Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 95 Records) |
Query Trace: CNTNAP2[original query] |
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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 |
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? Journal of experimental neuroscience 2018 11 12 1179069518809666. Canali Giorgia, Goutebroze Lauren |
A Schizophrenia-Related Genetic-Brain-Cognition Pathway Revealed in a Large Chinese Population. EBioMedicine 2018 Nov 37 471-482. Luo Na, Sui Jing, Chen Jiayu, Zhang Fuquan, Tian Lin, Lin Dongdong, Song Ming, Calhoun Vince D, Cui Yue, Vergara Victor M, Zheng Fanfan, Liu Jingyu, Yang Zhenyi, Zuo Nianming, Fan Lingzhong, Xu Kaibin, Liu Shengfeng, Li Jian, Xu Yong, Liu Sha, Lv Luxian, Chen Jun, Chen Yunchun, Guo Hua, Li Peng, Lu Lin, Wan Ping, Wang Huaning, Wang Huiling, Yan Hao, Yan Jun, Yang Yongfeng, Zhang Hongxing, Zhang Dai, Jiang Tian |
Sex differences in gene expression patterns associated with the APOE4 allele. F1000Research 2019 8 8 387. Hsu Michelle, Dedhia Mehek, Crusio Wim E, Delprato An |
Association of GDNF and CNTNAP2 gene variants with gambling. Journal of behavioral addictions 2019 Aug 1-8. Das Arundhuti, Pagliaroli Luca, Vereczkei Andrea, Kotyuk Eszter, Langstieh Banrida, Demetrovics Zsolt, Barta Csa |
Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population. Journal of ophthalmology 2019 2019 9687823. Ma Yi-Nu, Xie Ting-Yu, Chen Xue- |
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human mutation 2019 Feb . Zhou Wei-Zhen, Zhang Jie, Li Ziyi, Lin Xiaojing, Li Jiarui, Wang Sheng, Yang Changhong, Wu Qixi, Ye Adam Yongxin, Wang Meng, Wang Dandan, Pu Tad Zhengzhang, Wu Yu-Yu, Wei Lipi |
Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk.
Progress in neuro-psychopharmacology & biological psychiatry 2019 06 92 133-147. Wang Alex W, Avramopoulos Dimitrios, Lori Adriana, Mulle Jennifer, Conneely Karen, Powers Abigail, Duncan Erica, Almli Lynn, Massa Nicholas, McGrath John, Schwartz Ann C, Goes Fernando S, Weng Lei, Wang Ruihua, Yolken Robert, Ruczinski Ingo, Gillespie Charles F, Jovanovic Tanja, Ressler Kerry, Pulver Ann E, Pearce Brad |
Association between CNTNAP2 polymorphisms and autism: A family-based study in the chinese han population and a meta-analysis combined with GWAS data of psychiatric genomics consortium. Autism research : official journal of the International Society for Autism Research 2019 Jan . Zhang Tian, Zhang Jishui, Wang Ziqi, Jia Meixiang, Lu Tianlan, Wang Han, Yue Weihua, Zhang Dai, Li Jun, Wang Lifa |
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 |
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
