Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: Schizophrenia and NRXN1[original query] |
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Influence of neurexin 1 (NRXN1) polymorphisms in clozapine response. Human psychopharmacology 2010 Nov 25 (7-8): 582-5. Souza Renan P, Meltzer Herbert Y, Lieberman Jeffrey A, Le Foll Bernard, Kennedy James |
New copy number variations in schizophrenia. PloS one 2010 5 (10): e13422. Magri Chiara, Sacchetti Emilio, Traversa Michele, Valsecchi Paolo, Gardella Rita, Bonvicini Cristian, Minelli Alessandra, Gennarelli Massimo, Barlati Serg |
The putative functional rs1045881 marker of neurexin-1 in schizophrenia and clozapine response. Schizophrenia research 2011 Nov 132 (2-3): 121-4. Lett Tristram A P, Tiwari Arun K, Meltzer Herbert Y, Lieberman Jeffrey A, Potkin Steven G, Voineskos Aristotle N, Kennedy James L, Müller Daniel |
Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders. PloS one 2011 6 (6): e20982. Voineskos Aristotle N, Lett Tristram A P, Lerch Jason P, Tiwari Arun K, Ameis Stephanie H, Rajji Tarek K, Müller Daniel J, Mulsant Benoit H, Kennedy James |
A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population. Behavioral and brain functions : BBF 2011 7 (1): 7. Yue Weihua, Yang Yongfeng, Zhang Yanling, Lu Tianlan, Hu Xiaofeng, Wang Lifang, Ruan Yanyan, Lv Luxian, Zhang D |
Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients. Schizophrenia research 2011 Apr 127 (1-3): 35-40. Mühleisen Thomas W, Basmanav F Buket, Forstner Andreas J, Mattheisen Manuel, Priebe Lutz, Herms Stefan, Breuer Rene, Moebus Susanne, Nenadic Igor, Sauer Heinrich, Mössner Rainald, Maier Wolfgang, Rujescu Dan, Ludwig Michael, Rietschel Marcella, Nöthen Markus M, Cichon Sv |
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 |
High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy. BMC medical genetics 2011 Nov 12 (1): 1. Stewart LR, Hall AL, Kang SH, Shaw CA, Beaudet AL |
Genome-wide association study of multiplex schizophrenia pedigrees.
The American journal of psychiatry 2012 Sep 169 (9): 963-73. Levinson Douglas F, Shi Jianxin, Wang Kai, Oh Sang, Riley Brien, Pulver Ann E, Wildenauer Dieter B, Laurent Claudine, Mowry Bryan J, Gejman Pablo V, Owen Michael J, Kendler Kenneth S, Nestadt Gerald, Schwab Sibylle G, Mallet Jacques, Nertney Deborah, Sanders Alan R, Williams Nigel M, Wormley Brandon, Lasseter Virginia K, Albus Margot, Godard-Bauché Stephanie, Alexander Madeline, Duan Jubao, O'Donovan Michael C, Walsh Dermot, O'Neill Anthony, Papadimitriou George N, Dikeos Dimitris, Maier Wolfgang, Lerer Bernard, Campion Dominique, Cohen David, Jay Maurice, Fanous Ayman, Eichhammer Peter, Silverman Jeremy M, Norton Nadine, Zhang Nancy, Hakonarson Hakon, Gao Cynthia, Citri Ami, Hansen Mark, Ripke Stephan, , Dudbridge Frank, Holmans Peter |
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 |
Investigation of NRXN1 deletions: clinical and molecular characterization. American journal of medical genetics. Part A 2013 Apr 161 (4): 4. Dabell MP, Rosenfeld JA, Bader P, Escobar LF, El-Khechen D, Vallee SE, Dinulos MB, Curry C, Fisher J, Tervo R, Hannibal MC, Siefkas K, Wyatt PR, Hughes L, Smith R, Ellingwood S, Lacassie Y, Stroud T, Farrell SA, Sanchez-Lara PA, Randolph LM, Niyazov D, Stevens CA, Schoonveld C, Skidmore D, Mackay S, Miles JH, Moodley M, Huillet A, Neill NJ, Ellison JW, Ballif BC, Shaffer LG |
