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Volumn 26, Issue 4, 2004, Pages 294-304

Hierarchical Bayes Model for Random Haplotype and Family Effects in the Transmission of Fragile-X

Author keywords

CGG repeat; Expansion rates; Fragile X dynamic mutation; Haplotype associations; Markov chain Monte Carlo

Indexed keywords

CYTOSINE; FRAGILE X MENTAL RETARDATION PROTEIN; GUANINE;

EID: 2342628456     PISSN: 07410395     EISSN: None     Source Type: Journal    
DOI: 10.1002/gepi.10316     Document Type: Article
Times cited : (1)

References (42)
  • 1
    • 0028843825 scopus 로고
    • Population dynamics of meiotic/mitotic expansion model for the fragile X syndrome
    • Ashley EA, Sherman SL. 1995. Population dynamics of meiotic/mitotic expansion model for the fragile X syndrome. Am J Hum Genet 57:1414-1425.
    • (1995) Am J Hum Genet , vol.57 , pp. 1414-1425
    • Ashley, E.A.1    Sherman, S.L.2
  • 3
    • 0346205399 scopus 로고    scopus 로고
    • Markov chain Monte Carlo method and its application
    • Brooks SP. 1998. Markov chain Monte Carlo method and its application. Statistician 47:69-100.
    • (1998) Statistician , vol.47 , pp. 69-100
    • Brooks, S.P.1
  • 6
    • 0037084852 scopus 로고    scopus 로고
    • Premutation and intermediate-size FMRI alleles in 10,572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles
    • Dombrowski C, Lévesque S, Morel ML, Rouillard P, Morgan K, Rousseau F. 2002. Premutation and intermediate-size FMRI alleles in 10,572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. Hum Mol Genet 11:371-378.
    • (2002) Hum Mol Genet , vol.11 , pp. 371-378
    • Dombrowski, C.1    Lévesque, S.2    Morel, M.L.3    Rouillard, P.4    Morgan, K.5    Rousseau, F.6
  • 8
    • 0029916569 scopus 로고    scopus 로고
    • Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome
    • Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL. 1996. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. Hum Mol Genet 5:319-331.
    • (1996) Hum Mol Genet , vol.5 , pp. 319-331
    • Eichler, E.E.1    Macpherson, J.N.2    Murray, A.3    Jacobs, P.A.4    Chakravarti, A.5    Nelson, D.L.6
  • 11
    • 84972492387 scopus 로고
    • Inference from iterative simulation using multiple sequences
    • Gelman A, Rubin DB. 1992. Inference from iterative simulation using multiple sequences. Stat Sci 7:457-472.
    • (1992) Stat Sci , vol.7 , pp. 457-472
    • Gelman, A.1    Rubin, D.B.2
  • 15
    • 0001966753 scopus 로고    scopus 로고
    • Physical and behavioral phenotype
    • Hagerman RJ, Hagerman PJ, editors. Baltimore: Johns Hopkins University Press
    • Hagerman RJ. 2002. Physical and behavioral phenotype. In: Hagerman RJ, Hagerman PJ, editors. Fragile X syndrome: diagnosis, treatment and research, 3rd ed. Baltimore: Johns Hopkins University Press. p 3-109.
    • (2002) Fragile X Syndrome: Diagnosis, Treatment and Research, 3rd Ed. , pp. 3-109
    • Hagerman, R.J.1
  • 16
    • 0032424069 scopus 로고    scopus 로고
    • A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation
    • Huggins RM, Loesch DZ, Sherman SL. 1998. A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation. Ann Hum Genet 62:337-347.
    • (1998) Ann Hum Genet , vol.62 , pp. 337-347
    • Huggins, R.M.1    Loesch, D.Z.2    Sherman, S.L.3
  • 19
    • 0028802715 scopus 로고
    • Expansion of CGG repeat in fragile X depends on sex of the offspring: Genetic inferences