Nature communications 2019 01 10 (1): 376. Kilpeläinen Tuomas O, Bentley Amy R, Noordam Raymond, Sung Yun Ju, Schwander Karen, Winkler Thomas W, Jakupovic Hermina, Chasman Daniel I, Manning Alisa, Ntalla Ioanna, Aschard Hugues, Brown Michael R, de Las Fuentes Lisa, Franceschini Nora, Guo Xiuqing, Vojinovic Dina, Aslibekyan Stella, Feitosa Mary F, Kho Minjung, Musani Solomon K, Richard Melissa, Wang Heming, Wang Zhe, Bartz Traci M, Bielak Lawrence F, Campbell Archie, Dorajoo Rajkumar, Fisher Virginia, Hartwig Fernando P, Horimoto Andrea R V R, Li Changwei, Lohman Kurt K, Marten Jonathan, Sim Xueling, Smith Albert V, Tajuddin Salman M, Alver Maris, Amini Marzyeh, Boissel Mathilde, Chai Jin Fang, Chen Xu, Divers Jasmin, Evangelou Evangelos, Gao Chuan, Graff Mariaelisa, Harris Sarah E, He Meian, Hsu Fang-Chi, Jackson Anne U, Zhao Jing Hua, Kraja Aldi T, Kühnel Brigitte, Laguzzi Federica, Lyytikäinen Leo-Pekka, Nolte Ilja M, Rauramaa Rainer, Riaz Muhammad, Robino Antonietta, Rueedi Rico, Stringham Heather M, Takeuchi Fumihiko, van der Most Peter J, Varga Tibor V, Verweij Niek, Ware Erin B, Wen Wanqing, Li Xiaoyin, Yanek Lisa R, Amin Najaf, Arnett Donna K, Boerwinkle Eric, Brumat Marco, Cade Brian, Canouil Mickaël, Chen Yii-Der Ida, Concas Maria Pina, Connell John, de Mutsert Renée, de Silva H Janaka, de Vries Paul S, Demirkan Ayse, Ding Jingzhong, Eaton Charles B, Faul Jessica D, Friedlander Yechiel, Gabriel Kelley P, Ghanbari Mohsen, Giulianini Franco, Gu Chi Charles, Gu Dongfeng, Harris Tamara B, He Jiang, Heikkinen Sami, Heng Chew-Kiat, Hunt Steven C, Ikram M Arfan, Jonas Jost B, Koh Woon-Puay, Komulainen Pirjo, Krieger Jose E, Kritchevsky Stephen B, Kutalik Zoltán, Kuusisto Johanna, Langefeld Carl D, Langenberg Claudia, Launer Lenore J, Leander Karin, Lemaitre Rozenn N, Lewis Cora E, Liang Jingjing, , Liu Jianjun, Mägi Reedik, Manichaikul Ani, Meitinger Thomas, Metspalu Andres, Milaneschi Yuri, Mohlke Karen L, Mosley Thomas H, Murray Alison D, Nalls Mike A, Nang Ei-Ei Khaing, Nelson Christopher P, Nona Sotoodehnia, Norris Jill M, Nwuba Chiamaka Vivian, O'Connell Jeff, Palmer Nicholette D, Papanicolau George J, Pazoki Raha, Pedersen Nancy L, Peters Annette, Peyser Patricia A, Polasek Ozren, Porteous David J, Poveda Alaitz, Raitakari Olli T, Rich Stephen S, Risch Neil, Robinson Jennifer G, Rose Lynda M, Rudan Igor, Schreiner Pamela J, Scott Robert A, Sidney Stephen S, Sims Mario, Smith Jennifer A, Snieder Harold, Sofer Tamar, Starr John M, Sternfeld Barbara, Strauch Konstantin, Tang Hua, Taylor Kent D, Tsai Michael Y, Tuomilehto Jaakko, Uitterlinden André G, van der Ende M Yldau, van Heemst Diana, Voortman Trudy, Waldenberger Melanie, Wennberg Patrik, Wilson Gregory, Xiang Yong-Bing, Yao Jie, Yu Caizheng, Yuan Jian-Min, Zhao Wei, Zonderman Alan B, Becker Diane M, Boehnke Michael, Bowden Donald W, de Faire Ulf, Deary Ian J, Elliott Paul, Esko Tõnu, Freedman Barry I, Froguel Philippe, Gasparini Paolo, Gieger Christian, Kato Norihiro, Laakso Markku, Lakka Timo A, Lehtimäki Terho, Magnusson Patrik K E, Oldehinkel Albertine J, Penninx Brenda W J H, Samani Nilesh J, Shu Xiao-Ou, van der Harst Pim, Van Vliet-Ostaptchouk Jana V, Vollenweider Peter, Wagenknecht Lynne E, Wang Ya X, Wareham Nicholas J, Weir David R, Wu Tangchun, Zheng Wei, Zhu Xiaofeng, Evans Michele K, Franks Paul W, Gudnason Vilmundur, Hayward Caroline, Horta Bernardo L, Kelly Tanika N, Liu Yongmei, North Kari E, Pereira Alexandre C, Ridker Paul M, Tai E Shyong, van Dam Rob M, Fox Ervin R, Kardia Sharon L R, Liu Ching-Ti, Mook-Kanamori Dennis O, Province Michael A, Redline Susan, van Duijn Cornelia M, Rotter Jerome I, Kooperberg Charles B, Gauderman W James, Psaty Bruce M, Rice Kenneth, Munroe Patricia B, Fornage Myriam, Cupples L Adrienne, Rotimi Charles N, Morrison Alanna C, Rao Dabeeru C, Loos Ruth J |
