A. Heinen

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann et al. · Nature Genetics · 2024 · 47 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

A randomized, placebo controlled trial of prostacyclin (PGI2) in peripheral arterial disease

V. Hossman, A. Heinen, H. Auel et al. · Thrombosis Research · 1981 · 39 citations

Medicine, Cardiology, Pharmacology +11

Transition for adolescents with a rare disease: results of a nationwide German project

Corinna Grasemann, Jakob Höppner, Peter Burgard et al. · Orphanet Journal of Rare Diseases · 2023 · 25 citations · Full text

Medicine, Medical Education, Pediatrics +17

Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?

A. Heinen, Anja Schnabel, Normi Brück et al. · Lara D. Veeken · 2020 · 23 citations

Medicine, Dermatology, Immunology +14

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann et al. · medRxiv · 2023 · 15 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16