Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: GRM8[original query] |
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Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Apr 150B (3): 359-68. Chen Andrew C H, Tang Yongqiang, Rangaswamy Madhavi, Wang Jen C, Almasy Laura, Foroud Tatiana, Edenberg Howard J, Hesselbrock Victor, Nurnberger John, Kuperman Samuel, O'Connor Sean J, Schuckit Marc A, Bauer Lance O, Tischfield Jay, Rice John P, Bierut Laura, Goate Alison, Porjesz Berni |
Genome-wide association study of smoking initiation and current smoking. American journal of human genetics 2009 Mar 84 (3): 367-79. Vink Jacqueline M, Smit August B, de Geus Eco J C, Sullivan Patrick, Willemsen Gonneke, Hottenga Jouke-Jan, Smit Johannes H, Hoogendijk Witte J, Zitman Frans G, Peltonen Leena, Kaprio Jaakko, Pedersen Nancy L, Magnusson Patrik K, Spector Tim D, Kyvik Kirsten Ohm, Morley Katherine I, Heath Andrew C, Martin Nicholas G, Westendorp Rudi G J, Slagboom P Eline, Tiemeier Henning, Hofman Albert, Uitterlinden Andre G, Aulchenko Yurii S, Amin Najaf, van Duijn Cornelia, Penninx Brenda W, Boomsma Dorret |
Genome-wide association scan of trait depression.
Biological psychiatry 2010 Nov 68 (9): 811-7. Terracciano Antonio, Tanaka Toshiko, Sutin Angelina R, Sanna Serena, Deiana Barbara, Lai Sandra, Uda Manuela, Schlessinger David, Abecasis Gonçalo R, Ferrucci Luigi, Costa Paul |
Response to methadone maintenance treatment is associated with the MYOCD and GRM6 genes. Molecular diagnosis & therapy 2010 Jun 14 (3): 171-8. Fonseca Francina, Gratacòs Mònica, Escaramís Geòrgia, De Cid Rafael, Martín-Santos Rocío, Fernández-Espejo Emilio, Estivill Xavier, Torrens Mar |
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature genetics 2012 Jan 44 (1): 78-84. Elia Josephine, Glessner Joseph T, Wang Kai, Takahashi Nagahide, Shtir Corina J, Hadley Dexter, Sleiman Patrick M A, Zhang Haitao, Kim Cecilia E, Robison Reid, Lyon Gholson J, Flory James H, Bradfield Jonathan P, Imielinski Marcin, Hou Cuiping, Frackelton Edward C, Chiavacci Rosetta M, Sakurai Takeshi, Rabin Cara, Middleton Frank A, Thomas Kelly A, Garris Maria, Mentch Frank, Freitag Christine M, Steinhausen Hans-Christoph, Todorov Alexandre A, Reif Andreas, Rothenberger Aribert, Franke Barbara, Mick Eric O, Roeyers Herbert, Buitelaar Jan, Lesch Klaus-Peter, Banaschewski Tobias, Ebstein Richard P, Mulas Fernando, Oades Robert D, Sergeant Joseph, Sonuga-Barke Edmund, Renner Tobias J, Romanos Marcel, Romanos Jasmin, Warnke Andreas, Walitza Susanne, Meyer Jobst, Pálmason Haukur, Seitz Christiane, Loo Sandra K, Smalley Susan L, Biederman Joseph, Kent Lindsey, Asherson Philip, Anney Richard J L, Gaynor J William, Shaw Philip, Devoto Marcella, White Peter S, Grant Struan F A, Buxbaum Joseph D, Rapoport Judith L, Williams Nigel M, Nelson Stanley F, Faraone Stephen V, Hakonarson Hak |
A discovery resource of rare copy number variations in individuals with autism spectrum disorder. G3 (Bethesda, Md.) 2012 Dec 2 (12): 12. Prasad A, Merico D, Thiruvahindrapuram B, Wei J, Lionel AC, Sato D, Rickaby J, Lu C, Szatmari P, Roberts W, Fernandez BA, Marshall CR, Hatchwell E, Eis PS, Scherer SW |
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 |
Glutamatergic copy number variants and their role in attention-deficit/hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Sep 165B (6): 502-9. Akutagava-Martins Glaucia Chiyoko, Salatino-Oliveira Angelica, Genro Julia P, Contini Verônica, Polanczyk Guilherme, Zeni Cristian, Chazan Rodrigo, Kieling Christian, Anselmi Luciana, Menezes Ana M B, Grevet Eugênio H, Bau Claiton H D, Rohde Luis A, Hutz Mara |
A candidate syntenic genetic locus is associated with voluntary exercise levels in mice and humans. Behavioural brain research 2015 Jan 276 8-16. Kostrzewa E, Brandys M K, van Lith H A, Kas M J |
Heritability and molecular genetic basis of antisaccade eye tracking error rate: a genome-wide association study.
