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Wang S, Mandell JD, Kumar Y, et al. (2018) De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544
Wang S, Mandell JD, Kumar Y, et al. (2018) De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12
Pagliaroli L, Vereczkei A, Padmanabhuni SS, et al. (2017) Microrna Regulation Of Candidate Genes For Tourette Syndrome European Neuropsychopharmacology. 27: S453-S454
Padmanabhuni SS, Houssari R, Esserlind AL, et al. (2016) Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in Neuroscience. 10: 531
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
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
Zilhão NR, Padmanabhuni SS, Pagliaroli L, et al. (2015) Epigenome-Wide Association Study of Tic Disorders. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-11
Paschou P, Drineas P, Yannaki E, et al. (2014) Maritime route of colonization of Europe. Proceedings of the National Academy of Sciences of the United States of America. 111: 9211-6
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