Published in Genet Epidemiol on January 01, 1989
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The transmission/disequilibrium test: history, subdivision, and admixture. Am J Hum Genet (1995) 24.52
Use of unlinked genetic markers to detect population stratification in association studies. Am J Hum Genet (1999) 23.67
The TDT and other family-based tests for linkage disequilibrium and association. Am J Hum Genet (1996) 11.61
Mapping disease genes: family-based association studies. Am J Hum Genet (1995) 5.82
The role of HLA class II genes in insulin-dependent diabetes mellitus: molecular analysis of 180 Caucasian, multiplex families. Am J Hum Genet (1996) 2.90
Association mapping of disease loci, by use of a pooled DNA genomic screen. Am J Hum Genet (1997) 2.07
Relative predispositional effects (RPEs) of marker alleles with disease: HLA-DR alleles and Graves disease. Am J Hum Genet (1989) 2.03
Genetic analysis of type 1 diabetes using whole genome approaches. Proc Natl Acad Sci U S A (1995) 1.66
Linkage analysis versus association analysis: distinguishing between two models that explain disease-marker associations. Am J Hum Genet (1993) 1.61
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6. Am J Hum Genet (1997) 1.48
Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation chi-square (MASC) method: rejection of the unifying-shared-epitope hypothesis. Am J Hum Genet (1993) 1.07
Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers. Genetics (2003) 0.97
Statistical approaches to gene mapping. Am J Hum Genet (2000) 0.96
Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-chi 2 method. Am J Hum Genet (1995) 0.91
T-cell receptor genes and insulin-dependent diabetes mellitus (IDDM): no evidence for linkage from affected sib pairs. Am J Hum Genet (1990) 0.89
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate. Am J Hum Genet (1994) 0.87
Susceptibility to relapsing-progressive multiple sclerosis is associated with inheritance of genes linked to the variable region of the TcR beta locus: use of affected family-based controls. Am J Hum Genet (1998) 0.82
Involvement of human muscle acetylcholine receptor alpha-subunit gene (CHRNA) in susceptibility to myasthenia gravis. Proc Natl Acad Sci U S A (1994) 0.82
T cell receptor haplotypes in families of patients with insulin-dependent diabetes mellitus. Clin Exp Immunol (1993) 0.79
Linkage disequilibrium in the insulin gene region: size variation at the 5' flanking polymorphism and bimodality among "class I" alleles. Am J Hum Genet (1994) 0.78
The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families. J Med Genet (1992) 0.77
HLA disease associations: models for insulin dependent diabetes mellitus and the study of complex human genetic disorders. Annu Rev Genet (1988) 4.48
The role of HLA class II genes in insulin-dependent diabetes mellitus: molecular analysis of 180 Caucasian, multiplex families. Am J Hum Genet (1996) 2.90
Ancestral Asian source(s) of new world Y-chromosome founder haplotypes. Am J Hum Genet (1999) 2.89
Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus. Am J Hum Genet (1988) 2.88
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Hum Genet (1992) 2.41
Polymorphism, recombination, and linkage disequilibrium within the HLA class II region. J Immunol (1992) 2.39
A multilocus genotyping assay for candidate markers of cardiovascular disease risk. Genome Res (1999) 2.13
Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia. Placenta (2010) 2.09
Association mapping of disease loci, by use of a pooled DNA genomic screen. Am J Hum Genet (1997) 2.07
Relative predispositional effects (RPEs) of marker alleles with disease: HLA-DR alleles and Graves disease. Am J Hum Genet (1989) 2.03
Disequilibrium pattern analysis. I. Theory. Genetics (1987) 1.92
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients. Am J Hum Genet (1995) 1.78
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype? Am J Med Genet (1994) 1.76
HLA-DQ alpha allele and genotype frequencies in various human populations, determined by using enzymatic amplification and oligonucleotide probes. Am J Hum Genet (1990) 1.72
Characterization of recombination in the HLA class II region. Am J Hum Genet (1997) 1.69
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Hum Mol Genet (1995) 1.65
Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects. Am J Hum Genet (1998) 1.57
Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case-control study. Hum Reprod (2002) 1.55
A selective defect of interferon alpha production in human immunodeficiency virus-infected monocytes. J Exp Med (1990) 1.53
HLA DR-DQ associations with cervical carcinoma show papillomavirus-type specificity. Nat Genet (1994) 1.52
HLA class II alleles and susceptibility and resistance to insulin dependent diabetes mellitus in Mexican-American families. Nat Genet (1993) 1.50
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Hum Mol Genet (1993) 1.49
The association of specific HLA class I and II alleles with type 1 diabetes among Filipinos. Tissue Antigens (2002) 1.47
Intrachromosomal triplication of 15q11-q13. J Med Genet (1994) 1.43
Contrasting evolutionary histories among tightly linked HLA loci. Am J Hum Genet (1986) 1.39
Phenotype of maternal UPD(14) Am J Med Genet (1996) 1.38
The dynamics of X-inactivation skewing as women age. Clin Genet (2004) 1.37
HLA class I (A, B, C) and class II (DRB1, DQA1, DQB1, DPB1) alleles and haplotypes in the Han from southern China. Tissue Antigens (2007) 1.32
Association of HLA-DPB1*0301 with IDDM in Mexican-Americans. Diabetes (1996) 1.32
Evaluating DNA methylation and gene expression variability in the human term placenta. Placenta (2010) 1.30
Phenotype of triploid embryos. J Med Genet (2005) 1.27
Constrained disequilibrium values and hitchhiking in a three-locus system. Genetics (1998) 1.27
HLA diversity, differentiation, and haplotype evolution in Mesoamerican Natives. Hum Immunol (2001) 1.27
The causes and consequences of random and non-random X chromosome inactivation in humans. Clin Genet (2000) 1.24
