메뉴 건너뛰기




Volumn 32, Issue 6, 2008, Pages 505-512

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations

(19)  Sull, Jae Woong a   Liang, Kung Yee a   Hetmanski, Jacqueline B a   Fallin, Margaret Daniele a   Ingersoll, Roxann G a,b   Park, Jiwan c   Wu Chou, Yah Huei d   Chen, Philip K d   Chong, Samuel S e   Cheah, Felicia e   Yeow, Vincent f   Park, Beyoung Yun g   Jee, Sun Ha a,g   Jabs, Ethylin Wang b,h   Redett, Richard b   Jung, Euiju a   Ruczinski, Ingo a   Scott, Alan F b   Beaty, Terri H a  


Author keywords

Maternal transmission effects; Oral cleft; Parent of origin; RUNX2

Indexed keywords

DNA; TRANSCRIPTION FACTOR RUNX2;

EID: 51749084161     PISSN: 07410395     EISSN: 10982272     Source Type: Journal    
DOI: 10.1002/gepi.20323     Document Type: Article
Times cited : (30)

References (39)
  • 2
    • 13444269543 scopus 로고    scopus 로고
    • Haploview: Analysis and visualization of LD and haplotype maps
    • Barrett JC, Fry B, Maller J, Daly MJ. 2005. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21:263-265.
    • (2005) Bioinformatics , vol.21 , pp. 263-265
    • Barrett, J.C.1    Fry, B.2    Maller, J.3    Daly, M.J.4
  • 6
    • 1642383053 scopus 로고    scopus 로고
    • The complex genetics of cleft lip and palate
    • Cobourne MT. 2004. The complex genetics of cleft lip and palate. Eur J Orthod 26:7-16.
    • (2004) Eur J Orthod , vol.26 , pp. 7-16
    • Cobourne, M.T.1
  • 8
    • 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. 2004. 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 26:167-185.
    • (2004) Genet Epidemiol , vol.26 , pp. 167-185
    • Cordell, H.J.1    Barratt, B.J.2    Clayton, D.G.3
  • 10
    • 0023176710 scopus 로고
    • Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6
    • Eiberg H, Bixler D, Nielsen LS, Conneally PM, Mohr J. 1987. Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6. Clin Genet 32:129-132.
    • (1987) Clin Genet , vol.32 , pp. 129-132
    • Eiberg, H.1    Bixler, D.2    Nielsen, L.S.3    Conneally, P.M.4    Mohr, J.5
  • 13
    • 0038315197 scopus 로고    scopus 로고
    • Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian caseparent triads
    • Jugessur A, Wilcox AJ, Lie RT, Murray JC, Taylor JA, Ulvik A, Drevon CA, Vindenes HA, Abyholm FE. 2003. Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian caseparent triads. Am J Epidemiol 157:1083-1091.
    • (2003) Am J Epidemiol , vol.157 , pp. 1083-1091
    • Jugessur, A.1    Wilcox, A.J.2    Lie, R.T.3    Murray, J.C.4    Taylor, J.A.5    Ulvik, A.6    Drevon, C.A.7    Vindenes, H.A.8    Abyholm, F.E.9
  • 14
    • 33750575433 scopus 로고    scopus 로고
    • Core binding factor beta (CBFB) haploinsufficiency due to an interstitial deletion at 16q21q22 resulting in delayed cranial ossification, cleft palate, congenital heart anomalies, and feeding difficulties but favorable outcome
    • Khan A, Hyde RK, Dutra A, Mohide P, Liu P. 2006. Core binding factor beta (CBFB) haploinsufficiency due to an interstitial deletion at 16q21q22 resulting in delayed cranial ossification, cleft palate, congenital heart anomalies, and feeding difficulties but favorable outcome. Am J Med Genet A 140:2349-2354.
    • (2006) Am J Med Genet A , vol.140 , pp. 2349-2354
    • Khan, A.1    Hyde, R.K.2    Dutra, A.3    Mohide, P.4    Liu, P.5
  • 15
    • 0033814928 scopus 로고    scopus 로고
    • Implementing a unified approach to family-based tests of association
    • Laird NM, Horvath S, Xu X. 2000. Implementing a unified approach to family-based tests of association. Genet Epidemiol 19:S36-S42.
    • (2000) Genet Epidemiol , vol.19
    • Laird, N.M.1    Horvath, S.2    Xu, X.3
  • 16
    • 3242672318 scopus 로고    scopus 로고
    • Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, Ray A, Moreno L, Valencia C, Neiswanger K, Wyszynski DF, Bailey-Wilson JE, Albacha-Hejazi H, Beaty TH, McIntosh I, Hetmanski JB, Tunçbilek G, Edwards M, Harkin L, Scott R, Roddick LG. 2004. Meta-analysis of 13 genome scans reveals multiple cleft lip/ palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet 75:161-173.
    • Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, Ray A, Moreno L, Valencia C, Neiswanger K, Wyszynski DF, Bailey-Wilson JE, Albacha-Hejazi H, Beaty TH, McIntosh I, Hetmanski JB, Tunçbilek G, Edwards M, Harkin L, Scott R, Roddick LG. 2004. Meta-analysis of 13 genome scans reveals multiple cleft lip/ palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet 75:161-173.
  • 18
    • 0031954201 scopus 로고    scopus 로고
    • Prediction of liability to orofacial clefting using genetic and craniofacial data from parents
    • Mossey PA, Arngrimsson, R, McColl J, Vintiner GM, Connor JM. 1998. Prediction of liability to orofacial clefting using genetic and craniofacial data from parents. J Med Genet 35:371-378.
    • (1998) J Med Genet , vol.35 , pp. 371-378
    • Mossey, P.A.1    Arngrimsson, R.2    McColl, J.3    Vintiner, G.M.4    Connor, J.M.5
  • 20
    • 0036275126 scopus 로고    scopus 로고
    • BeadArray™ Technology: Enabling an accurate, cost-efficient approach to high-throughput genotyping
