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Eli Sprecher

Researcher Next ID · RN-042115

Researcher · Biochemistry, Genetics and Molecular Biology

Boston Children's Hospital

Boston, Israel

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Accepting doctoral researchersFunding unknown
Works count
538
Citation count
16,325
H-index
63
i10-index
269

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Skin and Cellular Biology Research
Autoimmune Bullous Skin Diseases
Wnt/β-catenin signaling in development and cancer
Hair Growth and Disorders
Genetic and rare skin diseases.

Publications

  • Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology ( EADV )

    Journal of the European Academy of Dermatology and Venereology · 2022 · https://doi.org/10.1111/jdv.18220

  • Association Between Vaccination With BNT162b2 and Incidence of Symptomatic and Asymptomatic SARS-CoV-2 Infections Among Health Care Workers

    JAMA · 2021 · https://doi.org/10.1001/jama.2021.7152

  • Updated S2K guidelines on the management of pemphigus vulgaris and foliaceus initiated by the european academy of dermatology and venereology (EADV)

    Journal of the European Academy of Dermatology and Venereology · 2020 · https://doi.org/10.1111/jdv.16752

  • Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

    British Journal of Dermatology · 2020 · https://doi.org/10.1111/bjd.18921

  • Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting

    Nature Genetics · 2013 · https://doi.org/10.1038/ng.2739

  • Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14

    The American Journal of Human Genetics · 2012 · https://doi.org/10.1016/j.ajhg.2012.05.010

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

    Journal of the American Academy of Dermatology · 2010 · https://doi.org/10.1016/j.jaad.2009.11.020

  • SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4

    The American Journal of Human Genetics · 2008 · https://doi.org/10.1016/j.ajhg.2007.08.005

  • Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis

    The American Journal of Human Genetics · 2005 · https://doi.org/10.1086/429844

  • Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

    Nature Genetics · 2004 · https://doi.org/10.1038/ng1358

Current projects

    No projects listed.