Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: GRID2[original query] |
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Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol. Pharmacogenetics and genomics 2011 Apr 21 (4): 206-16. Giegling Ina, Drago Antonio, Dolžan Vita, Plesni?ar Blanka Kores, Schäfer Martin, Hartmann Annette M, Sander Thomas, Toliat Mohammad Reza, Möller Hans-Jürgen, Stassen Hans H, Rujescu Dan, Serretti Alessand |
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study. Human genetics 2013 Jul 132 (7): 771-81. Beaty T H, Taub M A, Scott A F, Murray J C, Marazita M L, Schwender H, Parker M M, Hetmanski J B, Balakrishnan P, Mansilla M A, Mangold E, Ludwig K U, Noethen M M, Rubini M, Elcioglu N, Ruczinski |
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts.
Gut 2014 Sep . Ek Weronica E, Reznichenko Anna, Ripke Stephan, Niesler Beate, Zucchelli Marco, Rivera Natalia V, Schmidt Peter T, Pedersen Nancy L, Magnusson Patrik, Talley Nicholas J, Holliday Elizabeth G, Houghton Lesley, Gazouli Maria, Karamanolis George, Rappold Gudrun, Burwinkel Barbara, Surowy Harald, Rafter Joseph, Assadi Ghazaleh, Li Ling, Papadaki Evangelia, Gambaccini Dario, Marchi Santino, Colucci Rocchina, Blandizzi Corrado, Barbaro Raffaella, Karling Pontus, Walter Susanna, Ohlsson Bodil, Tornblom Hans, Bresso Francesca, Andreasson Anna, Dlugosz Aldona, Simren Magnus, Agreus Lars, Lindberg Greger, Boeckxstaens Guy, Bellini Massimo, Stanghellini Vincenzo, Barbara Giovanni, Daly Mark J, Camilleri Michael, Wouters Mira M, D'Amato Mau |
The human d2 glutamate receptor gene is not mutated in patients with spinocerebellar ataxia. Neural regeneration research 2014 May 9 (10): 1068-74. Huang Jinxiang, Lin Aiyu, Dong Haiyan, Wang Chaodo |
Copy number variation in Han Chinese individuals with autism spectrum disorder. Journal of neurodevelopmental disorders 2014 6 (1): 34. Gazzellone Matthew J, Zhou Xue, Lionel Anath C, Uddin Mohammed, Thiruvahindrapuram Bhooma, Liang Shuang, Sun Caihong, Wang Jia, Zou Mingyang, Tammimies Kristiina, Walker Susan, Selvanayagam Thanuja, Wei John, Wang Zhuozhi, Wu Lijie, Scherer Stephen |
SNPs in NRXN1 and CHRNA5 are associated to smoking and regulation of GABAergic and glutamatergic pathways. Pharmacogenomics 2016 Jun . Pérez-Rubio Gloria, Pérez-Rodríguez Martha E, Fernández-López Juan Carlos, Ramírez-Venegas Alejandra, García-Colunga Jesús, Ávila-Moreno Federico, Camarena Angel, Sansores Raúl H, Falfán-Valencia Ramc |
Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes. Translational psychiatry 2016 Feb 6 e739. Stevenson J M, Reilly J L, Harris M S H, Patel S R, Weiden P J, Prasad K M, Badner J A, Nimgaonkar V L, Keshavan M S, Sweeney J A, Bishop J |
Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis. Molecular psychiatry 2017 Aug . Authors are not available |
Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats. Obesity (Silver Spring, Md.) 2017 12 26 (1): 213-222. Keele Gregory R, Prokop Jeremy W, He Hong, Holl Katie, Littrell John, Deal Aaron, Francic Sanja, Cui Leilei, Gatti Daniel M, Broman Karl W, Tschannen Michael, Tsaih Shirng-Wern, Zagloul Maie, Kim Yunjung, Baur Brittany, Fox Joseph, Robinson Melanie, Levy Shawn, Flister Michael J, Mott Richard, Valdar William, Solberg Woods Leah |
A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
Sex differences in the genetic architecture of obsessive-compulsive disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 Nov . Khramtsova Ekaterina A, Heldman Raphael, Derks Eske M, Yu Dongmei, , Davis Lea K, Stranger Barbara |
Association of Gene Variations in Ionotropic Glutamate Receptor and Attention-Deficit/Hyperactivity Disorder in the Chinese Population: A Two-Stage Case-Control Study. Journal of attention disorders 2020 Feb 1087054720905089. Zhang Qi, Huang Xin, Chen Xin-Zhen, Li Shan-Ya-Wen, Yao Ting, Wu Ji |
Genome-wide association analysis of cognitive function in Danish long-lived individuals.
Mechanisms of ageing and development 2021 2 195 111463. Nygaard Marianne, Dowsett Joseph, McGue Matt, Christensen Kaare, Christiansen Lene, Tan Qihua, Mengel-From Jon |
Genome-Wide Association Study and Gene-Based Analysis of Participants With Hemophilia A and Inhibitors in the My Life, Our Future Research Repository. Frontiers in medicine 2022 7 9 903838. Lessard Samuel, He Chunla, Rajpal Deepak K, Klinger Katherine, Loh Christine, Harris Tim, Dumont Jennif |
Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. Genome medicine 2023 6 15 (1): 45. Zia Khan, Min Jung, Megan Crow, Rajat Mohindra, Vidya Maiya, Joshua S Kaminker, David H Hackos, G Scott Chandler, Mark I McCarthy, Tushar Bhanga |
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- Page last updated:Apr 16, 2024
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