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The role of genetic factors in age at natural menopause

Human reproduction (Oxford), 2001-09, Vol.16 (9), p.2014-2018

2001

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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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Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

Neurology, 2003-12, Vol.61 (12), p.1760-1765

2003

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Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3

Brain (London, England : 1878), 2004-11, Vol.127 (11), p.2551-2557

2004

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Numerical chromosomal abnormalities in equine embryos produced in vivo and in vitro

Molecular reproduction and development, 2005-09, Vol.72 (1), p.77-87

2005

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Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification

Clinical genetics, 2007-08, Vol.72 (2), p.122-129

2007

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Genome-wide linkage in a large dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13

Stroke (1970), 2004-10, Vol.35 (10), p.2276-2281

2004

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Neuregulin 1: genetic support for schizophrenia subtypes

Molecular psychiatry, 2004-12, Vol.9 (12), p.1061-1063

2004

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Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa

Human reproduction (Oxford), 1997-04, Vol.12 (4), p.752-754

1997

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Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

American journal of human genetics, 1989-12, Vol.45 (6), p.835-847

1989

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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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Identification of a new copper metabolism gene by positional cloning in a purebred dog population

Human molecular genetics, 2002-01, Vol.11 (2), p.165-173

2002

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Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only

Journal of medical genetics, 2000-12, Vol.37 (12), p.939-943

2000

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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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The effect of breed and intrauterine crowding on fetal erythropoiesis on day 35 of gestation in swine

Journal of animal science, 2003-09, Vol.81 (9), p.2352

2003

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A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21

Clinical genetics, 2009-05, Vol.75 (5), p.490-493

2009

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A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Nature (London), 1985-10, Vol.317 (6037), p.542-544

1985

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Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population

European journal of clinical investigation, 2003-12, Vol.33 (12), p.1070-1074

2003

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Anticipation in familial intracranial aneurysms in consecutive generations

European journal of human genetics : EJHG, 2003-10, Vol.11 (10), p.737-743

2003

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Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16

Human molecular genetics, 1999-03, Vol.8 (3), p.501-507

1999

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Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q

Oncogene, 1991-09, Vol.6 (9), p.1705-1711

1991

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Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations

Journal of medical genetics, 1989-09, Vol.26 (9), p.553-559

1989

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The PIP5K2A and RGS4 genes are differentially associated with deficit and non‐deficit schizophrenia

Genes, brain and behavior, 2007-03, Vol.6 (2), p.113-119

2007

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Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength

Neuromuscular disorders : NMD, 2008-11, Vol.18 (11), p.892-893

2008

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Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations

Cytogenetic and genome research, 2006-01, Vol.115 (3-4), p.254-261

2006

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The role of genetic factors in age at natural menopause

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

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3

Numerical chromosomal abnormalities in equine embryos produced in vivo and in vitro

Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification

Genome-wide linkage in a large dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13

Neuregulin 1: genetic support for schizophrenia subtypes

Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

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

Identification of a new copper metabolism gene by positional cloning in a purebred dog population

Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only

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

The effect of breed and intrauterine crowding on fetal erythropoiesis on day 35 of gestation in swine

A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population

Anticipation in familial intracranial aneurysms in consecutive generations

Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16

Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations

The PIP5K2A and RGS4 genes are differentially associated with deficit and non‐deficit schizophrenia

Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations

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