Published in Biom J on February 01, 2010
Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation. Biometrics (2011) 1.18
Candidate pathway based analysis for cleft lip with or without cleft palate. Stat Appl Genet Mol Biol (2012) 0.85
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature (2007) 144.95
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science (2008) 20.68
A HapMap harvest of insights into the genetics of common disease. J Clin Invest (2008) 18.31
Schizophrenia: a common disease caused by multiple rare alleles. Br J Psychiatry (2007) 7.00
Bayes factors for genome-wide association studies: comparison with P-values. Genet Epidemiol (2009) 4.33
A Bayesian measure of the probability of false discovery in genetic epidemiology studies. Am J Hum Genet (2007) 4.21
Reporting and interpretation in genome-wide association studies. Int J Epidemiol (2008) 2.73
Model selection based on logistic regression in a highly correlated candidate gene region. BMC Proc (2007) 1.66
Analysis of multiple SNPs in genetic association studies: comparison of three multi-locus methods to prioritize and select SNPs. Genet Epidemiol (2007) 1.21
Loss Function Based Ranking in Two-Stage, Hierarchical Models. Bayesian Anal (2006) 1.21
Empirical Bayes analysis of single nucleotide polymorphisms. BMC Bioinformatics (2008) 1.11
A new score statistic to test for association given linkage in affected sibling pair-control designs. BMC Proc (2007) 0.85
Influence of genotyping error in linkage mapping for complex traits--an analytic study. BMC Genet (2008) 0.83
Sensitive detection of chromosomal segments of distinct ancestry in admixed populations. PLoS Genet (2009) 6.36
Multiple loci associated with indices of renal function and chronic kidney disease. Nat Genet (2009) 4.78
Random-coil behavior and the dimensions of chemically unfolded proteins. Proc Natl Acad Sci U S A (2004) 4.44
Variants of DENND1B associated with asthma in children. N Engl J Med (2009) 4.18
Identifying interacting SNPs using Monte Carlo logic regression. Genet Epidemiol (2005) 4.18
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nat Genet (2011) 3.68
Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet (2012) 3.68
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet (2010) 3.63
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Am J Hum Genet (2009) 3.41
A genome-wide association study on African-ancestry populations for asthma. J Allergy Clin Immunol (2009) 2.53
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am J Hum Genet (2012) 2.53
Imputation methods to improve inference in SNP association studies. Genet Epidemiol (2006) 2.41
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J Am Coll Cardiol (2010) 2.17
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet (2012) 2.15
Nonmelanoma skin cancer and risk for subsequent malignancy. J Natl Cancer Inst (2008) 2.08
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. PLoS Genet (2011) 1.94
Protein folding: defining a "standard" set of experimental conditions and a preliminary kinetic data set of two-state proteins. Protein Sci (2005) 1.91
A multilevel model to address batch effects in copy number estimation using SNP arrays. Biostatistics (2010) 1.76
Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays. Ann Appl Stat (2008) 1.75
Recombination rates in admixed individuals identified by ancestry-based inference. Nat Genet (2011) 1.64
Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart. Genome Biol (2005) 1.64
Contact order and ab initio protein structure prediction. Protein Sci (2002) 1.59
Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan. BMC Bioinformatics (2006) 1.50
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genet Epidemiol (2011) 1.47
Using the R Package crlmm for Genotyping and Copy Number Estimation. J Stat Softw (2011) 1.41
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. Am J Hum Genet (2011) 1.35
The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans. BMC Genet (2011) 1.35
Adaptive evolution of the FADS gene cluster within Africa. PLoS One (2012) 1.34
Site-specific dimensions across a highly denatured protein; a single molecule study. J Mol Biol (2005) 1.25
Single nucleotide polymorphisms in inflammation-related genes and mortality in a community-based cohort in Washington County, Maryland. Am J Epidemiol (2008) 1.25
Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation. Biometrics (2011) 1.18
Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression. Blood (2011) 1.13
Hypothesis-driven candidate gene association studies: practical design and analytical considerations. Am J Epidemiol (2009) 1.12
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry (2012) 1.08
Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio. Hum Mutat (2007) 1.07
On the precision of experimentally determined protein folding rates and phi-values. Protein Sci (2006) 1.06
Two complex genotypes relevant to the kynurenine pathway and melanotropin function show association with schizophrenia and bipolar disorder. Schizophr Res (2009) 1.05
