Oostra BA - Search Results

1

EVI5 is a risk gene for multiple sclerosis.

Hoppenbrouwers IA, Aulchenko YS, Ebers GC, Ramagopalan SV, Oostra BA, van Duijn CM, Hintzen RQ. Hoppenbrouwers IA, et al. Among authors: oostra ba. Genes Immun. 2008 Jun;9(4):334-7. doi: 10.1038/gene.2008.22. Epub 2008 Apr 10. Genes Immun. 2008. PMID: 18401352

2

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: oostra ba. Mult Scler. 2007 Jan;13(1):17-24. doi: 10.1177/1352458506071216. Mult Scler. 2007. PMID: 17294607

3

Decreased systemic IL-7 and soluble IL-7Rα in multiple sclerosis patients.

Kreft KL, Verbraak E, Wierenga-Wolf AF, van Meurs M, Oostra BA, Laman JD, Hintzen RQ. Kreft KL, et al. Among authors: oostra ba. Genes Immun. 2012 Oct;13(7):587-92. doi: 10.1038/gene.2012.34. Epub 2012 Aug 23. Genes Immun. 2012. PMID: 22914435

4

N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam study.

Harhangi BS, Oostra BA, Heutink P, van Duijn CM, Hofman A, Breteler MM. Harhangi BS, et al. Among authors: oostra ba. J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):518-20. doi: 10.1136/jnnp.67.4.518. J Neurol Neurosurg Psychiatry. 1999. PMID: 10486401 Free PMC article.

5

CYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.

Harhangi BS, Oostra BA, Heutink P, van Duijn CM, Hofman A, Breteler MM. Harhangi BS, et al. Among authors: oostra ba. Mov Disord. 2001 Mar;16(2):290-3. doi: 10.1002/mds.1041. Mov Disord. 2001. PMID: 11295783 Clinical Trial.

6

Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.

Sleegers K, Roks G, Theuns J, Aulchenko YS, Rademakers R, Cruts M, van Gool WA, Van Broeckhoven C, Heutink P, Oostra BA, van Swieten JC, van Duijn CM. Sleegers K, et al. Among authors: oostra ba. Brain. 2004 Jul;127(Pt 7):1641-9. doi: 10.1093/brain/awh179. Epub 2004 May 6. Brain. 2004. PMID: 15130954

7

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: oostra ba. Neurology. 2005 Oct 25;65(8):1203-9. doi: 10.1212/01.wnl.0000178744.42953.b7. Epub 2005 Sep 14. Neurology. 2005. PMID: 16162858

8

Heritability of the function and structure of the arterial wall: findings of the Erasmus Rucphen Family (ERF) study.

Sayed-Tabatabaei FA, van Rijn MJ, Schut AF, Aulchenko YS, Croes EA, Zillikens MC, Pols HA, Witteman JC, Oostra BA, van Duijn CM. Sayed-Tabatabaei FA, et al. Among authors: oostra ba. Stroke. 2005 Nov;36(11):2351-6. doi: 10.1161/01.STR.0000185719.66735.dd. Epub 2005 Oct 20. Stroke. 2005. PMID: 16239631

9

Cerebrovascular risk factors do not contribute to genetic variance of cognitive function: the ERF study.

Sleegers K, de Koning I, Aulchenko YS, van Rijn MJ, Houben MP, Croes EA, van Swieten JC, Oostra BA, van Duijn CM. Sleegers K, et al. Among authors: oostra ba. Neurobiol Aging. 2007 May;28(5):735-41. doi: 10.1016/j.neurobiolaging.2006.03.012. Epub 2006 May 12. Neurobiol Aging. 2007. PMID: 16698126

10

STOX1 gene in pre-eclampsia and intrauterine growth restriction.

Berends AL, Bertoli-Avella AM, de Groot CJ, van Duijn CM, Oostra BA, Steegers EA. Berends AL, et al. Among authors: oostra ba. BJOG. 2007 Sep;114(9):1163-7. doi: 10.1111/j.1471-0528.2007.01414.x. Epub 2007 Jul 6. BJOG. 2007. PMID: 17617193

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