Human Genome Epidemiology Literature Finder
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Records 1 - 28 (of 28 Records) |
| Query Trace: Disease and NRXN1[original query] |
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| Recurrent CNVs disrupt three candidate genes in schizophrenia patients. American journal of human genetics 2008 Oct 83 (4): 504-10. Vrijenhoek Terry, Buizer-Voskamp Jacobine E, van der Stelt Inge, Strengman Eric, , Sabatti Chiara, Geurts van Kessel Ad, Brunner Han G, Ophoff Roel A, Veltman Joris |
| Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS genetics 2009 Jun 5 (6): e1000536. Bucan Maja, Abrahams Brett S, Wang Kai, Glessner Joseph T, Herman Edward I, Sonnenblick Lisa I, Alvarez Retuerto Ana I, Imielinski Marcin, Hadley Dexter, Bradfield Jonathan P, Kim Cecilia, Gidaya Nicole B, Lindquist Ingrid, Hutman Ted, Sigman Marian, Kustanovich Vlad, Lajonchere Clara M, Singleton Andrew, Kim Junhyong, Wassink Thomas H, McMahon William M, Owley Thomas, Sweeney John A, Coon Hilary, Nurnberger John I, Li Mingyao, Cantor Rita M, Minshew Nancy J, Sutcliffe James S, Cook Edwin H, Dawson Geraldine, Buxbaum Joseph D, Grant Struan F A, Schellenberg Gerard D, Geschwind Daniel H, Hakonarson Hak |
| A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS genetics 2009 Feb 5 (2): e1000373. Need Anna C, Ge Dongliang, Weale Michael E, Maia Jessica, Feng Sheng, Heinzen Erin L, Shianna Kevin V, Yoon Woohyun, Kasperavici?te Dalia, Gennarelli Massimo, Strittmatter Warren J, Bonvicini Cristian, Rossi Giuseppe, Jayathilake Karu, Cola Philip A, McEvoy Joseph P, Keefe Richard S E, Fisher Elizabeth M C, St Jean Pamela L, Giegling Ina, Hartmann Annette M, Möller Hans-Jürgen, Ruppert Andreas, Fraser Gillian, Crombie Caroline, Middleton Lefkos T, St Clair David, Roses Allen D, Muglia Pierandrea, Francks Clyde, Rujescu Dan, Meltzer Herbert Y, Goldstein David |
| 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 |
| Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. International journal of Alzheimer's disease 2011 2011 729478. Swaminathan Shanker, Kim Sungeun, Shen Li, Risacher Shannon L, Foroud Tatiana, Pankratz Nathan, Potkin Steven G, Huentelman Matthew J, Craig David W, Weiner Michael W, Saykin Andrew J, The Alzheimer's Disease Neuroimaging Initiative Adn |
| 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 |
| 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 |
| Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. Current Alzheimer research 2012 Sep 9 (7): 801-14. Swaminathan Shanker, Shen Li, Kim Sungeun, Inlow Mark, West John D, Faber Kelley M, Foroud Tatiana, Mayeux Richard, Saykin Andrew J, , |
| Identification of candidate intergenic risk loci in autism spectrum disorder. BMC genomics 2013 14 (1): 499. Walker Susan, Scherer Stephen |
| Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jun 162B (4): 388-403. Béna Frédérique, Bruno Damien L, Eriksson Mats, van Ravenswaaij-Arts Conny, Stark Zornitza, Dijkhuizen Trijnie, Gerkes Erica, Gimelli Stefania, Ganesamoorthy Devika, Thuresson Ann Charlotte, Labalme Audrey, Till Marianne, Bilan Frédéric, Pasquier Laurent, Kitzis Alain, Dubourgm Christele, Rossi Massimiliano, Bottani Armand, Gagnebin Maryline, Sanlaville Damien, Gilbert-Dussardier Brigitte, Guipponi Michel, van Haeringen Arie, Kriek Marjolein, Ruivenkamp Claudia, Antonarakis Stylianos E, Anderlid Britt Marie, Slater Howard R, Schoumans Jacqueli |
| Genetic study of neurexin and neuroligin genes in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2013 35 (2): 403-12. Martinez-Mir Amalia, González-Pérez Antonio, Gayán Javier, Antúnez Carmen, Marín Juan, Boada Mercé, Lopez-Arrieta Jesús María, Fernández Evaristo, Ramírez-Lorca Reposo, Sáez María Eugenia, Ruiz Agustín, Scholl Francisco G, Real Luis Migu |
| 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 |
| Enlisting hESCs to Interrogate Genetic Variants Associated with Neuropsychiatric Disorders. Cell stem cell 2015 Sep 17 (3): 253-4. Hyman Steven |
| [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 |
| Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology. NPJ genomic medicine 2024 12 9 (1): 67. Simone Montalbano, Morten Dybdahl Krebs, Anders Rosengren, Morteza Vaez, Kajsa-Lotta Georgii Hellberg, Preben B Mortensen, Anders D Børglum, Daniel H Geschwind, , Armin Raznahan, Wesley K Thompson, Dorte Helenius, Thomas Werge, Andrés Ingas |
| Genome-wide copy number variation association study in anorexia nervosa. Molecular psychiatry 2024 11 . Alicia Walker, Robert Karlsson, Jin P Szatkiewicz, Laura M Thornton, Zeynep Yilmaz, Virpi M Leppä, Androula Savva, Tian Lin, Julia Sidorenko, Allan McRae, George Kirov, Helena L Davies, Bengt T Fundín, Samuel J R A Chawner, Jie Song, Stina Borg, Jia Wen, Hunna J Watson, Melissa A Munn-Chernoff, Jessica H Baker, Scott Gordon, Wade H Berrettini, Harry Brandt, Steven Crawford, Katherine A Halmi, Allan S Kaplan, Walter H Kaye, James Mitchell, Michael Strober, D Blake Woodside, Nancy L Pedersen, Richard Parker, Jennifer Jordan, Martin A Kennedy, Andreas Birgegård, Mikael Landén, Nicholas G Martin, Patrick F Sullivan, Cynthia M Bulik, Naomi R Wr |
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