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Association Study of Single Nucleotide Polymorphisms on Chromosome 19q13 With Abdominal Aortic Aneurysm.
Published in:
Angiology, 2010, v. 61, n. 3, p. 243, doi. 10.1177/0003319709354752
By:
- Baas, Annette F.;
- Medic, Jelena;
- Van't Slot, Ruben;
- de Vries, Jean-Paul P. M.;
- Van Sambeek, Marc R. H. M.;
- Geelkerken, Bob H.;
- Boll, Bart P.;
- Grobbee, Diederick E.;
- Wijmenga, Cisca;
- Ruigrok, Ynte M.;
- Blankensteijn, Jan D.
Publication type:
Article
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
Published in:
Nature Genetics, 2008, v. 40, n. 1, p. 29, doi. 10.1038/ng.2007.52
By:
- van Es, Michael A.;
- van Vught, Paul W. J.;
- Blauw, Hylke M.;
- Franke, Lude;
- Saris, Christiaan G. J.;
- Van Den Bosch, Ludo;
- de Jong, Sonja W.;
- de Jong, Vianney;
- Baas, Frank;
- van't Slot, Ruben;
- Lemmens, Robin;
- Schelhaas, Helenius J.;
- Birve, Anna;
- Sleegers, Kristel;
- Van Broeckhoven, Christine;
- Schymick, Jennifer C.;
- Traynor, Bryan J.;
- Wokke, John H. J.;
- Wijmenga, Cisca;
- Robberecht, Wim
Publication type:
Article
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.
Published in:
Nature Genetics, 2005, v. 37, n. 12, p. 1341, doi. 10.1038/ng1680
By:
- Monsuur, Alienke J.;
- de Bakker, Paul I. W.;
- Alizadeh, Behrooz Z.;
- Zhernakova, Alexandra;
- Bevova, Marianna R.;
- Strengman, Eric;
- Franke, Lude;
- van't Slot, Ruben;
- van Belzen, Martine J.;
- Lavrijsen, Ineke C. M.;
- Diosdado, Begoña;
- Daly, Mark J.;
- Mulder, Chris J. J.;
- Mearin, M. Luisa;
- Meijer, Jos W. R.;
- Meijer, Gerrit A.;
- van Oort, Erica;
- Wapenaar, Martin C.;
- Koeleman, Bobby P. C.;
- Wijmenga, Cisca
Publication type:
Article
Genome-Wide Association Scan in HIV-1-Infected Individuals Identifying Variants Influencing Disease Course.
Published in:
PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022208
By:
- van Manen, Daniëlle;
- Delaneau, Olivier;
- Kootstra, Neeltje A.;
- Boeser-Nunnink, Brigitte D.;
- Limou, Sophie;
- Bol, Sebastiaan M.;
- Burger, Judith A.;
- Zwinderman, Aeilko H.;
- Moerland, Perry D.;
- Slot, Ruben van't;
- Zagury, Jean-François;
- van't Wout, Angélique B.;
- Schuitemaker, Hanneke
Publication type:
Article
Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus.
Published in:
European Journal of Human Genetics, 2013, v. 21, n. 5, p. 487, doi. 10.1038/ejhg.2012.206
By:
- Harakalova, Magdalena;
- van der Smagt, Jasper;
- de Kovel, Carolien G F;
- van't Slot, Ruben;
- Poot, Martin;
- Nijman, Isaac J;
- Medic, Jelena;
- Joziasse, Irene;
- Deckers, Jaap;
- Roos-Hesselink, Jolien W;
- Wessels, Marja W;
- Baars, Hubert F;
- Weiss, Marjan M;
- Pals, Gerard;
- Golmard, Lisa;
- Jeunemaitre, Xavier;
- Lindhout, Dick;
- Cuppen, Edwin;
- Baas, Annette F
Publication type:
Article
Discovery of variants unmasked by hemizygous deletions.
