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Volumn 18, Issue 1, 2015, Pages 86-91

VEGAS2: Software for more flexible gene-based testing

Author keywords

1, 000 genomes; GWAS; VEGAS; VEGAS2; X chromosome

Indexed keywords

3' UNTRANSLATED REGION; AFRICAN; AMERICAN; ARTICLE; ASIAN; AUTOSOME; CHROMOSOME 21; COMPUTER LANGUAGE; CONTROLLED STUDY; DATA ANALYSIS SOFTWARE; EUROPEAN; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SCREENING; GENOTYPE; HUMAN; HUMAN GENOME; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; VERSATILE GENE BASED ASSOCIATION STUDY 2; X CHROMOSOME; X CHROMOSOME INACTIVATION; BIOLOGICAL MODEL; COMPUTER INTERFACE; COMPUTER PROGRAM; COMPUTER SIMULATION; GENETICS; HAPLOTYPE MAP; INTERNET; ONLINE SYSTEM; PROCEDURES; SEXUAL DEVELOPMENT; STATISTICS AND NUMERICAL DATA; TWINS;

EID: 84922634287     PISSN: 18324274     EISSN: 18392628     Source Type: Journal    
DOI: 10.1017/thg.2014.79     Document Type: Article
Times cited : (218)

References (19)
  • 2
    • 84881647995 scopus 로고    scopus 로고
    • Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
    • Cheng, C. Y., Schache, M., Ikram, M. K., Young, T. L., Guggenheim, J. A., Vitart, V., . . . Baird, P. N. (2013). Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. American Journal of Human Genetics, 93, 264-277.
    • (2013) American Journal of Human Genetics , vol.93 , pp. 264-277
    • Cheng, C.Y.1    Schache, M.2    Ikram, M.K.3    Young, T.L.4    Guggenheim, J.A.5    Vitart, V.6    Baird, P.N.7
  • 4
    • 84883199435 scopus 로고    scopus 로고
    • An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease
    • Chu, X., Shen, M., Xie, F., Miao, X. J., Shou, W.H., Liu, L., . . . Huang, W. (2013). An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease. Journal of Medical Genetics, 50, 479-485.
    • (2013) Journal of Medical Genetics , vol.50 , pp. 479-485
    • Chu, X.1    Shen, M.2    Xie, F.3    Miao, X.J.4    Shou, W.H.5    Liu, L.6    Huang, W.7
  • 5
    • 52449118475 scopus 로고    scopus 로고
    • Testing for association on the X chromosome
    • Clayton, D. (2008). Testing for association on the X chromosome. Biostatistics, 9, 593-600.
    • (2008) Biostatistics , vol.9 , pp. 593-600
    • Clayton, D.1
  • 8
    • 84905650558 scopus 로고    scopus 로고
    • Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness
    • 163
    • Davidson, A. E., Cheong, S. S., Hysi, P. G., Venturini, C.,Plagnol, V., Ruddle, J. B., . . . Hardcastle, A. J. (2014). Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness. PLoS One, 9, e104,163.
    • (2014) PLoS One , vol.9 , pp. e104
    • Davidson, A.E.1    Cheong, S.S.2    Hysi, P.G.3    Venturini, C.4    Plagnol, V.5    Ruddle, J.B.6    Hardcastle, A.J.7
  • 13
    • 34347344976 scopus 로고    scopus 로고
    • A new multipoint method for genome-wide association studies by imputation of genotypes
    • Marchini, J., Howie, B., Myers, S., McVean, G., & Donnelly, P.(2007). A new multipoint method for genome-wide association studies by imputation of genotypes. Nature Genetics, 39, 906-913.
    • (2007) Nature Genetics , vol.39 , pp. 906-913
    • Marchini, J.1    Howie, B.2    Myers, S.3    McVean, G.4    Donnelly, P.5
  • 16
    • 84901743386 scopus 로고    scopus 로고
    • Chromosome X-wide association study identifies loci for fasting insulin and height and evidence for incomplete dosage compensation
    • Tukiainen, T., Pirinen, M., Sarin, A. P., Ladenvall, C., Kettunen,J., Lehtimaki, T., . . . Ripatti, S. (2014). Chromosome X-wide association study identifies loci for fasting insulin and height and evidence for incomplete dosage compensation. PLoS Genetics, 10, e1004127.
    • (2014) PLoS Genetics , vol.10
    • Tukiainen, T.1    Pirinen, M.2    Sarin, A.P.3    Ladenvall, C.4    Kettunen, J.5    Lehtimaki, T.6    Ripatti, S.7
  • 17
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • Wellcome Trust Case Control, C. (2007). Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature, 447, 661-678.
    • (2007) Nature , vol.447 , pp. 661-678
    • Wellcome Trust Case Control, C,1
  • 18
    • 84922623311 scopus 로고    scopus 로고
    • Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus
    • Zhang, Y., Zhang, J., Yang, J.,Wang, Y., Zhang, L., Zuo, X., . . . Yang, W. (2014). Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus. Human Molecular Genetics. Retrieved from http://hmg.oxfordjournals.org/citmgr?gca=hmg%3Bddu429v3.
    • (2014) Human Molecular Genetics
    • Zhang, Y.1    Zhang, J.2    Yang, J.3    Wang, Y.4    Zhang, L.5    Zuo, X.6    Yang, W.7
  • 19
    • 38049018997 scopus 로고    scopus 로고
    • Testing association for markers on the X chromosome
    • Zheng, G., Joo, J., Zhang, C., & Geller, N. L. (2007). Testing association for markers on the X chromosome. Genetic Epidemiology 31, 834-843.
    • (2007) Genetic Epidemiology , vol.31 , pp. 834-843
    • Zheng, G.1    Joo, J.2    Zhang, C.3    Geller, N.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.