Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: AUTS2[original query] |
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Autism and ultraconserved non-coding sequence on chromosome 7q. Psychiatric genetics 2006 1 16 (1): 19-23. Richler Esther, Reichert Jennifer G, Buxbaum Joseph D, McInnes Lynne Alis |
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. The British journal of psychiatry : the journal of mental science 2009 Jul 195 (1): 23-9. Hamshere M L, Green E K, Jones I R, Jones L, Moskvina V, Kirov G, Grozeva D, Nikolov I, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Breen G, St Clair D, Collier D A, Young A H, Ferrier I N, Farmer A, McGuffin P, , Holmans P A, Owen M J, O'Donovan M C, Craddock |
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Molecular psychiatry 2010 Jun 15 (6): 637-46. Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P |
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS genetics 2010 May 6 (5): e1000962. Mefford Heather C, Muhle Hiltrud, Ostertag Philipp, von Spiczak Sarah, Buysse Karen, Baker Carl, Franke Andre, Malafosse Alain, Genton Pierre, Thomas Pierre, Gurnett Christina A, Schreiber Stefan, Bassuk Alexander G, Guipponi Michel, Stephani Ulrich, Helbig Ingo, Eichler Evan |
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.
Proceedings of the National Academy of Sciences of the United States of America 2011 Apr 108 (17): 7119-24. Schumann Gunter, Coin Lachlan J, Lourdusamy Anbarasu, Charoen Pimphen, Berger Karen H, Stacey David, Desrivières Sylvane, Aliev Fazil A, Khan Anokhi A, Amin Najaf, Aulchenko Yurii S, Bakalkin Georgy, Bakker Stephan J, Balkau Beverley, Beulens Joline W, Bilbao Ainhoa, de Boer Rudolf A, Beury Delphine, Bots Michiel L, Breetvelt Elemi J, Cauchi Stéphane, Cavalcanti-Proença Christine, Chambers John C, Clarke Toni-Kim, Dahmen Norbert, de Geus Eco J, Dick Danielle, Ducci Francesca, Easton Alanna, Edenberg Howard J, Esko Tõnu, Esk Tõnu, Fernández-Medarde Alberto, Foroud Tatiana, Freimer Nelson B, Girault Jean-Antoine, Grobbee Diederick E, Guarrera Simonetta, Gudbjartsson Daniel F, Hartikainen Anna-Liisa, Heath Andrew C, Hesselbrock Victor, Hofman Albert, Hottenga Jouke-Jan, Isohanni Matti K, Kaprio Jaakko, Khaw Kay-Tee, Kuehnel Brigitte, Laitinen Jaana, Lobbens Stéphane, Luan Jian'an, Mangino Massimo, Maroteaux Matthieu, Matullo Giuseppe, McCarthy Mark I, Mueller Christian, Navis Gerjan, Numans Mattijs E, Núñez Alejandro, Nyholt Dale R, Onland-Moret Charlotte N, Oostra Ben A, O'Reilly Paul F, Palkovits Miklos, Penninx Brenda W, Polidoro Silvia, Pouta Anneli, Prokopenko Inga, Ricceri Fulvio, Santos Eugenio, Smit Johannes H, Soranzo Nicole, Song Kijoung, Sovio Ulla, Stumvoll Michael, Surakk Ida, Thorgeirsson Thorgeir E, Thorsteinsdottir Unnur, Troakes Claire, Tyrfingsson Thorarinn, Tönjes Anke, Uiterwaal Cuno S, Uitterlinden Andre G, van der Harst Pim, van der Schouw Yvonne T, Staehlin Oliver, Vogelzangs Nicole, Vollenweider Peter, Waeber Gerard, Wareham Nicholas J, Waterworth Dawn M, Whitfield John B, Wichmann Erich H, Willemsen Gonneke, Witteman Jacqueline C, Yuan Xin, Zhai Guangju, Zhao Jing H, Zhang Weihua, Martin Nicholas G, Metspalu Andres, Doering Angela, Scott James, Spector Tim D, Loos Ruth J, Boomsma Dorret I, Mooser Vincent, Peltonen Leena, Stefansson Kari, van Duijn Cornelia M, Vineis Paolo, Sommer Wolfgang H, Kooner Jaspal S, Spanagel Rainer, Heberlein Ulrike A, Jarvelin Marjo-Riitta, Elliott Pa |
Genetic analysis of AUTS2 as a susceptibility gene of heroin dependence. Drug and alcohol dependence 2013 Mar 128 (3): 238-42. Chen Yun-Hsiang, Liao Ding-Lieh, Lai Chih-Hao, Chen Chia-Hsia |
Increased de novo copy number variants in the offspring of older males. Translational psychiatry 2012 7 1 (8): e34. Flatscher-Bader T, Foldi C J, Chong S, Whitelaw E, Moser R J, Burne T H J, Eyles D W, McGrath J |
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.
