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Scope
Neurogenetics – the genetics of brain disorders may serve as a foundation for earlier, molecular diagnosis, fundamental neuroscience and future drug development. This Frontiers section focuses on research that capitalizes on human genetics to solve neurologic problems.
*For the submission of a Case Report please, send the manuscript draft to neurology@frontiersin.org for pre-evaluation. Any Case Reports submitted without a previous enquiry might experience delays, as they will be sent for assessment prior to peer review.
Scope
Neurogenetics – the genetics of brain disorders may serve as a foundation for earlier, molecular diagnosis, fundamental neuroscience and future drug development. This Frontiers section focuses on research that capitalizes on human genetics to solve neurologic problems. Ideally, submissions will have a translational bias and will marry aspects of clinical neurology, neuropathology, neurogenetics, molecular neuroscience, and neuropharmacology. Manuscripts are to include original research, provocative reviews, and perceptive syntheses, that are directive for the field.
Indexed in: PubMed, PubMed Central (PMC), Scopus, Google Scholar, DOAJ, CrossRef, Embase, CLOCKSS
PMCID: all published articles receive a PMCID
Neurogenetics welcomes submissions of the following article types: Brief Research Report, Case Report, Clinical Trial, Correction, Editorial, Erratum, Hypothesis and Theory, Methods, Mini Review, Opinion, Original Research, Perspective, Review, Specialty Grand Challenge, Study Protocol and Systematic Review.
All manuscripts must be submitted directly to the section Neurogenetics, where they are peer-reviewed by the Associate and Review Editors of the specialty section.
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Avenue du Tribunal Fédéral 34
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Switzerland
Tel +41(0)21 510 17 40
Fax +41 (0)21 510 17 01
For all queries regarding manuscripts in Review and potential conflicts of interest, please contact neurology.editorial.office@frontiersin.org
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