Neurology®Genetics Welcomes You to the AAN Annual Meeting!
About Neurology: Genetics
Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
The 2020 Impact Factor for Neurology: Genetics is 3.485.
Neurology: Genetics is indexed in PMC, Scopus, EMBASE, Google Scholar, DOAJ, CrossRef, Science Citation Index Expanded (SCIE), Web of Science®, and Current Contents®/Clinical Medicine.
Meet the Editors
Dr. Stefan M. Pulst, MD, Dr med, FAAN
Editor
Massimo Pandolfo, MD, FAAN
Deputy Editor
Alexandra Durr, MD, PhD
Associate Editor
Suman Jayadev, MD
Associate Editor
Margherita Milone, MD, PhD
Associate Editor
Raymond P. Roos, MD, FAAN
Associate Editor
Featured Infographics
Infographics are an exciting feature available across the Neurology® journals. We hope our readers will find them to be an engaging and convenient way to understand the information presented in the article. All infographics are created by a team of scientific writers and illustrators and undergo a rigorous review process involving input and feedback from the author and Neurology editors.
WGS and RNA Studies Diagnose Noncoding DMD Variants in Males With High Creatine Kinase
Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington disease
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy
Editor Selected Articles
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk
Brooke Rhead, Maria Bäärnhielm, Milena Gianfrancesco, et al.
Antisense oligonucleotides: A primer
Daniel R. Scoles, Eric V. Minikel, Stefan M. Pulst
Migraine polygenic risk score associates with efficacy of migraine-specific drugs
Lisette J.A. Kogelman, Ann-Louise Esserlind, Anne Francke Christensen, et al.
Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts
Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, et al.
Mitochondrial diseases in North America: An analysis of the NAMDC Registry
Emanuele Barca, Yuelin Long, Victoria Cooley, et al.
Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference?
Christiane Reitz, Ekaterina Rogaeva, Gary W. Beecham, et al.
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study
Anna Rubegni, Alessandro Malandrini, Claudia Dosi, et al.
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy
Asfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, Christopher Labos, Gerald Pfeffer
Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
Dr. Robert Pitceathly and Dr. William Macken
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Call for Submissions
Neurology: Genetics wants to review your research for publication! Learn more on how to prepare and submit your manuscript here.