Published in Ann Hum Genet on January 01, 1989
PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet (1998) 23.25
A random walk method for computing genetic location scores. Am J Hum Genet (1991) 3.45
Haplotyping the human T-cell receptor beta-chain gene complex by use of restriction fragment length polymorphisms. Proc Natl Acad Sci U S A (1990) 1.38
Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium. Am J Hum Genet (1991) 1.34
Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity. Am J Hum Genet (1993) 1.26
An optimal algorithm for automatic genotype elimination. Am J Hum Genet (1999) 0.95
Fitting mixture distributions to phenylthiocarbamide (PTC) sensitivity. Am J Hum Genet (1991) 0.75
PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet (1998) 23.25
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet (1995) 10.17
Computer programs for multilocus haplotyping of general pedigrees. Am J Hum Genet (1995) 4.51
Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees. Hum Hered (2001) 3.32
True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping. Am J Hum Genet (1997) 3.28
Similarity of DNA fingerprints due to chance and relatedness. Hum Hered (1993) 2.90
Nonparametric simulation-based statistics for detecting linkage in general pedigrees. Am J Hum Genet (1996) 2.57
Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene. Proc Natl Acad Sci U S A (1994) 2.54
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet (1999) 2.38
Genome-wide association scan for childhood caries implicates novel genes. J Dent Res (2011) 2.05
Two-locus models of disease: comparison of likelihood and nonparametric linkage methods. Am J Hum Genet (1993) 1.87
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. Am J Hum Genet (2000) 1.86
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci. Am J Hum Genet (2001) 1.82
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Nat Genet (1993) 1.78
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. Nat Genet (1993) 1.73
Linkage and association between inflammatory bowel disease and a locus on chromosome 12. Am J Hum Genet (1998) 1.64
Detection of tandem duplications and implications for linkage analysis. Am J Hum Genet (1994) 1.60
Invalidity of the Rao map function for three loci. Hum Hered (1994) 1.59
High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12. Am J Hum Genet (2000) 1.52
Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation. Am J Hum Genet (1997) 1.50
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet (1996) 1.47
A genome-wide screen for susceptibility loci in ankylosing spondylitis. Arthritis Rheum (1998) 1.41
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium. Am J Med Genet (1999) 1.31
Influence of the HLA-DRB1 locus on susceptibility and severity in rheumatoid arthritis. QJM (1996) 1.31
A survey of affected-sibship statistics for nonparametric linkage analysis. Am J Hum Genet (2001) 1.30
A primary linkage map of the human chromosome 11q22-23 region. Genomics (1990) 1.25
Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. Hum Mol Genet (1997) 1.24
The complexity of linkage analysis with neural networks. Hum Hered (2001) 1.20
Efficient strategies for genomic searching using the affected-pedigree-member method of linkage analysis. Am J Hum Genet (1994) 1.19
Genome-wide scan for adiposity-related phenotypes in adults from American Samoa. Int J Obes (Lond) (2007) 1.16
Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association. Am J Hum Genet (2001) 1.07
GWAS of dental caries patterns in the permanent dentition. J Dent Res (2012) 1.07
Polymorphisms of the CYP2D6 gene increase susceptibility to ankylosing spondylitis. Hum Mol Genet (2000) 1.05
The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn disease. Am J Hum Genet (2000) 1.01
A comparison of two algorithms, MultiMap and gene mapping system, for automated construction of genetic linkage maps. Genet Epidemiol (1999) 1.00
A whole genome linkage scan identifies multiple chromosomal regions influencing adiposity-related traits among Samoans. Ann Hum Genet (2008) 0.98
Linkage and association studies of the relationship between endometriosis and genes encoding the detoxification enzymes GSTM1, GSTT1 and CYP1A1. Mol Hum Reprod (2001) 0.97