Psychophysiology 2014 Dec 51 (12): 1272-84. Vaidyanathan Uma, Malone Stephen M, Donnelly Jennifer M, Hammer Micah A, Miller Michael B, McGue Matt, Iacono William |
The role of rs2237781 within GRM8 in eating behavior. Brain and behavior 2013 Sep 3 (5): 495-502. Gast Marie-Therese, Tönjes Anke, Keller Maria, Horstmann Annette, Steinle Nanette, Scholz Markus, Müller Ines, Villringer Arno, Stumvoll Michael, Kovacs Peter, Böttcher Yvon |
Expression and replication studies to identify new candidate genes involved in normal hearing function. PloS one 2014 9 (1): e85352. Girotto Giorgia, Vuckovic Dragana, Buniello Annalisa, Lorente-Cánovas Beatriz, Lewis Morag, Gasparini Paolo, Steel Karen |
A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.
PloS one 2014 10 (4): e0123654. Sanchez-Juan Pascual, Bishop Matthew T, Kovacs Gabor G, Calero Miguel, Aulchenko Yurii S, Ladogana Anna, Boyd Alison, Lewis Victoria, Ponto Claudia, Calero Olga, Poleggi Anna, Carracedo Ángel, van der Lee Sven J, Ströbel Thomas, Rivadeneira Fernando, Hofman Albert, Haïk Stéphane, Combarros Onofre, Berciano José, Uitterlinden Andre G, Collins Steven J, Budka Herbert, Brandel Jean-Philippe, Laplanche Jean Louis, Pocchiari Maurizio, Zerr Inga, Knight Richard S G, Will Robert G, van Duijn Cornelia |
Significant association of GRM7 and GRM8 genes with schizophrenia and major depressive disorder in the Han Chinese population. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2015 May . Li Wenjin, Ju Kang, Li Zhiqiang, He Kuanjun, Chen Jianhua, Wang Qingzhong, Yang Beimeng, An Lin, Feng Guoyin, Sun Weiming, Zhou Juan, Zhang Shasha, Song Pingping, Khan Raja, Ji Weidong, Shi Yongyo |
The molecular genetic architecture of attention deficit hyperactivity disorder. Molecular psychiatry 2015 Mar 20 (3): 289-97. Hawi Z, Cummins T D R, Tong J, Johnson B, Lau R, Samarrai W, Bellgrove M |
Association analysis of the GRM8 gene with schizophrenia in the Uygur Chinese population. Hereditas 2014 Dec 151 (6): 140-4. Zhang Lili, Zhong Xianjiang, An Zhiguo, Han Shuxian, Luo Xiao, Shi Yongyong, Yi Qizho |
Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2016 Sep . Gao Jianjun, Davis Lea K, Hart Amy B, Sanchez-Roige Sandra, Han Lide, Cacioppo John T, Palmer Abraham |
Mutation profiles in early-stage lung squamous cell carcinoma with clinical follow-up and correlation with markers of immune function. Annals of oncology : official journal of the European Society for Medical Oncology 2017 (1): 83-89. Choi M, Kadara H, Zhang J, Parra E R, Rodriguez-Canales J, Gaffney S G, Zhao Z, Behrens C, Fujimoto J, Chow C, Kim K, Kalhor N, Moran C, Rimm D, Swisher S, Gibbons D L, Heymach J, Kaftan E, Townsend J P, Lynch T J, Schlessinger J, Lee J, Lifton R P, Herbst R S, Wistuba I |
A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers.
