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Neurology. Genetics|December 25, 2019
Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosisLing Wei, Yanghua Tian, Yongping Chen, et al.
Neurology. Genetics|January 26, 2023
Neuropathology-Independent Association Between APOE Genotype and Cognitive Decline Rate in the Normal Aging-Early Alzheimer ContinuumJing Qian, Yiding Zhang, Rebecca A Betensky, et al.
Neurology. Genetics|March 27, 2020
ALS in Danish Registries: Heritability and links to psychiatric and cardiovascular disordersBetina B Trabjerg, Fleur C Garton, Wouter van Rheenen, et al.
Neurology. Genetics|October 16, 2020
Manifesting carriers of X-linked myotubular myopathy: Genetic modifiers modulating the phenotypeLucas Santos Souza, Camila Freitas Almeida, Guilherme Lopes Yamamoto, et al.
Neurology. Genetics|July 12, 2021
Effect of Body Weight on Age at Onset in Huntington Disease: A Mendelian Randomization StudyJorien M M van der Burg, Patrick Weydt, Georg Bernhard Landwehrmeyer, et al.
Neurology. Genetics|May 6, 2022
Biallelic ATOH1 Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing LossTanja Višnjar, Aleš Maver, Karin Writzl, et al.
Neurology. Genetics|June 3, 2022
Vanishing White Matter Disease Presenting as Dementia and Infertility: A Case ReportJasmine Parihar, Deepti Vibha, Roopa Rajan, et al.
Neurology. Genetics|June 17, 2022
Adult-Onset Sandhoff Disease in a Filipino Patient: Asymmetric Weakness, Whole HEXB Gene Deletion, and Coexisting MYH7 Pathogenic VariantGrayson Beecher, Teerin Liewluck, Margherita Milone
Neurology. Genetics|September 22, 2016
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis riskBrooke Rhead, Maria Bäärnhielm, Milena Gianfrancesco, et al.
Neurology. Genetics|June 8, 2017
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.
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