Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: ARHGEF3[original query] |
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Identification of a role for the ARHGEF3 gene in postmenopausal osteoporosis. American journal of human genetics 2008 Jun 82 (6): 1262-9. Mullin Ben H, Prince Richard L, Dick Ian M, Hart Deborah J, Spector Tim D, Dudbridge Frank, Wilson Scott |
A genome-wide association study identifies three loci associated with mean platelet volume.
American journal of human genetics 2009 Jan 84 (1): 66-71. Meisinger Christa, Prokisch Holger, Gieger Christian, Soranzo Nicole, Mehta Divya, Rosskopf Dieter, Lichtner Peter, Klopp Norman, Stephens Jonathan, Watkins Nicholas A, Deloukas Panos, Greinacher Andreas, Koenig Wolfgang, Nauck Matthias, Rimmbach Christian, Völzke Henry, Peters Annette, Illig Thomas, Ouwehand Willem H, Meitinger Thomas, Wichmann H-Erich, Döring Ange |
Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2010 Jun 21 (6): 1009-20. Li G H Y, Kung A W C, Huang Q |
Further genetic evidence suggesting a role for the RhoGTPase-RhoGEF pathway in osteoporosis. Bone 2009 Aug 45 (2): 387-91. Mullin Ben H, Prince Richard L, Mamotte Cyril, Spector Tim D, Hart Deborah J, Dudbridge Frank, Wilson Scott |
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci.
Arthritis and rheumatism 2011 Apr 63 (4): 884-93. Freudenberg Jan, Lee Hye-Soon, Han Bok-Ghee, Shin Hyoung Do, Kang Young Mo, Sung Yoon-Kyoung, Shim Seung-Cheol, Choi Chan-Bum, Lee Annette T, Gregersen Peter K, Bae Sang-Che |
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Human molecular genetics 2013 Jan . Li J, Glessner JT, Zhang H, Hou C, Wei Z, Bradfield JP, Mentch FD, Guo Y, Kim C, Xia Q, Chiavacci RM, Thomas KA, Qiu H, Grant SF, Furth SL, Hakonarson H, Sleiman PM |
Whole Exome Sequencing in Psoriasis Patients Contributes to Studies of Acitretin Treatment Difference. International journal of molecular sciences 2017 Jan 18 (2): . Zhou Xingchen, He Yijing, Kuang Yehong, Li Jie, Zhang Jianglin, Chen Mingliang, Chen Wangqing, Su Juan, Zhao Shuang, Liu Panpan, Chen Menglin, Shen Minxue, Chen Xiaoping, Zhu Wu, Chen Xia |
2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio.
Journal of human genetics 2017 Nov 62 (11): 979-988. Lin Bochao Danae, Carnero-Montoro Elena, Bell Jordana T, Boomsma Dorret I, de Geus Eco J, Jansen Rick, Kluft Cornelis, Mangino Massimo, Penninx Brenda, Spector Tim D, Willemsen Gonneke, Hottenga Jouke-J |
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
Secondary analyses for genome-wide association studies using expression quantitative trait loci.
Genetic epidemiology 2022 3 46 (3-4): 170-181. Ngwa Julius S, Yanek Lisa R, Kammers Kai, Kanchan Kanika, Taub Margaret A, Scharpf Robert B, Faraday Nauder, Becker Lewis C, Mathias Rasika A, Ruczinski In |
Genomic Variation Affecting MPV and PLT Count in Association with Development of Ischemic Stroke and Its Subtypes. Molecular neurobiology 2023 7 . Abhilash Ludhiadch, Sulena, Sandeep Singh, Sudip Chakraborty, Dixit Sharma, Mahesh Kulharia, Paramdeep Singh, Anjana Muns |
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- Page last updated:Apr 22, 2024
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