Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Syndrome and NRXN1[original query] |
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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. The American journal of psychiatry 2011 Mar 168 (3): 302-16. Levinson Douglas F, Duan Jubao, Oh Sang, Wang Kai, Sanders Alan R, Shi Jianxin, Zhang Nancy, Mowry Bryan J, Olincy Ann, Amin Farooq, Cloninger C Robert, Silverman Jeremy M, Buccola Nancy G, Byerley William F, Black Donald W, Kendler Kenneth S, Freedman Robert, Dudbridge Frank, Pe'er Itsik, Hakonarson Hakon, Bergen Sarah E, Fanous Ayman H, Holmans Peter A, Gejman Pablo |
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. European journal of human genetics : EJHG 2013 Mar 21 (3): 310-6. Boccuto Luigi, Lauri Maria, Sarasua Sara M, Skinner Cindy D, Buccella Daniela, Dwivedi Alka, Orteschi Daniela, Collins Julianne S, Zollino Marcella, Visconti Paola, Dupont Barb, Tiziano Danilo, Schroer Richard J, Neri Giovanni, Stevenson Roger E, Gurrieri Fiorella, Schwartz Charles |
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 |
Analysis of copy number variations at 15 schizophrenia-associated loci. The British journal of psychiatry : the journal of mental science 2013 Dec . Rees E, Walters JT, Georgieva L, Isles AR, Chambert KD, Richards AL, Mahoney-Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G |
Etiological yield of SNP microarrays in idiopathic intellectual disability. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2014 May 18 (3): 327-37. Utine G Eda, Halilo?lu Göknur, Volkan-Salanc? Bilge, Çetinkaya Arda, Kiper Pelin Ö, Alanay Yasemin, Akta? Dilek, Anlar Banu, Topçu Meral, Boduro?lu Koray, Alika?ifo?lu Mehm |
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 |
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, , |
Genetic predictors of antipsychotic response to lurasidone identified in a genome wide association study and by schizophrenia risk genes. Schizophrenia research 2018 02 192 194-204. Li Jiang, Yoshikawa Akane, Brennan Mark D, Ramsey Timothy L, Meltzer Herbert |
Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia. Schizophrenia bulletin 2019 5 46 (2): 328-335. Balakrishna Thivia, Curtis Dav |
Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis. Wellcome open research 2021 6 3 85. Newbury Dianne F, Simpson Nuala H, Thompson Paul A, Bishop Dorothy V |
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- Page last updated:Apr 16, 2024
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