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Volumn 162, Issue 7, 2005, Pages 676-685

Evaluation of offspring and maternal genetic effects on disease risk using a family-based approach: The "pent" design

Author keywords

Alleles; Epidemiologic methods; Genotype; Linkage (genetics); Linkage disequilibrium; Models, genetic; Models, statistical

Indexed keywords

DISEASE;

EID: 26444557985     PISSN: 00029262     EISSN: 14766256     Source Type: Journal    
DOI: 10.1093/aje/kwi249     Document Type: Article
Times cited : (25)

References (27)
  • 1
    • 0028844492 scopus 로고
    • Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
    • van der Put NMJ, Steegers-Theunissen RPM, Frosst P, et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995;346:1070-1.
    • (1995) Lancet , vol.346 , pp. 1070-1071
    • Van Der Put, N.M.J.1    Steegers-Theunissen, R.P.M.2    Frosst, P.3
  • 2
    • 0028803474 scopus 로고
    • A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
    • Whitehead AS, Gallagher P, Mills JL, et al. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. QJM 1995;88:763-6.
    • (1995) QJM , vol.88 , pp. 763-766
    • Whitehead, A.S.1    Gallagher, P.2    Mills, J.L.3
  • 3
    • 0030018760 scopus 로고    scopus 로고
    • 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
    • Ou CY, Stevenson RE, Brown VK, et al. 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 1996;63:610-14.
    • (1996) Am J Med Genet , vol.63 , pp. 610-614
    • Ou, C.Y.1    Stevenson, R.E.2    Brown, V.K.3
  • 4
    • 0029968027 scopus 로고    scopus 로고
    • Is mutated MTHFR a risk factor for neural tube defects?
    • Posey DL, Khoury MJ, Mulinare J, et al. Is mutated MTHFR a risk factor for neural tube defects? Lancet 1996;347:686-9.
    • (1996) Lancet , vol.347 , pp. 686-689
    • Posey, D.L.1    Khoury, M.J.2    Mulinare, J.3
  • 5
    • 0030938599 scopus 로고    scopus 로고
    • Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium
    • Mitchell LE. Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium. Am J Hum Genet 1997;60:1006-7.
    • (1997) Am J Hum Genet , vol.60 , pp. 1006-1007
    • Mitchell, L.E.1
  • 6
    • 0032211487 scopus 로고    scopus 로고
    • Distinguishing the effects of maternal and offspring genes through studies of "case-parent triads"
    • Wilcox AJ, Weinberg CR, Lie RT. Distinguishing the effects of maternal and offspring genes through studies of "case-parent triads." Am J Epidemiol 1998;148:893-901.
    • (1998) Am J Epidemiol , vol.148 , pp. 893-901
    • Wilcox, A.J.1    Weinberg, C.R.2    Lie, R.T.3
  • 7
    • 0031949066 scopus 로고    scopus 로고
    • A log-linear approach to case-parent-triad data: Assessing the effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
    • Weinberg CR, Wilcox AJ, Lie RT. A log-linear approach to case-parent-triad data: assessing the effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. Am J Hum Genet 1998;62:969-78.
    • (1998) Am J Hum Genet , vol.62 , pp. 969-978
    • Weinberg, C.R.1    Wilcox, A.J.2    Lie, R.T.3
  • 8
    • 0037318735 scopus 로고    scopus 로고
    • Studying parents and grandparents to assess genetic contributions to early-onset disease
    • Weinberg CR. Studying parents and grandparents to assess genetic contributions to early-onset disease. Am J Hum Genet 2003;72:438-47.
    • (2003) Am J Hum Genet , vol.72 , pp. 438-447
    • Weinberg, C.R.1
  • 9
    • 1842483890 scopus 로고    scopus 로고
    • Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects
    • Cordell HJ, Barratt BJ, Clayton DG. Case/pseudocontrol analysis in genetic association studies: a unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects. Genet Epidemiol 2004;26:167-85.
    • (2004) Genet Epidemiol , vol.26 , pp. 167-185
    • Cordell, H.J.1    Barratt, B.J.2    Clayton, D.G.3
  • 10
    • 0002629270 scopus 로고
    • Maximum likelihood from incomplete data via the EM algorithm
    • Dempster AP, Laird NM, Rubin DB. Maximum likelihood from incomplete data via the EM algorithm. J R Stat Soc (B) 1977;39:1-28.
    • (1977) J R Stat Soc (B) , vol.39 , pp. 1-28
    • Dempster, A.P.1    Laird, N.M.2    Rubin, D.B.3
  • 11
    • 0004215245 scopus 로고    scopus 로고
    • Cary, NC: SAS Institute, Inc
    • SAS Institute, Inc. SAS computer program, version 8.01. Cary, NC: SAS Institute, Inc, 1999.
    • (1999) SAS Computer Program, Version 8.01
  • 12
    • 0033362166 scopus 로고    scopus 로고
    • Allowing for missing parents in genetic studies of case-parent triads
    • Weinberg CR. Allowing for missing parents in genetic studies of case-parent triads. Am J Hum Genet 1999;64:1186-93.
    • (1999) Am J Hum Genet , vol.64 , pp. 1186-1193
    • Weinberg, C.R.1
  • 13
    • 0036517472 scopus 로고    scopus 로고