An optimal algorithm for automatic genotype elimination. Am J Hum Genet (1999) 0.95
Linkage methods for identifying genetic risk factors. World Rev Nutr Diet (1990) 0.94
Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome. Ann Neurol (1991) 0.92
Clustering tooth surfaces into biologically informative caries outcomes. J Dent Res (2012) 0.92
Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition. J Dent Res (2013) 0.91
Genetic epidemiology of bilateral breast cancer: a linkage analysis using the affected-pedigree-member method. Genet Epidemiol (1990) 0.89
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter. Am J Hum Genet (1998) 0.88
Mutational mechanisms for generating microsatellite allele-frequency distributions: an analysis of 4,558 markers. Am J Hum Genet (1998) 0.86
Discovery of cancer susceptibility genes: study designs, analytic approaches, and trends in technology. J Natl Cancer Inst Monogr (1999) 0.85
Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region. Am J Hum Genet (1998) 0.84
Parallel computation of genetic likelihoods using CRI-MAP, PVM, and a network of distributed workstations. Hum Hered (1995) 0.84
Human leptin locus (LEP) alleles and BMI in Samoans. Int J Obes Relat Metab Disord (2002) 0.83
Affected sib-pair analysis in endometriosis. Hum Reprod Update (2001) 0.83
Endrin food-poisoning. A report on four outbreaks caused by two separate shipments of endrin-contaminated flour. Bull World Health Organ (1967) 0.83
INSIG2 variants, dietary patterns and metabolic risk in Samoa. Eur J Clin Nutr (2012) 0.83
Comparison of allele-sharing statistics for general pedigrees. Genet Epidemiol (2000) 0.82
Improved programs for the affected-pedigree-member method of linkage analysis. Genet Epidemiol (1994) 0.82
Toward developing a genome-wide microsatellite marker set for linkage analysis in the rhesus macaque (Macaca mulatta): identification of 76 polymorphic markers. Am J Primatol (2001) 0.81
Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries. Caries Res (2014) 0.81
Consanguinity and relative-pair methods for linkage analysis. Am J Hum Genet (1998) 0.80
Use of MRI in genetic studies of endometriosis. Am J Med Genet (1997) 0.80
Interleukin 10 polymorphisms in ankylosing spondylitis. Genes Immun (2003) 0.79
A linkage study across the T cell receptor A and T cell receptor B loci in families with rheumatoid arthritis. Arthritis Rheum (1997) 0.78
Detecting heterogeneity with the affected-pedigree-member (APM) method. Genet Epidemiol (1993) 0.78
Magnetic resonance imaging to assess familial risk in relatives of women with endometriosis. Lancet (1998) 0.78
Association between endometriosis and N-acetyl transferase 2 polymorphisms in a UK population. Mol Hum Reprod (2001) 0.77
Molecular genetic investigations of autism. J Autism Dev Disord (1998) 0.77
An incremental algorithm for efficient multipoint linkage analysis. Hum Hered (1996) 0.77
Absence of a relationship between endometriosis and the N314D polymorphism of galactose-1-phosphate uridyl transferase in a UK population. Mol Hum Reprod (1999) 0.76
A likelihood-based analysis of consistent linkage of a disease locus to two nonsyntenic marker loci: osteogenesis imperfecta versus COL1A1 and COL1A2. Am J Hum Genet (1990) 0.76
Further concerns about the genetics of pre-eclampsia. Am J Hum Genet (1993) 0.75
Ulcerative colitis is more strongly linked to chromosome 12 than Crohn's disease. Gut (2001) 0.75
. . . and linguistic diversity. Nature (1998) 0.75
Pedigree selection and information content. Curr Protoc Hum Genet (2001) 0.75
Analysis of bipolar disorder using affected relatives. Genet Epidemiol (1997) 0.75
Molecular genetic analysis of Lubag. Adv Neurol (1998) 0.75
Genetic linkage studies of ataxia-telangiectasia: phenotypic blood markers. Dis Markers (1987) 0.75
Genetic models for linkage analysis of ataxia-telangiectasia. Princess Takamatsu Symp (1987) 0.75
Comparison of the affected-pedigree-member and lod-score methods. Prog Clin Biol Res (1989) 0.75
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q. Ann Neurol (1995) 0.75
Analysis of a complex oligogenic disease. Genet Epidemiol (1997) 0.75