Sinke RJ - Search Results

1

Accurate determination of microsatellite allele frequencies in pooled DNA samples.

Schnack HG, Bakker SC, van 't Slot R, Groot BM, Sinke RJ, Kahn RS, Pearson PL. Schnack HG, et al. Among authors: sinke rj. Eur J Hum Genet. 2004 Nov;12(11):925-34. doi: 10.1038/sj.ejhg.5201234. Eur J Hum Genet. 2004. PMID: 15305176

2

Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64.

Sinke RJ, Carlton VE, Juijn JA, Delhaas T, Bull L, van Berge Henegouwen GP, van Hattum J, Keller KM, Sinaasappel M, Bijleveld CM, Knol IE, Ploos van Amstel HK, Pearson PL, Berger R, Freimer NB, Houwen RH. Sinke RJ, et al. Hum Genet. 1997 Sep;100(3-4):382-7. doi: 10.1007/s004390050520. Hum Genet. 1997. PMID: 9272159 Free article.

3

Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.

Verbeek DS, Schelhaas JH, Ippel EF, Beemer FA, Pearson PL, Sinke RJ. Verbeek DS, et al. Among authors: sinke rj. Hum Genet. 2002 Oct;111(4-5):388-93. doi: 10.1007/s00439-002-0782-7. Epub 2002 Aug 30. Hum Genet. 2002. PMID: 12384780

4

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

Bakker SC, van der Meulen EM, Buitelaar JK, Sandkuijl LA, Pauls DL, Monsuur AJ, van 't Slot R, Minderaa RB, Gunning WB, Pearson PL, Sinke RJ. Bakker SC, et al. Among authors: sinke rj. Am J Hum Genet. 2003 May;72(5):1251-60. doi: 10.1086/375143. Epub 2003 Apr 4. Am J Hum Genet. 2003. PMID: 12679898 Free PMC article.

5

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.

van de Warrenburg BP, Verbeek DS, Piersma SJ, Hennekam FA, Pearson PL, Knoers NV, Kremer HP, Sinke RJ. van de Warrenburg BP, et al. Among authors: sinke rj. Neurology. 2003 Dec 23;61(12):1760-5. doi: 10.1212/01.wnl.0000098883.79421.73. Neurology. 2003. PMID: 14694043

6

Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations.

Verbeek DS, Piersma SJ, Hennekam EF, Ippel EF, Pearson PL, Sinke RJ. Verbeek DS, et al. Among authors: sinke rj. Eur J Hum Genet. 2004 Jun;12(6):441-6. doi: 10.1038/sj.ejhg.5201167. Eur J Hum Genet. 2004. PMID: 15026782

7

Neuregulin 1: genetic support for schizophrenia subtypes.

Bakker SC, Hoogendoorn ML, Selten JP, Verduijn W, Pearson PL, Sinke RJ, Kahn RS. Bakker SC, et al. Among authors: sinke rj. Mol Psychiatry. 2004 Dec;9(12):1061-3. doi: 10.1038/sj.mp.4001564. Mol Psychiatry. 2004. PMID: 15303101 Clinical Trial. No abstract available.

8

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.

Verbeek DS, van de Warrenburg BP, Wesseling P, Pearson PL, Kremer HP, Sinke RJ. Verbeek DS, et al. Among authors: sinke rj. Brain. 2004 Nov;127(Pt 11):2551-7. doi: 10.1093/brain/awh276. Epub 2004 Aug 11. Brain. 2004. PMID: 15306549

9

DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch families.

Bakker SC, van der Meulen EM, Oteman N, Schelleman H, Pearson PL, Buitelaar JK, Sinke RJ. Bakker SC, et al. Among authors: sinke rj. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):50-2. doi: 10.1002/ajmg.b.30089. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15389755

10

No association between 12 dopaminergic genes and schizophrenia in a large Dutch sample.

Hoogendoorn ML, Bakker SC, Schnack HG, Selten JP, Otten HG, Verduijn W, van der Heijden FM, Pearson PL, Kahn RS, Sinke RJ. Hoogendoorn ML, et al. Among authors: sinke rj. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):6-9. doi: 10.1002/ajmg.b.30147. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635698

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