Koeleman BP - Search Results

1

Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients.

van Eerde AM, Duran K, van Riel E, de Kovel CG, Koeleman BP, Knoers NV, Renkema KY, van der Horst HJ, Bökenkamp A, van Hagen JM, van den Berg LH, Wolffenbuttel KP, van den Hoek J, Feitz WF, de Jong TP, Giltay JC, Wijmenga C. van Eerde AM, et al. Among authors: koeleman bp. PLoS One. 2012;7(4):e31327. doi: 10.1371/journal.pone.0031327. Epub 2012 Apr 27. PLoS One. 2012. PMID: 22558067 Free PMC article.

2

Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux.

van Eerde AM, Koeleman BP, van de Kamp JM, de Jong TP, Wijmenga C, Giltay JC. van Eerde AM, et al. Among authors: koeleman bp. Pediatr Nephrol. 2007 Aug;22(8):1129-33. doi: 10.1007/s00467-007-0492-4. Epub 2007 May 12. Pediatr Nephrol. 2007. PMID: 17497182 Free PMC article.

3

Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis.

Kremer PH, Koeleman BP, Rinkel GJ, Diekstra FP, van den Berg LH, Veldink JH, Klijn CJ. Kremer PH, et al. Among authors: koeleman bp. J Neurol Neurosurg Psychiatry. 2016 Jul;87(7):693-6. doi: 10.1136/jnnp-2014-310094. Epub 2015 Aug 13. J Neurol Neurosurg Psychiatry. 2016. PMID: 26272027

4

Photoparoxysmal EEG response and genetic dissection of juvenile myoclonic epilepsy.

Koeleman BP, de Kovel CG, Kasteleijn-Nolst Trenité DG. Koeleman BP, et al. Epilepsy Behav. 2013 Jul;28 Suppl 1:S69-71. doi: 10.1016/j.yebeh.2012.07.016. Epilepsy Behav. 2013. PMID: 23756485 Review.

5

Polymorphisms in ACVRL1 and endoglin genes are not associated with sporadic and HHT-related brain AVMs in Dutch patients.

Boshuisen K, Brundel M, de Kovel CGF, Letteboer TG, Rinkel GJE, Westermann CJJ, Kim H, Pawlikowska L, Koeleman BPC, Klijn CJM. Boshuisen K, et al. Transl Stroke Res. 2013 Jun;4(3):375-378. doi: 10.1007/s12975-012-0231-4. Epub 2012 Nov 29. Transl Stroke Res. 2013. PMID: 24323303 Free PMC article.

6

Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population.

Zhernakova A, Eerligh P, Wijmenga C, Barrera P, Roep BO, Koeleman BP. Zhernakova A, et al. Among authors: koeleman bp. Genes Immun. 2005 Sep;6(6):459-61. doi: 10.1038/sj.gene.6364220. Genes Immun. 2005. PMID: 15875058

7

Lack of association between VEGF polymorphisms and ALS in a Dutch population.

Van Vught PW, Sutedja NA, Veldink JH, Koeleman BP, Groeneveld GJ, Wijmenga C, Uitdehaag BM, de Jong JM, Baas F, Wokke JH, Van den Berg LH. Van Vught PW, et al. Among authors: koeleman bp. Neurology. 2005 Nov 22;65(10):1643-5. doi: 10.1212/01.wnl.0000184514.39853.56. Neurology. 2005. PMID: 16301496

8

Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetes.

Zhernakova A, Alizadeh BZ, Eerligh P, Hanifi-Moghaddam P, Schloot NC, Diosdado B, Wijmenga C, Roep BO, Koeleman BP. Zhernakova A, et al. Among authors: koeleman bp. Genes Immun. 2006 Oct;7(7):544-9. doi: 10.1038/sj.gene.6364326. Epub 2006 Jul 20. Genes Immun. 2006. PMID: 16855620

9

CTLA4 is differentially associated with autoimmune diseases in the Dutch population.

Zhernakova A, Eerligh P, Barrera P, Wesoly JZ, Huizinga TW, Roep BO, Wijmenga C, Koeleman BP. Zhernakova A, et al. Among authors: koeleman bp. Hum Genet. 2005 Oct;118(1):58-66. doi: 10.1007/s00439-005-0006-z. Epub 2005 Jul 16. Hum Genet. 2005. PMID: 16025348

10

Association analysis of functional variants of the FcgRIIa and FcgRIIIa genes with type 1 diabetes, celiac disease and rheumatoid arthritis.

Alizadeh BZ, Valdigem G, Coenen MJ, Zhernakova A, Franke B, Monsuur A, van Riel PL, Barrera P, Radstake TR, Roep BO, Wijmenga C, Koeleman BP. Alizadeh BZ, et al. Among authors: koeleman bp. Hum Mol Genet. 2007 Nov 1;16(21):2552-9. doi: 10.1093/hmg/ddm194. Epub 2007 Jul 25. Hum Mol Genet. 2007. PMID: 17652100

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