Nicoline Hoogerbrugge
Nicoline Hoogerbrugge
Hoogleraar erfelijke kanker, medisch specialist
Verified email at
Cited by
Cited by
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes
C Troelstra, A van Gool, J de Wit, W Vermeulen, D Bootsma, ...
Cell 71 (6), 939-953, 1992
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, 2009
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
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
Subnuclear organization of the rat habenular complexes
KH Andres, MV Düring, RW Veh
Journal of Comparative Neurology 407 (1), 130-150, 1999
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 locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population
AC Antoniou, X Wang, ZS Fredericksen, L McGuffog, R Tarrell, ...
Nature genetics 42 (10), 885-892, 2010
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
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
The development of a short form of the EMBU: Its appraisal with students in Greece, Guatemala, Hungary and Italy
WA Arrindell, E Sanavio, G Aguilar, C Sica, C Hatzichristou, M Eisemann, ...
Personality and individual Differences 27 (4), 613-628, 1999
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
Genetical studies in pears
MB Crane, D Lewis
Journal of Genetics 43 (1-2), 31, 1942
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
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
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, ...
J Clin Oncol 30 (35), 4409-4415, 2012
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, 2015
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
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
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
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