Published in Hum Hered on January 03, 2006
KELVIN: a software package for rigorous measurement of statistical evidence in human genetics. Hum Hered (2011) 1.23
Fast and accurate calculation of a computationally intensive statistic for mapping disease genes. J Comput Biol (2009) 0.91
Practical considerations for dividing data into subsets prior to PPL analysis. Hum Hered (2008) 0.82
MLIP: using multiple processors to compute the posterior probability of linkage. BMC Bioinformatics (2008) 0.79
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet (2007) 14.05
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet (2012) 2.46
Identification of a schizophrenia-associated functional noncoding variant in NOS1AP. Am J Psychiatry (2009) 1.85
A major susceptibility locus for specific language impairment is located on 13q21. Am J Hum Genet (2002) 1.79
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene. Am J Med Genet B Neuropsychiatr Genet (2005) 1.64
HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity. Am J Hum Genet (2002) 1.51
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet (2011) 1.43
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment. Hum Hered (2004) 1.38
Evaluation of FOXP2 as an autism susceptibility gene. Am J Med Genet (2002) 1.25
The posterior probability of linkage allowing for linkage disequilibrium and a new estimate of disequilibrium between a trait and a marker. Hum Hered (2005) 1.24
Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage. Genet Epidemiol (2007) 1.21
Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7. Am J Med Genet B Neuropsychiatr Genet (2003) 1.20
SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility. J Clin Endocrinol Metab (2013) 1.12
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. J Med Genet (2010) 1.06
A new method for computing the multipoint posterior probability of linkage. Hum Hered (2004) 1.02
The emperor's new methods. Am J Hum Genet (2003) 0.99
Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set. Am J Hum Genet (2005) 0.98
Exploiting gene x gene interaction in linkage analysis. BMC Proc (2007) 0.95
Association statistics under the PPL framework. Genet Epidemiol (2010) 0.95
Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: application to the COGA families. BMC Genet (2005) 0.94
Expected monotonicity--a desirable property for evidence measures? Hum Hered (2010) 0.94
Fast and accurate calculation of a computationally intensive statistic for mapping disease genes. J Comput Biol (2009) 0.91
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc (2007) 0.89
A case of autism and uniparental disomy of chromosome 1. Hum Genet (2005) 0.89
Host-to-host variation of ecological interactions in polymicrobial infections. Phys Biol (2014) 0.88
Employing MCMC under the PPL framework to analyze sequence data in large pedigrees. Front Genet (2013) 0.85
Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky. Genet Epidemiol (2007) 0.82
Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci. J Neurodev Disord (2010) 0.81
Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies. Am J Psychiatry (2014) 0.80
Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis. Proc Natl Acad Sci U S A (2013) 0.80
Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16. Psychiatr Genet (2008) 0.79
MLIP: using multiple processors to compute the posterior probability of linkage. BMC Bioinformatics (2008) 0.79
In silico modeling of Itk activation kinetics in thymocytes suggests competing positive and negative IP4 mediated feedbacks increase robustness. PLoS One (2013) 0.79
Data-driven quantification of the robustness and sensitivity of cell signaling networks. Phys Biol (2013) 0.79
Calculation of multipoint likelihoods using flanking marker data: a simulation study. BMC Genet (2005) 0.77
Ascertainment bias in linkage analysis: comments on Ginsburg et al. Genet Epidemiol (2005) 0.77
Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations. BMC Genet (2005) 0.76
Genome-wide linkage analysis of blood pressure under locus heterogeneity. BMC Genet (2003) 0.76
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes. Hum Genet (2014) 0.75
A model-integrated multipoint Bayesian analysis of hypertension in the Framingham Heart Study data finds little evidence of linkage. BMC Genet (2003) 0.75
Is schizophrenia linked to chromosome 1q? Science (2002) 0.75