Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 67 Records) |
Query Trace: FOXP2[original query] |
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Segregating polymorphisms of FOXP2 are associated with measures of inner speech, speech fluency and strength of handedness in a healthy population. Brain and language 2017 Jun 173 33-40. Crespi Bernard, Read Silven, Hurd Pet |
Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population. Journal of neural transmission (Vienna, Austria : 1996) 2017 Apr . Rao Wenwang, Du Xiangdong, Zhang Yingyang, Yu Qiong, Hui Li, Yu Yaqin, Kou Changgui, Yin Guangzhong, Zhu Xiaomin, Man Lijuan, Soares Jair C, Zhang Xiang Ya |
The central nervous system patterning gene variants associated with clinical symptom severity of autism spectrum disorders. Journal of the Formosan Medical Association = Taiwan yi zhi 2017 1 116 (10): 755-764. Chien Yi-Ling, Wu Yu-Yu, Chen Hsin-I, Tsai Wen-Che, Chiu Yen-Nan, Liu Shih-Kai, Gau Susan Shur-F |
Meta-analysis of FOXP2 rs10447760 polymorphism with schizophrenia. Asian journal of psychiatry 2018 5 35 50-51. Chen Yan, Fang Xinyu, Wang Yewei, Zhang Ch |
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
No association between common genetic variation in FOXP2 and language impairment in schizophrenia. Psychiatry research 2019 01 271 590-597. McCarthy Nina S, Clark Melanie L, Jablensky Assen, Badcock Johanna |
The Association Between Genetic Variation in FOXP2 and Sensorimotor Control of Speech Production. Frontiers in neuroscience 2018 10 12 666. Zhang Siyun, Zhao Jiangli, Guo Zhiqiang, Jones Jeffery A, Liu Peng, Liu Hanj |
No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population. Psychiatric genetics 2018 Jan . Yin Jiajun, Jia Ningren, Liu Yansong, Jin Chunhui, Zhang Fuquan, Yu Shui, Wang Jun, Yuan Jianm |
FOXP2 contributes to the cognitive impairment in chronic patients with schizophrenia. Aging 2019 8 11 (16): 6440-6448. Lang Xiaoe, Zhang Wenzhong, Song Xinxin, Zhang Guangya, Du Xiangdong, Zhou Yongjie, Li Zezhi, Zhang Xiang Ya |
Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.
Translational psychiatry 2019 02 9 (1): 14. Arnau-Soler Aleix, Macdonald-Dunlop Erin, Adams Mark J, Clarke Toni-Kim, MacIntyre Donald J, Milburn Keith, Navrady Lauren, , , Hayward Caroline, McIntosh Andrew M, Thomson Pippa |
Deciphering the Biological Mechanisms Underlying the Genome-Wide Associations between Computerized Device Use and Psychiatric Disorders. Journal of clinical medicine 2019 11 8 (12): . Wendt Frank R, Muniz Carvalho Carolina, Pathak Gita A, Gelernter Joel, Polimanti Rena |
Toward Robust Functional Neuroimaging Genetics of Cognition. The Journal of neuroscience : the official journal of the Society for Neuroscience 2019 Sep . Uddén Julia, Hultén Annika, Bendtz Katarina, Mineroff Zachary, Kucera Katerina S, Vino Arianna, Fedorenko Evelina, Hagoort Peter, Fisher Simon |
FOXP2 expression and gray matter density in the male brains of patients with schizophrenia. Brain imaging and behavior 2020 Jul . Sanjuán Julio, Castro-Martínez Xochitl Helga, García-Martí Gracián, González-Fernández Javier, Sanz-Requena Roberto, Haro Josep María, Meana J Javier, Martí-Bonmatí Luis, Nacher Juan, Sebastiá-Ortega Noelia, Gilabert-Juan Javier, Moltó María Dolor |
Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancer.
Science advances 2020 May 6 (21): eaay5525. Du Mulong, Zheng Rui, Ma Gaoxiang, Chu Haiyan, Lu Jiafei, Li Shuwei, Xin Junyi, Tong Na, Zhang Gang, Wang Weizhi, Qiang Fulin, Gong Weida, Zhao Qinghong, Tao Guoquan, Chen Jinfei, Jia Zhifang, Jiang Jing, Jin Guangfu, Hu Zhibin, Shen Hongbing, Wang Meilin, Zhang Zhengdo |
A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank.
