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Johannes Zschocke

Professor of Human Genetics

Medical University of Innsbruck

Austria

Research Interests

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About

Johannes Zschocke is a Professor of Human Genetics at Medizinische Universität Innsbruck, Austria. His research areas include atopic dermatitis, breast cancer risk assessment, and Ehlers-Danlos syndromes, as evidenced by his recent publications. He is also involved in the genetic diagnosis of various inherited metabolic diseases and has contributed significantly to the understanding of hereditary conditions in clinical practice.

Articles (21)

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Collaborators (13)

Gunda Schwaninger

New York University

UNITED STATES

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Verena Peters

GERMANY

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Hauke Hillen

Assistant Professor

University Medical Center Göttingen

GERMANY

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Matthias Schmuth

Professor

Medical University of Innsbruck

AUSTRIA

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Katja Eckl

Senior Lecturer

Edge Hill University

UNITED KINGDOM

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Matthias R. Baumgartner

University of Zurich

SWITZERLAND

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Robert Gruber

Assoc. Prof

Tirol-Kliniken

AUSTRIA

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Lukas Forer

Assistant Professor

Medical University of Innsbruck

AUSTRIA

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Sandrine Dubrac

Medical University of Innsbruck

AUSTRIA

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Markus Andreas Keller

Assoc. Prof. (tenured) for Biochemical Genetics

Medical University of Innsbruck

AUSTRIA

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Peter H. Byers

Professor

University of Washington

UNITED STATES

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Andrew Wilkie

University of Oxford

UNITED KINGDOM

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Verena Vogi

AUSTRIA

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Johannes Zschocke

Research Interests

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Articles (21)

Harmonising the scope of practice for genetic counsellors in the D-A-CH region: a cross-border consensus for Germany, Austria, and Switzerland

Strategic Development of the Genetic Counselor Profession in Germany, Austria, and Switzerland: The Establishment of the GfH Genetic Counselor Commission

Reporting practices for secondary findings among ERN GENTURIS member institutions in 15 European countries

Mapping the Severity of Phenylalanine Hydroxylase Deficiency

Patients With Atopic Dermatitis Show Increased Clonal Hematopoiesis and Risk of Hematological Cancer

Integrating Polygenic Scores into Multifactorial Breast Cancer Risk Assessment: Insights from the First Year of Clinical Implementation in Western Austria

Stratification of Homologous Recombination Deficiency-Negative High-Grade Ovarian Cancer by the Type of Peritoneal Spread into Two Groups with Distinct Survival Outcomes

Clinical diagnosis of the monogenic Ehlers-Danlos syndromes

Editorial

Genetic diagnosis of the Ehlers-Danlos syndromes

Non-genetic diagnostic investigations in monogenic Ehlers-Danlos syndromes

Mendelian inheritance revisited: dominance and recessiveness in medical genetics

Guidelines in the JIMD: Evidence‐based practice for inherited metabolic disease

Correction to: Lost in promiscuity? An evolutionary and biochemical evaluation of HSD10 function in cardiolipin metabolism

Gregor Mendel and the concepts of dominance and recessiveness

Family History for Neurodegeneration in Multiple System Atrophy: Does it Indicate Susceptibility?

Lost in promiscuity? An evolutionary and biochemical evaluation of HSD10 function in cardiolipin metabolism

Array genotyping as diagnostic approach in medical genetics

The lipid environment modulates cardiolipin and phospholipid constitution in wild type and tafazzin‐deficient cells

The genetic counseling profession in Austria: Stakeholders’ perspectives

hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers

Collaborators (13)

Gunda Schwaninger

Verena Peters

Hauke Hillen

Matthias Schmuth

Katja Eckl

Matthias R. Baumgartner

Robert Gruber

Lukas Forer

Sandrine Dubrac

Markus Andreas Keller

Peter H. Byers

Andrew Wilkie

Verena Vogi

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