    • Oliphant A, Barker DL, Stuenlpnagel JR, Chee MS. 2002. BeadArray™ Technology: enabling an accurate, cost-efficient approach to high-throughput genotyping. Biotechniques 32:S56-S61.
    • (2002) Biotechniques , vol.32
    • Oliphant, A.1    Barker, D.L.2    Stuenlpnagel, J.R.3    Chee, M.S.4
  • 22
    • 0034054165 scopus 로고    scopus 로고
    • A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
    • Rabinowitz D, Laird N. 2000. A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered 50:211-223.
    • (2000) Hum Hered , vol.50 , pp. 211-223
    • Rabinowitz, D.1    Laird, N.2
  • 24
    • 0037224761 scopus 로고    scopus 로고
    • Detecting genotype combinations that increase risk for disease: Maternal-fetal genotype incompatibility test
    • Sinsheimer JS, Palmer CG, Woodward JA. 2003. Detecting genotype combinations that increase risk for disease: maternal-fetal genotype incompatibility test. Genet Epidemiol 24:1-13.
    • (2003) Genet Epidemiol , vol.24 , pp. 1-13
    • Sinsheimer, J.S.1    Palmer, C.G.2    Woodward, J.A.3
  • 25
    • 0027377799 scopus 로고
    • Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman RS, McGinnis RE, Ewens WJ. 1993. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 52:506-516.
    • (1993) Am J Hum Genet , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 26
    • 17844404045 scopus 로고    scopus 로고
    • Assessing maternal genetic associations: A comparison of the log-linear approach to case-parent triad data and a case-control approach
    • Starr JR, Hsu L, Schwartz SM. 2005. Assessing maternal genetic associations: a comparison of the log-linear approach to case-parent triad data and a case-control approach. Epidemiology 16:294-303.
    • (2005) Epidemiology , vol.16 , pp. 294-303
    • Starr, J.R.1    Hsu, L.2    Schwartz, S.M.3
  • 27
    • 3242782563 scopus 로고    scopus 로고
    • Conservation and expression of an alternative 3′ exon of Runx2 encoding a novel proline-rich C-terminal domain
    • Terry A, Kilbey A, Vaillant F, Stewart M, Jenkins A, Cameron E, Neil JC. 2004. Conservation and expression of an alternative 3′ exon of Runx2 encoding a novel proline-rich C-terminal domain. Gene 336:115-125.
    • (2004) Gene , vol.336 , pp. 115-125
    • Terry, A.1    Kilbey, A.2    Vaillant, F.3    Stewart, M.4    Jenkins, A.5    Cameron, E.6    Neil, J.C.7
  • 28
    • 0034028899 scopus 로고    scopus 로고
    • MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
    • van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK 2000. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet 24:342-343.
    • (2000) Nat Genet , vol.24 , pp. 342-343
    • van den Boogaard, M.J.1    Dorland, M.2    Beemer, F.A.3    van Amstel, H.K.4
  • 29
    • 0033925716 scopus 로고    scopus 로고
    • Testing for linkage disequilibrium, maternal effects, and imprinting with (in)complete case-parent triads, by use of the computer program LEM
    • van Den Cord EJ, Vermunt JK 2000. Testing for linkage disequilibrium, maternal effects, and imprinting with (in)complete case-parent triads, by use of the computer program LEM. Am J Hum Genet 66:335-338.
    • (2000) Am J Hum Genet , vol.66 , pp. 335-338
    • van Den Cord, E.J.1    Vermunt, J.K.2
  • 31
    • 0033362236 scopus 로고    scopus 로고
    • Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
    • Weinberg CR. 1999. Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. Am J Hum Genet 65:229-235.
    • (1999) Am J Hum Genet , vol.65 , pp. 229-235
    • Weinberg, C.R.1
  • 32
    • 25444463596 scopus 로고    scopus 로고
    • A hybrid design for studying genetic influences on risk of diseases with onset early in life
    • Weinberg CR, Umbach DM. 2005. A hybrid design for studying genetic influences on risk of diseases with onset early in life. Am J Hum Genet 77:627-636.
    • (2005) Am J Hum Genet , vol.77 , pp. 627-636
    • Weinberg, C.R.1    Umbach, D.M.2
  • 33
    • 0031949066 scopus 로고    scopus 로고
    • A log-linear approach to case-parent-triad data: Assessing 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. 1998. A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. Am J Hum Genet 62:969-978.
    • (1998) Am J Hum Genet , vol.62 , pp. 969-978
    • Weinberg, C.R.1    Wilcox, A.J.2    Lie, R.T.3
  • 35
    • 0038407464 scopus 로고    scopus 로고
    • What good is genomic imprinting: The function of parent-specific gene expression
    • Wilkins JF, Haig D. 2003. What good is genomic imprinting: the function of parent-specific gene expression. Nat Rev Genet 4:359-368.
    • (2003) Nat Rev Genet , vol.4 , pp. 359-368
    • Wilkins, J.F.1    Haig, D.2
  • 37
    • 0034934804 scopus 로고    scopus 로고
    • Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidecranial dysplasia and cleft lip
    • Yamachika E, Tsujigiwa H, Ishiwari Y, Mizukawa N, Nagai N, Sugahara T. 2001. Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidecranial dysplasia and cleft lip. J Oral Pathol Med 30:381-383.
    • (2001) J Oral Pathol Med , vol.30 , pp. 381-383
    • Yamachika, E.1    Tsujigiwa, H.2    Ishiwari, Y.3    Mizukawa, N.4    Nagai, N.5    Sugahara, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.