Bobby P C Koeleman
Bobby P C Koeleman
Medical Genetics, University Medical Center Utrecht, The Netherlands
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Mutation in blood coagulation factor V associated with resistance to activated protein C
RM Bertina, BPC Koeleman, T Koster, FR Rosendaal, RJ Dirven, ...
Nature 369 (6475), 64-67, 1994
50101994
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
BP Koeleman, PH Reitsma, CF Allaart, RM Bertina
6251994
15q13. 3 microdeletions increase risk of idiopathic generalized epilepsy
I Helbig, HC Mefford, AJ Sharp, M Guipponi, M Fichera, A Franke, ...
Nature genetics 41 (2), 160-162, 2009
5652009
Investigating neural primacy in Major Depressive Disorder: multivariate Granger causality analysis of resting-state fMRI time-series data
JP Hamilton, G Chen, ME Thomason, ME Schwartz, IH Gotlib
Molecular psychiatry 16 (7), 763-772, 2011
527*2011
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
4922018
Recurrent microdeletions at 15q11. 2 and 16p13. 11 predispose to idiopathic generalized epilepsies
CGF de Kovel, H Trucks, I Helbig, HC Mefford, C Baker, C Leu, C Kluck, ...
Brain 133 (1), 23-32, 2010
4082010
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
TRDJ Radstake, O Gorlova, B Rueda, JE Martin, BZ Alizadeh, ...
Nature genetics 42 (5), 426-429, 2010
3582010
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
AJ Monsuur, PIW de Bakker, BZ Alizadeh, A Zhernakova, MR Bevova, ...
Nature genetics 37 (12), 1341-1344, 2005
2742005
KIR in type 1 diabetes: disparate distribution of activating and inhibitory natural killer cell receptors in patients versus HLA-matched control subjects
AR van der Slik, BPC Koeleman, W Verduijn, GJ Bruining, BO Roep, ...
Diabetes 52 (10), 2639-2642, 2003
2662003
Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia
TGW Letteboer, JJ Mager, RJ Snijder, BPC Koeleman, D Lindhout, ...
Journal of medical genetics 43 (4), 371-377, 2006
2522006
Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases
A Zhernakova, BZ Alizadeh, M Bevova, MA van Leeuwen, MJH Coenen, ...
The American Journal of Human Genetics 81 (6), 1284-1288, 2007
2402007
Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation
M Firouzi, H Ramanna, B Kok, HJ Jongsma, BPC Koeleman, ...
Circulation research 95 (4), e29-e33, 2004
2182004
Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families?
BPC Koeleman, D Van Rumpt, K Hamulyak, PH Reitsma, RM Bertina
Thrombosis and haemostasis 74 (02), 580-583, 1995
2011995
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
1912014
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
O Gorlova, JE Martin, B Rueda, BPC Koeleman, J Ying, M Teruel, ...
PLoS Genet 7 (7), e1002178, 2011
1872011
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
O Gorlova, JE Martin, B Rueda, BPC Koeleman, J Ying, M Teruel, ...
PLoS Genet 7 (7), e1002178, 2011
1872011
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
O Gorlova, JE Martin, B Rueda, BPC Koeleman, J Ying, M Teruel, ...
PLoS Genet 7 (7), e1002178, 2011
1872011
Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies
F Dudbridge, BPC Koeleman
The American Journal of Human Genetics 75 (3), 424-435, 2004
1742004
Relative predispositional effects of HLA class II DRB1‐DQB1 haplotypes and genotypes on type 1 diabetes: a meta‐analysis
G Thomson, AM Valdes, JA Noble, I Kockum, MN Grote, J Najman, ...
Tissue antigens 70 (2), 110-127, 2007
1702007
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
A Suls, JA Jaehn, A Kecskés, Y Weber, S Weckhuysen, DC Craiu, ...
The American Journal of Human Genetics 93 (5), 967-975, 2013
1682013
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