Heutink P - Search Results

1

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.

Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, Varilo T, Peddle L, Rahman P, Piras G, Monne M, Murray S, Galver L, Peltonen L, Sabatti C, Collins A, Freimer N. Service S, et al. Among authors: heutink p. Nat Genet. 2006 May;38(5):556-60. doi: 10.1038/ng1770. Epub 2006 Apr 2. Nat Genet. 2006. PMID: 16582909

2

Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.

Bonifati V, Breedveld GJ, Squitieri F, Vanacore N, Brustenghi P, Harhangi BS, Montagna P, Cannella M, Fabbrini G, Rizzu P, van Duijn CM, Oostra BA, Meco G, Heutink P. Bonifati V, et al. Among authors: heutink p. Ann Neurol. 2002 Feb;51(2):253-6. doi: 10.1002/ana.10106. Ann Neurol. 2002. PMID: 11835383

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: heutink p. Diabetes. 2002 Mar;51(3):856-9. doi: 10.2337/diabetes.51.3.856. Diabetes. 2002. PMID: 11872691 Free article.

4

The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetes.

Njajou OT, Vaessen N, Oostra B, Heutink P, Van Duijn CM. Njajou OT, et al. Among authors: heutink p. Mol Genet Metab. 2002 Mar;75(3):290-1. doi: 10.1006/mgme.2002.3299. Mol Genet Metab. 2002. PMID: 11914044 No abstract available.

5

Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a Chinese kindred.

Zhao H, Tian Y, Breedveld G, Huang S, Zou Y, Y J, Chai J, Li H, Li M, Oostra BA, Lo WH, Heutink P. Zhao H, et al. Among authors: heutink p. Eur J Hum Genet. 2002 Mar;10(3):162-6. doi: 10.1038/sj.ejhg.5200790. Eur J Hum Genet. 2002. PMID: 11973619

6

Characterization of ZNF333, a novel double KRAB domain containing zinc finger gene on human chromosome 19p13.1.

Tian Y, Breedveld GJ, Huang S, Oostra BA, Heutink P, Lo WH. Tian Y, et al. Among authors: heutink p. Biochim Biophys Acta. 2002 Aug 19;1577(1):121-5. doi: 10.1016/s0167-4781(02)00397-4. Biochim Biophys Acta. 2002. PMID: 12151103

7

Gene finding in genetically isolated populations.

Heutink P, Oostra BA. Heutink P, et al. Hum Mol Genet. 2002 Oct 1;11(20):2507-15. doi: 10.1093/hmg/11.20.2507. Hum Mol Genet. 2002. PMID: 12351587 Review.

8

A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34.

Galjaard RJ, Smits AP, Tuerlings JH, Bais AG, Bertoli Avella AM, Breedveld G, de Graaff E, Oostra BA, Heutink P. Galjaard RJ, et al. Among authors: heutink p. Eur J Hum Genet. 2003 May;11(5):409-15. doi: 10.1038/sj.ejhg.5200982. Eur J Hum Genet. 2003. PMID: 12734547

9

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.

Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA; Tourette Syndrome Association International Consortium for Genetics. Verkerk AJ, et al. Among authors: heutink p. Genomics. 2003 Jul;82(1):1-9. doi: 10.1016/s0888-7543(03)00097-1. Genomics. 2003. PMID: 12809671

10

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. Among authors: heutink p. Mov Disord. 2003 Jul;18(7):751-7. doi: 10.1002/mds.10422. Mov Disord. 2003. PMID: 12815653

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