital Heidelberg2 papers (2021–2023)Arjen R. Mensenkamp · Eunice Kennedy Shriver National Institute of Child Health and Human Development2 papers (2019–2024)Arjen J. Witkamp · Utrecht University2 papers (2015–2023)Michael Hauptmann · Universitätsklinikum Brandenburg an der Havel1 papers (2012–2012) · 1 papers (2019–2019)