NTHL1 defines novel cancer syndrome

por Kuiper, Roland P., Hoogerbrugge, Nicoline
Publicado 2015

Finding all BRCA pathogenic mutation carriers: best practice models

por Hoogerbrugge, Nicoline, Jongmans, Marjolijn CJ
Publicado 2016

“Patient Journeys”: improving care by patient involvement

por Bolz-Johnson, Matt, Meek, Jelena, Hoogerbrugge, Nicoline
Publicado 2019

Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

por Tischkowitz, Marc, Colas, Chrystelle, Pouwels, Sjaak, Hoogerbrugge, Nicoline
Publicado 2020

Response to Tomao, Panici, and Tomao

por Vos, Janet R, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline
Publicado 2019

Group medical visits in the follow-up of women with a BRCA mutation: design of a randomized controlled trial

por Visser, Annemiek, Prins, Judith B, Hoogerbrugge, Nicoline, van Laarhoven, Hanneke WM
Publicado 2011

Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes

por Vos, Janet R., Giepmans, Lisette, Röhl, Claas, Geverink, Nicoline, Hoogerbrugge, Nicoline
Publicado 2018

Determinants of adherence to recommendations for cancer prevention among Lynch Syndrome mutation carriers: A qualitative exploration

por Visser, Annemiek, Vrieling, Alina, Murugesu, Laxsini, Hoogerbrugge, Nicoline, Kampman, Ellen, Hoedjes, Meeke
Publicado 2017

Universal genetic assessment for women with ovarian cancer not yet achieved: The promises of universal tumor DNA testing

por Witjes, Vera M., Vos, Janet R., Ligtenberg, Marjolijn J.L., Hoogerbrugge, Nicoline
Publicado 2021

Genetic testing for Lynch syndrome in the first year of colorectal cancer: a review of the psychological impact

por Landsbergen, Karin M., Prins, Judith B., Brunner, Han G., Kraaimaat, Floris W., Hoogerbrugge, Nicoline
Publicado 2009

A review on age‐related cancer risks in PTEN hamartoma tumor syndrome

por Hendricks, Linda A.J., Hoogerbrugge, Nicoline, Schuurs‐Hoeijmakers, Janneke H.M., Vos, Janet R.
Publicado 2020

Candidate Gene Discovery in Hereditary Colorectal Cancer and Polyposis Syndromes–Considerations for Future Studies

por te Paske, Iris B. A. W., Ligtenberg, Marjolijn J. L., Hoogerbrugge, Nicoline, de Voer, Richarda M.
Publicado 2020

The yield and effectiveness of breast cancer surveillance in women with PTEN Hamartoma Tumor Syndrome

por Hoxhaj, Alma, Drissen, Meggie M.C.M., Vos, Janet R., Bult, Peter, Mann, Ritse M., Hoogerbrugge, Nicoline
Publicado 2022

Focusing on Patient Needs and Preferences May Improve Genetic Counseling for Colorectal Cancer

por Salemink, Simone, Dekker, Nicky, Kets, Carolien M., van der Looij, Erica, van Zelst-Stams, Wendy A. G., Hoogerbrugge, Nicoline
Publicado 2013

Familial gastric cancer: detection of a hereditary cause helps to understand its etiology

por Vogelaar, Ingrid P, van der Post, Rachel S, Bisseling, Tanya M, van Krieken, J Han JM, Ligtenberg, Marjolijn JL, Hoogerbrugge, Nicoline
Publicado 2012

Highlights from the seventh European Multidisciplinary Colorectal Cancer Congress (EMCCC) 2014

por Punt, Cornelis JA, Nagtegaal, Iris D, van de Velde, Cornelis J, Beets-Tan, Regina, Cats, Annemieke, Hoogerbrugge, Nicoline, Marijnen, Corrie A
Publicado 2015

European Reference Networks: challenges and opportunities

por Tumiene, Birute, Graessner, Holm, Mathijssen, Irene MJ, Pereira, Alberto M, Schaefer, Franz, Scarpa, Maurizio, Blay, Jean-Yves, Dollfus, Helene, Hoogerbrugge, Nicoline
Publicado 2021

The added value of mammography in different age-groups of women with and without BRCA mutation screened with breast MRI

por Vreemann, Suzan, van Zelst, Jan C. M., Schlooz-Vries, Margrethe, Bult, Peter, Hoogerbrugge, Nicoline, Karssemeijer, Nico, Gubern-Mérida, Albert, Mann, Ritse M.
Publicado 2018

DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct

por Sie, Aisha S, Spruijt, Liesbeth, van Zelst-Stams, Wendy AG, Mensenkamp, Arjen R, Ligtenberg, Marjolijn J, Brunner, Han G, Prins, Judith B, Hoogerbrugge, Nicoline
Publicado 2012

Adequacy of family history taking in ovarian cancer patients: a population-based study

por van Altena, Anne M., van Aarle, Sandra, Kiemeney, Lambertus A. L. M., Hoogerbrugge, Nicoline, Massuger, Leon F. A. G., de Hullu, Joanne A.
Publicado 2012