| Year |
Citation |
Score |
| 2019 |
Alexander J, Ströbel T, Georgitsi M, Hönigschnabl S, Reiner A, Fischer P, Tsifintaris M, Paschou P, Kovacs GG. Neuropathology-driven Whole-genome Sequencing Study Points to Novel Candidate Genes for Healthy Brain Aging. Alzheimer Disease and Associated Disorders. PMID 30681437 DOI: 10.1097/Wad.0000000000000294 |
0.595 |
|
| 2017 |
Alexander J, Mantzaris D, Georgitsi M, Drineas P, Paschou P. Variant Ranker: a web-tool to rank genomic data according to functional significance. Bmc Bioinformatics. 18: 341. PMID 28716001 DOI: 10.1186/S12859-017-1752-3 |
0.611 |
|
| 2016 |
Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, et al. 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression. Molecular Psychiatry. PMID 27956742 DOI: 10.1038/Mp.2016.226 |
0.599 |
|
| 2016 |
Butler KM, da Silva C, Shafir Y, Weisfeld-Adams JD, Alexander JJ, Hegde M, Escayg A. De novo and inherited SCN8A epilepsy mutations detected by gene panel analysis. Epilepsy Research. 129: 17-25. PMID 27875746 DOI: 10.1016/J.Eplepsyres.2016.11.002 |
0.308 |
|
| 2016 |
Alexander J, Potamianou H, Xing J, Deng L, Karagiannidis I, Tsetsos F, Drineas P, Tarnok Z, Rizzo R, Wolanczyk T, Farkas L, Nagy P, Szymanska U, Androutsos C, Tsironi V, et al. Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Frontiers in Neuroscience. 10: 428. PMID 27708560 DOI: 10.3389/Fnins.2016.00428 |
0.728 |
|
| 2016 |
Forde NJ, Kanaan AS, Widomska J, Padmanabhuni SS, Nespoli E, Alexander J, Rodriguez Arranz JI, Fan S, Houssari R, Nawaz MS, Rizzo F, Pagliaroli L, Zilhäo NR, Aranyi T, Barta C, et al. 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. PMID 27601976 DOI: 10.3389/Fnins.2016.00384 |
0.745 |
|
| 2016 |
Tsetsos F, Padmanabhuni SS, Alexander J, Karagiannidis I, Tsifintaris M, Topaloudi A, Mantzaris D, Georgitsi M, Drineas P, Paschou P. Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis. Frontiers in Neuroscience. 10: 340. PMID 27499730 DOI: 10.3389/Fnins.2016.00340 |
0.699 |
|
| 2016 |
Alexander J, Kalev O, Mehrabian S, Traykov L, Raycheva M, Kanakis D, Drineas P, Lutz MI, Ströbel T, Penz T, Schuster M, Bock C, Ferrer I, Paschou P, Kovacs GG. Familial early-onset dementia with complex neuropathologic phenotype and genomic background. Neurobiology of Aging. 42: 199-204. PMID 27143436 DOI: 10.1016/J.Neurobiolaging.2016.03.012 |
0.651 |
|
| 2016 |
Karagiannidis I, Tsetsos F, Padmanabhuni SS, Alexander J, Georgitsi M, Paschou P. The Genetics of Gilles de la Tourette Syndrome: a Common Aetiological Basis with Comorbid Disorders? Current Behavioral Neuroscience Reports. 3: 218-231. DOI: 10.1007/S40473-016-0088-Z |
0.687 |
|
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