Ingrid Hausser

Overview

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

  845
  Citations

• Pathogenesis of cervical artery dissections Association with connective tissue abnormalities

  T. Brandt;E. Orberk;R. Weber;I. Werner

  352
  Citations

• Ultrastructural connective tissue abnormalities in patients with spontaneous cervicocerebral artery dissections

  Tobias Brandt;Ingrid Hausser;Erdem Orberk;Armin Grau

  312
  Citations

• Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagen

  Cassian Sitaru;Sidonia Mihai;Christoph Otto;Mircea T. Chiriac

  289
  Citations

• Mutations in PYCR1 cause cutis laxa with progeroid features

  Bruno Reversade;Nathalie Escande-Beillard;Aikaterini Dimopoulou;Bjorn Fischer

  276
  Citations

• PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans.

  Anaïs Grall;Eric Guaguère;Sandrine Planchais;Sandrine Planchais;Susanne Grond

  274
  Citations

• Integrin α3 mutations with kidney, lung, and skin disease

  Cristina Has;Giuseppina Spartà;Dimitra Kiritsi;Lisa Weibel

  261
  Citations

• Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease

  Vinzenz Oji;Katja-Martina Eckl;Karin Aufenvenne;Marc Nätebus

  247
  Citations

• 12R-lipoxygenase deficiency disrupts epidermal barrier function

  Nikolas Epp;Gerhard Fürstenberger;Karsten Müller;Silvia de Juanes

  239
  Citations

• A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy

  Anja Fritsch;Stefan Loeckermann;Johannes S. Kern;Attila Braun

  226
  Citations

• Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.

  A De Paepe;L Nuytinck;I Hausser;I Anton-Lamprecht

  220
  Citations

• Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length

  Katja-Martina Eckl;Katja-Martina Eckl;Rotem Tidhar;Holger Thiele;Vinzenz Oji

  196
  Citations

• Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification

  Ingrid Hausser;Ingrun Anton-Lamprecht

  188
  Citations

• ClpV recycles VipA/VipB tubules and prevents non‐productive tubule formation to ensure efficient type VI protein secretion

  Nicole Kapitein;Gabriele Bönemann;Aleksandra Pietrosiuk;Fabian Seyffer

  181
  Citations

• Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (Type VIIC) and common polymorphisms in the ADAMTS2 gene.

  Alain Colige;Lieve Nuytinck;Ingrid Hausser;Anthonie J. van Essen

  159
  Citations

• Keratin 1 maintains skin integrity and participates in an inflammatory network in skin through interleukin-18.

  Wera Roth;Vinod Kumar;Hans-Dietmar Beer;Miriam Richter

  150
  Citations

• Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

  Fransiska Malfait;Ariana Kariminejad;Tim Van Damme;Caroline Gauche

  149
  Citations

• New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations

  Bert Callewaert;Bert Callewaert;Marjolijn Renard;Vishwanathan Hucthagowder;Beate Albrecht

  148
  Citations

• Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrity.

  Johannes S Kern;Stefan Loeckermann;Anja Fritsch;Ingrid Hausser

  140
  Citations

• Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion

  Diana C. Blaydon;Daniela Nitoiu;Katja-Martina Eckl;Rita M. Cabral

  135
  Citations