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Neurology. Genetics|September 3, 2026
Multiple Sclerosis Misdiagnosis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: A Genotype-Misphenotype StudyDinith D Mendis, Sai Krishna Vallamchetla, Iris Vanessa Marin Collazo, et al.
Neurology. Genetics|September 30, 2026
Alternating Hemiplegia of Childhood: Development of a Disease-Specific Clinical Rating ScaleMichela Stagnaro, Carmen Fons, Eleni Panagiotakaki, et al.
Neurology. Genetics|September 30, 2026
Genetic Insights Into Protective Effects of GLP-1 Receptor Agonists on Stroke and Alzheimer Disease Across AncestriesIlana Caro-Châtelier, Muralidharan Sargurupremraj, Chengran Yang, et al.
Neurology. Genetics|September 17, 2026
Association of Bilateral Vestibulopathy With the ZNF91/LINC01224 Locus: A Genome-Wide Association StudyFelix L Heindl, Michael Strupp, Annette M Hartmann, et al.
Neurology. Genetics|October 6, 2026
Beyond Seizure Management in a Developmental Epileptic Encephalopathy: Expanding the SLC6A1 Neurodevelopmental Disorder PhenotypeMarie E Varnet, Hamza Dahshi, Kimberly Goodspeed, et al.
Neurology. Genetics|October 20, 2026
Erratum: Reduced Effect of APOE4 on White Matter Microstructure in an American Indian CommunityRené Labounek, Matti J Matheson, Corey Strong, et al.
Neurology. Genetics|October 20, 2026
Unraveling the Genotype-Phenotype Landscape of Kleefstra Syndrome Through EHMT1 Variant AnalysisJee Min Kim, Jong Ho Cha, Woojoong Kim, et al.
Neurology. Genetics|June 10, 2016
Defining the spectrum of frontotemporal dementias associated with TARDBP mutationsPaola Caroppo, Agnès Camuzat, Léna Guillot-Noel, et al.
Neurology. Genetics|April 29, 2016
Stabilization of the thermolabile variant S113L of carnitine palmitoyltransferase IILeila Motlagh, Ralph Golbik, Wolfgang Sippl, et al.
Neurology. Genetics|April 29, 2016
New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophyZhuoran Sun, Yasuyuki Ohta, Toru Yamashita, et al.
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