Published in Eur J Hum Genet on April 15, 2009
Mendel: the Swiss army knife of genetic analysis programs. Bioinformatics (2013) 1.85
Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia. Hum Hered (2011) 0.83
Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study. Invest Ophthalmol Vis Sci (2014) 0.80
Sympatric speciation in structureless environments. BMC Evol Biol (2016) 0.75
MENDELIAN PROPORTIONS IN A MIXED POPULATION. Science (1908) 60.99
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet (1974) 23.66
Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics (1992) 21.26
THE HARDY-WEINBERG LAW. Science (1943) 8.77
Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus. Am J Hum Genet (1998) 5.82
Some methods of estimating the inbreeding coefficient. Am J Hum Genet (1953) 5.04
Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet (2002) 4.89
An algorithm for automatic genotype elimination. Am J Hum Genet (1987) 4.18
Rational inferences about departures from Hardy-Weinberg equilibrium. Am J Hum Genet (2005) 4.15
A disequilibrium coefficient approach to Hardy-Weinberg testing. Biometrics (1989) 4.04
Testing heterozygote excess and deficiency. Genetics (1995) 3.80
Independence of VNTR alleles defined as fixed bins. Genetics (1992) 2.73
A comparison of tests for Hardy-Weinberg equilibrium. Biometrics (1980) 2.45
Searching for disease-susceptibility loci by testing for Hardy-Weinberg disequilibrium in a gene bank of affected individuals. Am J Epidemiol (2003) 2.27
Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data. Am J Hum Genet (2002) 2.15
Temporal and microgeographic variation in allozyme frequencies in a natural population of Drosophila buzzatii. Genetics (1986) 1.82
Testing for Hardy-Weinberg equilibrium in samples with related individuals. Genetics (2004) 1.75
The pedigree trimming problem. Hum Hered (2004) 1.00
SNPs and snails and puppy dogs' tails: analysis of SNP haplotype data using the gamete competition model. Ann Hum Genet (2001) 0.93
The variance for the disequilibrium coefficient in the individual Hardy-Weinberg test. Biometrics (1999) 0.91
Hardy-Weinberg testing of a single homozygous genotype. Genetics (2005) 0.86
Hardy-Weinberg analysis of a large set of published association studies reveals genotyping error and a deficit of heterozygotes across multiple loci. Hum Genomics (2008) 0.83
Survival quantitative trait locus fine mapping by measuring and testing for Hardy-Weinberg and linkage disequilibrium. Genetics (2007) 0.80
Fast model-based estimation of ancestry in unrelated individuals. Genome Res (2009) 15.63
Genome-wide association analysis by lasso penalized logistic regression. Bioinformatics (2009) 12.21
Prioritizing GWAS results: A review of statistical methods and recommendations for their application. Am J Hum Genet (2010) 5.39
Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet (2002) 4.89
Epigenetic predictor of age. PLoS One (2011) 3.46
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1). Nat Genet (2004) 2.86
Hierarchical phylogenetic models for analyzing multipartite sequence data. Syst Biol (2003) 2.84
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet (2002) 2.74
Association screening of common and rare genetic variants by penalized regression. Bioinformatics (2010) 2.67
Penalized estimation of haplotype frequencies. Bioinformatics (2008) 2.19
Enhancements to the ADMIXTURE algorithm for individual ancestry estimation. BMC Bioinformatics (2011) 2.16
Association testing with Mendel. Genet Epidemiol (2005) 1.96
Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome. BMC Syst Biol (2008) 1.93
Mendel: the Swiss army knife of genetic analysis programs. Bioinformatics (2013) 1.85
A quasi-Newton acceleration for high-dimensional optimization algorithms. Stat Comput (2011) 1.80
The value of avian genomics to the conservation of wildlife. BMC Genomics (2009) 1.63
Expression quantitative trait loci: replication, tissue- and sex-specificity in mice. Genetics (2010) 1.55
A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet (2002) 1.55
Models for estimating bayes factors with applications to phylogeny and tests of monophyly. Biometrics (2005) 1.53
Investigating the aspartic acid (D) repeat of asporin as a risk factor for osteoarthritis in a UK Caucasian population. Arthritis Rheum (2005) 1.48
Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids. Nat Genet (2008) 1.41
MM Algorithms for Some Discrete Multivariate Distributions. J Comput Graph Stat (2010) 1.36
Site and gender specificity of inheritance of bone mineral density. J Bone Miner Res (2003) 1.30
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. J Med Genet (2013) 1.26
Association testing in a linked region using large pedigrees. Am J Hum Genet (2005) 1.23
Characterizing bias in population genetic inferences from low-coverage sequencing data. Mol Biol Evol (2013) 1.22
Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20. Genet Med (2007) 1.22
Testing a molecular clock without an outgroup: derivations of induced priors on branch-length restrictions in a Bayesian framework. Syst Biol (2003) 1.21
Linkage analysis without defined pedigrees. Genet Epidemiol (2011) 1.20
Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21. Genome Res (2005) 1.20
Stability selection for genome-wide association. Genet Epidemiol (2011) 1.18
Genotype imputation via matrix completion. Genome Res (2012) 1.18
Inflammatory cytokine gene polymorphisms and increased risk of Parkinson disease. Arch Neurol (2007) 1.14
The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans. J Clin Invest (2011) 1.12
Oh brother, where art thou? A Bayes factor test for recombination with uncertain heritage. Syst Biol (2002) 1.11
Graphics Processing Units and High-Dimensional Optimization. Stat Sci (2010) 1.10
