Maike F Dohrn

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 27

Top Venues

Brain : a journal of neurology

Annals of clinical and translational neurology

Brain sciences

Journal of neurochemistry

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

Publications

Maike F Dohrn, Guney Bademci, Adriana P Rebelo, Médéric Jeanne, Nicholas A Borja, Danique Beijer, Matt C Danzi, Stephanie A Bivona, Paul Gueguen, Mohammad F Zafeer, null null, Mustafa Tekin, Stephan Züchner
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of clinical and translational neurology (2024)
Danique Beijer, Maike F Dohrn, Adriana P Rebelo, Matt C Danzi, Bianca Rose Grosz, Melina Ellis, Kishore Raj Kumar, Steve Vucic, Horia Vais, Jillian S Weissenrieder, Olesia Lunko, Usha Paudel, Leah C Simpson, Jacquelyn Raposo, Mario Saporta, Yeisha Arcia, Isaac Xu, Shawna Feely, Christopher J Record, Julian Blake, Mary M Reilly, Steven Scherer, Marina Kennerson, Yi-Chung Lee, J Kevin Foskett, Michael Shy, Stephan Zuchner
A recurrent missense variant in ITPR3 causes demyelinating Charcot-Marie-Tooth with variable severity. Brain : a journal of neurology (2024)
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, Jian J Li, Ethan K Tieu, Jessica Medina, Christopher Yanick, Jingyu Huang, Brendan Zotter, Juan I Young, Mario Saporta, Steven S Scherer, Katherina Walz, Stephan Zuchner
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain : a journal of neurology (2024)
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, Jian J Li, Ethan K Tieu, Jessica Medina, Christopher Yanick, Jingyu Huang, Brendan Zotter, Juan I Young, Mario Saporta, Steven S Scherer, Katherina Walz, Stephan Zuchner
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain : a journal of neurology 147 (9) (2024)
Maike F Dohrn, Guney Bademci, Adriana P Rebelo, Médéric Jeanne, Nicholas A Borja, Danique Beijer, Matt C Danzi, Stephanie A Bivona, Paul Gueguen, Mohammad F Zafeer, null null, Mustafa Tekin, Stephan Züchner
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of clinical and translational neurology 11 (4) (2024)
Maike F Dohrn, Guney Bademci, Adriana P Rebelo, Médéric Jeanne, Nicholas A Borja, Danique Beijer, Matt C Danzi, Stephanie A Bivona, Paul Gueguen, Mohammad F Zafeer, null null, Mustafa Tekin, Stephan Züchner
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of clinical and translational neurology 11 (4) (2024)
Maike F Dohrn, Guney Bademci, Adriana P Rebelo, Médéric Jeanne, Nicholas A Borja, Danique Beijer, Matt C Danzi, Stephanie A Bivona, Paul Gueguen, Mohammad F Zafeer, null null, Mustafa Tekin, Stephan Züchner
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of clinical and translational neurology 11 (4) (2024)
Adriana P Rebelo, Clemer Abad, Maike F Dohrn, Jian J Li, Ethan K Tieu, Jessica Medina, Christopher Yanick, Jingyu Huang, Brendan Zotter, Juan I Young, Mario Saporta, Steven S Scherer, Katherina Walz, Stephan Zuchner
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain : a journal of neurology (2024)
Maike F Dohrn, Guney Bademci, Adriana P Rebelo, Médéric Jeanne, Nicholas A Borja, Danique Beijer, Matt C Danzi, Stephanie A Bivona, Paul Gueguen, Mohammad F Zafeer, null null, Mustafa Tekin, Stephan Züchner
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism. Annals of clinical and translational neurology (2024)
Vance P Lemmon, Maike F Dohrn, Sarah Fazal, Danique Beijer, Adriana P Rebelo, Vivian Cintra, Stephan Zuchner
