John Alexander
Affiliations: | Department of Molecular Biology and Genetics, Democritus University of Thrace |
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| Alexander J, Ströbel T, Georgitsi M, et al. (2019) Neuropathology-driven Whole-genome Sequencing Study Points to Novel Candidate Genes for Healthy Brain Aging. Alzheimer Disease and Associated Disorders |
| Alexander J, Mantzaris D, Georgitsi M, et al. (2017) Variant Ranker: a web-tool to rank genomic data according to functional significance. Bmc Bioinformatics. 18: 341 |
| Le Guennec K, Quenez O, Nicolas G, et al. (2016) 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression. Molecular Psychiatry |
| Butler KM, da Silva C, Shafir Y, et al. (2016) De novo and inherited SCN8A epilepsy mutations detected by gene panel analysis. Epilepsy Research. 129: 17-25 |
| Alexander J, Potamianou H, Xing J, et al. (2016) Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Frontiers in Neuroscience. 10: 428 |
| Forde NJ, Kanaan AS, Widomska J, et al. (2016) TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome. Frontiers in Neuroscience. 10: 384 |
| Tsetsos F, Padmanabhuni SS, Alexander J, et al. (2016) Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis. Frontiers in Neuroscience. 10: 340 |
| Alexander J, Kalev O, Mehrabian S, et al. (2016) Familial early-onset dementia with complex neuropathologic phenotype and genomic background. Neurobiology of Aging. 42: 199-204 |
| Karagiannidis I, Tsetsos F, Padmanabhuni SS, et al. (2016) The Genetics of Gilles de la Tourette Syndrome: a Common Aetiological Basis with Comorbid Disorders? Current Behavioral Neuroscience Reports. 3: 218-231 |