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Jason H. Moore
Articles in Scholarly Journals [Incomplete List]
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis
Genetic Epidemiology, vol. 32, no. 3, pp. 187–203, 2008
Interleukin-1 gene complex single nucleotide polymorphisms in systemic sclerosis: A further step ahead
Human Immunology, vol. 69, no. 3, pp. 187–192, 2008
DNA Repair Polymorphisms Modify Bladder Cancer Risk: A Multi-factor Analytic Strategy
Human Heredity, vol. 65, no. 2, pp. 105–118, 2008
Acceleration of Cardiovascular Disease by a Dysfunctional Prostacyclin Receptor Mutation: Potential Implications for Cyclooxygenase-2 Inhibition
Circulation Research, vol. 102, no. 8, pp. 986–993, 2008
Symbolic Modeling of Epistasis
Human Heredity, vol. 63, no. 2, pp. 120–133, 2007
Selective repression of retinoic acid target genes by RIP140 during induced tumor cell differentiation of pluripotent human embryonal carcinoma cells
Molecular Cancer, vol. 6, no. 1, p. 57, 2007
Correlation Between Genetic Variations in Hox Clusters and Hirschsprung's Disease
Annals of Human Genetics, vol. 71, no. 4, pp. 526–536, 2007
Gender-specific correlations of plasminogen activator inhibitor-1 and tissue plasminogen activator levels with cardiovascular disease-related traits
Journal of Thrombosis and Haemostasis, vol. 5, no. 2, pp. 313–320, 2007
Characterization of MicroRNA Expression Levels and Their Biological Correlates in Human Cancer Cell Lines
Cancer Research, vol. 67, no. 6, pp. 2456–2468, 2007
Specific Polymorphic Variation in the Mitochondrial Genome and Increased In-Hospital Mortality After Severe Trauma
Annals of Surgery, vol. 246, no. 3, pp. 406–414, 2007
Genomics and proteomics of lung disease: conference summary
AJP: Lung Cellular and Molecular Physiology, vol. 293, no. 1, pp. L45–L51, 2007
Evaporative cooling feature selection for genotypic data involving interactions
Bioinformatics, vol. 23, no. 16, pp. 2113–2120, 2007
Application of HapMap data to the evaluation of 8 candidate genes for pediatric slow transit constipation
Journal of Pediatric Surgery, vol. 42, no. 4, pp. 666–671, 2007
A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction
Genetic Epidemiology, vol. 31, no. 4, pp. 306–315, 2007
Genetic programming neural networks: A powerful bioinformatics tool for human genetics
Applied Soft Computing, vol. 7, no. 1, pp. 471–479, 2007
Renin–angiotensin system gene polymorphisms and coronary artery disease in a large angiographic cohort: Detection of high order gene–gene interaction
Atherosclerosis, vol. 195, no. 1, pp. 172–180, 2007
Epistatic effects of polymorphisms in genes from the renin-angiotensin, bradykinin, and fibrinolytic systems on plasma t-PA and PAI-1 levels
Genomics, vol. 89, no. 3, pp. 362–369, 2007
Identification of a two-loci epistatic interaction associated with susceptibility to rheumatoid arthritis through reverse engineering and multifactor dimensionality reduction
Genomics, vol. 90, no. 1, pp. 6–13, 2007
Bioinformatics
Journal of Cellular Physiology, vol. 213, no. 2, pp. 365–369, 2007
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels
Human Genetics, vol. 121, no. 2, pp. 243–256, 2007
The effects of polymorphisms in genes from the renin–angiotensin, bradykinin, and fibrinolytic systems on plasma t-PA and PAI-1 levels are dependent on environmental context
Human Genetics, vol. 122, no. 3-4, pp. 275–281, 2007
Genomic mining for complex disease traits with “random chemistry”
Genetic Programming and Evolvable Machines, vol. 8, no. 4, pp. 395–411, 2007
A novel method to identify gene–gene effects in nuclear families: the MDR-PDT
Genetic Epidemiology, vol. 30, no. 2, pp. 111–123, 2006
Elevated male European and female African contributions to the genomes of African American individuals
Human Genetics, vol. 120, no. 5, pp. 713–722, 2006
A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility
Journal of Theoretical Biology, vol. 241, no. 2, pp. 252–261, 2006
Cytokine Expression Patterns Associated with Systemic Adverse Events following Smallpox Immunization
The Journal of Infectious Diseases, vol. 194, no. 4, pp. 444–453, 2006
Hybrid grammar-based approach to nonlinear dynamical system identification from biological time series
Physical Review E, vol. 73, no. 2, 2006
The gender-specific role of polymorphisms from the fibrinolytic, renin-angiotensin, and bradykinin systems in determining plasma t-PA and PAI-1 levels
