Heutink P - Search Results

1

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, Stefansson H, Liu X, Pliner H, Lee JH, Cheng R; International Parkinson's Disease Genomics Consortium (IPDGC); Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI); 23andMe; GenePD; NeuroGenetics Research Consortium (NGRC); Hussman Institute of Human Genomics (HIHG); Ashkenazi Jewish Dataset Investigator; Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE); North American Brain Expression Consortium (NABEC); United Kingdom Brain Expression Consortium (UKBEC); Greek Parkinson's Disease Consortium; Alzheimer Genetic Analysis Group; Ikram MA, Ioannidis JP, Hadjigeorgiou GM, Bis JC, Martinez M, Perlmutter JS, Goate A, Marder K, Fiske B, Sutherland M, Xiromerisiou G, Myers RH, Clark LN, Stefansson K, Hardy JA, Heutink P, Chen H, Wood NW, Houlden H, Payami H, Brice A, Scott WK, Gasser T, Bertram L, Eriksson N, Foroud T, Singleton AB. Nalls MA, et al. Among authors: heutink p. Nat Genet. 2014 Sep;46(9):989-93. doi: 10.1038/ng.3043. Epub 2014 Jul 27. Nat Genet. 2014. PMID: 25064009 Free PMC article.

2

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.

3

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.

4

Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight.

Vaessen N, Janssen JA, Heutink P, Hofman A, Lamberts SW, Oostra BA, Pols HA, van Duijn CM. Vaessen N, et al. Among authors: heutink p. Lancet. 2002 Mar 23;359(9311):1036-7. doi: 10.1016/s0140-6736(02)08067-4. Lancet. 2002. PMID: 11937187

5

Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristics.

Njajou OT, de Jong G, Berghuis B, Vaessen N, Snijders PJ, Goossens JP, Wilson JH, Breuning MH, Oostra BA, Heutink P, Sandkuijl LA, van Duijn CM. Njajou OT, et al. Among authors: heutink p. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):439-43. doi: 10.1006/bcmd.2002.0581. Blood Cells Mol Dis. 2002. PMID: 12547233

6

Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21-22.

Savioz A, Riederer BM, Heutink P, Rizzu P, Tolnay M, Kövari E, Probst A, Riederer Ir, Bouras C, Leuba G. Savioz A, et al. Among authors: heutink p. Neurobiol Dis. 2003 Feb;12(1):46-55. doi: 10.1016/s0969-9961(02)00011-6. Neurobiol Dis. 2003. PMID: 12609488

7

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.

Hague S, Rogaeva E, Hernandez D, Gulick C, Singleton A, Hanson M, Johnson J, Weiser R, Gallardo M, Ravina B, Gwinn-Hardy K, Crawley A, St George-Hyslop PH, Lang AE, Heutink P, Bonifati V, Hardy J, Singleton A. Hague S, et al. Among authors: heutink p. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685

8

The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes.

Macedo MG, Anar B, Bronner IF, Cannella M, Squitieri F, Bonifati V, Hoogeveen A, Heutink P, Rizzu P. Macedo MG, et al. Among authors: heutink p. Hum Mol Genet. 2003 Nov 1;12(21):2807-16. doi: 10.1093/hmg/ddg304. Epub 2003 Sep 2. Hum Mol Genet. 2003. PMID: 12952867

9

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: heutink p. Diabetes. 2003 Dec;52(12):3001-4. doi: 10.2337/diabetes.52.12.3001. Diabetes. 2003. PMID: 14633863

10

Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.

Bertoli-Avella AM, Giroud-Benitez JL, Bonifati V, Alvarez-Gonzalez E, Heredero-Baute L, van Duijn CM, Heutink P. Bertoli-Avella AM, et al. Among authors: heutink p. Mov Disord. 2003 Nov;18(11):1240-9. doi: 10.1002/mds.10534. Mov Disord. 2003. PMID: 14639663

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