Holger Hoehn

Biochemistry, Genetics and Molecular Biology · Life Sciences

43h-index6.4kcitations183works2.02yr avg
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Research Topics

DNA Repair Mechanisms(73), Genomic variations and chromosomal abnormalities(29), Prenatal Screening and Diagnostics(27), Chromosomal and Genetic Variations(26), Carcinogens and Genotoxicity Assessment(24)

Publications183 total

Cell Cycle Analysis via BrdU-Hoechst Flow Cytometry — Principles and Applications
2024· 2 cited
Living related liver transplantation in an adult patient with hepatocellular adenoma and carcinoma 13 years after bone marrow transplantation for <scp>F</scp>anconi anemia: A case report
Hepatology Research·2013· 11 citedOpen Access
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
Human Genetics·2010· 101 citedOpen Access
Genotype–phenotype correlations in Fanconi anemia
Mutation research. Fundamental and molecular mechanisms of mutagenesis·2009· 143 cited
Expression analysis and functional activity of interleukin-7 splice variants
Genes and Immunity·2008· 41 cited
Spectral karyotyping and SNP microarray analysis define uniparental disomy (UPD) as a novel mutational mechanism in MSI- and CSI-colorectal cancers.
PubMed·2008· 1 citedOpen Access
Spectral Karyotyping and SNP Microarray Analysis Define Uniparental Disomy (UPD) as a Novel Mutational Mechanism in MSI- and CSI-Colorectal Cancers
Analytical Cellular Pathology·2008Open Access
Neoplasia, Ageing, and Genetic Instability due to Defective Caretaker Genes
Analytical Cellular Pathology·2008Open Access
Neoplasia, ageing, and genetic instability due to defective caretaker genes.
PubMed·2008· 2 citedOpen Access
Genetic instability syndromes with progeroid features
Zeitschrift für Gerontologie und Geriatrie·2007· 21 cited
Fanconi Anemia
Monographs in human genetics·2007· 11 cited
Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype
The American Journal of Human Genetics·2007· 134 citedOpen Access
Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure
Orphanet Journal of Rare Diseases·2007· 78 citedOpen Access
Contents / Editorial / Preface
Monographs in human genetics·2007Open Access
Subject Index
Monographs in human genetics·2007Open Access
Revertant Mosaicism in Fanconi Anemia: Natural Gene Therapy at Work
Monographs in human genetics·2007· 3 cited
Disruption of the FA/BRCA pathway in bladder cancer
Cytogenetic and Genome Research·2007· 39 cited
Milestones in Fanconi Anemia Research
Monographs in human genetics·2007· 3 cited
Applications of Cell Cycle Testing in Fanconi Anemia
Monographs in human genetics·2007· 6 cited
The spectrum of WRN mutations in Werner syndrome patients Communicated by Mark Paalman This article is a US government work and, as such, is in the public domain in the United States of America.
2006
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Frequent Co-authors

Detlev Schindler(16), George M. Martin(15), Darrell Salk(7), Eileen Bryant(7), Martin Poot(6), Thomas H. Norwood(6), Hans Joenje(5), Richard Friedl(4), Kit Sing Au(4), Peter S. Rabinovitch(4), Manfred Kubbies(4), Helmut Hanenberg(3), Sarah Herterich(3), Kornelia Neveling(3), Reinhard Kalb(3), Judith G. Hall(3), Johan P. de Winter(2), Quinten Waisfisz(2), Martin Digweed(2), M Gross(2)