Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 95 Records) |
Query Trace: NRXN1[original query] |
---|
Somatic mutations in ZFHX4 gene are associated with poor overall survival of Chinese esophageal squamous cell carcinoma patients. Scientific reports 2017 Jul 7 (1): 4951. Qing Tao, Zhu Sibo, Suo Chen, Zhang Lei, Zheng Yuanting, Shi Lemi |
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 |
Neurexin gene family variants as risk factors for autism spectrum disorder. Autism research : official journal of the International Society for Autism Research 2018 01 11 (1): 37-43. Wang Jia, Gong Jianhua, Li Li, Chen Yanlin, Liu Lingfei, Gu HuaiTing, Luo Xiu, Hou Fang, Zhang Jiajia, Song Ranr |
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants. Genetics in medicine : official journal of the American College of Medical Genetics 2018 9 21 (4): 816-825. Pizzo Lucilla, Jensen Matthew, Polyak Andrew, Rosenfeld Jill A, Mannik Katrin, Krishnan Arjun, McCready Elizabeth, Pichon Olivier, Le Caignec Cedric, Van Dijck Anke, Pope Kate, Voorhoeve Els, Yoon Jieun, Stankiewicz Pawe?, Cheung Sau Wai, Pazuchanics Damian, Huber Emily, Kumar Vijay, Kember Rachel L, Mari Francesca, Curró Aurora, Castiglia Lucia, Galesi Ornella, Avola Emanuela, Mattina Teresa, Fichera Marco, Mandarà Luana, Vincent Marie, Nizon Mathilde, Mercier Sandra, Bénéteau Claire, Blesson Sophie, Martin-Coignard Dominique, Mosca-Boidron Anne-Laure, Caberg Jean-Hubert, Bucan Maja, Zeesman Susan, Nowaczyk Ma?gorzata J M, Lefebvre Mathilde, Faivre Laurence, Callier Patrick, Skinner Cindy, Keren Boris, Perrine Charles, Prontera Paolo, Marle Nathalie, Renieri Alessandra, Reymond Alexandre, Kooy R Frank, Isidor Bertrand, Schwartz Charles, Romano Corrado, Sistermans Erik, Amor David J, Andrieux Joris, Girirajan Santho |
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 Aug . Rizzo Ambra, Alfei Enrico, Zibordi Federica, Saletti Veronica, Zorzi Giovanna, Freri Elena, Estienne Margherita, Girgenti Vita, D'Arrigo Stefano, Esposito Silvia, Buldrini Barbara, Moroni Isabella, Milani Donatella, Granata Tiziana, Ardissone Anna, Eoli Marica, Molteni Bruna, Bigoni Stefania, Pantaleoni Chiara, Nardocci Nardo, Sciacca Francesca Lui |
Significance of neurexin and neuroligin polymorphisms in regulating risk of Hirschsprung's disease. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2018 Apr . Li Yanhong, Liu Hui, Dong Yub |
An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder. Molecular psychiatry 2018 Apr . Williams Sarah M, An Joon Yong, Edson Janette, Watts Michelle, Murigneux Valentine, Whitehouse Andrew J O, Jackson Colin J, Bellgrove Mark A, Cristino Alexandre S, Claudianos Charl |
Identification of Key Genes and Pathways Associated with RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis. Medical science monitor : international medical journal of experimental and clinical research 2018 Oct 24 7100-7108. Zhu Fangxiao, Huang Rui, Li Jing, Liao Xiwen, Huang Yumei, Lai Yongro |
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 |
Data on genotype frequency for SNPs associated to age of smoking onset and successful smoking cessation treatment. Data in brief 2019 Jun 24 103893. Pérez-Rubio Gloria, López-Flores Luis Alberto, Ramírez-Venegas Alejandra, Sansores Raúl H, Falfán-Valencia Ramc |
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 |
Genetic variants as risk factors for cigarette smoking at an early age and relapse to smoking cessation treatment: A pilot study. Gene 2019 Feb 694 93-96. Pérez-Rubio Gloria, López-Flores Luis Alberto, García-Carmona Salvador, García-Gómez Leonor, Noé-Díaz Valeri, Ambrocio-Ortiz Enrique, Nava-Quiroz Karol J, Morales-González Fernando, Del Angel-Pablo Alma D, Ramírez-Venegas Alejandra, Sansores Raúl H, Falfán-Valencia Ramc |