Residues participating in the protein folding nucleus do not exhibit preferential evolutionary conservation. J Mol Biol (2002) 1.02
Evidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate. Hum Genet (2010) 1.01
Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations. Genet Epidemiol (2008) 1.01
Testing SNPs and sets of SNPs for importance in association studies. Biostatistics (2010) 1.01
Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans. Genet Epidemiol (2012) 0.98
Cruciferous vegetable intake and lung cancer risk: a nested case-control study matched on cigarette smoking. Cancer Epidemiol Biomarkers Prev (2010) 0.98
Statistical inference from multiple iTRAQ experiments without using common reference standards. J Proteome Res (2013) 0.97
A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry. J Hum Genet (2011) 0.97
African ancestry is a risk factor for asthma and high total IgE levels in African admixed populations. Genet Epidemiol (2013) 0.97
The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate. Cleft Palate Craniofac J (2011) 0.96
SNPchip: R classes and methods for SNP array data. Bioinformatics (2007) 0.93
Alcohol dehydrogenase genetic polymorphisms, low-to-moderate alcohol consumption, and risk of breast cancer. Alcohol Clin Exp Res (2007) 0.93
Associations of classic Kaposi sarcoma with common variants in genes that modulate host immunity. Cancer Epidemiol Biomarkers Prev (2006) 0.93
African and non-African admixture components in African Americans and an African Caribbean population. Genet Epidemiol (2010) 0.93
A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease. BMC Med Genomics (2010) 0.91
The plasma proteome identifies expected and novel proteins correlated with micronutrient status in undernourished Nepalese children. J Nutr (2013) 0.91
Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study. BMC Med Genet (2009) 0.90
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. Am J Med Genet A (2012) 0.90
Hepcidin and iron status among pregnant women in Bangladesh. Asia Pac J Clin Nutr (2008) 0.89
Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD. Hum Genet (2012) 0.88
A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk. BMC Genet (2014) 0.88
Incorporating genotype uncertainties into the genotypic TDT for main effects and gene-environment interactions. Genet Epidemiol (2012) 0.88
Detection of SNP-SNP interactions in trios of parents with schizophrenic children. Genet Epidemiol (2010) 0.88
Performance assessment of copy number microarray platforms using a spike-in experiment. Bioinformatics (2011) 0.88
Logic regression and its extensions. Adv Genet (2010) 0.87
Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol (2013) 0.87
Fast detection of de novo copy number variants from SNP arrays for case-parent trios. BMC Bioinformatics (2012) 0.86
BMP4 was associated with NSCL/P in an Asian population. PLoS One (2012) 0.86
Haplotype block partitioning as a tool for dimensionality reduction in SNP association studies. BMC Genomics (2008) 0.85
Candidate pathway based analysis for cleft lip with or without cleft palate. Stat Appl Genet Mol Biol (2012) 0.85
Copy number variants of GSTM1 and GSTT1 in relation to lung cancer risk in a prospective cohort study. Ann Epidemiol (2009) 0.85
DNA repair gene variants in relation to overall cancer risk: a population-based study. Carcinogenesis (2012) 0.84
Metabolomic profiling of urine: response to a randomised, controlled feeding study of select fruits and vegetables, and application to an observational study. Br J Nutr (2013) 0.84
Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations. BMC Genet (2014) 0.83
A population-based study of hedgehog pathway gene variants in relation to the dual risk of basal cell carcinoma plus another cancer. Cancer Epidemiol (2012) 0.82
The association between skin characteristics and skin cancer prevention behaviors. Cancer Epidemiol Biomarkers Prev (2009) 0.82
X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts. Eur J Oral Sci (2013) 0.81
A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. J Invest Dermatol (2012) 0.81
Importance measures for epistatic interactions in case-parent trios. Ann Hum Genet (2010) 0.79
R classes and methods for SNP array data. Methods Mol Biol (2010) 0.79
Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. Birth Defects Res A Clin Mol Teratol (2012) 0.78
Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies. Biom J (2014) 0.78
Efficient simulation of epistatic interactions in case-parent trios. Hum Hered (2013) 0.77
ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population. Chin Med J (Engl) (2012) 0.76
A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts. Birth Defects Res A Clin Mol Teratol (2015) 0.76
Cross-platform Comparison of Two Pancreatic Cancer Phenotypes. Cancer Inform (2010) 0.75
Detecting disease variants in case-parent trio studies using the bioconductor software package trio. Genet Epidemiol (2014) 0.75
Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations. Eur J Hum Genet (2013) 0.75