Sinke RJ - Search Results

1

Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome.

Vorstman JA, Chow EW, Ophoff RA, van Engeland H, Beemer FA, Kahn RS, Sinke RJ, Bassett AS. Vorstman JA, et al. Among authors: sinke rj. Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):430-3. doi: 10.1002/ajmg.b.30827. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18646052 Free PMC article.

2

Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency.

Sjarif DR, Sinke RJ, Duran M, Beemer FA, Kleijer WJ, Ploos van Amstel JK, Poll-The BT. Sjarif DR, et al. Among authors: sinke rj. J Med Genet. 1998 Aug;35(8):650-6. doi: 10.1136/jmg.35.8.650. J Med Genet. 1998. PMID: 9719371 Free PMC article.

3

Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia.

Schelhaas HJ, Ippel PF, Hageman G, Sinke RJ, van der Laan EN, Beemer FA. Schelhaas HJ, et al. Among authors: sinke rj. J Neurol. 2001 Feb;248(2):113-20. doi: 10.1007/s004150170245. J Neurol. 2001. PMID: 11284128

4

Association between an agouti-related protein gene polymorphism and anorexia nervosa.

Vink T, Hinney A, van Elburg AA, van Goozen SH, Sandkuijl LA, Sinke RJ, Herpertz-Dahlmann BM, Hebebrand J, Remschmidt H, van Engeland H, Adan RA. Vink T, et al. Among authors: sinke rj. Mol Psychiatry. 2001 May;6(3):325-8. doi: 10.1038/sj.mp.4000854. Mol Psychiatry. 2001. PMID: 11326303

5

Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.

Sinke RJ, Ippel EF, Diepstraten CM, Beemer FA, Wokke JH, van Hilten BJ, Knoers NV, van Amstel HK, Kremer HP. Sinke RJ, et al. Arch Neurol. 2001 Nov;58(11):1839-44. doi: 10.1001/archneur.58.11.1839. Arch Neurol. 2001. PMID: 11708993

6

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

7

[Developmental disorder in girls due to Rett syndrome].

Pruissen DM, Sinke RJ, Terhal PA, Beemer FA, Peters AC. Pruissen DM, et al. Among authors: sinke rj. Ned Tijdschr Geneeskd. 2003 Aug 9;147(32):1560-3. Ned Tijdschr Geneeskd. 2003. PMID: 12942847 Dutch.

8

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.

9

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

10

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

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