Journal Report

NEUROLOGY-GENETICS

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Journal Information
Journal Title
NEUROLOGY-GENETICS
Publisher
LIPPINCOTT WILLIAMS & WILKINS
ISSN
2376-7839
E-ISSN
2376-7839
Database
Clarivate
Domain
Not available
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓
2018
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Cerebrotendinous Xanthomatosis
Héctor Rubén Martínez-Hernández, Leonel Villa-Villegas, Carlos Eduardo Piña-Avilés et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200443
Duchenne Muscular Dystrophy and Delandistrogene Moxeparvovec Gene Therapy in Children
Breno Bopp Antonello, Fabio Cargnelutti Fontoura, Anna Luiza Braga Albuquerque et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200444
Mortality of Individuals With <i>PRNP</i> Variants Associated With Prion Disease in the United States, 1998–2024
Yuan Lian, Keisi Kotobelli, Katie Glisic et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200461
Unraveling the Genotype-Phenotype Landscape of Kleefstra Syndrome Through <i>EHMT1</i> Variant Analysis
Jee Min Kim, Jong Ho Cha, Woojoong Kim et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200445
Quantification of Neuromotor Control in <i>STXBP1</i> -Related Disorders With Wearable Sensors
Julie M. Orlando, Bintou Bane, Torrey Chisari et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200439
Nationwide Implementation of Newborn Screening for Spinal Muscular Atrophy in Canada
Hugh J. McMillan, Homira Osman, Kristin Kernohan et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200451
Clinical and Genetic Spectrum of <i>ATP1A3</i> -Related Disorders
Victor Rebelo Procaci, Raphael Pinheiro Camurugy da Hora, Anna Maria Gomes et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200459
Reduced Effect of <i>APOE4</i> on White Matter Microstructure in an American Indian Community
René Labounek, Matti J. Matheson, Corey Strong et al.
2026-12 Vol. 12 Issue 6
DOI: 10.1212/nxg.0000000000200438
Two Cases of Multiple Sclerosis in a Family With X-Linked Charcot-Marie-Tooth Disease
Marija Menih, Tanja Hojs Fabjan, Aleš Maver et al.
2026-10 Vol. 12 Issue 5
DOI: 10.1212/nxg.0000000000200426
Genetic Screening of Colombian Patients With Early-Onset Parkinson Disease
Tobias M. Franz, Marios Gavrielatos, Ysabella Wijaya et al.
2026-10 Vol. 12 Issue 5
DOI: 10.1212/nxg.0000000000200427
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Printed: October 27, 2026 02:25