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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

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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