Association of the APOLIPOPROTEIN A1/C3/A4/A5 gene cluster with triglyceride levels and LDL particle size in familial combined hyperlipidemia. Circ Res (2004) 1.07
HLA-B maternal-fetal genotype matching increases risk of schizophrenia. Am J Hum Genet (2006) 1.04
RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility. Am J Hum Genet (2002) 1.03
Replication of GWAS associations for GAK and MAPT in Parkinson's disease. Ann Hum Genet (2010) 1.03
Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer. Clin Cancer Res (2009) 1.02
Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples. Circ Cardiovasc Genet (2009) 1.01
Differential destruction of stem cells: implications for targeted cancer stem cell therapy. Cancer Res (2009) 1.01
USF1 contributes to high serum lipid levels in Dutch FCHL families and U.S. whites with coronary artery disease. Arterioscler Thromb Vasc Biol (2007) 1.01
RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. Ann Appl Stat (2010) 1.01
The pedigree trimming problem. Hum Hered (2004) 1.00
Household organophosphorus pesticide use and Parkinson's disease. Int J Epidemiol (2013) 0.98
Genetic variation in immune regulation and DNA repair pathways and stomach cancer in China. Cancer Epidemiol Biomarkers Prev (2009) 0.97
A Path Algorithm for Constrained Estimation. J Comput Graph Stat (2013) 0.97
Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex. PLoS One (2010) 0.96
The v-MFG test: investigating maternal, offspring and maternal-fetal genetic incompatibility effects on disease and viability. Genet Epidemiol (2006) 0.95
A high-throughput method for cloning and sequencing human immunodeficiency virus type 1 integration sites. J Virol (2006) 0.94
A Poisson model for random multigraphs. Bioinformatics (2010) 0.94
Codon and rate variation models in molecular phylogeny. Mol Biol Evol (2002) 0.94
Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study. J Deaf Stud Deaf Educ (2010) 0.93
Single nucleotide polymorphisms of 8 inflammation-related genes and their associations with smoking-related cancers. Int J Cancer (2010) 0.93
CCL3 genotype and current depression increase risk of HIV-associated dementia. Neurobehav HIV Med (2009) 0.93
Modeling maternal-offspring gene-gene interactions: the extended-MFG test. Genet Epidemiol (2010) 0.93
Vocabulon: a dictionary model approach for reconstruction and localization of transcription factor binding sites. Bioinformatics (2004) 0.93
Powerful allele sharing statistics for nonparametric linkage analysis. Hum Hered (2004) 0.91
Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers. Carcinogenesis (2010) 0.90
Allowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects. Hum Hered (2006) 0.90
Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans. Arterioscler Thromb Vasc Biol (2009) 0.90
Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses. Genetics (2011) 0.89
RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order. Eur J Hum Genet (2004) 0.88
Galanin preproprotein is associated with elevated plasma triglycerides. Arterioscler Thromb Vasc Biol (2008) 0.88
Functional paraoxonase 1 variants modify the risk of Parkinson's disease due to organophosphate exposure. Environ Int (2013) 0.88
Functional polymorphisms in dopamine-related genes: effect on neurocognitive functioning in HIV+ adults. J Clin Exp Neuropsychol (2011) 0.88
Using the maternal-fetal genotype incompatibility test to assess non-inherited maternal HLA-DRB1 antigen coding alleles as rheumatoid arthritis risk factors. BMC Proc (2007) 0.88
Merging microsatellite data. J Comput Biol (2006) 0.88
Reconstructing ancestral haplotypes with a dictionary model. J Comput Biol (2006) 0.87
Chromosome 19p13 loci in Finnish migraine with aura families. Am J Med Genet B Neuropsychiatr Genet (2005) 0.86
A dictionary model for haplotyping, genotype calling, and association testing. Genet Epidemiol (2007) 0.86
Mendel-GPU: haplotyping and genotype imputation on graphics processing units. Bioinformatics (2012) 0.86
Expression of the placental transcriptome in maternal nutrient reduction in baboons is dependent on fetal sex. J Nutr (2013) 0.85
Extinction models for cancer stem cell therapy. Math Biosci (2011) 0.85
The longitudinal and interactive effects of HIV status, stimulant use, and host genotype upon neurocognitive functioning. J Neurovirol (2014) 0.85
Pesticides that inhibit the ubiquitin-proteasome system: effect measure modification by genetic variation in SKP1 in Parkinson׳s disease. Environ Res (2013) 0.85
Effects of genome-wide copy number variation on expression in mammalian cells. BMC Genomics (2011) 0.85
Effect of pre-test genetic counseling for deaf adults on knowledge of genetic testing. J Genet Couns (2011) 0.85
Mixed effects models for quantitative trait loci mapping with inbred strains. Genetics (2008) 0.84
Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia. J Lipid Res (2004) 0.84
Sex steroid metabolism polymorphisms and mammographic density in pre- and early perimenopausal women. Breast Cancer Res (2009) 0.84
Directed mammalian gene regulatory networks using expression and comparative genomic hybridization microarray data from radiation hybrids. PLoS Comput Biol (2009) 0.84
The chromosome 11 region from strain 129 provides protection from sex reversal in XYPOS mice. Genetics (2008) 0.84
Bayesian Gaussian Mixture Models for High-Density Genotyping Arrays. J Am Stat Assoc (2008) 0.84
Genetic association analysis of RHOB and TXNDC3 in osteoarthritis. Am J Hum Genet (2007) 0.84
A powerful score test to detect positive selection in genome-wide scans. Eur J Hum Genet (2010) 0.84
Estrogen receptor alpha and matrix metalloproteinase 2 polymorphisms and age-related maculopathy in older women. Am J Epidemiol (2008) 0.84
Reconstructing DNA copy number by joint segmentation of multiple sequences. BMC Bioinformatics (2012) 0.84