Pancreatic ductal adenocarcinomas from Mexican patients present a distinct genomic mutational pattern. Molecular biology reports 2020 6 47 (7): 5175-5184. Sanchez Paulina, Espinosa Magali, Maldonado Vilma, Barquera Rodrigo, Belem-Gabiño Nayeli, Torres Javier, Cravioto Adrian, Melendez-Zajgla Jor |
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific reports 2020 Feb 10 (1): 3198. Bacchelli Elena, Cameli Cinzia, Viggiano Marta, Igliozzi Roberta, Mancini Alice, Tancredi Raffaella, Battaglia Agatino, Maestrini Ele |
Genomic Diversity in Sporadic Breast Cancer in a Latin American Population. Genes 2020 10 11 (11): . Brignoni Lucía, Cappetta Mónica, Colistro Valentina, Sans Mónica, Artagaveytia Nora, Bonilla Carolina, Bertoni Bernar |
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population. Genes 2020 Oct 11 (10): . Khalid Madiha, Raza Hashim, M Driessen Terri, J Lee Paul, Tejwani Leon, Sami Abdul, Nawaz Muhammad, Mehmood Baig Shahid, Lim Janghoo, Kaukab Raja Ghaza |
Common variant of CNTNAP2 gene modulate the social performances and functional connectivity of posterior right temporoparietal junction. Social cognitive and affective neuroscience 2020 Jan . Bai Tongjian, Zhang Long, Xie Xiaohui, Xiao Guixian, Huang Wanling, Li Dandan, Zu Meidan, Wei Lin, Zuo Xianbo, J I Gong-Jun, Hu Panpan, Zhu Chunyan, Qiu Bensheng, Tian Yanghua, Wang K |
Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder. NeuroImage. Clinical 2021 7 31 102729. Chien Yi-Ling, Chen Yu-Chieh, Gau Susan Shur-F |
Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder. Behavioural neurology 2021 7 2021 4150926. Fang Fang, Ge Minxia, Liu Jun, Zhang Zengyu, Yu Hong, Zhu Shuilong, Xu Liwei, Shao Li |
CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis. Human cell 2021 5 34 (5): 1410-1423. Uddin Mohammad Sarowar, Azima Atkia, Aziz Md Abdul, Aka Tutun Das, Jafrin Sarah, Millat Md Shalahuddin, Siddiqui Shafayet Ahmed, Uddin Md Giash, Hussain Md Saddam, Islam Mohammad Safiq |
Common variants of the autism-associated CNTNAP2 gene contribute to the modulatory effect of social function mediated by temporal cortex. Behavioural brain research 2021 Apr 409 113319. Li Dandan, Zhang Long, Bai Tongjian, Huang Wanling, Ji Gong-Jun, Yang Tingting, Zhang Yifan, Tian Yanghua, Qiu Bensheng, Wang K |
A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability. PloS one 2021 12 16 (12): e0260548. Shiota Yuka, Hirosawa Tetsu, Yoshimura Yuko, Tanaka Sanae, Hasegawa Chiaki, Iwasaki Sumie, An Kyung-Min, Soma Daiki, Sano Masuhiko, Yokoyama Shigeru, Kikuchi Mitsu |
Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population. Genes 2021 Oct 12 (10): . Bocharova Anna, Vagaitseva Kseniya, Marusin Andrey, Zhukova Natalia, Zhukova Irina, Minaycheva Larisa, Makeeva Oksana, Stepanov Vad |
Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL.
