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Volumn 5, Issue , 2015, Pages

Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myeloma

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MODEL; CASE CONTROL STUDY; CLINICAL TRIAL; GENETIC PREDISPOSITION; GENETIC VARIATION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; HUMAN; HUMAN GENOME; MULTIPLE MYELOMA; PATHOLOGY; PHENOTYPE; QUANTITATIVE TRAIT; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84937879795     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep12473     Document Type: Article
Times cited : (16)

References (26)
  • 2
    • 0037148921 scopus 로고    scopus 로고
    • A long-term study of prognosis in monoclonal gammopathy of undetermined significance
    • Kyle, R. A. et al. A long-term study of prognosis in monoclonal gammopathy of undetermined significance. N Engl J Med 346, 564-9 (2002).
    • (2002) N Engl J Med , vol.346 , pp. 564-569
    • Kyle, R.A.1
  • 3
    • 33746364172 scopus 로고    scopus 로고
    • Familial risks and temporal incidence trends of multiple myeloma
    • Altieri, A., Chen, B., Bermejo, J. L., Castro, F. & Hemminki, K. Familial risks and temporal incidence trends of multiple myeloma. Eur J Cancer 42, 1661-70 (2006).
    • (2006) Eur J Cancer , vol.42 , pp. 1661-1670
    • Altieri, A.1    Chen, B.2    Bermejo, J.L.3    Castro, F.4    Hemminki, K.5
  • 4
    • 84895802141 scopus 로고    scopus 로고
    • Inherited genetic susceptibility to multiple myeloma
    • Morgan, G. J. et al. Inherited genetic susceptibility to multiple myeloma. Leukemia 28, 518-24 (2014).
    • (2014) Leukemia , vol.28 , pp. 518-524
    • Morgan, G.J.1
  • 5
    • 84655166569 scopus 로고    scopus 로고
    • Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk
    • Broderick, P. et al. Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. Nat Genet 44, 58-61 (2012).
    • (2012) Nat Genet , vol.44 , pp. 58-61
    • Broderick, P.1
  • 6
    • 84885022887 scopus 로고    scopus 로고
    • Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
    • Chubb, D. et al. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nat Genet 45, 1221-5 (2013).
    • (2013) Nat Genet , vol.45 , pp. 1221-1225
    • Chubb, D.1
  • 7
    • 84878596524 scopus 로고    scopus 로고
    • The CCND1 c.870G> A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
    • Weinhold, N. et al. The CCND1 c.870G> A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nat Genet 45, 522-5 (2013).
    • (2013) Nat Genet , vol.45 , pp. 522-525
    • Weinhold, N.1
  • 8
    • 78650856517 scopus 로고    scopus 로고
    • GCTA: A tool for genome-wide complex trait analysis
    • Yang, J., Lee, S. H., Goddard, M. E. & Visscher, P. M. GCTA: a tool for genome-wide complex trait analysis. Am J Hum Genet 88, 76-82 (2011).
    • (2011) Am J Hum Genet , vol.88 , pp. 76-82
    • Yang, J.1    Lee, S.H.2    Goddard, M.E.3    Visscher, P.M.4
  • 9
    • 84883170802 scopus 로고    scopus 로고
    • Genome-wide complex trait analysis (GCTA): Methods, data analyses, and interpretations
    • Yang, J., Lee, S. H., Goddard, M. E. & Visscher, P. M. Genome-wide complex trait analysis (GCTA): methods, data analyses, and interpretations. Methods Mol Biol 1019, 215-36 (2013).
    • (2013) Methods Mol Biol , vol.1019 , pp. 215-236
    • Yang, J.1    Lee, S.H.2    Goddard, M.E.3    Visscher, P.M.4
  • 10
    • 79957588287 scopus 로고    scopus 로고
    • Genome partitioning of genetic variation for complex traits using common SNPs
    • Yang, J. et al. Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet 43, 519-25 (2011).
    • (2011) Nat Genet , vol.43 , pp. 519-525
    • Yang, J.1
  • 11
    • 84916623158 scopus 로고    scopus 로고
    • Measuring missing heritability: Inferring the contribution of common variants
    • Golan, D., Lander, E. S. & Rosset, S. Measuring missing heritability: Inferring the contribution of common variants. Proceedings of the National Academy of Sciences 111, E5272-E5281 (2014).
    • (2014) Proceedings of the National Academy of Sciences , vol.111 , pp. E5272-E5281
    • Golan, D.1    Lander, E.S.2    Rosset, S.3
  • 12
    • 84911369978 scopus 로고    scopus 로고
    • Most common 'sporadic' cancers have a significant germline genetic component
    • Lu, Y. et al. Most common 'sporadic' cancers have a significant germline genetic component. Hum Mol Genet 23, 6112-8 (2014).
    • (2014) Hum Mol Genet , vol.23 , pp. 6112-6118
    • Lu, Y.1
  • 13
    • 84873031286 scopus 로고    scopus 로고
    • Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis
    • Lee, S. H. et al. Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Hum Mol Genet 22, 832-41 (2013).
    • (2013) Hum Mol Genet , vol.22 , pp. 832-841
    • Lee, S.H.1
  • 14
    • 77954140531 scopus 로고    scopus 로고
    • Common SNPs explain a large proportion of the heritability for human height
    • Yang, J. et al. Common SNPs explain a large proportion of the heritability for human height. Nat Genet 42, 565-9 (2010).
    • (2010) Nat Genet , vol.42 , pp. 565-569
    • Yang, J.1
  • 15
    • 0034969437 scopus 로고    scopus 로고
    • Are rare variants responsible for susceptibility to complex diseases?
    • Pritchard, J. K. Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69, 124-37 (2001).
    • (2001) Am J Hum Genet , vol.69 , pp. 124-137
    • Pritchard, J.K.1
  • 16
    • 79955650000 scopus 로고    scopus 로고
    • The prognostic significance of cytogenetics and molecular profiling in multiple myeloma
    • Sawyer, J. R. The prognostic significance of cytogenetics and molecular profiling in multiple myeloma. Cancer Genet 204, 3-12 (2011).
    • (2011) Cancer Genet , vol.204 , pp. 3-12
    • Sawyer, J.R.1
  • 17
    • 79959841853 scopus 로고    scopus 로고
    • Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
    • Do, C. B. et al. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet 7, e1002141 (2011).
    • (2011) PLoS Genet , vol.7 , pp. e1002141
    • Do, C.B.1
  • 18
    • 84875703379 scopus 로고    scopus 로고
    • Large-scale genotyping identifies 41 new loci associated with breast cancer risk
    • 361-1-2
    • Michailidou, K. et al. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet 45, 353-61 361-1-2 (2013).
    • (2013) Nat Genet , vol.45 , pp. 353-361
    • Michailidou, K.1
  • 19
    • 84875739291 scopus 로고    scopus 로고
    • Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
    • 391-1-2
    • Eeles, R. A. et al. Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. Nat Genet 45, 385-91 391-1-2 (2013).
    • (2013) Nat Genet , vol.45 , pp. 385-391
    • Eeles, R.A.1
  • 20
    • 84875707717 scopus 로고    scopus 로고
    • GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer
    • 370-1-2
    • Pharoah, P. D. et al. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. Nat Genet 45, 362-70 370-1-2 (2013).
    • (2013) Nat Genet , vol.45 , pp. 362-370
    • Pharoah, P.D.1
  • 21
    • 79955793051 scopus 로고    scopus 로고
    • Polygenic susceptibility to prostate and breast cancer: Implications for personalised screening
    • Pashayan, N. et al. Polygenic susceptibility to prostate and breast cancer: implications for personalised screening. Br J Cancer 104, 1656-63 (2011).
    • (2011) Br J Cancer , vol.104 , pp. 1656-1663
    • Pashayan, N.1
  • 22
    • 84859972113 scopus 로고    scopus 로고
    • MyelomA genetics international consortium
    • Morgan, G. et al. MyelomA Genetics International Consortium. Leuk Lymphoma 53, 796-800 (2012).
    • (2012) Leuk Lymphoma , vol.53 , pp. 796-800
    • Morgan, G.1
  • 23
    • 78650174738 scopus 로고    scopus 로고
    • First-line treatment with zoledronic acid as compared with clodronic acid in multiple myeloma (MRC Myeloma IX): A randomised controlled trial
    • Morgan, G. J. et al. First-line treatment with zoledronic acid as compared with clodronic acid in multiple myeloma (MRC Myeloma IX): a randomised controlled trial. Lancet 376, 1989-99 (2010).
    • (2010) Lancet , vol.376 , pp. 1989-1999
    • Morgan, G.J.1
  • 24
    • 32144461525 scopus 로고    scopus 로고
    • Cohort profile: 1958 British birth cohort (National Child Development Study)
    • Power, C. & Elliott, J. Cohort profile: 1958 British birth cohort (National Child Development Study). Int J Epidemiol 35, 34-41 (2006).
    • (2006) Int J Epidemiol , vol.35 , pp. 34-41
    • Power, C.1    Elliott, J.2
  • 25
    • 27644546712 scopus 로고    scopus 로고
    • Population structure, differential bias and genomic control in a large-scale, case-control association study
    • Clayton, D. G. et al. Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat Genet 37, 1243-6 (2005).
    • (2005) Nat Genet , vol.37 , pp. 1243-1246
    • Clayton, D.G.1
  • 26
    • 77955405475 scopus 로고    scopus 로고
    • Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
    • McLaren, W. et al. Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 26, 2069-70 (2010).
    • (2010) Bioinformatics , vol.26 , pp. 2069-2070
    • McLaren, W.1


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