World's Best Scientists 2026 revealed!

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Genetics

D-Index
76
Citations
24717
World Ranking
1814
National Ranking
134

Overview

Bernhard Zabel is affiliated with the University of Freiburg in Germany. Their research is primarily situated within Biochemistry, Genetics and Molecular Biology, with a focus on Molecular Biology and Cancer Research as subfields. The scientist's work centers on topics including Cancer-related molecular mechanisms research, RNA modifications and cancer, and RNA Research and Splicing.

Zabel's research outputs include contributions to the field of non-coding RNA, exemplified by their recent paper titled "Uncovering pathways regulating chondrogenic differentiation of CHH fibroblasts", published in 2021 in the journal Non-coding RNA Research. This publication has been cited multiple times, reflecting engagement within the scientific community.

Frequent collaborators in their research activities include:

  • Alzbeta Chabronova
  • Guus van den Akker
  • Mandy M.F. Meekels-Steinbusch
  • Franziska Friedrich
  • Andy Cremers

The primary publication venue associated with Zabel is Non-coding RNA Research. The scientist's focused research areas span several molecular biology topics, notably around RNA function and cancer-related mechanisms, aligning with both their subfield and main thematic interests.

Zabel's research intersects molecular biology and cancer research disciplines, addressing mechanisms at the RNA level that contribute to cancer development and progression. Their work on RNA modifications links molecular detail with broader disease contexts, reflecting a multi-dimensional approach within genetics and molecular biology.

No awards or book publications are recorded in the available data.

Best Publications

  • LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development

    Y. Q. Gong;R. B. Slee;N. Fukai;G. Rawadi

  • Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

    S Mundlos;S Mundlos;F Otto;C Mundlos;C Mundlos;J.B Mulliken

  • Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

    Thomas Wagner;Jutta Wirth;Jobst Meyer;Bernhard Zabel

  • Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

    E. V. Semina;R. Reiter;N. J. Leysens;W. L. M. Alward

  • Nosology and classification of genetic skeletal disorders : 2010 revision

    Matthew L. Warman;Valerie Cormier-Daire;Christine Hall;Deborah Krakow;Deborah Krakow

  • Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.

    Sabine Endele;Georg Rosenberger;Kirsten Geider;Bernt Popp

  • Regulation of chondrocyte differentiation by Cbfa1.

    I.S Kim;F Otto;B Zabel;S Mundlos

  • Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

    Sandra D. Dreyer;Guang Zhou;Antonio Baldini;Andreas Winterpacht

  • Glucose/galactose malabsorption caused by a defect in the Na + /glucose cotransporter

    E. Turk;B. Zabel;S. Mundlos;J. Dyer

  • Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations.

    Nabeel Bardeesy;David Falkoff;Mary-Jane Petruzzi;Norma Nowak

  • TRPM5 is a transient Ca2+-activated cation channel responding to rapid changes in [Ca2+]i.

    D Prawitt;Mahealani K Monteilh-Zoller;Lili R Brixel;Christian Spangenberg

  • Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux

    Cynthia F. Bartels;Hülya Bükülmez;Hülya Bükülmez;Pius Padayatti;David K. Rhee

  • Nuclear localization of the protein encoded by the Wilms' tumor gene WT1 in embryonic and adult tissues

    Stefan Mundlos;Jerry Pelletier;André Darveau;Michael Bachmann

  • Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I.

    P. Momeni;G. Glöckner;O. Schmidt;D. Von Holtum

  • The type II collagenopathies: A spectrum of chondrodysplasias

    J. Spranger;A. Winterpacht;B. Zabel

  • Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

    Bärbel Dittrich;Karin Buiting;Bernd Korn;Sarah Rickard

  • PAX8, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms’ tumors

    Andrej Poleev;Helmut Fickenscher;Stefan Mundlos;Andreas Winterpacht

  • Mutations in WNT1 Cause Different Forms of Bone Fragility

    Katharina Keupp;Filippo Beleggia;Hülya Kayserili;Aileen M. Barnes

  • A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein.

    Yiu-mo Chan;Ingrun Anton-Lamprecht;Qian-Chun Yu;Andreas Jackel

  • Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

    H.-J. Lüdecke;J. Schaper;P. Meinecke;P. Momeni

Frequent Co-Authors

Stefan Mundlos
Stefan Mundlos Max Planck Society
Brendan Lee
Brendan Lee Baylor College of Medicine
Jerry Pelletier
Jerry Pelletier McGill University
Andrea Superti-Furga
Andrea Superti-Furga University of Lausanne
Geert Mortier
Geert Mortier University of Antwerp
Matthew L. Warman
Matthew L. Warman Boston Children's Hospital
Sheila Unger
Sheila Unger University of Lausanne
Jan G. Hengstler
Jan G. Hengstler TU Dortmund University
Valérie Cormier-Daire
Valérie Cormier-Daire Necker-Enfants Malades Hospital

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