Hans Joenje

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Publications in SciGraph latest 50 shown

  • 2016-12 Letter to the editor for “Update of the human and mouse Fanconi anemia genes” in HUMAN GENOMICS
  • 2015-12 Update of the human and mouse Fanconi anemia genes in HUMAN GENOMICS
  • 2015-12 A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51 in NATURE COMMUNICATIONS
  • 2014-12 Coregulation of FANCA and BRCA1 in human cells in SPRINGERPLUS
  • 2012-12 Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma in FAMILIAL CANCER
  • 2011-07 Metabolism: Alcohol, DNA and disease in NATURE
  • 2011-02 SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype in NATURE GENETICS
  • 2009-12 Lack of large genomic deletions in BRIP1, PALB2, and FANCD2 genes in BRCA1/2 negative familial breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2008-01 Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2007-02 Fanconi anemia is associated with a defect in the BRCA2 partner PALB2 in NATURE GENETICS
  • 2005-09 The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J in NATURE GENETICS
  • 2005-09 A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M in NATURE GENETICS
  • 2005-05 Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion in NATURE GENETICS
  • 2004-11 Apparent absence of BRCA2 protein in a proportion of acute myeloid leukemia cell lines in LEUKEMIA
  • 2004-11 X-linked inheritance of Fanconi anemia complementation group B in NATURE GENETICS
  • 2003-10 A novel ubiquitin ligase is deficient in Fanconi anemia in NATURE GENETICS
  • 2003-05 Disruption of the Fanconi anemia–BRCA pathway in cisplatin-sensitive ovarian tumors in NATURE MEDICINE
  • 2002-12 Analysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays in BMC HEMATOLOGY
  • 2002-07 Impaired DNA damage-induced nuclear Rad51 foci formation uniquely characterizes Fanconi anemia group D1 in ONCOGENE
  • 2001-06 The emerging genetic and molecular basis of Fanconi anaemia in NATURE REVIEWS GENETICS
  • 2001-04 Connecting Fanconi anemia to BRCA1 in NATURE MEDICINE
  • 2001-03 Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemia in FAMILIAL CANCER
  • 2000-11 Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-04 Cloning and characterization of murine Fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary in MAMMALIAN GENOME
  • 2000-01 The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM in NATURE GENETICS
  • 1999-08 Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism in NATURE GENETICS
  • 1999-01 Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1998-11 The Fanconi anaemia group G gene FANCG is identical with XRCC9 in NATURE GENETICS
  • 1998-09 Localisation of a Fanconi anaemia gene to chromosome 9p in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1998-07 Subtyping Analysis of Fanconi Anemia by Immunoblotting and Retroviral Gene Transfer in MOLECULAR MEDICINE
  • 1996-12 Erratum: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA in NATURE GENETICS
  • 1996-12 Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene in HUMAN GENETICS
  • 1996-11 Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA in NATURE GENETICS
  • 1996-09 Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant in HUMAN GENETICS
  • 1996-05 Fanconi anaemia in Italy: High prevalence of complementation group A in two geographic clusters in HUMAN GENETICS
  • 1996-03 Fanconi anaemia complementation groups in Germany and The Netherlands in HUMAN GENETICS
  • 1996-03 Immortalization of four new fanconi anemia fibroblast cell lines by an improved procedure in SOMATIC CELL AND MOLECULAR GENETICS
  • 1995-11 Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3 in NATURE GENETICS
  • 1995-11 Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p in NATURE GENETICS
  • 1991-01 Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-clichloro-platinum (II) in Fanconi anemia lymphocyte cultures in HUMAN GENETICS
  • 1989-08 Effect of N-acetylcysteine on the antiproliferative action of X-rays or bleomycin in cultured human lung tumor cells in JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
  • 1989 Oxygen Metabolism and Chromosomal Breakage in Fanconi Anemia in FANCONI ANEMIA
  • 1987-09 Antioxidant status of Fanconi anemia fibroblasts in HUMAN GENETICS
  • 1987-02 Abstract of papers in PHARMACEUTISCH WEEKBLAD
  • 1986-12 Oxygen-induced cytogenetic instability in normal human lymphocytes in HUMAN GENETICS
  • 1986 Introduction: Oxygen Metabolism, DNA Repair, and the Origin of Spontaneous Genetic Instability in ANTIMUTAGENESIS AND ANTICARCINOGENESIS MECHANISMS
  • 1985-11 Differential sensitivity of Fanconi anaemia lymphocytes to the clastogenic action of cis-diamminedichloroplatinum (II) and trans-diamminedichloroplatinum (II) in HUMAN GENETICS
  • 1985-01 Characterization of an oxygen-tolerant cell line derived from Chinese hamster ovary in CELL AND TISSUE RESEARCH
  • 1983-12 Effect of oxygen tension on chromosomal aberrations in Fanconi anaemia in HUMAN GENETICS
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