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Volumn 50, Issue 3, 2011, Pages 377-379

Of 508 Mice and 40,000 Humans

Author keywords

[No Author keywords available]

Indexed keywords

EDITORIAL; ELECTROCARDIOGRAM; EPISTASIS; EXPERIMENTAL MOUSE; GENE MUTATION; GENETIC ASSOCIATION; HEART RATE; HEART VENTRICLE TACHYCARDIA; HERITABILITY; HUMAN; HUMAN GENETICS; LINKAGE ANALYSIS; NONHUMAN; PLEIOTROPY; PR INTERVAL; PRIORITY JOURNAL; QRS COMPLEX; QUANTITATIVE TRAIT LOCUS; SINGLE NUCLEOTIDE POLYMORPHISM; SUDDEN DEATH; TRIPLE HELIX;

EID: 79551601027     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yjmcc.2010.12.008     Document Type: Editorial
Times cited : (1)

References (37)
  • 1
    • 0038267112 scopus 로고    scopus 로고
    • Out-of-hospital cardiac arrest-the relevance of heart failure. The Maastricht Circulatory Arrest Registry
    • Gorgels A.P., Gijsbers C., de Vreede-Swagemakers J., Lousberg A., Wellens H.J. Out-of-hospital cardiac arrest-the relevance of heart failure. The Maastricht Circulatory Arrest Registry. Eur Heart J 2003, 24:1204-1209.
    • (2003) Eur Heart J , vol.24 , pp. 1204-1209
    • Gorgels, A.P.1    Gijsbers, C.2    de Vreede-Swagemakers, J.3    Lousberg, A.4    Wellens, H.J.5
  • 2
    • 0033586647 scopus 로고    scopus 로고
    • Predicting sudden death in the population: the Paris Prospective Study I
    • Jouven X., Desnos M., Guerot C., Ducimetière P. Predicting sudden death in the population: the Paris Prospective Study I. Circulation 1999, 99:1978-1983.
    • (1999) Circulation , vol.99 , pp. 1978-1983
    • Jouven, X.1    Desnos, M.2    Guerot, C.3    Ducimetière, P.4
  • 4
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Wang Q., Shen J., Splawski I., Atkinson D., Li Z., Robinson J.L., et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995, 80:805-811.
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1    Shen, J.2    Splawski, I.3    Atkinson, D.4    Li, Z.5    Robinson, J.L.6
  • 5
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • Wang Q., Curran M.E., Splawski I., Burn T.C., Millholland J.M., VanRaay T.J., et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 1996, 12:17-23.
    • (1996) Nat Genet , vol.12 , pp. 17-23
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3    Burn, T.C.4    Millholland, J.M.5    VanRaay, T.J.6
  • 6
    • 25144503454 scopus 로고    scopus 로고
    • Genetics of cardiac arrhythmias
    • Wilde A.A.M., Bezzina C.R. Genetics of cardiac arrhythmias. Heart 2005, 91:1352-1358.
    • (2005) Heart , vol.91 , pp. 1352-1358
    • Wilde, A.A.M.1    Bezzina, C.R.2
  • 8
    • 14644439232 scopus 로고    scopus 로고
    • QT interval is a heritable quantitative trait with evidence of linkage to chromosome 3 in a genome-wide linkage analysis: the Framingham Heart Study
    • Newton-Cheh C., Larson M.G., Corey D.C., Benjamin E.J., Herbert A.G., Levy D., et al. QT interval is a heritable quantitative trait with evidence of linkage to chromosome 3 in a genome-wide linkage analysis: the Framingham Heart Study. Heart Rhythm 2005, 2:277-284.
    • (2005) Heart Rhythm , vol.2 , pp. 277-284
    • Newton-Cheh, C.1    Larson, M.G.2    Corey, D.C.3    Benjamin, E.J.4    Herbert, A.G.5    Levy, D.6
  • 13
    • 43249106694 scopus 로고    scopus 로고
    • Augmentation of J waves and electrical storms in patients with early repolarization
    • Nam G., Kim Y., Antzelevitch C. Augmentation of J waves and electrical storms in patients with early repolarization. N Engl J Med 2008, 358:2078-2079.
    • (2008) N Engl J Med , vol.358 , pp. 2078-2079
    • Nam, G.1    Kim, Y.2    Antzelevitch, C.3
  • 15
    • 33845708766 scopus 로고    scopus 로고
    • Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD
    • Remme C.A., Verkerk A.O., Nuyens D., van Ginneken A.C.G., van Brunschot S., Belterman C.N.W., et al. Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD. Circulation 2006, 114:2584-2594.
    • (2006) Circulation , vol.114 , pp. 2584-2594
    • Remme, C.A.1    Verkerk, A.O.2    Nuyens, D.3    van Ginneken, A.C.G.4    van Brunschot, S.5    Belterman, C.N.W.6
  • 16
    • 67649871391 scopus 로고    scopus 로고
    • Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy
    • Remme C.A., Scicluna B.P., Verkerk A.O., Amin A.S., van Brunschot S., Beekman L., et al. Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy. Circ Res 2009, 104:1283-1292.
    • (2009) Circ Res , vol.104 , pp. 1283-1292
    • Remme, C.A.1    Scicluna, B.P.2    Verkerk, A.O.3    Amin, A.S.4    van Brunschot, S.5    Beekman, L.6
  • 17
    • 0035576885 scopus 로고    scopus 로고
    • Sensitized polygenic trait analysis
    • Matin A., Nadeau J.H. Sensitized polygenic trait analysis. Trends Genet 2001, 17:727-731.
    • (2001) Trends Genet , vol.17 , pp. 727-731
    • Matin, A.1    Nadeau, J.H.2
  • 18
    • 77952405802 scopus 로고    scopus 로고
    • Genetics of complex disorders