Deep structured learning for variant prioritization in Mendelian diseases. Nature communications 14 (1) (2023)
Tabea M Dyong, Burkhard Gess, Christina Dumke, Roman Rolke, Maike F Dohrn
Carbamazepine for Chronic Muscle Pain: A Retrospective Assessment of Indications, Side Effects, and Treatment Response. Brain sciences 13 (1) (2023)
Tabea M Dyong, Burkhard Gess, Christina Dumke, Roman Rolke, Maike F Dohrn
Carbamazepine for Chronic Muscle Pain: A Retrospective Assessment of Indications, Side Effects, and Treatment Response. Brain sciences 13 (1) (2023)
Tabea M Dyong, Burkhard Gess, Christina Dumke, Roman Rolke, Maike F Dohrn
Carbamazepine for Chronic Muscle Pain: A Retrospective Assessment of Indications, Side Effects, and Treatment Response. Brain sciences 13 (1) (2023)
Maike F Dohrn, Danique Beijer, Museer A Lone, Elif Bayraktar, Piraye Oflazer, Rotem Orbach, Sandra Donkervoort, A Reghan Foley, Aubrey Rose, Michael Lyons, Raymond J Louie, Kenneth Gable, Teresa Dunn, Sitong Chen, Matt C Danzi, Matthis Synofzik, Carsten G Bönnemann, Ayse Nazli Basak, Thorsten Hornemann, Stephan Zuchner
Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis. Journal of neurology, neurosurgery, and psychiatry (2023)
Abdoulaye Yalcouyé, Adriana P Rebelo, Lassana Cissé, Lynette Rives, Salia Bamba, Joy Cogan, Kevin Esoh, Salimata Diarra, Kimberly M Ezell, Abdoulaye Taméga, Cheick O Guinto, Maike F Dohrn, Rizwan Hamid, Kenneth H Fischbeck, Stephan Zuchner, Guida Landouré
Novel variant in CADM3 causes Charcot-Marie-Tooth disease. Brain communications 5 (5) (2023)
Annette Lischka, Katja Eggermann, Christopher J Record, Maike F Dohrn, Petra Laššuthová, Florian Kraft, Matthias Begemann, Daniela Dey, Eggermann Thomas, Danique Beijer, Jana Šoukalová, Matilde Laura, Alexander M Rossor, Radim Mazanec, Jonas Van Lent, Pedro José Tomaselli, Martin Ungelenk, Karlien Y Debus, Shawna M E Feely, Dieter Gläser, Sujatha Jagadeesh, Madelena Martin, Geeta M Govindaraj, Pratibha Singhi, Revanth Baineni, Niranjan Biswal, Marisol Ibarra-Ramírez, Maryse Bonduelle, Burkhard Gess, Juan Romero Sánchez, Renu Suthar, Vrajesh Udani, Atchayaram Nalini, Gopikrishnan Unnikrishnan, Wilson Marques Junior, Sandra Mercier, Vincent Procaccio, Céline Bris, Beena Suresh, Vaishnavi Reddy, Mariola Skorupinska, Nathalie Bonello-Palot, Fanny Mochel, Georg Dahl, Karthika Sasidharan, Fiji M Devassikutty, Sheela Nampoothiri, Maria J Rodovalho Doriqui, Wolfgang Müller-Felber, Katharina Vill, Tobias B Haack, Andreas Dufke, Michael Abele, Rolf Stucka, Saima Siddiqi, Noor Ullah, Stephanie Spranger, Deborah Chiabrando, Behiye S Bolgül, Yesim Parman, Pavel Seeman, Angelika Lampert, Jörg B Schulz, John N Wood, James J Cox, Michaela Auer-Grumbach, Vincent Timmerman, Jonathan de Winter, Andreas C Themistocleous, Michael Shy, David L H Bennett, Jonathan Baets, Christian A Hübner, Enrico Leipold, Stephan Züchner, Miriam Elbracht, Arman Çakar, Jan Senderek, Thorsten Hornemann, C Geoffrey Woods, Mary M Reilly, Ingo Kurth
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies. Brain : a journal of neurology (2023)
Tabea M Dyong, Burkhard Gess, Christina Dumke, Roman Rolke, Maike F Dohrn
Carbamazepine for Chronic Muscle Pain: A Retrospective Assessment of Indications, Side Effects, and Treatment Response. Brain sciences 13 (1) (2023)
Maike F Dohrn, Corina Heller, Diana Zengeler, Carolin D Obermaier, Saskia Biskup, Joachim Weis, Stefan Nikolin, Kristl G Claeys, Ulrike Schöne, Danique Beijer, Natalie Winter, Pascal Achenbach, Burkhard Gess, Jörg B Schulz, Lejla Mulahasanovic
