Nicoline Hoogerbrugge
Nicoline Hoogerbrugge
Hoogleraar erfelijke kanker, medisch specialist
Подтвержден адрес электронной почты в домене gen.umcn.nl
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Hyperglycemia in the acute phase of stroke is not caused by stress.
F Van Kooten, N Hoogerbrugge, P Naarding, PJ Koudstaal
Stroke 24 (8), 1129-1132, 1993
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
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