Antje Bornemann

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

Karsten M. Strauss, L. Miguel Martins, Hélène Plun‐Favreau et al. · Human Molecular Genetics · 2005 · 563 citations · Full text

Mitophagy, Mitochondrial Dysfunction, Genetics +16

Absence of integrin α7 causes a novel form of muscular dystrophy

Ulríke Mayer, Gesine Saher, Reinhard Fässler et al. · Nature Genetics · 1997 · 443 citations

Skeletal Muscle, Medicine, Physiology +6

A Functional Role of HLA-G Expression in Human Gliomas: An Alternative Strategy of Immune Escape

Heinz Wiendl, Meike Mitsdoerffer, Valeska Hofmeister et al. · The Journal of Immunology · 2002 · 327 citations · Full text

CD19-Targeting CAR T Cells for Myositis and Interstitial Lung Disease Associated With Antisynthetase Syndrome

Ann‐Christin Pecher, Luca Hensen, Reinhild Klein et al. · JAMA · 2023 · 207 citations · Full text

Ubiquitylation of synphilin-1 and α-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease

Esti Liani, Allon Eyal, Eyal Avraham et al. · Proceedings of the National Academy of Sciences · 2004 · 188 citations · Full text