HuGE Literature Finder
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron 2017 Jun 94 (6): 1101-1111.e7. Huang Alden Y, Yu Dongmei, Davis Lea K, Sul Jae Hoon, Tsetsos Fotis, Ramensky Vasily, Zelaya Ivette, Ramos Eliana Marisa, Osiecki Lisa, Chen Jason A, McGrath Lauren M, Illmann Cornelia, Sandor Paul, Barr Cathy L, Grados Marco, Singer Harvey S, Nöthen Markus M, Hebebrand Johannes, King Robert A, Dion Yves, Rouleau Guy, Budman Cathy L, Depienne Christel, Worbe Yulia, Hartmann Andreas, Müller-Vahl Kirsten R, Stuhrmann Manfred, Aschauer Harald, Stamenkovic Mara, Schloegelhofer Monika, Konstantinidis Anastasios, Lyon Gholson J, McMahon William M, Barta Csaba, Tarnok Zsanett, Nagy Peter, Batterson James R, Rizzo Renata, Cath Danielle C, Wolanczyk Tomasz, Berlin Cheston, Malaty Irene A, Okun Michael S, Woods Douglas W, Rees Elliott, Pato Carlos N, Pato Michele T, Knowles James A, Posthuma Danielle, Pauls David L, Cox Nancy J, Neale Benjamin M, Freimer Nelson B, Paschou Peristera, Mathews Carol A, Scharf Jeremiah M, Coppola Giovanni, , |
Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in neuroscience 2016 10 531. Padmanabhuni Shanmukha S, Houssari Rayan, Esserlind Ann-Louise, Olesen Jes, Werge Thomas M, Hansen Thomas F, Bertelsen Birgitte, Tsetsos Fotis, Paschou Peristera, Tümer Zeyn |
CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. PloS one 2013 8 (3): e59061. Nag Abhishek, Bochukova Elena G, Kremeyer Barbara, Campbell Desmond D, Muller Heike, Valencia-Duarte Ana V, Cardona Julio, Rivas Isabel C, Mesa Sandra C, Cuartas Mauricio, Garcia Jharley, Bedoya Gabriel, Cornejo William, Herrera Luis D, Romero Roxana, Fournier Eduardo, Reus Victor I, Lowe Thomas L, Farooqi I Sadaf, , Mathews Carol A, McGrath Lauren M, Yu Dongmei, Cook Ed, Wang Kai, Scharf Jeremiah M, Pauls David L, Freimer Nelson B, Plagnol Vincent, Ruiz-Linares Andr |
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