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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

American journal of human genetics, 2003-05, Vol.72 (5), p.1251-1260

2003

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PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

American journal of human genetics, 2001-09, Vol.69 (3), p.629-634

2001

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Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

Journal of medical genetics, 2004-09, Vol.41 (9), p.652-657

2004

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

Molecular psychiatry, 2001-05, Vol.6 (3), p.325-328

2001

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Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura

Neurology, 2001-04, Vol.56 (8), p.1028-1032

2001

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A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

Nature genetics, 2001-07, Vol.28 (3), p.213-214

2001

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Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling

European journal of human genetics : EJHG, 1999-09, Vol.7 (6), p.713-716

1999

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Linkage-Disequilibrium Mapping of Disease Genes by Reconstruction of Ancestral Haplotypes in Founder Populations

American journal of human genetics, 1999-06, Vol.64 (6), p.1728-1738

1999

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Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

Nature genetics, 1994-12, Vol.8 (4), p.380-386

1994

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Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

Nature genetics, 1995-07, Vol.10 (3), p.351-353

1995

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An Apolipoprotein CIII Haplotype Protective Against Hypertriglyceridemia is Specified by Promoter and 3' Untranslated Region Polymorphisms

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (10), p.4562-4566

1993

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Clinical and genetic heterogeneity in benign hereditary chorea

Neurology, 2002-08, Vol.59 (4), p.579-584

2002

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Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23

Nature genetics, 1996-04, Vol.12 (4), p.436-441

1996

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Melanocortin-1 Receptor Variant R151C Modifies Melanoma Risk in Dutch Families with Melanoma

American journal of human genetics, 2001-10, Vol.69 (4), p.774-779

2001

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Score test for detecting linkage to quantitative traits

Genetic epidemiology, 2002-04, Vol.22 (4), p.345-355

2002

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A Genome-Wide Scan in Type 2 Diabetes Mellitus Provides Independent Replication of a Susceptibility Locus on 18p11 and Suggests the Existence of Novel Loci on 2q12 and 19q13

The journal of clinical endocrinology and metabolism, 2003-05, Vol.88 (5), p.2223-2230

2003

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Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

Nature genetics, 1993-12, Vol.5 (4), p.359-362

1993

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Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

Nature genetics, 1992-08, Vol.1 (5), p.368-371

1992

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A Gly15Arg Mutation in the Interleukin-10 Gene Reduces Secretion of Interleukin-10 in Crohn Disease

Scandinavian journal of gastroenterology, 2003-01, Vol.38 (6), p.611-617

2003

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Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

Genes and immunity, 2004-05, Vol.5 (3), p.215-220

2004

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Hereditary Vascular Retinopathy, Cerebroretinal Vasculopathy, and Hereditary Endotheliopathy with Retinopathy, Nephropathy, and Stroke Map to a Single Locus on Chromosome 3p21.1-p21.3

American journal of human genetics, 2001-08, Vol.69 (2), p.447-453

2001

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Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11

Human molecular genetics, 1994-01, Vol.3 (1), p.167-171

1994

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The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27

American journal of human genetics, 1999-09, Vol.65 (3), p.728-734

1999

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Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

Human genetics, 1995-11, Vol.96 (5), p.604-608

1995

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Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci

Journal of thrombosis and haemostasis, 2003-08, Vol.1 (8), p.1771-1776

2003

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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

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

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling

Linkage-Disequilibrium Mapping of Disease Genes by Reconstruction of Ancestral Haplotypes in Founder Populations

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

An Apolipoprotein CIII Haplotype Protective Against Hypertriglyceridemia is Specified by Promoter and 3' Untranslated Region Polymorphisms

Clinical and genetic heterogeneity in benign hereditary chorea

Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23

Melanocortin-1 Receptor Variant R151C Modifies Melanoma Risk in Dutch Families with Melanoma

Score test for detecting linkage to quantitative traits

A Genome-Wide Scan in Type 2 Diabetes Mellitus Provides Independent Replication of a Susceptibility Locus on 18p11 and Suggests the Existence of Novel Loci on 2q12 and 19q13

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

A Gly15Arg Mutation in the Interleukin-10 Gene Reduces Secretion of Interleukin-10 in Crohn Disease

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

Hereditary Vascular Retinopathy, Cerebroretinal Vasculopathy, and Hereditary Endotheliopathy with Retinopathy, Nephropathy, and Stroke Map to a Single Locus on Chromosome 3p21.1-p21.3

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11

The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci

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