Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and GRIK2[original query] |
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| Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease. Human genetics 2006 Sep 120 (2): 285-92. Metzger Silke, Bauer Peter, Tomiuk Jürgen, Laccone Franco, Didonato Stefano, Gellera Cinzia, Mariotti Caterina, Lange Herwig W, Weirich-Schwaiger Helga, Wenning Gregor K, Seppi Klaus, Melegh Bela, Havasi Viktoria, Balikó Laszlo, Wieczorek Stefan, Zaremba Jacek, Hoffman-Zacharska Dorota, Sulek Anna, Basak A Nazli, Soydan Esra, Zidovska Jana, Kebrdlova Vera, Pandolfo Massimo, Ribaï Pascale, Kadasi Ludovit, Kvasnicova Marta, Weber Bernhard H F, Kreuz Friedmar, Dose Matthias, Stuhrmann Manfred, Riess Ol |
| TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochemical and biophysical research communications 2012 Aug 424 (3): 404-8. Lee Ji-Hyun, Lee Jong-Min, Ramos Eliana Marisa, Gillis Tammy, Mysore Jayalakshmi S, Kishikawa Shotaro, Hadzi Tiffany, Hendricks Audrey E, Hayden Michael R, Morrison Patrick J, Nance Martha, Ross Christopher A, Margolis Russell L, Squitieri Ferdinando, Gellera Cinzia, Gomez-Tortosa Estrella, Ayuso Carmen, Suchowersky Oksana, Trent Ronald J, McCusker Elizabeth, Novelletto Andrea, Frontali Marina, Jones Randi, Ashizawa Tetsuo, Frank Samuel, Saint-Hilaire Marie-Helene, Hersch Steven M, Rosas Herminia D, Lucente Diane, Harrison Madaline B, Zanko Andrea, Abramson Ruth K, Marder Karen, Sequeiros Jorge, Landwehrmeyer G Bernhard, , Shoulson Ira, , Myers Richard H, MacDonald Marcy E, Gusella James |
| Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human molecular genetics 2012 Aug 21 (15): 3513-23. Griswold Anthony J, Ma Deqiong, Cukier Holly N, Nations Laura D, Schmidt Mike A, Chung Ren-Hua, Jaworski James M, Salyakina Daria, Konidari Ioanna, Whitehead Patrice L, Wright Harry H, Abramson Ruth K, Williams Scott M, Menon Ramkumar, Martin Eden R, Haines Jonathan L, Gilbert John R, Cuccaro Michael L, Pericak-Vance Margaret |
| Genetic heterogeneity of asthma phenotypes identified by a clustering approach. The European respiratory journal 2014 Feb 43 (2): 439-52. Siroux Valérie, González Juan R, Bouzigon Emmanuelle, Curjuric Ivan, Boudier Anne, Imboden Medea, Anto Josep Maria, Gut Ivo, Jarvis Deborah, Lathrop Mark, Omenaas Ernst Reidar, Pin Isabelle, Wjst Mathias, Demenais Florence, Probst-Hensch Nicole, Kogevinas Manolis, Kauffmann Franci |
| A non-parametric approach for detecting gene-gene interactions associated with age-at-onset outcomes. BMC genetics 2014 15 79. Li Ming, Gardiner Joseph C, Breslau Naomi, Anthony James C, Lu Qi |
| [Glutamate receptors genes polymorphism and the risk of paranoid schizophrenia in Russians and tatars from the Republic of Bashkortostan]. Molekuliarnaia biologiia 0 48 (5): 771-81. Gareeva A E, Khusnutdinova E |
| Multiplex PCR Analysis of 17 (11 Novels) STR Markers Linked to Six Autosomal Recessive Intellectual Disability Genes in Iranian Population. Clinical laboratory 2016 62 (1-2): 31-8. Shirin Ghadami, Maryam Abiri, Farideh Zonozi Rishsefid, Javad Tavakkoly-Bazzaz, Sirous Zeina |
Genomewide Gene-by-Sex Interaction Scans Identify ADGRV1 for Sex Differences in Opioid Dependent African Americans.
Scientific reports 2019 Dec 9 (1): 18070. Yang Bao-Zhu, Zhou Hang, Cheng Zhongshan, Kranzler Henry R, Gelernter Jo |
| Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.
Progress in neuro-psychopharmacology & biological psychiatry 2021 Jul 110393. Wang Kesheng, Xu Chun, Smith Amanda, Xiao Danqing, Navia R Osvaldo, Lu Yongke, Xie Changchun, Piamjariyakul Ubolrat, |
- Page last reviewed:Feb 1, 2024
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