Snijders PJ - Search Results

1

A clinical-genetic study of Parkinson's disease in a genetically isolated community.

Dekker MC, van Swieten JC, Houwing-Duistermaat JJ, Snijders PJ, Boeren E, Hofman A, Breteler MM, Heutink P, Oostra BA, van Duijn CM. Dekker MC, et al. Among authors: snijders pj. J Neurol. 2003 Sep;250(9):1056-62. doi: 10.1007/s00415-003-0151-z. J Neurol. 2003. PMID: 14504966

2

Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population.

van Rijn MJ, Slooter AJ, Schut AF, Isaacs A, Aulchenko YS, Snijders PJ, Kappelle LJ, van Swieten JC, Oostra BA, van Duijn CM. van Rijn MJ, et al. Among authors: snijders pj. Neurology. 2005 Oct 25;65(8):1203-9. doi: 10.1212/01.wnl.0000178744.42953.b7. Epub 2005 Sep 14. Neurology. 2005. PMID: 16162858

3

A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands.

Vaessen N, Heutink P, Houwing-Duistermaat JJ, Snijders PJ, Rademaker T, Testers L, Batstra MR, Sandkuijl LA, van Duijn CM, Oostra BA. Vaessen N, et al. Among authors: snijders pj. Diabetes. 2002 Mar;51(3):856-9. doi: 10.2337/diabetes.51.3.856. Diabetes. 2002. PMID: 11872691 Free article.

4

A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands.

Aulchenko YS, Vaessen N, Heutink P, Pullen J, Snijders PJ, Hofman A, Sandkuijl LA, Houwing-Duistermaat JJ, Edwards M, Bennett S, Oostra BA, van Duijn CM. Aulchenko YS, et al. Among authors: snijders pj. Diabetes. 2003 Dec;52(12):3001-4. doi: 10.2337/diabetes.52.12.3001. Diabetes. 2003. PMID: 14633863

5

Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the Netherlands.

Bertoli-Avella AM, Dekker MC, Aulchenko YS, Houwing-Duistermaat JJ, Simons E, Testers L, Pardo LM, Rademaker TA, Snijders PJ, van Swieten JC, Bonifati V, Heutink P, van Duijn CM, Oostra BA. Bertoli-Avella AM, et al. Among authors: snijders pj. Hum Genet. 2006 Mar;119(1-2):51-60. doi: 10.1007/s00439-005-0108-7. Epub 2005 Dec 14. Hum Genet. 2006. PMID: 16369765

6

PET neuroimaging and mutations in the DJ-1 gene.

Dekker MC, Eshuis SA, Maguire RP, Veenma-van der Duijn L, Pruim J, Snijders PJ, Oostra BA, van Duijn CM, Leenders KL. Dekker MC, et al. Among authors: snijders pj. J Neural Transm (Vienna). 2004 Dec;111(12):1575-81. doi: 10.1007/s00702-004-0165-4. Epub 2004 Jun 21. J Neural Transm (Vienna). 2004. PMID: 15565491

7

Familial clustering of multiple sclerosis in a Dutch genetic isolate.

Hoppenbrouwers IA, Cortes LM, Aulchenko YS, Sintnicolaas K, Njajou O, Snijders PJ, Oostra BA, van Duijn CM, Hintzen RQ. Hoppenbrouwers IA, et al. Among authors: snijders pj. Mult Scler. 2007 Jan;13(1):17-24. doi: 10.1177/1352458506071216. Mult Scler. 2007. PMID: 17294607

8

Novel strategy to identify genetic risk factors for COPD severity: a genetic isolate.

van Diemen CC, Postma DS, Aulchenko YS, Snijders PJ, Oostra BA, van Duijn CM, Boezen HM. van Diemen CC, et al. Among authors: snijders pj. Eur Respir J. 2010 Apr;35(4):768-75. doi: 10.1183/09031936.00054408. Epub 2009 Sep 24. Eur Respir J. 2010. PMID: 19797132 Free article.

9

Clinical features and neuroimaging of PARK7-linked parkinsonism.

Dekker M, Bonifati V, van Swieten J, Leenders N, Galjaard RJ, Snijders P, Horstink M, Heutink P, Oostra B, van Duijn C. Dekker M, et al. Mov Disord. 2003 Jul;18(7):751-7. doi: 10.1002/mds.10422. Mov Disord. 2003. PMID: 12815653

10

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

Njajou OT, Vaessen N, Joosse M, Berghuis B, van Dongen JW, Breuning MH, Snijders PJ, Rutten WP, Sandkuijl LA, Oostra BA, van Duijn CM, Heutink P. Njajou OT, et al. Among authors: snijders pj. Nat Genet. 2001 Jul;28(3):213-4. doi: 10.1038/90038. Nat Genet. 2001. PMID: 11431687

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