Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: GRM1[original query] |
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Genetic analysis of the GRM1 gene in human melanoma susceptibility. European journal of human genetics : EJHG 2007 Nov 15 (11): 1176-82. Ortiz Pablo, Vanaclocha Francisco, López-Bran Eduardo, Esquivias José Ignacio, López-Estebaranz José Luis, Martín-González Manuel, Arrue Itziar, García-Romero Diana, Ochoa Carolina, González-Perez Antonio, Ruiz Agustin, Real Luis Migu |
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 |
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 |
Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes. Psychoneuroendocrinology 2012 Apr 37 (4): 565-75. Menke Andreas, Sämann Philipp, Kloiber Stefan, Czamara Darina, Lucae Susanne, Hennings Johannes, Heck Angela, Kohli Martin A, Czisch Michael, Müller-Myhsok Bertram, Holsboer Florian, Binder Elisabeth |
Deleterious GRM1 mutations in schizophrenia. PloS one 2012 7 (3): e32849. Ayoub Mohammed Akli, Angelicheva Dora, Vile David, Chandler David, Morar Bharti, Cavanaugh Juleen A, Visscher Peter M, Jablensky Assen, Pfleger Kevin D G, Kalaydjieva Lu |
Metabotropic glutamate receptor 1 expression and its polymorphic variants associate with breast cancer phenotypes. PloS one 2013 8 (7): e69851. Mehta Madhura S, Dolfi Sonia C, Bronfenbrener Roman, Bilal Erhan, Chen Chunxia, Moore Dirk, Lin Yong, Rahim Hussein, Aisner Seena, Kersellius Romona D, Teh Jessica, Chen Suzie, Toppmeyer Deborah L, Medina Dan J, Ganesan Shridar, Vazquez Alexei, Hirshfield Kim |
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 |
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human genetics 2014 Jun 133 (6): 781-92. Waltes Regina, Duketis Eftichia, Knapp Michael, Anney Richard J L, Huguet Guillaume, Schlitt Sabine, Jarczok Tomasz A, Sachse Michael, Kämpfer Laura M, Kleinböck Tina, Poustka Fritz, Bölte Sven, Schmötzer Gabriele, Voran Anette, Huy Ellen, Meyer Jobst, Bourgeron Thomas, Klauck Sabine M, Freitag Christine M, Chiocchetti Andreas |
Frequency of alcohol consumption in humans; the role of metabotropic glutamate receptors and downstream signaling pathways. Translational psychiatry 2015 5 e586. Meyers J L, Salling M C, Almli L M, Ratanatharathorn A, Uddin M, Galea S, Wildman D E, Aiello A E, Bradley B, Ressler K, Koenen K |
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 |
Kynurenine pathway and cognitive impairments in schizophrenia: Pharmacogenetics of galantamine and memantine. Schizophrenia research. Cognition 2016 Jun 4 4-9. Koola Maju Math |
Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia. Clinical genetics 2016 Apr . Barresi S, Niceta M, Alfieri P, Brankovich V, Piccini G, Bruselles A, Barone M R, Cusmai R, Tartaglia M, Bertini E, Zanni |
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 |
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 |
Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes. Psychiatry and clinical neurosciences 2018 10 73 (1): 11-19. Ganesh Suhas, Ahmed P Husayn, Nadella Ravi K, More Ravi P, Seshadri Manasa, Viswanath Biju, Rao Mahendra, Jain Sanjeev, , Mukherjee Odi |
Genotype, resilience and function and physical activity post hip fracture. International journal of orthopaedic and trauma nursing 2019 Mar . Resnick Barbara, Klinedinst N Jennifer, Yerges-Armstrong Laura, Magaziner Jay, Orwig Denise, Hochberg Marc C, Gruber-Baldini Ann L, Dorsey Susan |
Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study. Journal of neural transmission (Vienna, Austria : 1996) 2019 Dec 126 (12): 1679-1693. Waltes Regina, Freitag Christine M, Herlt Timo, Lempp Thomas, Seitz Christiane, Palmason Haukur, Meyer Jobst, Chiocchetti Andreas |
The impact of Mendelian sleep and circadian genetic variants in a population setting. PLoS genetics 2022 9 18 (9): e1010356. Weedon Michael N, Jones Samuel E, Lane Jacqueline M, Lee Jiwon, Ollila Hanna M, Dawes Amy, Tyrrell Jess, Beaumont Robin N, Partonen Timo, Merikanto Ilona, Rich Stephen S, Rotter Jerome I, Frayling Timothy M, Rutter Martin K, Redline Susan, Sofer Tamar, Saxena Richa, Wood Andrew |
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