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 |
Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain. Schizophrenia research 2014 Oct 159 (1): 107-13. Ivorra José Luis, Rivero Olga, Costas Javier, Iniesta Raquel, Arrojo Manuel, Ramos-Ríos Ramón, Carracedo Angel, Palomo Tomas, Rodriguez-Jimenez Roberto, Cervilla Jorge, Gutiérrez Blanca, Molina Esther, Arango Celso, Alvarez Mar, Pascual Juan C, Pérez Víctor, Saiz Pilar Alejandra, García-Portilla María Paz, Bobes Julio, González-Pinto Ana, Zorrilla Iñaki, Haro Josep María, Bernardo Miguel, Baca-García Enrique, González José Carlos, Hoenicka Janet, Moltó María Dolores, Sanjuán Jul |
Identification of candidate single-nucleotide polymorphisms in NRXN1 related to antipsychotic treatment response in patients with schizophrenia. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2014 Aug 39 (9): 2170-8. Jenkins Aaron, Apud José A, Zhang Fengyu, Decot Heather, Weinberger Daniel R, Law Amanda |
Copy number variants and therapeutic response to antidepressant medication in major depressive disorder. The pharmacogenomics journal 2014 Aug 14 (4): 395-9. Tansey K E, Rucker J J H, Kavanagh D H, Guipponi M, Perroud N, Bondolfi G, Domenici E, Evans D M, Hauser J, Henigsberg N, Jerman B, Maier W, Mors O, O'Donovan M, Peters T J, Placentino A, Rietschel M, Souery D, Aitchison K J, Craig I, Farmer A, Wendland J R, Malafosse A, Lewis G, Kapur S, McGuffin P, Uher |
[The Role of Neurotrophins and Neurexins Genes in the Risk of Paranoid Schizophrenia in Russians and Tatars]. Genetika 2015 Jul 51 (7): 799-811. Gareeva A E, Traks T, Koks S, Khusnutdinova E |
Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility. Journal of psychiatric research 0 66-67 38-44. Suárez-Rama José Javier, Arrojo Manuel, Sobrino Beatriz, Amigo Jorge, Brenlla Julio, Agra Santiago, Paz Eduardo, Brión María, Carracedo Ángel, Páramo Mario, Costas Javi |
Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family. European journal of medical genetics 2015 Nov . Duong Linh Tt, Hoeffding Louise K, Petersen Kirsten B, Knudsen Charlotte D, Thygesen Johan H, Klitten Laura L, Tommerup Niels, Ingason Andrés, Werge Thom |
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature genetics 2016 Nov . , |
Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese. Biological psychiatry 2015 Nov . Li Zhiqiang, Chen Jianhua, Xu Yifeng, Yi Qizhong, Ji Weidong, Wang Peng, Shen Jiawei, Song Zhijian, Wang Meng, Yang Ping, Wang Qingzhong, Feng Guoyin, Liu Benxiu, Sun Wensheng, Xu Qi, Li Baojie, He Lin, He Guang, Li Wenjin, Wen Zujia, Liu Ke, Huang Fang, Zhou Juan, Ji Jue, Li Xingwang, Shi Yongyo |
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 |
High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder. BMC medical genomics 2017 Nov 10 (1): 68. Grünblatt Edna, Oneda Beatrice, Ekici Arif B, Ball Juliane, Geissler Julia, Uebe Steffen, Romanos Marcel, Rauch Anita, Walitza Susan |
Association study between the neurexin-1 gene and tardive dyskinesia. Human psychopharmacology 2017 Jan 32 (1): . Lanning Rachel, Lett Tristram A, Tiwari Arun K, Brandl Eva J, de Luca Vincenzo, Voineskos Aristotle N, Potkin Steven G, Lieberman Jeffrey A, Meltzer Herbert Y, Müller Daniel J, Remington Gary, Kennedy James L, Zai Clement |
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.
