Laboratory of Genome Variation and Genetic Epidemiology

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Publications (John Alexander)

  1. Alexander J, Strobel T, Georgitsi M, Honigschnabl S, Reiner A, Fischer P, Tsifintaris M, Paschou P, Kovacs GG (2019). Neuropathology-driven Whole-genome Sequencing Study Points to Novel Candidate Genes for Healthy Brain Aging. Alzheimer Dis Assoc Disord 2019;33:7–14.
  2. 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 (2017).
  3. Le Guennec, K, O Quenez, G Nicolas, D Wallon, S Rousseau, A-C Richard, J Alexander, et al. 2016. “17q21.31 Duplication Causes Prominent Tau-Related Dementia with Increased MAPT Expression.” Mol Psychiatry. Macmillan Publishers Limited, part of Springer Nature. http://dx.doi.org/10.1038/mp.2016.226.
  4. Alexander J, Potamianou H, Xing J, Deng L, Karagiannidis I, Tsetsos F, Drineas P, Zsanett T, Rizzo R, Wolanczyk T, Farkas L, Nagy P, Szymanska U, Androutsos C, Tsironi V, Koumoula A, Barta C, Sandor P, Barr C, Tischfield J, Paschou P, Heiman G, Georgitsi M. (2016). Targeted re-sequencing approach of candidate genes implicates rare potentially functional variants in Tourette Syndrome etiology. Frontiers in Neuroscience.
  5. Alexander, J., Kalev, O., Mehrabian, S., Traykov, L., Raycheva, M., Kanakis, D., et al. (2016). Familial early-onset dementia with complex neuropathological phenotype and genomic background. Neurobiol. Aging.2016.
  6. N. J. Forde, A. S. Kanaan, J. Widomska, S. S. Padmanabhuni, E. Nespoli, J. Alexander, J. Rodriguez Arranz, S. Fan, R. Houssari, M. S. Nawaz, N. R. Zilhao, L. Pagliaroli, F. Rizzo, T. Aranyi, C. Barta, T. M. Boeckers, D. I. Boomsma, W. R. Buisman, J. K. Buitelaar, D. Cath, A. Dietrich, N. Driessen, P. Drineas, M. Dunlap, S. Gerasch, J. Glennon, B. Hengerer, O. A. van den Heuvel, C.e Jespersgaard, H. E. Moller, K. R. Müller-Vahl, T. Openneer, G. Poelmans, P. J. W. Pouwels, J. M. Scharf, H. Stefansson, Z. Tumer, D. Veltman, Y. D van der Werf, P. J. Hoekstra, A. Ludolph, and P. Paschou (2016) TS-EUROTRAIN: A European-wide investigation and training network on the aetiology and pathophysiology of Gilles de la Tourette Syndrome, Frontiers in Neuroscience, 10, article 384, 2016.
  7. Karagiannidis I, Tsetsos F, Padmanabhuni SS, Alexander J, Georgitsi M, Paschou P (2016). The Genetics of Gilles de la Tourette Syndrome: a Common Aetiological Basis with Comorbid Disorders? Current Behavioral Neuroscience Reports 1–14
  8. F. Tsetsos, S. S. Padmanabhuni, J. Alexander, I. Karagiannidis, M. Tsifintaris, A. Topaloudi, D. Mantzaris, M. Georgitsi, P. Drineas, and P. Paschou, Meta-analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder provides support for a shared genetic basis, Frontiers in Neuroscience, accepted, 2016.
  9. Olivier M, Weninger A, Ardin M, Huskova H, Castells X, Vallée MP, McKay J, Nedelko T, Muehlbauer K-R, Marusawa H, Alexander J, Hazelwood L, Byrnes G, Hollstein M, Zavadil J. Modelling mutational landscapes of human cancers in vitro. Sci Rep. 2014 Jan;4:4482. doi:10.1038/srep04482 PMID: 24670820