High-resolution HLA class I typing in the CEPH families: analysis of linkage disequilibrium among HLA loci. Tissue Antigens (2000) 1.23
Common and well-documented HLA alleles: 2012 update to the CWD catalogue. Tissue Antigens (2013) 1.22
Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies. Am J Hum Genet (2002) 1.20
Maternal uniparental disomy 22 has no impact on the phenotype. Am J Hum Genet (1994) 1.16
Reduced recombination and paternal age effect in Klinefelter syndrome. Hum Genet (1992) 1.15
Molecular mapping of a recombination hotspot located in the second intron of the human TAP2 locus. Am J Hum Genet (1995) 1.12
Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. Am J Hum Genet (1997) 1.12
A specific HLA-DP beta allele is associated with pauciarticular juvenile rheumatoid arthritis but not adult rheumatoid arthritis. Proc Natl Acad Sci U S A (1989) 1.11
Infection of human gastrointestinal cells by HIV-1. AIDS Res Hum Retroviruses (1990) 1.11
Testing for segregation distortion in the HLA complex. Biometrics (1994) 1.11
Evolution of HLA class II molecules: Allelic and amino acid site variability across populations. Genetics (1999) 1.10
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia. J Med Genet (2005) 1.08
Disequilibrium pattern analysis. II. Application to Danish HLA A and B locus data. Genetics (1987) 1.08
Prenatal and perinatal environmental influences on the human fetal and placental epigenome. Clin Pharmacol Ther (2012) 1.04
Genetic variability and linkage disequilibrium within the HLA-DP region: analysis of 15 different populations. Tissue Antigens (2001) 1.03
Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome. Am J Med Genet (1999) 1.03
A multilocus genotyping assay for cardiovascular disease. Clin Chem Lab Med (1998) 1.01
Influence of host genetics on the severity of coccidioidomycosis. Emerg Infect Dis (1999) 0.99
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications. Hum Mol Genet (1994) 0.97
Genes within the HLA class II region confer both predisposition and resistance to primary biliary cirrhosis. Tissue Antigens (1994) 0.96
Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion. Am J Hum Genet (1999) 0.96
Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss. Hum Reprod (2010) 0.95
Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA data. Genetics (1991) 0.94
A comprehensive search for segregation distortion in HLA. Hum Immunol (1987) 0.94
HLA class II linkage disequilibrium and haplotype evolution in the Cayapa Indians of Ecuador. Am J Hum Genet (1995) 0.93
Major histocompatibility complex class II haplotypes and linkage disequilibrium values observed in the CEPH families. Hum Immunol (1994) 0.93
Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies. Am J Med Genet (2002) 0.93
African-American HLA class II allele and haplotype diversity. Tissue Antigens (1997) 0.92
Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13). Am J Med Genet (2001) 0.91
HLA and IDDM predisposition: new aspects. Genet Epidemiol Suppl (1986) 0.91
Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy. Eur J Hum Genet (1998) 0.91
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line. Am J Med Genet (2000) 0.90
Genetic variability and linkage disequilibrium within the DP region in the CEPH families. Hum Immunol (1997) 0.89
Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters. Am J Med Genet (2001) 0.89
Gene conversion in the evolution of both the H-2 and Qa class I genes of the murine major histocompatibility complex. Genetics (1990) 0.89
Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth. Clin Genet (2013) 0.89
An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features. Clin Dysmorphol (1994) 0.89
Prenatal viral exposure followed by adult stress produces glucose intolerance in a mouse model. Diabetologia (2006) 0.89
Inheritance of insulin-dependent diabetes. Nature (1988) 0.88
Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences. Am J Med Genet (1996) 0.87
Molecular analysis of the role of the HLA class II genes DRB1, DQA1, DQB1, and DPB1 in susceptibility to Lyme arthritis. Hum Immunol (1991) 0.87
Knowing when you don't know enough: children's judgements about ambiguous information. Cognition (1982) 0.86
Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios. Prenat Diagn (1997) 0.86
The extent, mechanism, and consequences of genetic variation, for recombination rate. Am J Hum Genet (1996) 0.86
The association of skewed X chromosome inactivation with aneuploidy in humans. Cytogenet Genome Res (2005) 0.86
Review: A high capacity of the human placenta for genetic and epigenetic variation: implications for assessing pregnancy outcome. Placenta (2011) 0.86
Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus. Eur J Pediatr (1995) 0.86
Exclusively paternal X chromosomes in a girl with short stature. Hum Genet (1993) 0.85
The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders. Clin Genet (2011) 0.85
PCR/oligonucleotide probe typing of HLA class II alleles in a Filipino population reveals an unusual distribution of HLA haplotypes. Am J Hum Genet (1994) 0.85
XIST expression and X-chromosome inactivation in human preimplantation embryos. Am J Hum Genet (1997) 0.84
Multipoint genetic mapping with uniparental disomy data. Am J Hum Genet (2000) 0.84
Autoimmune thyroid disease in type I diabetic families. Genet Epidemiol (1989) 0.84
Multiple origins of X chromosome tetrasomy. J Med Genet (1994) 0.84
Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation. Hum Reprod (2012) 0.83
Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases. Am J Med Genet (1999) 0.83
Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases. Am J Med Genet (1996) 0.83
Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism. J Med Genet (2003) 0.83
Parental origin of the supernumerary chromosome in trisomy 18. Clin Genet (1993) 0.83
Boredom at school. Br J Educ Psychol (1975) 0.82
A selective defect of interferon alpha production in human immunodeficiency virus-infected monocytes. J Exp Med (1991) 0.82
Immunogenetics. Viruses, cancer and the MHC. Nature (1992) 0.82