Підписатись
Mathieu Platteel
Mathieu Platteel
UMCG dept. of Genetics
Підтверджена електронна адреса в umcg.nl
Назва
Посилання
Посилання
Рік
Multiple common variants for celiac disease influencing immune gene expression
PCA Dubois, G Trynka, L Franke, KA Hunt, J Romanos, A Curtotti, ...
Nature genetics 42 (4), 295-302, 2010
12092010
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ...
Nature genetics 43 (12), 1193-1201, 2011
9402011
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Nature genetics 46 (8), 818-825, 2014
7102014
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
4582010
Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA
RSN Fehrmann, RC Jansen, JH Veldink, HJ Westra, D Arends, ...
PLoS genetics 7 (8), e1002197, 2011
4342011
Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-κB signalling
G Trynka, A Zhernakova, J Romanos, L Franke, KA Hunt, G Turner, ...
Gut 58 (8), 1078-1083, 2009
2432009
HLA-A*02 is associated with a reduced risk and HLA-A*01 with an increased risk of developing EBV+ Hodgkin lymphoma
M Niens, RF Jarrett, B Hepkema, IM Nolte, A Diepstra, M Platteel, ...
Blood, The Journal of the American Society of Hematology 110 (9), 3310-3315, 2007
2072007
Common and different genetic background for rheumatoid arthritis and coeliac disease
MJH Coenen, G Trynka, S Heskamp, B Franke, CC van Diemen, ...
Human molecular genetics 18 (21), 4195-4203, 2009
1792009
Cell specific eQTL analysis without sorting cells
HJ Westra, D Arends, T Esko, MJ Peters, C Schurmann, K Schramm, ...
PLoS genetics 11 (5), e1005223, 2015
1372015
Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’
P Deelen, A Menelaou, EM Van Leeuwen, A Kanterakis, F Van Dijk, ...
European Journal of Human Genetics 22 (11), 1321-1326, 2014
1222014
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants
JY Hehir-Kwa, T Marschall, WP Kloosterman, LC Francioli, JA Baaijens, ...
Nature communications 7 (1), 1-10, 2016
1042016
Understanding human immune function using the resources from the Human Functional Genomics Project
MG Netea, LAB Joosten, Y Li, V Kumar, M Oosting, S Smeekens, ...
Nature medicine 22 (8), 831-833, 2016
712016
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
EM Van Leeuwen, LC Karssen, J Deelen, A Isaacs, C Medina-Gomez, ...
Nature communications 6 (1), 6065, 2015
512015
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly
A Kim, C Savary, C Dubourg, W Carré, C Mouden, H Hamdi-Roze, ...
Brain 142 (1), 35-49, 2019
472019
PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype–phenotype associations
MK Ten Kate, M Platteel, R Mulder, P Terpstra, GAF Nicolaes, PH Reitsma, ...
Human mutation 29 (7), 939-947, 2008
412008
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant
R Almeida, I Ricaño-Ponce, V Kumar, P Deelen, A Szperl, G Trynka, ...
Human molecular genetics 23 (9), 2481-2489, 2014
392014
Wellcome Trust Case Control Consortium (WTCCC)
G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ...
Thelma BK, Cukrowska B, Urcelay E, Bilbao JR, Mearin ML, Barisani D, Barrett …, 2011
372011
Susceptibility to chronic mucus hypersecretion, a genome wide association study
AE Dijkstra, J Smolonska, M Van Den Berge, C Wijmenga, P Zanen, ...
PloS one 9 (4), e91621, 2014
342014
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease
I Ricaño-Ponce, J Gutierrez-Achury, AF Costa, P Deelen, A Kurilshikov, ...
European Journal of Human Genetics 28 (3), 313-323, 2020
302020
A framework for the detection of de novo mutations in family-based sequencing data
LC Francioli, M Cretu-Stancu, KV Garimella, M Fromer, WP Kloosterman, ...
European Journal of Human Genetics 25 (2), 227-233, 2017
292017
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