Holger Hoehn

Overview

Best Publications

• The Fanconi anaemia group G gene FANCG is identical with XRCC9.

  de Winter Jp;Waisfisz Q;Rooimans Ma;van Berkel Cg

  481
  Citations

• Cytogenetics of Werner’s syndrome cultured skin fibroblasts: variegated translocation mosaicism

  D Salk;K Au;H Hoehn;G M Martin

  338
  Citations

• Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines.

  Martin PooT;Holger Hoehn;Thomas M. Rünger;George M. Martin;George M. Martin

  298
  Citations

• The spectrum of WRN mutations in Werner syndrome patients

  Shurong Huang;Lin Lee;Nancy B. Hanson;Catherine Lenaerts

  249
  Citations

• Morphological and biochemical heterogeneity of amniotic fluid cells in culture.

  Holger Hoehn;Holger Hoehn;Darrell Salk;Darrell Salk

  214
  Citations

• Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction

  M Gross;H Hanenberg;S Lobitz;R Friedl

  212
  Citations

• BrdU-Hoechst flow cytometry: a unique tool for quantitative cell cycle analysis.

  P.S. Rabinovitch;M. Kubbies;Y.C. Chen;D. Schindler

  203
  Citations

• Variegated translocation mosaicism in human skin fibroblast cultures

  H. Hoehn;E.M. Bryant;K. Au;T.H. Norwood

  203
  Citations

• Second report on chicken genes and chromosomes 2005

  Michael Schmid;I. Nanda;H. Hoehn;M. Schartl

  192
  Citations

• Cultivated cells from diagnostic amniocentesis in second trimester pregnancies. I. Clonal morphology and growth potential.

  Holger Hoehn;Eileen M. Bryant;Laurence E. Karp;George M. Martin

  185
  Citations

• Genotype-phenotype correlations in Fanconi anemia.

  Kornelia Neveling;Daniela Endt;Holger Hoehn;Detlev Schindler

  175
  Citations

• Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype

  Reinhard Kalb;Kornelia Neveling;Holger Hoehn;Hildegard Schneider

  167
  Citations

• Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts

  D Salk;D Salk;E Bryant;K Au;H Hoehn;H Hoehn

  148
  Citations

• Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia.

  Helga Seyschab;Richard Friedl;Yujie Sun;Detlev Schindler

  136
  Citations

• Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells.

  M Kubbies;D Schindler;H Hoehn;A Schinzel

  127
  Citations

• Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.

  M. Wijker;N. V. Morgan;S. Herterich;C. G M Van Berkel

  120
  Citations

• Significance of phenotypic and chromosomal abnormalities in X‐linked mental retardation (Martin‐Bell or Renpenning syndrome)

  M. Jennings;J. G. Hall;H. Hoehn;Jürgen Herrmann

  110
  Citations

• WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.

  Katrin Friedrich;Lin Lee;Dru F. Leistritz;Gudrun Nürnberg

  104
  Citations

• Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes.

  R A Pagon;J G Hall;S L Davenport;J Aase

  98
  Citations

• Cellular Aging in Werner's Syndrome: A Unique Phenotype?

  Thomas H. Norwood;Holger Hoehn;Darrell Salk;George M. Martin

  98
  Citations