Human molecular genetics 2020 May 29 (8): 1396-1404. Meng Weihua, Chan Brian W, Harris Cameron, Freidin Maxim B, Hebert Harry L, Adams Mark J, Campbell Archie, Hayward Caroline, Zheng Hua, Zhang Xianwei, Colvin Lesley A, Hales Tim G, Palmer Colin N A, Williams Frances M K, McIntosh Andrew, Smith Blair |
Genomic influences on self-reported childhood maltreatment.
Translational psychiatry 2020 Jan 10 (1): 38. Dalvie Shareefa, Maihofer Adam X, Coleman Jonathan R I, Bradley Bekh, Breen Gerome, Brick Leslie A, Chen Chia-Yen, Choi Karmel W, Duncan Laramie E, Guffanti Guia, Haas Magali, Harnal Supriya, Liberzon Israel, Nugent Nicole R, Provost Allison C, Ressler Kerry J, Torres Katy, Amstadter Ananda B, Bryn Austin S, Baker Dewleen G, Bolger Elizabeth A, Bryant Richard A, Calabrese Joseph R, Delahanty Douglas L, Farrer Lindsay A, Feeny Norah C, Flory Janine D, Forbes David, Galea Sandro, Gautam Aarti, Gelernter Joel, Hammamieh Rasha, Jett Marti, Junglen Angela G, Kaufman Milissa L, Kessler Ronald C, Khan Alaptagin, Kranzler Henry R, Lebois Lauren A M, Marmar Charles, Mavissakalian Matig R, McFarlane Alexander, Donnell Meaghan O', Orcutt Holly K, Pietrzak Robert H, Risbrough Victoria B, Roberts Andrea L, Rothbaum Alex O, Roy-Byrne Peter, Ruggiero Ken, Seligowski Antonia V, Sheerin Christina M, Silove Derrick, Smoller Jordan W, Stein Murray B, Teicher Martin H, Ursano Robert J, Van Hooff Miranda, Winternitz Sherry, Wolff Jonathan D, Yehuda Rachel, Zhao Hongyu, Zoellner Lori A, Stein Dan J, Koenen Karestan C, Nievergelt Caroline |
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
The neural basis of nonword repetition in children with developmental speech or language disorder: An fMRI study. Neuropsychologia 2020 1 138 107312. Pigdon Lauren, Willmott Catherine, Reilly Sheena, Conti-Ramsden Gina, Liegeois Frederique, Connelly Alan, Morgan Angela |
Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression. Brain : a journal of neurology 2021 9 145 (2): 770-786. Li Shiwu, Li Jiao, Liu Jiewei, Wang Junyang, Li Xiaoyan, Huo Yongxia, Li Yifan, Liu Yixing, Li Ming, Xiao Xiao, Luo Xiong-Ji |
Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes. Noro psikiyatri arsivi 2021 9 58 (3): 171-175. Yalçintepe Sinem, Görker I??k, Demir Selma, Atli Emine ?kbal, Atli Engin, Tozkir Hilmi, Süt Necdet, Özen Yasemin, Eker Damla, Mail Çisem, Güler Hazal Sezginer, Zhuri Drenushe, Gurkan Hak |
Predicted regulatory SNPs reveal potential drug targets and novel companion diagnostics in psoriasis. Journal of translational autoimmunity 2021 4 100096. Ruiz Ramírez Andrea Virginia, Flores-Saiffe Farías Adolfo, Chávez Álvarez Rocío Del Carmen, Prado Montes de Oca Ernes |
The genetic determinants of language network dysconnectivity in drug-naïve early stage schizophrenia. NPJ schizophrenia 2021 Mar 7 (1): 18. Du Jingnan, Palaniyappan Lena, Liu Zhaowen, Cheng Wei, Gong Weikang, Zhu Mengmeng, Wang Jijun, Zhang Jie, Feng Jianfe |
Sexual dimorphism in the relationship between Forkhead-Box P2 and BMI with cognitive deficits in schizophrenia. Frontiers in aging neuroscience 2022 8 14 920352. Yang Mi, Cui Ying, Xue Mei, Forster Mattew T, Lang Xiaoe, Xiu Meihong, Li Zezhi, Zhang Xiangya |
Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia? Annals of the New York Academy of Sciences 2022 8 1517 (1): 279-285. Peretz Isabelle, Ross Jay, Bourassa Cynthia V, Perreault Louis-Philippe Lemieux, Dion Patrick A, Weiss Michael W, Felezeu Mihaela, Rouleau Guy A, Dubé Marie-Pier |
Dissecting the cross-trait effects of the FOXP2 GWAS hit on clinical and brain phenotypes in adults with ADHD. European archives of psychiatry and clinical neuroscience 2022 3 . Meyer Gabriela Pessin, da Silva Bruna Santos, Bandeira Cibele Edom, Tavares Maria Eduarda Araujo, Cupertino Renata Basso, Oliveira Eduarda Pereira, Müller Diana, Kappel Djenifer B, Teche Stefania Pigatto, Vitola Eduardo Schneider, Rohde Luis Augusto, Rovaris Diego Luiz, Grevet Eugenio Horacio, Bau Claiton Henrique Dot |
Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Molecular psychiatry 2022 10 27 (11): 4453-4463. Tielbeek Jorim J, Uffelmann Emil, Williams Benjamin S, Colodro-Conde Lucía, Gagnon Éloi, Mallard Travis T, Levitt Brandt E, Jansen Philip R, Johansson Ada, Sallis Hannah M, Pistis Giorgio, Saunders Gretchen R B, Allegrini Andrea G, Rimfeld Kaili, Konte Bettina, Klein Marieke, Hartmann Annette M, Salvatore Jessica E, Nolte Ilja M, Demontis Ditte, Malmberg Anni L K, Burt S Alexandra, Savage Jeanne E, Sugden Karen, Poulton Richie, Harris Kathleen Mullan, Vrieze Scott, McGue Matt, Iacono William G, Mota Nina Roth, Mill Jonathan, Viana Joana F, Mitchell Brittany L, Morosoli Jose J, Andlauer Till F M, Ouellet-Morin Isabelle, Tremblay Richard E, Côté Sylvana M, Gouin Jean-Philippe, Brendgen Mara R, Dionne Ginette, Vitaro Frank, Lupton Michelle K, Martin Nicholas G, , , Castelao Enrique, Räikkönen Katri, Eriksson Johan G, Lahti Jari, Hartman Catharina A, Oldehinkel Albertine J, Snieder Harold, Liu Hexuan, Preisig Martin, Whipp Alyce, Vuoksimaa Eero, Lu Yi, Jern Patrick, Rujescu Dan, Giegling Ina, Palviainen Teemu, Kaprio Jaakko, Harden Kathryn Paige, Munafò Marcus R, Morneau-Vaillancourt Geneviève, Plomin Robert, Viding Essi, Boutwell Brian B, Aliev Fazil, Dick Danielle M, Popma Arne, Faraone Stephen V, Børglum Anders D, Medland Sarah E, Franke Barbara, Boivin Michel, Pingault Jean-Baptiste, Glennon Jeffrey C, Barnes J C, Fisher Simon E, Moffitt Terrie E, Caspi Avshalom, Polderman Tinca J C, Posthuma Daniel |
The FoxP1 gene regulates lung function, production of matrix metalloproteinases and inflammatory mediators, and viability of lung epithelia. Respiratory research 2022 Oct 23 (1): 281. Andreas Alexis, Maloy Abby, Nyunoya Toru, Zhang Yingze, Chandra Div |
Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data.
Translational psychiatry 2022 1 12 (1): 17. Meng Peilin, Ye Jing, Chu Xiaomeng, Cheng Bolun, Cheng Shiqiang, Liu Li, Yang Xuena, Liang Chujun, Zhang Fe |
Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder. Psychiatric genetics 2023 1 33 (1): 8-19. Yaz?c? Merve, Yekta? Çi?dem, Eröz Recep, Kaplan Karakaya Elif Sümeyra, Sar?gedik En |
Linked OXTR Variants Are Associated with Social Behavior Differences in Bonobos (Pan paniscus). bioRxiv : the preprint server for biology 2024 1 . Sara A Skiba, Alek Hansen, Ryan McCall, Azeeza Byers, Sarah Waldron, Amanda J Epping, Jared P Taglialatela, Martin L Huds |
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- Page last updated:Apr 16, 2024
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