Andries Westerveld

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Publications in SciGraph latest 50 shown

  • 2009-12 Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2003-10 Anticipation in familial intracranial aneurysms in consecutive generations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-07 Duplication and transposition of the NF1 pseudogene regions on chromosomes 2, 14, and 22 in HUMAN GENETICS
  • 2000-12 Microsatellite instability and promoter methylation as possible causes of NF1 gene inactivation in neurofibromas in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-03 Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-12 Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter–22q11.2 in BRITISH JOURNAL OF CANCER
  • 1999-10 Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) in NATURE GENETICS
  • 1996-06 Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus in HUMAN GENETICS
  • 1996-03 No mutations found byRET mutation scanning in sporadic and hereditary neuroblastoma in HUMAN GENETICS
  • 1995-11 Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3 in NATURE GENETICS
  • 1995-07 Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene in HUMAN GENETICS
  • 1994-10 Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosis in BRITISH JOURNAL OF CANCER
  • 1993-08 Corrigendum: Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification in NATURE GENETICS
  • 1993-06 Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N–myc amplification in NATURE GENETICS
  • 1993-04 In situ glucose-6-phosphate dehydrogenase activity during development of pre-implantation mouse embryos in JOURNAL OF MOLECULAR HISTOLOGY
  • 1991-07 New distal marker closely linked to the fragile X locus in HUMAN GENETICS
  • 1991 Molecular, Cytogenetic and Linkage Analysis of Chromosome 11p Regions Involved in Wilms’ Tumour and Associated Congenital Diseases in RECENT PROGRESS IN THE GENETIC EPIDEMIOLOGY OF CANCER
  • 1989 Molecular Genetic Dissection of Mammalian Excision Repair in DNA REPAIR MECHANISMS AND THEIR BIOLOGICAL IMPLICATIONS IN MAMMALIAN CELLS
  • 1989 Genetic Heterogeneity in Inherited Disorders with a Generalized Impairment of Peroxisomal Functions: Visualization by Immunofluorescence Microscopy of Peroxisome Assembly After Somatic Cell Fusion of Complementary Cell Lines in MOLECULAR BASIS OF MEMBRANE-ASSOCIATED DISEASES
  • 1989 Functions, Biogenesis and Pathology of Peroxisomes in Man in ORGANELLES IN EUKARYOTIC CELLS
  • 1989 Isolation and Characterization of Genes Involved in Mammalian Excision Repair in DNA DAMAGE AND REPAIR
  • 1988 Complementation Analysis of Peroxisomal Diseases: Kinetics of Assembly of Peroxisomes After Fusion of Complementary Cell Lines from Patients Deficient in Peroxisomes in LIPID STORAGE DISORDERS
  • 1987 Complementation Analysis of Peroxisomal Diseases by Somatic Cell Fusion in PEROXISOMES IN BIOLOGY AND MEDICINE
  • 1986-12 Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells in HUMAN GENETICS
  • 1985-04 The chromosomal localization of human β-galactosidase revisited: a locus for β-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22 in HUMAN GENETICS
  • 1984-08 Molecular cloning of a human DNA repair gene in NATURE
  • 1983-09 Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies in HUMAN GENETICS
  • 1983 Localization of Genes Involved in DNA Repair on Human Chromosomes by Using Cell Fusion in THE USE OF HUMAN CELLS FOR THE EVALUATION OF RISK FROM PHYSICAL AND CHEMICAL AGENTS
  • 1982-02 Expression of human hprt gene on the inactive X chromosome after DNA-mediated gene transfer in NATURE
  • 1981-07 Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations in HUMAN GENETICS
  • 1980-05 Regional assignment of the gene locus for steroid sulfatase in HUMAN GENETICS
  • 1980-02 The genetic defect in the various types of human β-galactosidase deficiency in HUMAN GENETICS
  • 1979-10 Assignment of structural β-galactosidase loci to human chromosomes 3 and 22 in HUMAN GENETICS
  • 1978-01 A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids in HUMAN GENETICS
  • 1978-01 Localization of a gene for human α-galactosidase B (=N-Acetyl-α-D-Galactosaminidase) on chromosome 22 in HUMAN GENETICS
  • 1977-07 Regional localization of aβ-galactosidase locus on human chromosome 22 in SOMATIC CELL GENETICS
  • 1977-01 Characterization of α-galactosidase isoenzymes in normal and fabry human-Chinese hamster somatic cell hybrids in HUMAN GENETICS
  • 1977-01 Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybrids in HUMAN GENETICS
  • 1974-05 Claim that two human linkage groups carry different loci for GPT and LDH withdrawn in NATURE
  • 1973-09 Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids in HUMANGENETIK
  • 1972-12 Two New Linkage Groups in Man, both carrying Different Loci for Lactate Dehydrogenase and Glutamic-Pyruvic Transaminase in NATURE
  • 1972-11 X-Linkage of Human α-Galactosidase in NATURE
  • 1972-08 Evidence for linkage of 3-phosphoglycerate kinase, hypoxanthine-guanine-phosphoribosyl transferase, and glucose 6-phosphate dehydrogenase loci in Chinese hamster cells studied by using a relationship between gene multiplicity and enzyme activity in BIOCHEMICAL GENETICS
  • 1972-03 Evidence for Linkage between Human Loci for 6-Phosphogluconate Dehydrogenase and Phosphoglucomutase1 in Man–Chinese Hamster Somatic Cell Hybrids in NATURE
  • 1971-12 Evidence for linkage between glucose 6-phosphate dehydrogenase and hypoxanthine-guanine-phosphoribosyl transferase loci in Chinese hamster cells in BIOCHEMICAL GENETICS
  • 1971-11 Loss of Human Genetic Markers in Man-Chinese Hamster Somatic Cell Hybrids in NATURE
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