    • A comprehensive review of genetic association studies
    • Hirschhorn JN, Lohmueller K, Byrne E, et al. A comprehensive review of genetic association studies. Genet Med 2002;4:45-61.
    • (2002) Genet Med , vol.4 , pp. 45-61
    • Hirschhorn, J.N.1    Lohmueller, K.2    Byrne, E.3
  • 15
    • 0042881041 scopus 로고    scopus 로고
    • Mathematical multi-locus approaches to localizing complex human trait genes
    • Hoh J, Ott J. Mathematical multi-locus approaches to localizing complex human trait genes. Nat Rev Genet 2003;4:701-9.
    • (2003) Nat Rev Genet , vol.4 , pp. 701-709
    • Hoh, J.1    Ott, J.2
  • 16
    • 0345411335 scopus 로고    scopus 로고
    • The ubiquitous nature of epistasis in determining susceptibility to common human diseases
    • Moore JH. The ubiquitous nature of epistasis in determining susceptibility to common human diseases. Hum Hered 2003;56:73-82.
    • (2003) Hum Hered , vol.56 , pp. 73-82
    • Moore, J.H.1
  • 17
    • 0037433052 scopus 로고    scopus 로고
    • Multifactorial dimensionality reduction software for detecting gene-gene and gene-environment interactions
    • Hahn LW, Ritchie MD, Moore JH. Multifactorial dimensionality reduction software for detecting gene-gene and gene-environment interactions. Bioinformatics 2003;19:376-82.
    • (2003) Bioinformatics , vol.19 , pp. 376-382
    • Hahn, L.W.1    Ritchie, M.D.2    Moore, J.H.3
  • 18
    • 0346101571 scopus 로고    scopus 로고
    • Power estimation for multiple SNP association test of case-control study and application
    • Hao K, Xu X, Laird N, et al. Power estimation for multiple SNP association test of case-control study and application. Genet Epidemiol 2004;26:22-30.
    • (2004) Genet Epidemiol , vol.26 , pp. 22-30
    • Hao, K.1    Xu, X.2    Laird, N.3
  • 19
    • 0345689434 scopus 로고    scopus 로고
    • Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers
    • Wille A, Hoh J, Ott J. Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers. Genet Epidemiol 2003;25:350-9.
    • (2003) Genet Epidemiol , vol.25 , pp. 350-359
    • Wille, A.1    Hoh, J.2    Ott, J.3
  • 20
    • 0034190659 scopus 로고    scopus 로고
    • 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A HuGE review
    • Botto LD, Yang Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review. Am J Epidemiol 2000;151:862-77.
    • (2000) Am J Epidemiol , vol.151 , pp. 862-877
    • Botto, L.D.1    Yang, Q.2
  • 21
    • 0003463062 scopus 로고    scopus 로고
    • Hyattsville, MD: National Center for Health Statistics, Centers for Disease Control and Prevention
    • US Department of Health and Human Services. Vital statistics of the United States, 1999: natality. Hyattsville, MD: National Center for Health Statistics, Centers for Disease Control and Prevention, 2001. (http://www.cdc.gov/nchs/datawh/statab/unpubd/natality/natab99.htm).
    • (2001) Vital Statistics of the United States, 1999: Natality
  • 22
    • 0036918343 scopus 로고    scopus 로고
    • RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility
    • Palmer CGS, Turuunen JA, Sinsheimer JS, et al. RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility. Am J Hum Genet 2002;71:1312-19.
    • (2002) Am J Hum Genet , vol.71 , pp. 1312-1319
    • Palmer, C.G.S.1    Turuunen, J.A.2    Sinsheimer, J.S.3
  • 24
    • 3142714601 scopus 로고    scopus 로고
    • Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia
    • Vefring H, Lie RT, Odegard R, et al. Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia. Epidemiology 2004;15:317-22.
    • (2004) Epidemiology , vol.15 , pp. 317-322
    • Vefring, H.1    Lie, R.T.2    Odegard, R.3
  • 25
    • 0842346181 scopus 로고    scopus 로고
    • Lipoprotein concentrations in newborns are associated with allelic variants in their mothers
    • Descamps OS, Bruniaux M, Guilmot PF, et al. Lipoprotein concentrations in newborns are associated with allelic variants in their mothers. Atherosclerosis 2004;172:287-98.
    • (2004) Atherosclerosis , vol.172 , pp. 287-298
    • Descamps, O.S.1    Bruniaux, M.2    Guilmot, P.F.3
  • 26
    • 0036271829 scopus 로고    scopus 로고
    • Oocyte-specific genes regulate follicle formation, fertility and early mouse development
    • Dean J. Oocyte-specific genes regulate follicle formation, fertility and early mouse development. J Reprod Immunol 2002;53:171-80.
    • (2002) J Reprod Immunol , vol.53 , pp. 171-180
    • Dean, J.1
  • 27
    • 0037313184 scopus 로고    scopus 로고
    • Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition
    • Wu X, Viveiros MM, Eppig JJ, et al. Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition. Nat Genetic 2003;33:187-91.
    • (2003) Nat Genetic , vol.33 , pp. 187-191
    • Wu, X.1    Viveiros, M.M.2    Eppig, J.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.