    • Kere J. Genetics of complex disorders. Biochem Biophys Res Commun 2010, 396:143-146.
    • (2010) Biochem Biophys Res Commun , vol.396 , pp. 143-146
    • Kere, J.1
  • 19
    • 33745237158 scopus 로고    scopus 로고
    • A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
    • Arking D.E., Pfeufer A., Post W., Kao W.H.L., Newton-Cheh C., Ikeda M., et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet 2006, 38:644-651.
    • (2006) Nat Genet , vol.38 , pp. 644-651
    • Arking, D.E.1    Pfeufer, A.2    Post, W.3    Kao, W.H.L.4    Newton-Cheh, C.5    Ikeda, M.6
  • 21
    • 63449109595 scopus 로고    scopus 로고
    • Common variants at ten loci modulate the QT interval duration in the QTSCD Study
    • Pfeufer A., Sanna S., Arking D.E., Müller M., Gateva V., Fuchsberger C., et al. Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat Genet 2009, 41:407-414.
    • (2009) Nat Genet , vol.41 , pp. 407-414
    • Pfeufer, A.1    Sanna, S.2    Arking, D.E.3    Müller, M.4    Gateva, V.5    Fuchsberger, C.6
  • 23
    • 84947899543 scopus 로고    scopus 로고
    • Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
    • Sotoodehnia N., Isaacs A., de Bakker P.I.W., Dörr M., Newton-Cheh C., Nolte I.M., et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet 2010, 42(12):1068-1076.
    • (2010) Nat Genet , vol.42 , Issue.12 , pp. 1068-1076
    • Sotoodehnia, N.1    Isaacs, A.2    de Bakker, P.I.W.3    Dörr, M.4    Newton-Cheh, C.5    Nolte, I.M.6
  • 25
    • 67349188883 scopus 로고    scopus 로고
    • A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
    • Cho Y.S., Go M.J., Kim Y.J., Heo J.Y., Oh J.H., Ban H., et al. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat Genet 2009, 41:527-534.
    • (2009) Nat Genet , vol.41 , pp. 527-534
    • Cho, Y.S.1    Go, M.J.2    Kim, Y.J.3    Heo, J.Y.4    Oh, J.H.5    Ban, H.6
  • 28
    • 0001740245 scopus 로고
    • Regression towards mediocrity hereditary stature
    • Galton F. Regression towards mediocrity hereditary stature. J. Anthropol. Inst. 1886, 15:246-263.
    • (1886) J. Anthropol. Inst. , vol.15 , pp. 246-263
    • Galton, F.1
  • 29
    • 0001077470 scopus 로고
    • The correlation between relatives on the supposition of Mendelian inheritance
    • Fisher R.A. The correlation between relatives on the supposition of Mendelian inheritance. Trans Roy Soc Edin 1918.
    • (1918) Trans Roy Soc Edin
    • Fisher, R.A.1
  • 30
    • 77957947562 scopus 로고    scopus 로고
    • Hundreds of variants clustered in genomic loci and biological pathways affect human height
    • Lango Allen H., Estrada K., Lettre G., Berndt S.I., Weedon M.N., Rivadeneira F., et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010, 467:832-838.
    • (2010) Nature , vol.467 , pp. 832-838
    • Lango Allen, H.1    Estrada, K.2    Lettre, G.3    Berndt, S.I.4    Weedon, M.N.5    Rivadeneira, F.6
  • 31
    • 77951702343 scopus 로고    scopus 로고
    • Genetic heterogeneity in human disease
    • McClellan J., King M. Genetic heterogeneity in human disease. Cell 2010, 141:210-217.
    • (2010) Cell , vol.141 , pp. 210-217
    • McClellan, J.1    King, M.2
  • 33
    • 70349629971 scopus 로고    scopus 로고
    • Using biological networks to search for interacting loci in genome-wide association studies
    • Emily M., Mailund T., Hein J., Schauser L., Schierup M.H. Using biological networks to search for interacting loci in genome-wide association studies. Eur J Hum Genet 2009, 17:1231-1240.
    • (2009) Eur J Hum Genet , vol.17 , pp. 1231-1240
    • Emily, M.1    Mailund, T.2    Hein, J.3    Schauser, L.4    Schierup, M.H.5
  • 34
    • 77956793795 scopus 로고    scopus 로고
    • Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice
    • Milan D.J., Lubitz S.A., Kääb S., Ellinor P.T. Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice. Heart Rhythm 2010, 7:1141-1148.
    • (2010) Heart Rhythm , vol.7 , pp. 1141-1148
    • Milan, D.J.1    Lubitz, S.A.2    Kääb, S.3    Ellinor, P.T.4
  • 35
    • 15944376562 scopus 로고    scopus 로고
    • Strategies for mapping and cloning quantitative trait genes in rodents
    • Flint J., Valdar W., Shifman S., Mott R. Strategies for mapping and cloning quantitative trait genes in rodents. Nat Rev Genet 2005, 6:271-286.
    • (2005) Nat Rev Genet , vol.6 , pp. 271-286
    • Flint, J.1    Valdar, W.2    Shifman, S.3    Mott, R.4
  • 36
    • 77952422980 scopus 로고    scopus 로고
    • Congenic and bioinformatics analyses resolved a major-effect Fob3b QTL on mouse Chr 15 into two closely linked loci
    • Prevoršek Z., Gorjanc G., Paigen B., Horvat S. Congenic and bioinformatics analyses resolved a major-effect Fob3b QTL on mouse Chr 15 into two closely linked loci. Mamm Genome 2010, 21:172-185.
    • (2010) Mamm Genome , vol.21 , pp. 172-185
    • Prevoršek, Z.1    Gorjanc, G.2    Paigen, B.3    Horvat, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.