Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: RGS7[original query] |
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Association analysis of Rgs7 variants with panic disorder. Journal of neural transmission (Vienna, Austria : 1996) 2009 Nov 116 (11): 1523-8. Hohoff Christa, Neumann Anna, Domschke Katharina, Jacob Christian, Maier Wolfgang, Fritze Jürgen, Bandelow Borwin, Krakowitzky Petra, Rothermundt Matthias, Arolt Volker, Deckert Jürg |
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis. Genes and immunity 2009 Oct 10 (7): 624-30. McCauley J L, Zuvich R L, Bradford Y, Kenealy S J, Schnetz-Boutaud N, Gregory S G, Hauser S L, Oksenberg J R, Mortlock D P, Pericak-Vance M A, Haines J |
Association of polymorphisms in RGS4 and expression of RGS transcripts in the brains of human alcoholics. Brain research 2010 Jun 1340 1-9. Ho Ada M-C, MacKay Rachel K, Dodd Peter R, Lewohl Joanne |
Genetic variations in the regulator of G-protein signaling genes are associated with survival in late-stage non-small cell lung cancer. PloS one 2011 6 (6): 6. Dai J, Gu J, Lu C, Lin J, Stewart D, Chang D, Roth JA, Wu X |
New gene variants associated with venous thrombosis: a replication study in White and Black Americans. Journal of thrombosis and haemostasis : JTH 2011 Mar 9 (3): 489-95. Austin H, De Staercke C, Lally C, Bezemer I D, Rosendaal F R, Hooper W |
Multiple hits for the association of uterine fibroids on human chromosome 1q43. PloS one 2013 8 (3): e58399. Aissani Brahim, Wiener Howard, Zhang K |
Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH interval. Endocrine-related cancer 2015 Aug 22 (4): 633-43. Aissani Brahim, Zhang Kui, Mensenkamp Arjen R, Menko Fred H, Wiener Howard |
Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait. European journal of human genetics : EJHG 2015 Oct 23 (10): 1378-83. Frani? Sanja, Groen-Blokhuis Maria M, Dolan Conor V, Kattenberg Mathijs V, Pool René, Xiao Xiangjun, Scheet Paul A, Ehli Erik A, Davies Gareth E, van der Sluis Sophie, Abdellaoui Abdel, Hansell Narelle K, Martin Nicholas G, Hudziak James J, van Beijsterveldt Catherina E M, Swagerman Suzanne C, Hulshoff Pol Hilleke E, de Geus Eco J C, Bartels Meike, Ropers H Hilger, Hottenga Jouke-Jan, Boomsma Dorret |
Association of frequent genetic variants in platelet activation pathway genes with large-vessel ischemic stroke in Polish population. Platelets 2017 Jan 28 (1): 66-73. Postula Marek, Janicki Piotr K, Milanowski Lukasz, Pordzik Justyna, Eyileten Ceren, Karlinski Michal, Wylezol Pawel, Solarska Marta, Czlonkowka Anna, Kurkowska-Jastrzebka Iwona, Sugino Shigekazu, Imamura Yuka, Mirowska-Guzel Dagma |
Fine Mapping of the Body Fat QTL on Human Chromosome 1q43. PloS one 2016 11 (4): e0153794. Aissani Brahim, Wiener Howard W, Zhang K |
A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians.
Diabetes 2017 May . Piaggi Paolo, Masindova Ivica, Muller Yunhua L, Mercader Josep, Wiessner Gregory B, Chen Peng, , Kobes Sayuko, Hsueh Wen-Chi, Mongalo Milliejoan, Knowler William C, Krakoff Jonathan, Hanson Robert L, Bogardus Clifton, Baier Leslie |
Thrombogenesis-associated genetic determinants as predictors of thromboembolism and prognosis in cervical cancer. Scientific reports 2023 6 13 (1): 9519. Beatriz Vieira Neto, Valéria Tavares, José Brito da Silva, Joana Liz-Pimenta, Inês Soares Marques, Luísa Carvalho, Lurdes Salgado, Deolinda Pereira, Rui Medeir |
Identification of genetic variants associated with anterior cruciate ligament rupture and AKC standard coat color in the Labrador Retriever. BMC genomic data 2023 10 24 (1): 60. B T Lee, L A Baker, M Momen, H Terhaar, E E Binversie, S J Sample, Peter Mu |
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- Page last updated:Apr 22, 2024
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