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Neurology. Genetics|July 20, 2019
HACE1 deficiency leads to structural and functional neurodevelopmental defectsVanja Nagy, Ronja Hollstein, Tsung-Pin Pai, et al.Neurology. Genetics|July 20, 2019
Congenital myopathies in the adult neuromuscular clinic: Diagnostic challenges and pitfallsStefan Nicolau, Teerin Liewluck, Jennifer A Tracy, et al.Neurology. Genetics|February 10, 2017
A gain-of-function mutation in the GRIK2 gene causes neurodevelopmental deficitsYomayra F Guzmán, Keri Ramsey, Jacob R Stolz, et al.Neurology. Genetics|March 14, 2019
Genomic variation in educational attainment modifies Alzheimer disease riskNeha S Raghavan, Badri Vardarajan, Richard MayeuxNeurology. Genetics|April 22, 2017
20th Workshop of the International Stroke Genetics Consortium, November 3-4, 2016, Milan, Italy: 2016.036 ISGC research prioritiesDaniel Woo, Stephanie Debette, Christopher AndersonNeurology. Genetics|March 18, 2021
Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal PolyneuropathyHelene Bruhn, Kristin Samuelsson, Florian A Schober, et al.Neurology. Genetics|May 5, 2018
Somatic GNAQ mutation in the forme fruste of Sturge-Weber syndromeMichael S Hildebrand, A Simon Harvey, Stephen Malone, et al.Neurology. Genetics|August 16, 2018
Axon reflex-mediated vasodilation is reduced in proportion to disease severity in TTR-FAPIrène Calero-Romero, Marc R Suter, Bernard Waeber, et al.Neurology. Genetics|August 16, 2018
Association study between multiple system atrophy and TREM2 p.R47HKotaro Ogaki, Michael G Heckman, Shunsuke Koga, et al.Neurology. Genetics|November 21, 2022
Relationships of APOE Genotypes With Small RNA and Protein Cargo of Brain Tissue Extracellular Vesicles From Patients With Late-Stage ADYiyao Huang, Tom A P Driedonks, Lesley Cheng, et al.Pageof 88