Neuronal impact of patient-specific aberrant NRXN1? splicing. Nature genetics 2019 12 51 (12): 1679-1690. Flaherty Erin, Zhu Shijia, Barretto Natalie, Cheng Esther, Deans P J Michael, Fernando Michael B, Schrode Nadine, Francoeur Nancy, Antoine Alesia, Alganem Khaled, Halpern Madeline, Deikus Gintaras, Shah Hardik, Fitzgerald Megan, Ladran Ian, Gochman Peter, Rapoport Judith, Tsankova Nadejda M, McCullumsmith Robert, Hoffman Gabriel E, Sebra Robert, Fang Gang, Brennand Kristen |
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 |
Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
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 |
The influence of NRXN1 on systemizing and the brain structure in healthy adults. Brain imaging and behavior 2021 Sep . Shiota Yuka, Matsudaira Izumi, Takeuchi Hikaru, Ono Chiaki, Tomita Hiroaki, Kawashima Ryuta, Taki Yasuyu |
Genetic Variants in Smoking-Related Genes in Two Smoking Cessation Programs: A Cross-Sectional Study. International journal of environmental research and public health 2021 Jun 18 (12): . Pérez-Rubio Gloria, López-Flores Luis Alberto, Cupertino Ana Paula, Cartujano-Barrera Francisco, Reynales-Shigematsu Luz Myriam, Ramírez Mariana, Ellerbeck Edward F, Rodríguez-Bolaños Rosibel, Falfan-Valencia Ramc |
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 |
Timing of chronic obstructive pulmonary disease diagnosis in lung cancer prognosis: a clinical and genomic-based study. Translational lung cancer research 2021 Mar 10 (3): 1209-1220. Dai Jie, He Yanqi, Maneenil Kunlatida, Liu Han, Liu Ming, Guo Qian, Bennett Amy C, Stoddard Shawn M, Wampfler Jason A, Jiang Gening, Yang Pi |
Investigation of the genetic effect of 56 tobacco-smoking susceptibility genes on DNA methylation and RNA expression in human brain. Frontiers in psychiatry 2022 9 13 924062. Yang Zhongli, Yang Jiekun, Mao Ying, Li Ming |
Synthesis of genetic association studies on autism spectrum disorders using a genetic model-free approach. Psychiatric genetics 2022 3 32 (3): 91-104. Mpoulimari Ioanna, Zintzaras Eli |
Identification of a Five-Gene Panel to Assess Prognosis for Gastric Cancer. BioMed research international 2022 2022 5593619. Li Shuxin, Mao Qianqian, Zhang Zixuan, Wang Yuqi, Chen Duoxuan, Chen Zhenwen, Lu Jian |
The role of the KIBRA and APOE genes in developing spatial abilities in humans. Vavilovskii zhurnal genetiki i selektsii 2021 Dec 25 (8): 839-846. Kazantseva A V, Enikeeva R F, Davydova Yu D, Mustafin R N, Takhirova Z R, Malykh S B, Lobaskova M M, Tikhomirova T N, Khusnutdinova E |
A single nucleotide polymorphism-based formula to predict the risk of propofol TCI concentration being over 4?µg?mL at the time of loss of consciousness. The pharmacogenomics journal 2022 1 22 (2): 109-116. Zheng Zhuoling, Xue Faling, Wang Haini, He Yongqi, Zhang Lingyi, Ma Wudi, Zhang Caibin, Guan Yanping, Ye Fang, Wen Yongzi, Li Xiaoyan, Huang Min, Huang Wenqi, Wang Zhongxing, Li Jia |
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 |
Allelic contribution of Nrxn1? to autism-relevant behavioral phenotypes in mice. PLoS genetics 2023 2 19 (2): e1010659. Xu Bing, Ho Yugong, Fasolino Maria, Medina Joanna, O'Brien William Timothy, Lamonica Janine M, Nugent Erin, Brodkin Edward S, Fuccillo Marc V, Bucan Maja, Zhou Zhaol |
TNS1 and NRXN1 Genes Interacting With Early-Life Smoking Exposure in Asthma-Plus-Eczema Susceptibility. Allergy, asthma & immunology research 2023 11 15 (6): 779-794. Patricia Margaritte-Jeannin, Raphaël Vernet, Ashley Budu-Aggrey, Markus Ege, Anne-Marie Madore, Christophe Linhard, Hamida Mohamdi, Erika von Mutius, Raquell Granell, Florence Demenais, Cathrine Laprise, Emmanuelle Bouzigon, Marie-Hélène Dizi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: