Published in Genet Epidemiol on January 01, 2005
A generalized family-based association test for dichotomous traits. Am J Hum Genet (2009) 1.70
Quantitative trait linkage analysis using Gaussian copulas. Genetics (2006) 1.18
Calculating asymptotic significance levels of the constrained likelihood ratio test with application to multivariate genetic linkage analysis. Stat Appl Genet Mol Biol (2009) 0.99
Robust score statistics for QTL linkage analysis. Am J Hum Genet (2008) 0.90
Identifying variants that contribute to linkage for dichotomous and quantitative traits in extended pedigrees. BMC Proc (2011) 0.75
Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. JAMA (2009) 12.35
The Collaborative Cross, a community resource for the genetic analysis of complex traits. Nat Genet (2004) 9.37
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
A postgenomic method for predicting essential genes at subsaturation levels of mutagenesis: application to Mycobacterium tuberculosis. Proc Natl Acad Sci U S A (2003) 3.70
Ascertainment adjustment in complex diseases. Genet Epidemiol (2002) 3.63
Genetic architecture of complex traits: large phenotypic effects and pervasive epistasis. Proc Natl Acad Sci U S A (2008) 3.56
Genotypic analysis of HIV-1 drug resistance at the limit of detection: virus production without evolution in treated adults with undetectable HIV loads. J Infect Dis (2004) 3.30
Genetic analysis of complex traits in the emerging Collaborative Cross. Genome Res (2011) 3.25
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios. Am J Hum Genet (2005) 3.03
Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. Am J Psychiatry (2007) 2.84
A new standard genetic map for the laboratory mouse. Genetics (2009) 2.78
The recombinational anatomy of a mouse chromosome. PLoS Genet (2008) 2.66
Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy. Invest Ophthalmol Vis Sci (2005) 2.54
BayesMendel: an R environment for Mendelian risk prediction. Stat Appl Genet Mol Biol (2004) 2.34
SNP-specific array-based allele-specific expression analysis. Genome Res (2008) 2.30
Prevalence and correlates of hoarding behavior in a community-based sample. Behav Res Ther (2008) 2.16
Crossover interference underlies sex differences in recombination rates. Trends Genet (2007) 2.04
The identification of OCD-related subgroups based on comorbidity. Biol Psychiatry (2003) 2.00
R/qtl: high-throughput multiple QTL mapping. Bioinformatics (2010) 1.99
Poor performance of bootstrap confidence intervals for the location of a quantitative trait locus. Genetics (2006) 1.99
A model selection approach for the identification of quantitative trait loci in experimental crosses, allowing epistasis. Genetics (2008) 1.91
Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13. Invest Ophthalmol Vis Sci (2006) 1.90
A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32. Invest Ophthalmol Vis Sci (2006) 1.81
Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein. Proc Natl Acad Sci U S A (2005) 1.80
Spectrum of heart disease associated with murine and human GATA4 mutation. J Mol Cell Cardiol (2007) 1.71
Coffee intake and risk of hypertension: the Johns Hopkins precursors study. Arch Intern Med (2002) 1.58
Modifiers of von Willebrand factor identified by natural variation in inbred strains of mice. Blood (2009) 1.58
Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1-q25.3. Am J Ophthalmol (2002) 1.56
Further development of YBOCS dimensions in the OCD Collaborative Genetics study: symptoms vs. categories. Psychiatry Res (2008) 1.54
Cross-reactive T cells are involved in rapid clearance of 2009 pandemic H1N1 influenza virus in nonhuman primates. PLoS Pathog (2011) 1.52
Genetic dissection of a model complex trait using the Drosophila Synthetic Population Resource. Genome Res (2012) 1.51
Empirically derived latent classes of tobacco dependence syndromes observed in recent-onset tobacco smokers: epidemiological evidence from a national probability sample survey. Nicotine Tob Res (2004) 1.47
An SNP-Based Linkage Map for Zebrafish Reveals Sex Determination Loci. G3 (Bethesda) (2011) 1.42
Breed distribution and history of canine mdr1-1Delta, a pharmacogenetic mutation that marks the emergence of breeds from the collie lineage. Proc Natl Acad Sci U S A (2004) 1.41
Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22. Am J Hum Genet (2003) 1.40
Sports ability in young men and the incidence of cardiovascular disease. Am J Med (2002) 1.39
The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. Am J Hum Genet (2003) 1.37
Genome Reshuffling for Advanced Intercross Permutation (GRAIP): simulation and permutation for advanced intercross population analysis. PLoS One (2008) 1.33
Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families. Am J Hum Genet (2004) 1.29
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia. Am J Hum Genet (2009) 1.27
Oral clefts, maternal smoking, and TGFA: a meta-analysis of gene-environment interaction. Cleft Palate Craniofac J (2005) 1.25
Quantitative trait loci x maternal cytoplasmic environment interaction for development rate in Oncorhynchus mykiss. Genetics (2006) 1.23
High-throughput computer vision introduces the time axis to a quantitative trait map of a plant growth response. Genetics (2013) 1.22
Significance thresholds for quantitative trait locus mapping under selective genotyping. Genetics (2007) 1.22
Familiality of factor analysis-derived YBOCS dimensions in OCD-affected sibling pairs from the OCD Collaborative Genetics Study. Biol Psychiatry (2006) 1.22
FMR1 CGG expansions: prevalence and sex ratios. Am J Med Genet B Neuropsychiatr Genet (2013) 1.19
betaA3/A1-crystallin in astroglial cells regulates retinal vascular remodeling during development. Mol Cell Neurosci (2007) 1.18
