Sandkuijl LA - Search Results

1

Variance-component analysis of obesity in type 2 diabetes confirms loci on chromosomes 1q and 11q.

van Tilburg JH, Sandkuijl LA, Strengman E, Pearson PL, van Haeften TW, Wijmenga C. van Tilburg JH, et al. Among authors: sandkuijl la. Obes Res. 2003 Nov;11(11):1290-4. doi: 10.1038/oby.2003.175. Obes Res. 2003. PMID: 14627748 Free article.

2

A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9.

van Belzen MJ, Vrolijk MM, Meijer JW, Crusius JB, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: sandkuijl la. Am J Gastroenterol. 2004 Mar;99(3):466-71. doi: 10.1111/j.1572-0241.2004.04072.x. Am J Gastroenterol. 2004. PMID: 15056087

3

A major non-HLA locus in celiac disease maps to chromosome 19.

Van Belzen MJ, Meijer JW, Sandkuijl LA, Bardoel AF, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. Van Belzen MJ, et al. Among authors: sandkuijl la. Gastroenterology. 2003 Oct;125(4):1032-41. doi: 10.1016/s0016-5085(03)01205-8. Gastroenterology. 2003. PMID: 14517787

4

Rapid N-acetyltransferase 2 imputed phenotype and smoking may increase risk of colorectal cancer in women (Netherlands).

van der Hel OL, Bueno de Mesquita HB, Sandkuijl L, van Noord PA, Pearson PL, Grobbee DE, Peeters PH. van der Hel OL, et al. Cancer Causes Control. 2003 Apr;14(3):293-8. doi: 10.1023/a:1023601922106. Cancer Causes Control. 2003. PMID: 12814209

5

Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy.

Weigell-Weber M, Sarra GM, Kotzot D, Sandkuijl L, Messmer E, Hergersberg M. Weigell-Weber M, et al. Arch Ophthalmol. 2003 Aug;121(8):1184-8. doi: 10.1001/archopht.121.8.1184. Arch Ophthalmol. 2003. PMID: 12912698 Free article.

6

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

7

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

8

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

9

Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33.

Hong KS, McInnes LA, Service SK, Song T, Lucas J, Silva S, Fournier E, León P, Molina J, Reus VI, Sandkuijl LA, Freimer NB. Hong KS, et al. Among authors: sandkuijl la. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):83-6. doi: 10.1002/ajmg.b.20091. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755450

10

An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21.

Aaltonen J, Björses P, Sandkuijl L, Perheentupa J, Peltonen L. Aaltonen J, et al. Nat Genet. 1994 Sep;8(1):83-7. doi: 10.1038/ng0994-83. Nat Genet. 1994. PMID: 7987397

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