Frontiers in psychiatry 2018 9 290. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yu Younger W-Y, Yang Albert C, Tsai Shih-J |
An Exome-wide Association Study for Type 2 Diabetes-Attributed End-Stage Kidney Disease in African Americans. Kidney international reports 2018 Jul 3 (4): 867-878. Guan Meijian, Keaton Jacob M, Dimitrov Latchezar, Hicks Pamela J, Xu Jianzhao, Palmer Nicholette D, Wilson James G, Freedman Barry I, Bowden Donald W, Ng Maggie C |
Cardiac arrhythmia and neuroexcitability gene variants in resected brain tissue from patients with sudden unexpected death in epilepsy (SUDEP). NPJ genomic medicine 2018 4 3 9. Friedman Daniel, Kannan Kasthuri, Faustin Arline, Shroff Seema, Thomas Cheddhi, Heguy Adriana, Serrano Jonathan, Snuderl Matija, Devinsky Orr |
Genomic sequencing and editing revealed the GRM8 signaling pathway as potential therapeutic targets of squamous cell lung cancer. Cancer letters 2019 Feb 442 53-67. Zhang Panpan, Kang Bin, Xie Guoyun, Li Shaolei, Gu Ying, Shen Yue, Zhao Xin, Ma Yuanyuan, Li Fuqiang, Si Jiahui, Wang Jian, Chen Jinfeng, Yang Huanming, Xu Xun, Yang Y |
TCF4 and GRM8 gene polymorphisms and risk of schizophrenia in an Iranian population: a case-control study. Molecular biology reports 2018 Oct . Tavakkoly-Bazzaz Javad, Azarnezhad Asaad, Mousavi Negar, Salehipour Pouya, Shahsavand Ananloo Esmaeil, Alizadeh Fatem |
GRM8 genotype is associated with externalizing disorders and greater inter-trial variability in brain activation during a response inhibition task. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2020 Apr 131 (6): 1180-1186. Bauer Lance O, Covault Jonathan |
Association between the group III metabotropic glutamate receptor gene polymorphisms and attention-deficit/hyperactivity disorder and functional exploration of risk loci. Journal of psychiatric research 2020 Oct 132 65-71. Zhang Qi, Chen Xinzhen, Li Shanyawen, Yao Ting, Wu Ji |
EGFR-Mutated Squamous Cell Lung Cancer and Its Association With Outcomes. Frontiers in oncology 2021 7 11 680804. Jin Rui, Peng Ling, Shou Jiawei, Wang Jin, Jin Yin, Liang Fei, Zhao Jing, Wu Mengmeng, Li Qin, Zhang Bin, Wu Xiaoying, Lan Fen, Xia Lixia, Yan Junrong, Shao Yang, Stebbing Justin, Shen Huahao, Li Wen, Xia Ya |
Disease patterns of coronary heart disease and type 2 diabetes harbored distinct and shared genetic architecture. Cardiovascular diabetology 2022 12 21 (1): 276. Xiao Han, Ma Yujia, Zhou Zechen, Li Xiaoyi, Ding Kexin, Wu Yiqun, Wu Tao, Chen Dafa |
Genetic loci implicated in meta-analysis of body shape in Africans.
Nutrition, metabolism, and cardiovascular diseases : NMCD 2022 4 32 (6): 1511-1518. Nakabuye Mariam, Kamiza Abram Bunya, Soremekun Opeyemi, Machipisa Tafadzwa, Cohen Emmanuel, Pirie Fraser, Nashiru Oyekanmi, Young Elizabeth, Sandhu Manjinder S, Motala Ayesha A, Chikowore Tinashe, Fatumo Seg |
A pilot study on glutamate receptor and carrier gene variants and risk of childhood autism spectrum. Metabolic brain disease 2023 8 . Jun Liu, Jing Yan, Fei Qu, Weiming Mo, Hong Yu, Pingfang Hu, Zengyu Zha |
Genetic Markers Associated with Milk Production and Thermotolerance in Holstein Dairy Cows Managed in a Heat-Stressed Environment. Biology 2023 5 12 (5): . Ricardo Zamorano-Algandar, Juan F Medrano, Milton G Thomas, R Mark Enns, Scott E Speidel, Miguel A Sánchez-Castro, Guillermo Luna-Nevárez, José C Leyva-Corona, Pablo Luna-Nevár |
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- Page last updated:Apr 22, 2024
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