A randomised placebo-controlled trial of a traditional Chinese herbal formula in the treatment of primary dysmenorrhoea. PLoS One (2007) 1.17
A comprehensive linkage map of the dog genome. Genetics (2009) 1.17
Body mass index and risk of incident hypertension over the life course: the Johns Hopkins Precursors Study. Circulation (2012) 1.17
Quantitative trait linkage analysis by generalized estimating equations: unification of variance components and Haseman-Elston regression. Genet Epidemiol (2004) 1.16
Haplotype probabilities for multiple-strain recombinant inbred lines. Genetics (2006) 1.16
Meiotic recombination in human oocytes. PLoS Genet (2009) 1.15
Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations. Eur J Hum Genet (2009) 1.14
Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval. Genetics (2006) 1.14
Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder. Am J Hum Genet (2004) 1.13
Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease. Hum Mol Genet (2005) 1.13
Mapping expression in randomized rodent genomes. Nat Genet (2005) 1.12
High-resolution quantitative trait locus mapping reveals sign epistasis controlling ovariole number between two Drosophila species. Genetics (2006) 1.12
Multipoint affected sibpair linkage methods for localizing susceptibility genes of complex diseases. Genet Epidemiol (2003) 1.12
Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations. Genetics (2006) 1.11
Systems genetics of susceptibility to obesity-induced diabetes in mice. Physiol Genomics (2011) 1.10
An imprinted locus epistatically influences Nstr1 and Nstr2 to control resistance to nerve sheath tumors in a neurofibromatosis type 1 mouse model. Cancer Res (2006) 1.08
Clinical and molecular characterization of the bladder exstrophy-epispadias complex: analysis of 232 families. BJU Int (2004) 1.08
Psychiatric and psychosocial predictors of substance use disorders among adolescents: longitudinal study. Br J Psychiatry (2007) 1.06
Clinical correlates of recurrent major depression in obsessive-compulsive disorder. Depress Anxiety (2004) 1.05
Variation in genomic recombination rates among heterogeneous stock mice. Genetics (2009) 1.04
SNPs made routine. Nat Methods (2004) 1.04
R/qtlDesign: inbred line cross experimental design. Mamm Genome (2007) 1.03
Extralymphoid CD8+ T cells resident in tissue from simian immunodeficiency virus SIVmac239{Delta}nef-vaccinated macaques suppress SIVmac239 replication ex vivo. J Virol (2010) 1.02
Familiality of novel factorial dimensions of schizophrenia. Arch Gen Psychiatry (2009) 1.02
Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms. Hum Genet (2009) 1.01
Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations. Genet Epidemiol (2008) 1.01
Genetic resistance to diet-induced obesity in chromosome substitution strains of mice. Mamm Genome (2010) 1.00
Particle effects on heart-rate regulation in senescent mice. Inhal Toxicol (2004) 0.99
Characterization of killer immunoglobulin-like receptor genetics and comprehensive genotyping by pyrosequencing in rhesus macaques. BMC Genomics (2011) 0.99
A simple method for combining genetic mapping data from multiple crosses and experimental designs. PLoS One (2007) 0.98
Multiple polymorphic loci determine basal hepatic and splenic iron status in mice. Hepatology (2006) 0.97
Novel autoantigens in autoimmune hypophysitis. Clin Endocrinol (Oxf) (2008) 0.97
Multipoint linkage mapping using sibpairs: non-parametric estimation of trait effects with quantitative covariates. Genet Epidemiol (2005) 0.97
Efficient imputation of missing markers in low-coverage genotyping-by-sequencing data from multiparental crosses. Genetics (2014) 0.96
Patterns of recombination activity on mouse chromosome 11 revealed by high resolution mapping. PLoS One (2010) 0.96
Five latent factors underlying schizophrenia: analysis and relationship to illnesses in relatives. Schizophr Bull (2004) 0.95
Nuclear cataract shows significant familial aggregation in an older population after adjustment for possible shared environmental factors. Invest Ophthalmol Vis Sci (2004) 0.95
Differential MHC class I expression in distinct leukocyte subsets. BMC Immunol (2011) 0.94
Arlm1 is a male-specific modifier of astrocytoma resistance on mouse Chr 12. Neuro Oncol (2012) 0.93
Alcohol consumption and domain-specific cognitive function in older adults: longitudinal data from the Johns Hopkins Precursors Study. J Gerontol B Psychol Sci Soc Sci (2010) 0.93
Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder. Am J Med Genet B Neuropsychiatr Genet (2011) 0.93
Factor analysis of the Yale-Brown Obsessive Compulsive Scale in a family study of obsessive-compulsive disorder. Depress Anxiety (2007) 0.91
A major locus conferring susceptibility to infection by Streptococcus pneumoniae in mice. Mamm Genome (2003) 0.91
Multiple loci contribute to genome-wide recombination levels in male mice. Mamm Genome (2010) 0.90
xQTL workbench: a scalable web environment for multi-level QTL analysis. Bioinformatics (2012) 0.90
Selective genotyping and phenotyping strategies in a complex trait context. Genetics (2009) 0.90
The C. savignyi genetic map and its integration with the reference sequence facilitates insights into chordate genome evolution. Genome Res (2008) 0.89
Incorporation of covariates into multipoint linkage disequilibrium mapping in case-control studies. Genet Epidemiol (2008) 0.88
Detection of SNP-SNP interactions in trios of parents with schizophrenic children. Genet Epidemiol (2010) 0.88
Incorporating covariates into multipoint association mapping in the case-parent design. Hum Hered (2010) 0.88
Acute-phase CD8 T cell responses that select for escape variants are needed to control live attenuated simian immunodeficiency virus. J Virol (2013) 0.87
Sex-specific clinical correlates of hoarding in obsessive-compulsive disorder. Behav Res Ther (2008) 0.87