    • Loesch DZ, Huggins RM, Petrovic V, Slater H. 1995. Expansion of CGG repeat in fragile X depends on sex of the offspring: genetic inferences. Am J Hum Genet 57:1408-1413.
    • (1995) Am J Hum Genet , vol.57 , pp. 1408-1413
    • Loesch, D.Z.1    Huggins, R.M.2    Petrovic, V.3    Slater, H.4
  • 24
    • 0027416537 scopus 로고
    • Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes
    • Oudet C, Mornet E, Serre JL, Thomas F, Lentes-Zengerling S, Kretz C, Deluchat C, Tejadu I, Boue J, Boue A, Mandel JL. 1993. Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes. Am J Hum Genet 52:297-304.
    • (1993) Am J Hum Genet , vol.52 , pp. 297-304
    • Oudet, C.1    Mornet, E.2    Serre, J.L.3    Thomas, F.4    Lentes-Zengerling, S.5    Kretz, C.6    Deluchat, C.7    Tejadu, I.8    Boue, J.9    Boue, A.10    Mandel, J.L.11
  • 31
    • 0029896679 scopus 로고    scopus 로고
    • Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females
    • Sherman SL, Meadows KL, Ashley AE. 1996. Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females. Am J Med Genet 64:256-260.
    • (1996) Am J Med Genet , vol.64 , pp. 256-260
    • Sherman, S.L.1    Meadows, K.L.2    Ashley, A.E.3
  • 32
  • 33
    • 0028074287 scopus 로고
    • Sequence analysis of the fragile X trinucleotide repeat: Implications for the origin of the fragile X mutation
    • Snow K, Tester DJ, Knuckeberg KE, Schaid DJ, Thibodeau SN. 1994. Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation. Hum Mol Genet 3:1543-1551.
    • (1994) Hum Mol Genet , vol.3 , pp. 1543-1551
    • Snow, K.1    Tester, D.J.2    Knuckeberg, K.E.3    Schaid, D.J.4    Thibodeau, S.N.5
  • 36
    • 0003393711 scopus 로고    scopus 로고
    • Release 5.0. College Station, TX: Stata Corp.
    • STATA Statistical Software. 1997. Release 5.0. College Station, TX: Stata Corp.
    • (1997) STATA Statistical Software
  • 37
    • 0036091566 scopus 로고    scopus 로고
    • Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range
    • Sullivan AK, Crawford DC, Scott EH, Leslie ML, Sherman SL. 2002. Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range. Am J Hum Genet 70:1532-1544.
    • (2002) Am J Hum Genet , vol.70 , pp. 1532-1544
    • Sullivan, A.K.1    Crawford, D.C.2    Scott, E.H.3    Leslie, M.L.4    Sherman, S.L.5
  • 38
    • 84942951309 scopus 로고
    • Molecular predictors of involvement of fragile X females
    • Taylor AK, Safanda MZ, Fall C. 1994. Molecular predictors of involvement of fragile X females. J Am Med Assoc 271:507-514.
    • (1994) J Am Med Assoc , vol.271 , pp. 507-514
    • Taylor, A.K.1    Safanda, M.Z.2    Fall, C.3
  • 39
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP, et al. 1991. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65:905-914.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.1    Pieretti, M.2    Sutcliffe, J.S.3    Fu, Y.H.4    Kuhl, D.P.5    Pizzuti, A.6    Reiner, O.7    Richards, S.8    Victoria, M.F.9    Zhang, F.P.10
  • 42
    • 0030008960 scopus 로고    scopus 로고
    • Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes
    • Zhong N, Ju W, Pietrofesa J, Wang D, Dobkin C, Brown WT. 1996. Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes. Am J Med Genet 64:261-265.
    • (1996) Am J Med Genet , vol.64 , pp. 261-265
    • Zhong, N.1    Ju, W.2    Pietrofesa, J.3    Wang, D.4    Dobkin, C.5    Brown, W.T.6


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