- Title
- Solving unsolved rare neurological diseases-a Solve-RD viewpoint
- Creators
- Rebecca Schüle - European Reference Network for Rare Neurological Diseases, Tübingen, Germany. rebecca.schuele-freyer@uni-tuebingen.deDagmar Timmann - Department of Neurology and Center for Translational Neuro- and Behavioral Sciences (C-TNBS), University Hospital Essen, Essen, GermanyCorrie E Erasmus - Department of Pediatric Neurology, Radboud University Medical Center, Amalia Children's Hospital, Donders Institute for Brain, Cognition and Behavior, Nijmegen, The NetherlandsJennifer Reichbauer - German Center for Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, GermanyMelanie Wayand - German Center for Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, GermanyBart van de Warrenburg - Department of Neurology, Donders Centre for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The NetherlandsLudger Schöls - European Reference Network for Rare Neurological Diseases, Tübingen, GermanyCarlo Wilke - German Center for Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, GermanyAndrea Bevot - Department of Pediatric Neurology and Developmental Medicine, University Children's Hospital, Tübingen, GermanyStephan Zuchner - Dr. John T. Macdonald Foundation Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USASergi Beltran - Facultat de Biologia, Departament de Genètica, Microbiologia i Estadística, Universitat de Barcelona (UB), Barcelona, SpainSteven Laurie - CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, SpainLeslie Matalonga - CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, SpainHolm Graessner - Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, GermanyMatthis Synofzik - European Reference Network for Rare Neurological Diseases, Tübingen, GermanySolve-RD-DITF-RND
- Publication Details
- European journal of human genetics : EJHG
- Grant note
- 825575 / EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) PT13/0001/0044 / Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) 779257 / EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) R01NS072248 / U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) PT17/0009/0019 / Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III)
- Academic Unit
- Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics
- Language
- English
- Resource Type
- Journal article
- PMID
- 33972714
- Record Identifier
- 991031600089002976
Journal article
Solving unsolved rare neurological diseases-a Solve-RD viewpoint
European journal of human genetics : EJHG
2021-05-10
PMID: 33972714
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- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.189 Genome Studies
- 1.189.597 BRCA1
- Web Of Science research areas
- Biochemistry & Molecular Biology
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
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Source: InCites