G. Ommen

发表

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

J. Sutcliffe, S. Richards, G. Riggins, 1991, Cell.

Supplementary Information Whole-genome sequence variation , population structure and demographic history of the Dutch population

Pieter B. T. Neerincx, Jeroen F. J. Laros, David van Enckevort, 2022 .

Chromosomal localization and preliminary characterization of the human gene encoding insulin-like growth factor II

G. Ommen, J. Sussenbach, G. van Ommen, 2004, Human Genetics.

Rapid detection of BRCA1 mutations by the protein truncation test

J. Klijn, P. Devilee, J. D. Dunnen, 1995, Nature Genetics.

A high-quality reference panel reveals the complexity and distribution of structural genome changes in a human population

Morris A. Swertz, Jasmijn A. Baaijens, Victor Guryev, 2016, bioRxiv.

Screening for BRCA2 mutations in 81 Dutch breast–ovarian cancer families

M. Stratton, G. Bignell, J. Klijn, 1999, British Journal of Cancer.

The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B

P. Reitsma, G. Ommen, E. Bakker, 2005, Annals of Hematology.

Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions

C. Heyting, G. Ommen, P. Pearson, 1987, Human Genetics.

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study

A. Covone, C. Broeckhoven, K. Bushby, 2004, Human Genetics.

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

Peter Devilee, Ronald van Eijk, Tamara Peelen, 1997, Nature Genetics.

Transcription in yeast mitochondria: Isolation and physical mapping of messenger RNAs for subunits of cytochrome c oxidase and ATPase

L. Grivell, A. Moorman, G. Ommen, 1978, Molecular and General Genetics MGG.

Fine structure physical mapping of 4S RNA genes on mitochondrial DNA ofSaccharomyces cerevisiae

P. Borst, G. Ommen, G. Groot, 1977, Molecular and General Genetics MGG.

The human thyroglobulin gene: A polymorphic marker localized distal to C-MYC on chromosome 8 band q24

F. Baas, G. Ommen, P. Pearson, 2004, Human Genetics.

The association of mTOR and familial longevity in the blood transcriptome is not reflected in primary skin fibroblasts

P. Slagboom, G. Ommen, A. Maier, 2014 .

Making ends meet

G. Ommen, 1994, Nature Genetics.

PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

H. Willard, L. Kunkel, K. Davies, 1985, The Lancet.

Mutations affecting RNA splicing and the interaction of gene expression of the yeast mitochondrial loci cob and oxi-3

L. Grivell, M. D. Haan, E. Roosendaal, 1980, Cell.

Transcription maps of mtdnas of two strains of saccharomyces: transcription of strain-specific insertions; complex rna maturation and splicing

L. Grivell, G. Ommen, G. Groot, 1979, Cell.

Yeast mitochondrial RNA does not contain poly(A)

L. Grivell, R. Flavell, G. Ommen, 1974, Nature.

Carrier detection in X‐linked ocular albinism of the Nettleship‐Falls type by DNA analysis

G. Ommen, A. Gal, E. Bleeker-Wagemakers, 1992, Clinical genetics.

Splice point sequence and transcripts of the intervening sequence in the mitochondrial 21S ribosomal RNA gene of yeast

H. Tabak, P. Borst, G. Ommen, 1980, Cell.

Molecular Xp deletion in a male: suggestion of a locus for hypogonadotropic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci

G. Ommen, U. Pettersson, G. V. Ommen, 1989, Clinical genetics.

Overexpression of subunit c, the main component of the storage material in Juvenile Neuronal Ceroid Lipofuscinosis (JNCL), causes disruption of mitochondria in C. elegans and subsequent death

P. Taschner, G. Ommen, D. Peters, 2008 .

Making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis

G. Ommen, G. D. Voer, De Voer, 2008 .

Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype

P. Taschner, G. Ommen, D. Peters, 2005, Journal of Inherited Metabolic Disease.

A targeted mouse Brca1 mutation removing the last BRCT repeat results in apoptosis and embryonic lethality at the headfold stage

P. Devilee, C. Cornelisse, R. Fodde, 2001, Oncogene.

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Dennis E Bulman, Ronald van Eijk, Peter J Oefner, 1996, Cell.

Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus

T. Cremer, T. Ried, M. Cremer, 2004, Human Genetics.

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

F. Baas, G. Ommen, J. D. Vijlder, 2004, Human Genetics.

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

M. Wapenaar, G. Ommen, P. Pearson, 1985, Human Genetics.

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome

A. Monaco, L. Kunkel, G. Ommen, 1986, Cell.

Prenatal diagnosis of Duchenne muscular dystrophy: A three-year experience in a rapidly evolving field

G. Ommen, P. Pearson, E. Bakker, 1989, Journal of Inherited Metabolic Disease.

Fluorescent labelling of cRNA for microarray applications

Floor de Kort, P. Hoen, J. D. Dunnen, 2003 .

Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia

B. Dutrillaux, G. Ommen, J. Kaplan, 1988, Human Genetics.

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type

G. Ommen, A. Bergen, A. Gal, 1991, Human Genetics.

The Physical Map of Yeast Mitochondrial DNA Anno 1977 (A Review)

L. Grivell, A. Moorman, C. Heyting, 1977 .

The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kb

Frank Baas, Gert-Jan B.van Ommen, Hennie Bikker, 1986, Nucleic Acids Res..

Huntingtin with an expanded polyglutamine repeat affects the Jab1-p27(Kip1) pathway

R. Roos, G. Ommen, J. Dorsman, 2012, Neurobiology of Disease.

Understanding the low uptake of presymptomatic DNA testing for Huntington's disease

G. Ommen, A. Tibben, F. Verhage, 1992, The Lancet.

intermediate and reduced penetrance New problems in testing for Huntington ' s disease :

G. Ommen, M. Niermeijer, 2001 .

Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome

C. Wadelius, G. Holmgren, G. Ommen, 1989, Human Genetics.

A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis

J. Osinga, G. Ommen, H. Scheffer, 1995, Human Genetics.

The Presymptomatic Diagnosis of Huntington’s Disease Using Molecular Techniques, Applications and New Developments

G. Ommen, P. Pearson, A. Verwest, 1989 .

progression in Huntington disease interact to affect clinical severity and HTT Normal and mutant

T. Stijnen, G. Ommen, N. Aziz, 2009 .

Corrigendum Familial Resemblance for Serum Metabolite Concentrations — Corrigendum

G. Willemsen, D. Boomsma, M. Beekman, 2013 .

Borderline repeat expansion in Huntington's disease

G. Ommen, M. Losekoot, K. E. Rooij, 1993, The Lancet.

Rapid identification of mutations in the IDS gene of Hunter patients: Analysis of mRNA by the protein truncation test

G. Ommen, F. Hogervorst, A. C. V. D. Tuijn, 1994 .

PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

H. Willard, L. Kunkel, K. Davies, 1985, The Lancet.

Small N-terminal mutant huntingtin fragments, but not wild type, are mainly present in monomeric form: Implications for pathogenesis

R. Roos, G. Ommen, J. Dorsman, 2006, Experimental Neurology.

Exclusion ofEpidermal GrowthFactor andHigh-Resolution Physical Mapping acrosstheRieger Syndrome Locus

G. Ommen, C. Lindgren, C. Murray, 1996 .

University of Groningen Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families

C. Wijmenga, M. Stoneking, C. Duijn, 2016 .