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Nicoline Hoogerbrugge
Nicoline Hoogerbrugge
Hoogleraar erfelijke kanker, medisch specialist
Bestätigte E-Mail-Adresse bei gen.umcn.nl
Titel
Zitiert von
Zitiert von
Jahr
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results
SE Plon, DM Eccles, D Easton, WD Foulkes, M Genuardi, MS Greenblatt, ...
Human mutation 29 (11), 1282-1291, 2008
10492008
A conservative and minimally invasive approach to necrotizing pancreatitis improves outcome
HC Van Santvoort, OJ Bakker, TL Bollen, MG Besselink, UA Ali, ...
Gastroenterology 141 (4), 1254-1263, 2011
9582011
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
MJL Ligtenberg, RP Kuiper, TL Chan, M Goossens, KM Hebeda, ...
Nature genetics 41 (1), 112-117, 2009
9372009
Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers
RS van der Post, IP Vogelaar, F Carneiro, P Guilford, D Huntsman, ...
Journal of medical genetics 52 (6), 361-374, 2015
6702015
Deficient mismatch repair system in patients with sporadic advanced colorectal cancer
M Koopman, GAM Kortman, L Mekenkamp, MJL Ligtenberg, ...
British journal of cancer 100 (2), 266-273, 2009
6162009
Cancer risks in BRCA2 families: estimates for sites other than breast and ovary
CJ Van Asperen, RM Brohet, EJ Meijers-Heijboer, N Hoogerbrugge, ...
Journal of medical genetics 42 (9), 711-719, 2005
5272005
The effect of growth hormone administration in growth hormone deficient adults on bone, protein, carbohydrate and lipid homeostasis, as well as on body composition
A Binnerts, GR Swart, JHP Wilson, N Hoogerbrugge, HAP Pois, ...
Clinical endocrinology 37 (1), 79-87, 1992
4181992
A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer
RDA Weren, MJL Ligtenberg, CM Kets, RM De Voer, ETP Verwiel, ...
Nature genetics 47 (6), 668-671, 2015
4112015
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general …
AC Antoniou, X Wang, ZS Fredericksen, L McGuffog, R Tarrell, ...
Nature genetics 42 (10), 885-892, 2010
4082010
Hereditary diffuse gastric cancer: updated clinical practice guidelines
VR Blair, M McLeod, F Carneiro, DG Coit, JL D'Addario, JM van Dieren, ...
The Lancet Oncology 21 (8), e386-e397, 2020
3772020
TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
MWG Ruijs, S Verhoef, MA Rookus, R Pruntel, AH van der Hout, ...
Journal of medical genetics 47 (6), 421-428, 2010
3742010
Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors
AR Mensenkamp, IP Vogelaar, WAG van Zelst–Stams, M Goossens, ...
Gastroenterology 146 (3), 643-646. e8, 2014
3642014
Risks of less common cancers in proven mutation carriers with lynch syndrome
C Engel, M Loeffler, V Steinke, N Rahner, E Holinski-Feder, W Dietmaier, ...
Journal of Clinical Oncology 30 (35), 4409-4415, 2012
3642012
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
MJE Kempers, RP Kuiper, CW Ockeloen, PO Chappuis, P Hutter, ...
The lancet oncology 12 (1), 49-55, 2011
3552011
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ...
Nature genetics 47 (2), 164-171, 2015
3242015
Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
AC Antoniou, J Beesley, L McGuffog, OM Sinilnikova, S Healey, ...
Cancer research 70 (23), 9742-9754, 2010
2602010
BRCA1-Associated Breast Cancers Present Differently From BRCA2-Associated and Familial Cases: Long-Term Follow-Up of the Dutch MRISC Screening Study
AJ Rijnsburger, IM Obdeijn, R Kaas, MMA Tilanus-Linthorst, C Boetes, ...
Journal of clinical oncology 28 (36), 5265-5273, 2010
2392010
Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers
RS Van der Post, LA Kiemeney, MJL Ligtenberg, JA Witjes, ...
Journal of medical genetics 47 (7), 464-470, 2010
2372010
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
SW Ten Broeke, RM Brohet, CM Tops, HM van der Klift, ME Velthuizen, ...
Journal of Clinical Oncology 33 (4), 319-325, 2015
2362015
Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)
M Nielsen, PF Franken, T Reinards, MM Weiss, A Wagner, H Van der Klift, ...
Journal of medical genetics 42 (9), e54-e54, 2005
2312005
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