Ellen Knierim

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 5

Top Topics

Photodynamic Therapy

Congenital Heart Disease

Binding Protein

Top Venues

Journal of neurology

Acta neuropathologica

European journal of human genetics : EJHG

Cerebral cortex (New York, N.Y. : 1991)

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

Publications

Nina-Maria Wilpert, Ana Luisa de A Marcelino, Ellen Knierim, Pasquale Incoronato, Elisa Sanchez-Sendin, Olga Staudacher, Anne Drenckhahn, Petra Bittigau, Jakob Kreye, Harald Prüss, Markus Schuelke, Andrea A Kühn, Angela M Kaindl, Marc Nikolaus
Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2. Journal of neurology (2023)
Ellen Knierim, Johannes Vogt, Michael Kintscher, Alexey Ponomarenko, Jan Baumgart, Prateep Beed, Tatiana Korotkova, Thorsten Trimbuch, Axel Panzer, Ortrud K Steinlein, Ulrich Stephani, Andrew Escayg, Mahmoud E Koko, Yuanyuan Liu, Holger Lerche, Dietmar Schmitz, Robert Nitsch, Markus Schuelke
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype. Cerebral cortex (New York, N.Y. : 1991) (2023)
Marc Nikolaus, Arend Koch, Werner Stenzel, Sefer Elezkurtaj, Felix Sahm, Anna Tietze, Laura Stöffler, Jakob Kreye, Pablo Hernáiz Driever, Ulrich W Thomale, Angela M Kaindl, Markus Schuelke, Ellen Knierim
Atypical NMDA receptor expression in a diffuse astrocytoma, MYB- or MYBL1-altered as a trigger for autoimmune encephalitis. Acta neuropathologica 144 (2) (2022)
Sarah Paisdzior, Ellen Knierim, Gunnar Kleinau, Heike Biebermann, Heiko Krude, Rachel Straussberg, Markus Schuelke
A New Mechanism in THRA Resistance: The First Disease-Associated Variant Leading to an Increased Inhibitory Function of THRA2. International journal of molecular sciences 22 (10) (2021)
Markus Buelow, David Süßmuth, Laurie D Smith, Omid Aryani, Claudia Castiglioni, Werner Stenzel, Enrico Bertini, Markus Schuelke, Ellen Knierim
Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum. European journal of human genetics : EJHG 29 (7) (2021)