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Biology and Biochemistry

D-Index
68
Citations
17020
World Ranking
7770
National Ranking
143

Overview

Daniel Hohl is affiliated with the University of Lausanne in Switzerland. Their research primarily spans the fields of medicine and biochemistry, genetics, and molecular biology. Within these domains, they have contributed extensively to molecular biology, dermatology, genetics, epidemiology, and cell biology.

The scientist's work focuses on several key topics, including:

  • Hedgehog Signaling Pathway Studies
  • Genetic and rare skin diseases.
  • Cutaneous lymphoproliferative disorders research
  • Cancer and Skin Lesions
  • Skin and Cellular Biology Research
  • Genetic and Kidney Cyst Diseases
  • Nonmelanoma Skin Cancer Studies

Among their recent publications are:

  • "Birt-Hogg-Dubé syndrome," 2020, European Respiratory Review
  • "Netherton Syndrome: Insights into Pathogenesis and Clinical Implications," 2020, Journal of Investigative Dermatology
  • "Immune modules to guide diagnosis and personalized treatment of inflammatory skin diseases," 2024, Nature Communications
  • "HOPX Exhibits Oncogenic Activity during Squamous Skin Carcinogenesis," 2021, Journal of Investigative Dermatology
  • "Challenges in Treating Genodermatoses: New Therapies at the Horizon," 2022, Frontiers in Pharmacology

Hohl frequently collaborates with several coauthors, including Marcel Huber, Gabriela Blanchard, Elena Chiticariu, Fanny Morice-Picard, and P. Vabres.

Their work is commonly published in journals such as:

  • Journal of Investigative Dermatology
  • Zenodo (CERN European Organization for Nuclear Research)
  • Journal of the European Academy of Dermatology and Venereology
  • Dermatology Practical & Conceptual
  • Oncotarget

Best Publications

  • Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009

    Vinzenz Oji;Gianluca Tadini;Masashi Akiyama;Claudine Blanchet Bardon

  • Identification of the familial cylindromatosis tumour-suppressor gene.

    Graham R. Bignell;William Warren;Sheila Seal;Meiko Takahashi

  • Cutaneous cancer stem cell maintenance is dependent on beta-catenin signalling.

    Ilaria Malanchi;Hector Peinado;Deepika Kassen;Thomas Hussenet

  • Mutations of keratinocyte transglutaminase in lamellar ichthyosis.

    Marcel Huber;Irmingard Rettler;Katja Bernasconi;Edgar Frenk

  • The Inflammasome Mediates UVB-Induced Activation and Secretion of Interleukin-1β by Keratinocytes

    Laurence Feldmeyer;Martin Keller;Gisela Niklaus;Daniel Hohl

  • Identification of a major keratinocyte cell envelope protein, loricrin.

    Thomas Mehrel;Daniel Hohl;Joseph A. Rothnagel;Mary A. Longley

  • Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

    Gabriele Richard;Lisa E. Smith;Regina A. Bailey;Peter Itin

  • Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis

    J. A. Rothnagel;A. M. Dominey;L. D. Dempsey;M. A. Longley

  • Characterization of human loricrin. Structure and function of a new class of epidermal cell envelope proteins.

    D Hohl;T Mehrel;U Lichti;M L Turner

  • Notch1 is a p53 target gene involved in human keratinocyte tumor suppression through negative regulation of ROCK1/2 and MRCKα kinases

    Karine Lefort;Anna Mandinova;Paola Ostano;Vihren Kolev

  • The human epidermal differentiation complex: cornified envelope precursors, S100 proteins and the 'fused genes' family.

    Magdalini Kypriotou;Marcel Huber;Daniel Hohl

  • Lessons from Loricrin-Deficient Mice: Compensatory Mechanisms Maintaining Skin Barrier Function in the Absence of a Major Cornified Envelope Protein

    Peter J. Koch;Pierre A. de Viragh;Pierre A. de Viragh;Elisabeth Scharer;Elisabeth Scharer;Donnie Bundman

  • Incidence of bullous pemphigoid and pemphigus in Switzerland: a 2-year prospective study.

    G Marazza;H C Pham;L Schärer;P P Pedrazzetti

  • Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda

    Fabrice Chimienti;Ronald C. Hogg;Laure Plantard;Caroline Lehmann

  • Skin Colonization by Staphylococcus aureus Precedes the Clinical Diagnosis of Atopic Dermatitis in Infancy

    Patrick Meylan;Caroline Lang;Sophie Mermoud;Alexandre Johannsen

  • Cornified Cell Envelope

    Daniel Hohl

  • LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome

    Emmanuelle Bitoun;Alessia Micheloni;Laurence Lamant;Chrystelle Bonnart

  • Transcription of the Human Loricrin Gene In Vitro Is Induced by Calcium and Cell Density and Suppressed by Retinoic Acid

    Daniel Hohl;Ulrike Lichti;Ulrike Lichti;Dirk Breitkreutz;Dirk Breitkreutz;Peter M. Steinert;Peter M. Steinert

  • Mutations in the gene encoding SLURP-1 in Mal de Meleda

    Judith Fischer;Bakar Bouadjar;Roland Heilig;Marcel Huber

  • The Small Proline-Rich Proteins Constitute a Multigene Family of Differentially Regulated Cornified Cell Envelope Precursor Proteins

    Daniel Hohl;Pierre A. de Viragh;Françoise Arniguet-Barras;Susan Gibbs

Frequent Co-Authors

Dennis R. Roop
Dennis R. Roop University of Colorado Anschutz Medical Campus
Sabine Werner
Sabine Werner ETH Zurich
Joseph A. Rothnagel
Joseph A. Rothnagel University of Queensland
Daniel Bertrand
Daniel Bertrand University of Geneva
Irene M. Leigh
Irene M. Leigh University of Dundee
Alain Hovnanian
Alain Hovnanian Imagine Institute for Genetic Diseases
Akemi Ishida-Yamamoto
Akemi Ishida-Yamamoto Asahikawa Medical University
Peter M. Steinert
Peter M. Steinert National Institutes of Health
Hajime Iizuka
Hajime Iizuka Asahikawa Medical University
Matthias Schmuth
Matthias Schmuth Innsbruck Medical University

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