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers. Neurological research and practice 4 (1) (2022)
Maike F Dohrn, Adriana P Rebelo, Siddharth Srivastava, Gerarda Cappuccio, Smigiel Robert, Alka Malhotra, Donald Basel, Ingrid M B H van de Laar, Rinze Frederik Neuteboom, Coranne Aarts-Tesselaar, Sonal Mahida, Nicola Brunetti-Pierri, Ryan J Taft, Stephan Züchner
De Novo ATP1A1 Variants in an Early-Onset Complex Neurodevelopmental Syndrome. Neurology 98 (11) (2022)
Maike F Dohrn, Jessica Medina, Karmele R Olaciregui Dague, Ernst Hund
Are we creating a new phenotype? Physiological barriers and ethical considerations in the treatment of hereditary transthyretin-amyloidosis. Neurological research and practice 3 (1) (2021)
Maike F Dohrn, Gisa Ellrichmann, Rastislav Pjontek, Carsten Lukas, Jens Panse, Ralf Gold, Jörg B Schulz, Burkhard Gess, Simone C Tauber
Progressive multifocal leukoencephalopathy and immune reconstitution inflammatory syndrome in seven patients with sarcoidosis: a critical discussion of treatment and prognosis. Therapeutic advances in neurological disorders 14 (2021)
Yuliia V Nikonishyna, Nadine J Ortner, Teresa Kaserer, Jessica Hoffmann, Saskia Biskup, Manuel Dafotakis, Kathrin Reetz, Jörg B Schulz, Jörg Striessnig, Maike F Dohrn
Novel CACNA1A Variant p.Cys256Phe Disrupts Disulfide Bonds and Causes Spinocerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society (2021)
Maike F Dohrn, Ulrike Schöne, Charlotte Küppers, Deborah Christen, Jörg B Schulz, Burkhard Gess, Simone Tauber
Immunoglobulins to mitigate paraneoplastic Lambert Eaton Myasthenic Syndrome under checkpoint inhibition in Merkel cell carcinoma. Neurological research and practice 2 (2020)
Maike F Dohrn, Michaela Auer-Grumbach, Ralf Baron, Frank Birklein, Fabiola Escolano-Lozano, Christian Geber, Nicolai Grether, Tim Hagenacker, Ernst Hund, Juliane Sachau, Matthias Schilling, Jens Schmidt, Wilhelm Schulte-Mattler, Claudia Sommer, Markus Weiler, Gilbert Wunderlich, Katrin Hahn
Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature. Journal of neurology 268 (10) (2020)
Maike F Dohrn, Sandra Ihne, Ute Hegenbart, Jessica Medina, Stephan L Züchner, Teresa Coelho, Katrin Hahn
Targeting transthyretin - Mechanism-based treatment approaches and future perspectives in hereditary amyloidosis. Journal of neurochemistry 156 (6) (2020)
Maike F Dohrn, Juan Pedro Bolaños
Does APC/CCDH1 control the human brain size?: An Editorial Highlight for 'A novel human Cdh1 mutation impairs anaphase-promoting complex/cyclosome (APC/C) activity resulting in microcephaly, psychomotor retardation, and epilepsy' on page 103. Journal of neurochemistry 151 (1) (2019)
Maike F Dohrn, Nicola Glöckle, Lejla Mulahasanovic, Corina Heller, Julia Mohr, Christine Bauer, Erik Riesch, Andrea Becker, Florian Battke, Konstanze Hörtnagel, Thorsten Hornemann, Saranya Suriyanarayanan, Markus Blankenburg, Jörg Bernhard Schulz, Kristl G Claeys, Burkhard Gess, Istvan Katona, Andreas Ferbert, Debora Vittore, Alexander Grimm, Stefan Wolking, Ludger Schöls, Holger Lerche, G Christoph Korenke, Dirk Fischer, Bertold Schrank, Urania Kotzaeridou, Gerhard Kurlemann, Bianca Dräger, Anja Schirmacher, Peter Young, Beate Schlotter-Weigel, Saskia Biskup
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies. Journal of neurochemistry 143 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Maike F Dohrn