Search details
1.
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.
Nat Genet
; 32(2): 235-6, 2002 Oct.
Article
in English
| MEDLINE | ID: mdl-12355084
2.
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.
Nat Genet
; 35(4): 315-7, 2003 Dec.
Article
in English
| MEDLINE | ID: mdl-14634647
3.
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.
Circ Res
; 92(1): 14-22, 2003 Jan 10.
Article
in English
| MEDLINE | ID: mdl-12522116
4.
A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands.
Diabetes
; 52(12): 3001-4, 2003 Dec.
Article
in English
| MEDLINE | ID: mdl-14633863
5.
A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands.
Diabetes
; 51(3): 856-9, 2002 Mar.
Article
in English
| MEDLINE | ID: mdl-11872691
6.
Candidate gene approach in association studies: would the factor V Leiden mutation have been found by this approach?
Eur J Hum Genet
; 12(6): 478-82, 2004 Jun.
Article
in English
| MEDLINE | ID: mdl-15054398
7.
Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.
Eur J Hum Genet
; 10(4): 271-5, 2002 Apr.
Article
in English
| MEDLINE | ID: mdl-12032736
8.
Linkage disequilibrium in young genetically isolated Dutch population.
Eur J Hum Genet
; 12(7): 527-34, 2004 Jul.
Article
in English
| MEDLINE | ID: mdl-15054401
9.
Differential immunogenicity of paternal HLA Class I antigens in pregnant women.
Hum Immunol
; 64(6): 600-6, 2003 Jun.
Article
in English
| MEDLINE | ID: mdl-12770790
10.
Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy.
Arch Ophthalmol
; 121(8): 1184-8, 2003 Aug.
Article
in English
| MEDLINE | ID: mdl-12912698
11.
Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations.
Psychiatr Genet
; 14(1): 13-23, 2004 Mar.
Article
in English
| MEDLINE | ID: mdl-15091311
12.
Linkage and association studies of IL1B and IL1RN gene polymorphisms in preeclampsia.
Hypertens Pregnancy
; 21(1): 23-38, 2002.
Article
in English
| MEDLINE | ID: mdl-12044341
13.
Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
; 141B(4): 367-73, 2006 Jun 05.
Article
in English
| MEDLINE | ID: mdl-16652356
14.
Cost-effective designs for linkage disequilibrium mapping of complex traits.
Am J Hum Genet
; 72(5): 1213-20, 2003 May.
Article
in English
| MEDLINE | ID: mdl-12696019
15.
Variance-component analysis of obesity in type 2 diabetes confirms loci on chromosomes 1q and 11q.
Obes Res
; 11(11): 1290-4, 2003 Nov.
Article
in English
| MEDLINE | ID: mdl-14627748
16.
Rapid N-acetyltransferase 2 imputed phenotype and smoking may increase risk of colorectal cancer in women (Netherlands).
Cancer Causes Control
; 14(3): 293-8, 2003 Apr.
Article
in English
| MEDLINE | ID: mdl-12814209
17.
A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9.
Am J Gastroenterol
; 99(3): 466-71, 2004 Mar.
Article
in English
| MEDLINE | ID: mdl-15056087
18.
Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophy.
Am J Hum Genet
; 75(1): 44-53, 2004 Jul.
Article
in English
| MEDLINE | ID: mdl-15154112
19.
Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33.
Am J Med Genet B Neuropsychiatr Genet
; 125B(1): 83-6, 2004 Feb 15.
Article
in English
| MEDLINE | ID: mdl-14755450
20.
A major non-HLA locus in celiac disease maps to chromosome 19.
Gastroenterology
; 125(4): 1032-41, 2003 Oct.
Article
in English
| MEDLINE | ID: mdl-14517787