Human genetics 2013 Oct 132 (10): 1141-51. Kapoor Manav, Wang Jen-Chyong, Wetherill Leah, Le Nhung, Bertelsen Sarah, Hinrichs Anthony L, Budde John, Agrawal Arpana, Bucholz Kathleen, Dick Danielle, Harari Oscar, Hesselbrock Victor, Kramer John, Nurnberger John I, Rice John, Saccone Nancy, Schuckit Marc, Tischfield Jay, Porjesz Bernice, Edenberg Howard J, Bierut Laura, Foroud Tatiana, Goate Alis |
Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene. PloS one 2013 8 (2): e57199. Chojnicka Izabela, Gajos Krzysztof, Strawa Katarzyna, Broda Gra?yna, Fudalej Sylwia, Fudalej Marcin, Stawi?ski Piotr, Pawlak Aleksandra, Krajewski Pawe?, Wojnar Marcin, P?oski Raf |
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. American journal of human genetics 2013 Feb 92 (2): 210-20. Beunders Gea, Voorhoeve Els, Golzio Christelle, Pardo Luba M, Rosenfeld Jill A, Talkowski Michael E, Simonic Ingrid, Lionel Anath C, Vergult Sarah, Pyatt Robert E, van de Kamp Jiddeke, Nieuwint Aggie, Weiss Marjan M, Rizzu Patrizia, Verwer Lucilla E N I, van Spaendonk Rosalina M L, Shen Yiping, Wu Bai-lin, Yu Tingting, Yu Yongguo, Chiang Colby, Gusella James F, Lindgren Amelia M, Morton Cynthia C, van Binsbergen Ellen, Bulk Saskia, van Rossem Els, Vanakker Olivier, Armstrong Ruth, Park Soo-Mi, Greenhalgh Lynn, Maye Una, Neill Nicholas J, Abbott Kristin M, Sell Susan, Ladda Roger, Farber Darren M, Bader Patricia I, Cushing Tom, Drautz Joanne M, Konczal Laura, Nash Patricia, de Los Reyes Emily, Carter Melissa T, Hopkins Elizabeth, Marshall Christian R, Osborne Lucy R, Gripp Karen W, Thrush Devon Lamb, Hashimoto Sayaka, Gastier-Foster Julie M, Astbury Caroline, Ylstra Bauke, Meijers-Heijboer Hanne, Posthuma Danielle, Menten Björn, Mortier Geert, Scherer Stephen W, Eichler Evan E, Girirajan Santhosh, Katsanis Nicholas, Groffen Alexander J, Sistermans Erik |
The clinical significance of small copy number variants in neurodevelopmental disorders. Journal of medical genetics 2014 Oct 51 (10): 677-88. Asadollahi Reza, Oneda Beatrice, Joset Pascal, Azzarello-Burri Silvia, Bartholdi Deborah, Steindl Katharina, Vincent Marie, Cobilanschi Joana, Sticht Heinrich, Baldinger Rosa, Reissmann Regina, Sudholt Irene, Thiel Christian T, Ekici Arif B, Reis André, Bijlsma Emilia K, Andrieux Joris, Dieux Anne, FitzPatrick David, Ritter Susanne, Baumer Alessandra, Latal Beatrice, Plecko Barbara, Jenni Oskar G, Rauch Ani |
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families. Neurogenetics 2014 May 15 (2): 117-27. Egger Gerald, Roetzer Katharina M, Noor Abdul, Lionel Anath C, Mahmood Huda, Schwarzbraun Thomas, Boright Oliver, Mikhailov Anna, Marshall Christian R, Windpassinger Christian, Petek Erwin, Scherer Stephen W, Kaschnitz Wolfgang, Vincent John |
The evidence for the contribution of the autism susceptibility candidate 2 (AUTS2) gene in heroin dependence susceptibility. Journal of molecular neuroscience : MN 2014 Dec 54 (4): 811-9. Dang Wei, Zhang Qian, Zhu Yong-Sheng, Lu Xiao-Y |
Association study identifying a new susceptibility gene (AUTS2) for schizophrenia. International journal of molecular sciences 2014 15 (11): 19406-16. Zhang Bao, Xu Yue-Hong, Wei Shu-Guang, Zhang Hong-Bo, Fu Dong-Ke, Feng Zu-Fei, Guan Fang-Lin, Zhu Yong-Sheng, Li Sheng-B |
A genome-wide association study of antidepressant response in Koreans.
Translational psychiatry 2015 5 e633. Myung W, Kim J, Lim S-W, Shim S, Won H-H, Kim Seonwoo, Kim Sangha, Lee M-S, Chang H S, Kim J-W, Carroll B J, Kim D |
Association between AUTS2 haplotypes and alcohol dependence in a Japanese population. Acta neuropsychiatrica 2016 Jan 1-7. Narita Shin, Nagahori Kenta, Nishizawa Daisuke, Yoshihara Eiji, Kawai Atsuko, Ikeda Kazutaka, Iwahashi Kazuhi |
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.