European journal of endocrinology 2021 4 184 (6): 847-856. Wittekind Dirk Alexander, Scholz Markus, Kratzsch Jürgen, Löffler Markus, Horn Katrin, Kirsten Holger, Witte Veronica, Villringer Arno, Kluge Micha |
PTPRD and CNTNAP2 as markers of tumor aggressiveness in oligodendrogliomas. Scientific reports 2022 8 12 (1): 14083. Rautajoki Kirsi J, Jaatinen Serafiina, Tiihonen Aliisa M, Annala Matti, Vuorinen Elisa M, Kivinen Anni, Rauhala Minna J, Maass Kendra K, Pajtler Kristian W, Yli-Harja Olli, Helén Pauli, Haapasalo Joonas, Haapasalo Hannu, Zhang Wei, Nykter Mat |
Genetics of autism spectrum disorder: an umbrella review of systematic reviews and meta-analyses. Translational psychiatry 2022 6 12 (1): 249. Qiu Shuang, Qiu Yingjia, Li Yan, Cong Xianli |
A Pilot Study of Whole-Blood Transcriptomic Analysis to Identify Genes Associated with Repetitive Low-Level Blast Exposure in Career Breachers. Biomedicines 2022 3 10 (3): . Vorn Rany, Edwards Katie A, Hentig James, Yun Sijung, Kim Hyung-Suk, Lai Chen, Devoto Christina, Yarnell Angela M, Polejaeva Elena, Dell Kristine C, LoPresti Matthew L, Walker Peter, Carr Walter, Stone James R, Ahlers Stephen T, Gill Jessica |
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 |
Genetic contributions to female gout and hyperuricemia using genome-wide association study and polygenic risk score analyses.
Rheumatology (Oxford, England) 2022 6 . Lin Chien-Yu, Chang Ya-Sian, Liu Ting-Yuan, Huang Chung-Ming, Chung Chin-Chun, Chen Yu-Chia, Tsai Fuu-Jen, Chang Jan-Gowth, Chang Shun-J |
Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder. Gene 2023 8 147723. Yulian Fang, Yaqiong Cui, Zhaoqing Yin, Mengzhu Hou, Pan Guo, Hanjie Wang, Nan Liu, Chunquan Cai, Mingbang Wa |
Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder. Human genetics 2023 5 . Gianluca D'Onofrio, Andrea Accogli, Mariasavina Severino, Haluk Caliskan, Tomislav Kokotovi?, Antonela Blazekovic, Kristina Gotovac Jercic, Silvana Markovic, Tamara Zigman, Krnjak Goran, Nina Bariši?, Vlasta Duranovic, Ana Ban, Fran Borovecki, Danijela Petkovi? Ramadža, Ivo Bari?, Walid Fazeli, Peter Herkenrath, Carla Marini, Roberta Vittorini, Vykuntaraju Gowda, Arjan Bouman, Clarissa Rocca, Issam Azmi Alkhawaja, Bibi Nazia Murtaza, Malik Mujaddad Ur Rehman, Chadi Al Alam, Gisele Nader, Maria Margherita Mancardi, Thea Giacomini, Siddharth Srivastava, Javeria Raza Alvi, Hoda Tomoum, Sara Matricardi, Michele Iacomino, Antonella Riva, Marcello Scala, Francesca Madia, Angela Pistorio, Vincenzo Salpietro, Carlo Minetti, Jean-Baptiste Rivière, Myriam Srour, Stephanie Efthymiou, Reza Maroofian, Henry Houlden, Sonja Catherine Vernes, Federico Zara, Pasquale Striano, Vanja Na |
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- Page last updated:Apr 16, 2024
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