11 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544. PMID 30566877 DOI: 10.1016/j.celrep.2018.12.024  0.64
2018 Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, et al. 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. PMID 30257206 DOI: 10.1016/j.celrep.2018.08.082  0.64
2016 Padmanabhuni SS, Houssari R, Esserlind AL, Olesen J, Werge TM, Hansen TF, Bertelsen B, Tsetsos F, Paschou P, Tümer Z. Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in Neuroscience. 10: 531. PMID 27920664 DOI: 10.3389/fnins.2016.00531  0.64
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  0.64
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  0.64
2015 Zilhão NR, Padmanabhuni SS, Pagliaroli L, Barta C, Smit DJ, Cath D, Nivard MG, Baselmans BM, van Dongen J, Paschou P, Boomsma DI. Epigenome-Wide Association Study of Tic Disorders. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-11. PMID 26499864 DOI: 10.1017/thg.2015.72  0.64
2015 Nazaryan L, Bertelsen B, Padmanabhuni SS, Debes NM, LuCamp, Have CT, Tümer Z. Association study between CDH2 and Gilles de la Tourette syndrome in a Danish cohort. Psychiatry Research. 228: 974-5. PMID 26032459 DOI: 10.1016/j.psychres.2015.05.010  0.64
2014 Saleem M, Padmanabhuni SS, Ngomo AC, Iqbal A, Almeida JS, Decker S, Deus HF. TopFed: TCGA tailored federated query processing and linking to LOD. Journal of Biomedical Semantics. 5: 47. PMID 25937882 DOI: 10.1186/2041-1480-5-47  0.64
2014 Paschou P, Drineas P, Yannaki E, Razou A, Kanaki K, Tsetsos F, Padmanabhuni SS, Michalodimitrakis M, Renda MC, Pavlovic S, Anagnostopoulos A, Stamatoyannopoulos JA, Kidd KK, Stamatoyannopoulos G. Maritime route of colonization of Europe. Proceedings of the National Academy of Sciences of the United States of America. 111: 9211-6. PMID 24927591 DOI: 10.1073/pnas.1320811111  0.64
2013 Guo J, Hammar M, Oberg L, Padmanabhuni SS, Bjäreland M, Dalevi D. Combining evidence of preferential gene-tissue relationships from multiple sources. Plos One. 8: e70568. PMID 23950964 DOI: 10.1371/journal.pone.0070568  0.64
2013 Saleem M, Padmanabhuni SS, Ngomo ACN, Almeida JS, Decker S, Deus HF. Linked cancer genome atlas database Acm International Conference Proceeding Series. 129-134. DOI: 10.1145/2506182.2506200  0.64
Show low-probability matches.