Translational psychiatry 2019 09 9 (1): 230. Alliey-Rodriguez Ney, Grey Tamar A, Shafee Rebecca, Asif Huma, Lutz Olivia, Bolo Nicolas R, Padmanabhan Jaya, Tandon Neeraj, Klinger Madeline, Reis Katherine, Spring Jonathan, Coppes Lucas, Zeng Victor, Hegde Rachal R, Hoang Dung T, Bannai Deepthi, Nawaz Uzma, Henson Philip, Liu Siyuan, Gage Diane, McCarroll Steven, Bishop Jeffrey R, Hill Scot, Reilly James L, Lencer Rebekka, Clementz Brett A, Buckley Peter, Glahn David C, Meda Shashwath A, Narayanan Balaji, Pearlson Godfrey, Keshavan Matcheri S, Ivleva Elena I, Tamminga Carol, Sweeney John A, Curtis David, Badner Judith A, Keedy Sarah, Rapoport Judith, Liu Chunyu, Gershon Elliot |
Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia. Schizophrenia bulletin 2019 5 46 (2): 328-335. Balakrishna Thivia, Curtis Dav |
Neurexin 3 transmembrane and soluble isoform expression and splicing haplotype are associated with neuron inflammasome and Alzheimer's disease. Alzheimer's research & therapy 2019 Mar 11 (1): 28. Hishimoto Akitoyo, Pletnikova Olga, Lang Doyle Lu, Troncoso Juan C, Egan Josephine M, Liu Qing-Ro |
A large data resource of genomic copy number variation across neurodevelopmental disorders. NPJ genomic medicine 2019 4 26. Zarrei Mehdi, Burton Christie L, Engchuan Worrawat, Young Edwin J, Higginbotham Edward J, MacDonald Jeffrey R, Trost Brett, Chan Ada J S, Walker Susan, Lamoureux Sylvia, Heung Tracy, Mojarad Bahareh A, Kellam Barbara, Paton Tara, Faheem Muhammad, Miron Karin, Lu Chao, Wang Ting, Samler Kozue, Wang Xiaolin, Costain Gregory, Hoang Ny, Pellecchia Giovanna, Wei John, Patel Rohan V, Thiruvahindrapuram Bhooma, Roifman Maian, Merico Daniele, Goodale Tara, Drmic Irene, Speevak Marsha, Howe Jennifer L, Yuen Ryan K C, Buchanan Janet A, Vorstman Jacob A S, Marshall Christian R, Wintle Richard F, Rosenberg David R, Hanna Gregory L, Woodbury-Smith Marc, Cytrynbaum Cheryl, Zwaigenbaum Lonnie, Elsabbagh Mayada, Flanagan Janine, Fernandez Bridget A, Carter Melissa T, Szatmari Peter, Roberts Wendy, Lerch Jason, Liu Xudong, Nicolson Rob, Georgiades Stelios, Weksberg Rosanna, Arnold Paul D, Bassett Anne S, Crosbie Jennifer, Schachar Russell, Stavropoulos Dimitri J, Anagnostou Evdokia, Scherer Stephen |
Genotype Variations of rs13381800 in TCF4 Gene and rs17039988 in NRXN1 Gene among a Sample of Iranian Patients with Schizophrenia. Iranian journal of psychiatry 2020 2 14 (4): 265-273. Agahi Mohadeseh, Noormohammadi Zahra, Salahshourifar Iman, Mahdavi Hezaveh Nilouf |
The clinical relevance of intragenic NRXN1 deletions. Journal of medical genetics 2020 1 57 (5): 347-355. Cosemans Nele, Vandenhove Laura, Vogels Annick, Devriendt Koenraad, Van Esch Hilde, Van Buggenhout Griet, Olivié Hilde, de Ravel Thomy, Ortibus Els, Legius Eric, Aerssens Peter, Breckpot Jeroen, R Vermeesch Joris, Shen Sanbing, Fitzgerald Jacqueline, Gallagher Louise, Peeters Hil |
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell genomics 2023 8 3 (8): 100356. Eduardo A Maury, Maxwell A Sherman, Giulio Genovese, Thomas G Gilgenast, Tushar Kamath, S J Burris, Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, Andrew Chess, Steven A McCarroll, Po-Ru Loh, Jennifer E Phillips-Cremins, Kristen J Brennand, Evan Z Macosko, James T R Walters, Michael O'Donovan, Patrick Sullivan, , , Jonathan Sebat, Eunjung A Lee, Christopher A Wal |
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- Page last updated:Apr 16, 2024
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