Published in:
European Journal of Human Genetics, 2012, v. 20, n. 7, p. 748, doi. 10.1038/ejhg.2011.263
By:
- Hochstenbach, Ron;
- Poot, Martin;
- Nijman, Isaac J;
- Renkens, Ivo;
- Duran, Karen J;
- van'T Slot, Ruben;
- van Binsbergen, Ellen;
- van der Zwaag, Bert;
- Vogel, Maartje J;
- Terhal, Paulien A;
- Ploos van Amstel, Hans Kristian;
- Kloosterman, Wigard P;
- Cuppen, Edwin
Publication type:
Article
Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations.
Published in:
European Journal of Human Genetics, 2011, v. 19, n. 6, p. 682, doi. 10.1038/ejhg.2011.2
By:
- Einarsdottir, Elisabet;
- Bevova, Marianna R.;
- Zhernakova, Alexandra;
- Monsuur, Alienke;
- Koskinen, Lotta L. E.;
- Slot, Ruben van't;
- Mulder, Chris;
- Mearin, M. Luisa;
- Korponay-Szabo, Ilma R.;
- Kaukinen, Katri;
- Kurppa, Kalle;
- Kere, Juha;
- Mäki, Markku;
- Wijmenga, Cisca;
- Saavalainen, Päivi
Publication type:
Article
Accurate determination of microsatellite allele frequencies in pooled DNA samples.
Published in:
European Journal of Human Genetics, 2004, v. 12, n. 11, p. 925, doi. 10.1038/sj.ejhg.5201234
By:
- Schnack, Hugo G;
- Bakker, Steven C;
- van't Slot, Ruben;
- Groot, Bart M;
- Sinke, Richard J;
- Kahn, Rene S;
- Pearson, Peter L
Publication type:
Article
Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy.
Published in:
PLoS Genetics, 2011, v. 7, n. 7, p. 1, doi. 10.1371/journal.pgen.1002178
By:
- Gorlova, Olga;
- Martin, Jose-Ezequiel;
- Rueda, Blanca;
- Koeleman, Bobby P. C.;
- Ying, Jun;
- Teruel, Maria;
- Diaz-Gallo, Lina-Marcela;
- Broen, Jasper C.;
- Vonk, Madelon C.;
- Simeon, Carmen P.;
- Alizadeh, Behrooz Z.;
- Coenen, Marieke J. H.;
- Voskuyl, Alexandre E.;
- Schuerwegh, Annemie J.;
- van Riel, Piet L. C. M.;
- Vanthuyne, Marie;
- Van't Slot, Ruben;
- Italiaander, Annet;
- Ophoff, Roel A.;
- Hunzelmann, Nicolas
Publication type:
Article
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 20, p. 4091, doi. 10.1093/hmg/ddq323
By:
- Blauw, Hylke M.;
- Al-Chalabi, Ammar;
- Andersen, Peter M.;
- van Vught, Paul W.J.;
- Diekstra, Frank P.;
- van Es, Michael A.;
- Saris, Christiaan G.J.;
- Groen, Ewout J.N.;
- van Rheenen, Wouter;
- Koppers, Max;
- van't Slot, Ruben;
- Strengman, Eric;
- Estrada, Karol;
- Rivadeneira, Fernando;
- Hofman, Albert;
- Uitterlinden, Andre G.;
- Kiemeney, Lambertus A.;
- Vermeulen, Sita H.M.;
- Birve, Anna;
- Waibel, Stefan
Publication type:
Article
Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 22, p. 3361, doi. 10.1093/hmg/ddl412
By:
- Ruigrok, Ynte M.;
- Rinkel, Gabriël J.E.;
- van't Slot, Ruben;
- Wolfs, Marcel;
- Tang, Song;
- Wijmenga, Cisca
Publication type:
Article
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.
Published in:
Neurogenetics, 2010, v. 11, n. 1, p. 81, doi. 10.1007/s10048-009-0205-1
By:
- Poot, Martin;
- Beyer, Vera;
- Schwaab, Ira;
- Damatova, Natalja;
- van’t Slot, Ruben;
- Prothero, Jo;
- Holder, Sue E.;
- Haaf, Thomas
Publication type:
Article

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