Andreas Busjahn

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 4

Top Venues

Nutrients

Nature genetics

The International journal of eating disorders

HealthTwiSt GmbH

This page only lists publications with an associated author ORCID identifier.

Affiliation History

HealthTwiSt GmbH Jan 01 2003

Germany

CEO

Publications

Martina Pech, Christoph U Correll, Janine Schmidt, Almut Zeeck, Tobias Hofmann, Andreas Busjahn, Verena Haas
The Relationship between Patient Self-Reported, Pre-Morbid Physical Activity and Clinical Outcomes of Inpatient Treatment in Youth with Anorexia Nervosa: A Pilot Study. Nutrients 16 (12) (2024)
Martina Pech, Christoph U Correll, Janine Schmidt, Almut Zeeck, Tobias Hofmann, Andreas Busjahn, Verena Haas
The Relationship between Patient Self-Reported, Pre-Morbid Physical Activity and Clinical Outcomes of Inpatient Treatment in Youth with Anorexia Nervosa: A Pilot Study. Nutrients 16 (12) (2024)
Verena Haas, Katja Wechsung, Vivien Kaiser, Janine Schmidt, Klemens Raile, Andreas Busjahn, Daniel Le Grange, Christoph U Correll
Comparing family-based treatment with inpatient treatment in youth with anorexia nervosa eligible for hospitalization: A 12-month feasibility study. The International journal of eating disorders (2023)
Philipp G Maass, Atakan Aydin, Friedrich C Luft, Carolin Schächterle, Anja Weise, Sigmar Stricker, Carsten Lindschau, Martin Vaegler, Fatimunnisa Qadri, Hakan R Toka, Herbert Schulz, Peter M Krawitz, Dmitri Parkhomchuk, Jochen Hecht, Irene Hollfinger, Yvette Wefeld-Neuenfeld, Eireen Bartels-Klein, Astrid Mühl, Martin Kann, Herbert Schuster, David Chitayat, Martin G Bialer, Thomas F Wienker, Jürg Ott, Katharina Rittscher, Thomas Liehr, Jens Jordan, Ghislaine Plessis, Jens Tank, Knut Mai, Ramin Naraghi, Russell Hodge, Maxwell Hopp, Lars O Hattenbach, Andreas Busjahn, Anita Rauch, Fabrice Vandeput, Maolian Gong, Franz Rüschendorf, Norbert Hübner, Hermann Haller, Stefan Mundlos, Nihat Bilginturan, Matthew A Movsesian, Enno Klussmann, Okan Toka, Sylvia Bähring
PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature genetics 47 (6) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Andreas Busjahn