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Genetics

D-Index
85
Citations
25249
World Ranking
1314
National Ranking
49

Overview

Hans Joenje is affiliated with VU University Medical Center in the Netherlands and has contributed to research primarily within the fields of Biochemistry, Genetics, and Molecular Biology. Their work spans several subfields including Molecular Biology, Plant Science, and Genetics.

The research topics most associated with Hans Joenje's publications encompass:

  • DNA Repair Mechanisms
  • CRISPR and Genetic Engineering
  • Chromosomal and Genetic Variations
  • Hemoglobinopathies and Related Disorders

Hans Joenje's recent publications include the following papers:

  • "BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia," 2022, published in Scientific Reports
  • "Publisher Correction: BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia," 2022, published in Scientific Reports

The primary venue for their publications is Scientific Reports, where at least two of their papers have appeared.

Hans Joenje frequently collaborates with other researchers. The most common co-authors include:

  • Josephine C. Dorsman
  • Khashayar Roohollahi
  • Yvonne de Jong
  • Govind Pai
  • Mohamad Amr Zaini

Best Publications

  • Biallelic Inactivation of BRCA2 in Fanconi Anemia

    Niall G. Howlett;Toshiyasu Taniguchi;Susan Olson;Barbara Cox

  • The emerging genetic and molecular basis of Fanconi anaemia

    Hans Joenje;Ketan J. Patel

  • A novel ubiquitin ligase is deficient in Fanconi anemia

    Amom Ruhikanta Meetei;Johan P de Winter;Annette L Medhurst;Michael Wallisch

  • Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors.

    Toshiyasu Taniguchi;Marc Tischkowitz;Najim Ameziane;Shirley V. Hodgson

  • Doxorubicin (adriamycin): a critical review of free radical-dependent mechanisms of cytotoxicity.

    H.G. Keizer;H.M. Pinedo;G.J. Schuurhuis;H. Joenje

  • Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

    Bing Xia;Josephine C Dorsman;Najim Ameziane;Yne de Vries

  • A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

    Amom Ruhikanta Meetei;Annette L Medhurst;Chen Ling;Yutong Xue

  • The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.

    Marieke Levitus;Quinten Waisfisz;Barbara C Godthelp;Yne de Vries

  • Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

    J R Foe;M A Rooimans;L Bosnoyan-Collins;N Alon

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

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

  • A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome.

    Amom Ruhikanta Meetei;Salvatore Sechi;Michael Wallisch;Dafeng Yang

  • Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion

    Hugo Vega;Hugo Vega;Quinten Waisfisz;Miriam Gordillo;Miriam Gordillo;Norio Sakai

  • SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

    C. Stoepker;K. Hain;B. Schuster;Y. Hilhorst-Hofstee

  • X-linked inheritance of Fanconi anemia complementation group B

    Amom Ruhikanta Meetei;Marieke Levitus;Yutong Xue;Annette L Medhurst

  • Identification of FAAP24, a Fanconi Anemia Core Complex Protein that Interacts with FANCM

    Alberto Ciccia;Chen Ling;Rachel Coulthard;Zhijiang Yan

  • Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia

    Hans Joenje;Fré Arwert;Aldur W. Eriksson;Han de Koning

  • The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

    de Winter Jp;Rooimans Ma;van Der Weel L;van Berkel Cg

  • Evidence for at Least Eight Fanconi Anemia Genes

    Hans Joenje;Anneke B. Oostra;Mario Wijker;Franca M. di Summa

  • Association of complementation group and mutation type with clinical outcome in Fanconi anemia

    Laurence Faivre;Philippe Guardiola;Cathryn Lewis;Inderjeet Dokal

  • Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

    Marieke Levitus;Marieke Levitus;Martin A. Rooimans;Martin A. Rooimans;Jûrgen Steltenpool;Jûrgen Steltenpool;Nicolle F. C. Cool;Nicolle F. C. Cool

Frequent Co-Authors

Johan P. de Winter
Johan P. de Winter VU University Medical Center
Fré Arwert
Fré Arwert VU University Medical Center
Quinten Waisfisz
Quinten Waisfisz Vrije Universiteit Amsterdam
Christopher G. Mathew
Christopher G. Mathew King's College London
Gerard Pals
Gerard Pals Vrije Universiteit Amsterdam
Weidong Wang
Weidong Wang National Institutes of Health
Detlev Schindler
Detlev Schindler University of Würzburg
Neil V. Morgan
Neil V. Morgan University of Birmingham
Alan D. D'Andrea
Alan D. D'Andrea Dana-Farber Cancer Institute
Anna Savoia
Anna Savoia University of Trieste

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