Molecular psychiatry 2017 May . Jorgenson E, Thai K K, Hoffmann T J, Sakoda L C, Kvale M N, Banda Y, Schaefer C, Risch N, Mertens J, Weisner C, Choquet |
Comprehensive molecular profiling of 718 Multiple Myelomas reveals significant differences in mutation frequencies between African and European descent cases. PLoS genetics 2017 Nov 13 (11): e1007087. Manojlovic Zarko, Christofferson Austin, Liang Winnie S, Aldrich Jessica, Washington Megan, Wong Shukmei, Rohrer Daniel, Jewell Scott, Kittles Rick A, Derome Mary, Auclair Daniel, Craig David Wesley, Keats Jonathan, Carpten John |
No Association between the Polymorphism rs6943555 in the AUTS2 Gene and Personality Traits in Japanese University Students. Psychiatry investigation 2017 Sep 14 (5): 681-686. Narita Shin, Ikeda Kazutaka, Nishizawa Daisuke, Yoshihara Eiji, Numajiri Maki, Onozawa Yuuya, Ohtani Nobuyo, Iwahashi Kazuhi |
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 |
Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population. Journal of cellular and molecular medicine 2018 Jan . Zhang Yan, Xie Xiaoli, Zeng Jixiao, Wu Qiang, Zhang Ruizhong, Zhu Deli, Xia Huim |
Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients. Frontiers in genetics 2019 5 10 434. Balicza Péter, Varga Noémi Ágnes, Bolgár Bence, Pentelényi Klára, Bencsik Renáta, Gál Anikó, Gézsi András, Prekop Csilla, Molnár Viktor, Molnár Mária Jud |
Genome-wide association study of germline variants and breast cancer-specific mortality.
British journal of cancer 2019 Mar 120 (6): 647-657. Escala-Garcia Maria, Guo Qi, Dörk Thilo, Canisius Sander, Keeman Renske, Dennis Joe, Beesley Jonathan, Lecarpentier Julie, Bolla Manjeet K, Wang Qin, Abraham Jean, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Auer Paul L, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Bermisheva Marina, Bernstein Leslie, Blomqvist Carl, Boeckx Bram, Bojesen Stig E, Bonanni Bernardo, Børresen-Dale Anne-Lise, Brauch Hiltrud, Brenner Hermann, Brentnall Adam, Brinton Louise, Broberg Per, Brock Ian W, Brucker Sara Y, Burwinkel Barbara, Caldas Carlos, Caldés Trinidad, Campa Daniele, Canzian Federico, Carracedo Angel, Carter Brian D, Castelao Jose E, Chang-Claude Jenny, Chanock Stephen J, Chenevix-Trench Georgia, Cheng Ting-Yuan David, Chin Suet-Feung, Clarke Christine L, , Cordina-Duverger Emilie, Couch Fergus J, Cox David G, Cox Angela, Cross Simon S, Czene Kamila, Daly Mary B, Devilee Peter, Dunn Janet A, Dunning Alison M, Durcan Lorraine, Dwek Miriam, Earl Helena M, Ekici Arif B, Eliassen A Heather, Ellberg Carolina, Engel Christoph, Eriksson Mikael, Evans D Gareth, Figueroa Jonine, Flesch-Janys Dieter, Flyger Henrik, Gabrielson Marike, Gago-Dominguez Manuela, Galle Eva, Gapstur Susan M, García-Closas Montserrat, García-Sáenz José A, Gaudet Mia M, George Angela, Georgoulias Vassilios, Giles Graham G, Glendon Gord, Goldgar David E, González-Neira Anna, Alnæs Grethe I Grenaker, Grip Mervi, Guénel Pascal, Haeberle Lothar, Hahnen Eric, Haiman Christopher A, Håkansson Niclas, Hall Per, Hamann Ute, Hankinson Susan, Harkness Elaine F, Harrington Patricia A, Hart Steven N, Hartikainen Jaana M, Hein Alexander, Hillemanns Peter, Hiller Louise, Holleczek Bernd, Hollestelle Antoinette, Hooning Maartje J, Hoover Robert N, Hopper John L, Howell Anthony, Huang Guanmengqian, Humphreys Keith, Hunter David J, Janni Wolfgang, John Esther M, Jones Michael E, Jukkola-Vuorinen Arja, Jung Audrey, Kaaks Rudolf, Kabisch Maria, Kaczmarek Katarzyna, Kerin Michael J, Khan Sofia, Khusnutdinova Elza, Kiiski Johanna I, Kitahara Cari M, Knight Julia A, Ko Yon-Dschun, Koppert Linetta B, Kosma Veli-Matti, Kraft Peter, Kristensen