메뉴 건너뛰기




Volumn 141, Issue 6, 2006, Pages 643-647

Rh and ABO maternal-fetal incompatibility and risk of autism

Author keywords

Antibodies, log linear model; Autism; Genotype; Immune incompatibility

Indexed keywords

ALLELE; ARTICLE; AUTISM; BLOOD GROUP ABO INCOMPATIBILITY; FEMALE; GENE LOCUS; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RHESUS INCOMPATIBILITY; STATISTICAL MODEL;

EID: 33748948935     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30391     Document Type: Article
Times cited : (10)

References (19)
  • 1
    • 4243175068 scopus 로고
    • Studies of blood group antibodies, V. Fractionation of examples of anti-B, anti-A,B, anti-P, anti-Jka, anti-Lea, anti-D, anti-CD, anti-K, anti-Fya, anti-s and anti-Good
    • Abelson NM, Rawson AJ. 1961. Studies of blood group antibodies, V. Fractionation of examples of anti-B, anti-A,B, anti-P, anti-Jka, anti-Lea, anti-D, anti-CD, anti-K, anti-Fya, anti-s and anti-Good. Transfusion 1:116-123.
    • (1961) Transfusion , vol.1 , pp. 116-123
    • Abelson, N.M.1    Rawson, A.J.2
  • 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
  • 3
    • 1942500225 scopus 로고    scopus 로고
    • Thimerosal and autism? A plausible hypothesis that should not be dismissed
    • Blaxill MF, Redwood L, Bessler M. 2004. Thimerosal and autism? A plausible hypothesis that should not be dismissed. Medical Hypotheses 62:643-845.
    • (2004) Medical Hypotheses , vol.62 , pp. 643-845
    • Blaxill, M.F.1    Redwood, L.2    Bessler, M.3
  • 4
    • 0025860203 scopus 로고
    • Epidemiology of Rh hemolytic disease of the newborn in the United States
    • Chavez GF, Mulinare J, Edmonds LD. 1991. Epidemiology of Rh hemolytic disease of the newborn in the United States. JAMA 265:3270-3274.
    • (1991) JAMA , vol.265 , pp. 3270-3274
    • Chavez, G.F.1    Mulinare, J.2    Edmonds, L.D.3
  • 5
    • 0021906488 scopus 로고
    • Failure of passively administered anti-Rh to prevent secondary Rh responses
    • de Silva M, Contreras M, Mollison PL. 1985. Failure of passively administered anti-Rh to prevent secondary Rh responses. Vox Sang 48:178-180.
    • (1985) Vox Sang , vol.48 , pp. 178-180
    • Silva, M.1    Contreras, M.2    Mollison, P.L.3
  • 6
    • 2342611056 scopus 로고    scopus 로고
    • ABO and Rh(D) phenotype frequencies of different racial/ethnic groups in the United States
    • Garratty G, Glynn SA, McEntire R. 2004. ABO and Rh(D) phenotype frequencies of different racial/ethnic groups in the United States. Transfusion 44:703-706.
    • (2004) Transfusion , vol.44 , pp. 703-706
    • Garratty, G.1    Glynn, S.A.2    McEntire, R.3
  • 7
    • 0033814303 scopus 로고    scopus 로고
    • Bilirubin oxidation in brain
    • Hansen TW. 2000. Bilirubin oxidation in brain. Mol Genet Metab 71:411-417.
    • (2000) Mol Genet Metab , vol.71 , pp. 411-417
    • Hansen, T.W.1
  • 8
    • 0035055544 scopus 로고    scopus 로고
    • The family based association test method: Strategies for studying general genotype-phenotype associations
    • Horvath S, Xu X, Laird NM. 2001. The family based association test method: Strategies for studying general genotype-phenotype associations. Eur J Hum Genet 9:301-306.
    • (2001) Eur J Hum Genet , vol.9 , pp. 301-306
    • Horvath, S.1    Xu, X.2    Laird, N.M.3
  • 9
    • 0035320002 scopus 로고    scopus 로고
    • Prenatal, perinatal, and neonatal factors in autism, pervasive developmental disorder-not otherwise specified, and the general population
    • Juul-Dam N, Townsend J, Courchesne E. 2001. Prenatal, perinatal, and neonatal factors in autism, pervasive developmental disorder-not otherwise specified, and the general population. Pediatrics 107:E63.
    • (2001) Pediatrics , vol.107
    • Juul-Dam, N.1    Townsend, J.2    Courchesne, E.3
  • 13
    • 0038064292 scopus 로고    scopus 로고
    • Heritable and nonheritable risk factors for autism spectrum disorders
    • Newschaffer CJ, Fallin D, Lee NL. 2002. Heritable and nonheritable risk factors for autism spectrum disorders. Epidemiol Rev 24:137-153.
    • (2002) Epidemiol Rev , vol.24 , pp. 137-153
    • Newschaffer, C.J.1    Fallin, D.2    Lee, N.L.3
  • 14
    • 0034888213 scopus 로고    scopus 로고
    • Polymorphism and recombination events at the ABO locus: A major challenge for genomic ABO blood grouping strategies
    • Olsson ML, Chester MA. 2001. Polymorphism and recombination events at the ABO locus: A major challenge for genomic ABO blood grouping strategies. Transfus Med 11:295-313.
    • (2001) Transfus Med , vol.11 , pp. 295-313
    • Olsson, M.L.1    Chester, M.A.2
  • 16
    • 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
  • 18
    • 0034659823 scopus 로고    scopus 로고
    • RHD gene deletion occurred in the Rhesus box
    • Wagner FF, Flegel WA. 2000. RHD gene deletion occurred in the Rhesus box. Blood 95:3662-3668.
    • (2000) Blood , vol.95 , pp. 3662-3668
    • Wagner, F.F.1    Flegel, W.A.2
  • 19
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.