Vessela N, Krüger Ute, Kühl Tabea, Lambrechts Diether, Le Marchand Loic, Lee Eunjung, Lejbkowicz Flavio, Li Lian, Lindblom Annika, Lindström Sara, Linet Martha, Lissowska Jolanta, Lo Wing-Yee, Loibl Sibylle, Lubinski Jan, Lux Michael P, MacInnis Robert J, Maierthaler Melanie, Maishman Tom, Makalic Enes, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martinez Maria Elena, Mavroudis Dimitrios, McLean Catriona, Meindl Alfons, Middha Pooja, Miller Nicola, Milne Roger L, Moreno Fernando, Mulligan Anna Marie, Mulot Claire, Nassir Rami, Neuhausen Susan L, Newman William T, Nielsen Sune F, Nordestgaard Børge G, Norman Aaron, Olsson Håkan, Orr Nick, Pankratz V Shane, Park-Simon Tjoung-Won, Perez Jose I A, Pérez-Barrios Clara, Peterlongo Paolo, Petridis Christos, Pinchev Mila, Prajzendanc Karoliona, Prentice Ross, Presneau Nadege, Prokofieva Darya, Pylkäs Katri, Rack Brigitte, Radice Paolo, Ramachandran Dhanya, Rennert Gadi, Rennert Hedy S, Rhenius Valerie, Romero Atocha, Roylance Rebecca, Saloustros Emmanouil, Sawyer Elinor J, Schmidt Daniel F, Schmutzler Rita K, Schneeweiss Andreas, Schoemaker Minouk J, Schumacher Fredrick, Schwentner Lukas, Scott Rodney J, Scott Christopher, Seynaeve Caroline, Shah Mitul, Simard Jacques, Smeets Ann, Sohn Christof, Southey Melissa C, Swerdlow Anthony J, Talhouk Aline, Tamimi Rulla M, Tapper William J, Teixeira Manuel R, Tengström Maria, Terry Mary Beth, Thöne Kathrin, Tollenaar Rob A E M, Tomlinson Ian, Torres Diana, Truong Thérèse, Turman Constance, Turnbull Clare, Ulmer Hans-Ulrich, Untch Michael, Vachon Celine, van Asperen Christi J, van den Ouweland Ans M W, van Veen Elke M, Wendt Camilla, Whittemore Alice S, Willett Walter, Winqvist Robert, Wolk Alicja, Yang Xiaohong R, Zhang Yan, Easton Douglas F, Fasching Peter A, Nevanlinna Heli, Eccles Diana M, Pharoah Paul D P, Schmidt Marjanka |
A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction. PloS one 2019 14 (11): e0224399. Levran Orna, Randesi Matthew, Rotrosen John, Ott Jurg, Adelson Miriam, Kreek Mary Jean |
Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
Molecular biology reports 2020 Oct 47 (10): 7623-7632. Alsubaie Laila M, Alsuwat Hind Saleh, Almandil Noor B, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
Effect of AUTS2 gene rs6943555 variant in male patients with schizophrenia in a Turkish population. Gene 2020 6 756 144913. Ozsoy Filiz, Karakus Nevin Balci, Yigit Serbulent, Kulu Muber |
Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population.
Journal of cellular and molecular medicine 2020 Nov . Niu Yuguang, Xie Chengyong, Du Zhenhua, Zeng Jifeng, Chen Hongxia, Jin Liang, Zhang Qing, Yu Huiying, Wang Yahui, Ping Jie, Yang Chenning, Liu Xinyi, Li Yuanfeng, Zhou Gangqi |
Evaluation of candidate genes in a Chinese cohort of atypical Rolandic epilepsy. Epileptic disorders : international epilepsy journal with videotape 2021 Jul . Hu Xiaoyue, Tang Jihong, Hua Ying, Wang Yanping, Huang Ji |
Trans-ancestry, Bayesian Meta-analysis Discovers 20 Novel Risk Loci for Inflammatory Bowel Disease in an African American, East Asian, and European Cohort. Human molecular genetics 2022 10 . Cordero Roberto Y, Cordero Jennifer B, Stiemke Andrew B, Datta Lisa W, Buyske Steven, Kugathasan Subra, McGovern Dermot P B, Brant Steven R, Simpson Claire |
Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2023 11 . Eun Suk Jung, David Ellinghaus, Frauke Degenhardt, Akira Meguro, Seik-Soon Khor, Sören Mucha, Mareike Wendorff, Simonas Juzenas, Nobuhisa Mizuki, Katsushi Tokunaga, Seung Won Kim, Min Goo Lee, Stefan Schreiber, Won Ho Kim, Andre Franke, Jae Hee Che |
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