Thrombosis and Haemostasis, 2006
BMC Bioinformatics, vol. 7, no. 1, p. 204, 2006
Transcriptional Profiling in Coronary Artery Disease: Indications for Novel Markers of Coronary Collateralization
Circulation, vol. 114, no. 17, pp. 1811–1820, 2006
Single-Nucleotide Polymorphisms for Diagnosis of Salt-Sensitive Hypertension
Clinical Chemistry, vol. 52, no. 3, pp. 352–360, 2006
Machine Learning for Detecting Gene-Gene Interactions
Applied Bioinformatics, vol. 5, no. 2, pp. 77–88, 2006
BMC Medical Genetics, vol. 7, no. 1, p. 39, 2006
Diabetic Nephropathy Is Associated With Gene Expression Levels of Oxidative Phosphorylation and Related Pathways
Diabetes, vol. 55, no. 6, pp. 1826–1831, 2006
BMC Genomics, vol. 6, no. 1, p. 42, 2005
The Interaction of Four Genes in the Inflammation Pathway Significantly Predicts Prostate Cancer Risk
Cancer Epidemiology Biomarkers & Prevention, vol. 14, no. 11, pp. 2563–2568, 2005
Relative impact of CYP3A genotype and concomitant medication on the severity of atorvastatin-induced muscle damage
Pharmacogenetics and Genomics, vol. 15, no. 6, pp. 415–421, 2005
Concordance of multiple analytical approaches demonstrates a complex relationship between DNA repair gene SNPs, smoking and bladder cancer susceptibility
Carcinogenesis, vol. 27, no. 5, pp. 1030–1037, 2005
A global view of epistasis
Nature Genetics, vol. 37, no. 1, Article ID ng0105-13, 1 pages, 2005
Combinatorial Pharmacogenetics
Nature Reviews Drug Discovery, vol. 4, no. 11, Article ID nrd1874, 7 pages, 2005
Analysis of the RELN gene as a genetic risk factor for autism
Molecular Psychiatry, vol. 10, no. 6, Article ID 4001614, 8 pages, 2005
Connecting the dots between genes, biochemistry, and disease susceptibility: systems biology modeling in human genetics
Molecular Genetics and Metabolism, vol. 84, no. 2, pp. 104–111, 2005
Traversing the conceptual divide between biological and statistical epistasis: systems biology and a more modern synthesis
BioEssays, vol. 27, no. 6, pp. 637–646, 2005
The Challenges of Whole-Genome Approaches to Common Diseases
JAMA: The Journal of the American Medical Association, vol. 291, no. 13, pp. 1642–1643, 2004
The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings?
BioEssays, vol. 26, no. 2, pp. 170–179, 2004
Co-localization of differentially expressed genes and shared susceptibility loci in human autoimmunity
Genetic Epidemiology, vol. 27, no. 2, pp. 162–172, 2004
Multifactor-dimensionality reduction shows a two-locus interaction associated with Type 2 diabetes mellitus
Diabetologia, vol. 47, no. 3, pp. 549–554, 2004
Reporting of model validation procedures in human studies of genetic interactions
Nutrition, vol. 20, no. 1, pp. 69–73, 2004
Genetics, statistics and human disease: analytical retooling for complexity
Trends in Genetics, vol. 20, no. 12, pp. 640–647, 2004
Activation of cryptic 3' splice sites within introns of cellular genes following gene entrapment
Nucleic Acids Research, vol. 32, no. 9, pp. 2912–2924, 2004
Linear dynamic features of ambulatory blood pressure in a population-based study
Blood Pressure Monitoring, vol. 9, no. 5, pp. 259–267, 2004
Routine discovery of complex genetic models using genetic algorithms
Applied Soft Computing, vol. 4, no. 1, pp. 79–86, 2004
A High-Density Admixture Map for Disease Gene Discovery in African Americans
The American Journal of Human Genetics, vol. 74, no. 5, pp. 1001–1013, 2004
Association of Homozygous Wild-Type Glutathione S-Transferase M1 Genotype with Increased Breast Cancer Risk
Cancer Research, vol. 64, no. 4, pp. 1233–1236, 2004
Renin-Angiotensin System Gene Polymorphisms and Atrial Fibrillation
Circulation, vol. 109, no. 13, pp. 1640–1646, 2004
Multilocus Analysis of Hypertension: A Hierarchical Approach
Human Heredity, vol. 57, no. 1, pp. 28–38, 2004
Arthritis Research & Therapy, vol. 6, no. 3, p. 120, 2004
BMC Bioinformatics, vol. 5, no. 1, p. 49, 2004
Computational analysis of gene-gene interactions using multifactor dimensionality reduction
Expert Review of Molecular Diagnostics, vol. 4, no. 6, pp. 795–803, 2004
Integrated analysis of genetic, genomic and proteomic data
Expert Review of Proteomics, vol. 1, no. 1, pp. 67–75, 2004
Gene Expression Profiles in Human Autoimmune Disease
Current Pharmaceutical Design, vol. 9, no. 23, pp. 1905–1917, 2003
BMC Bioinformatics, vol. 4, no. 1, p. 28, 2003
The Ubiquitous Nature of Epistasis in Determining Susceptibility to Common Human Diseases
Human Heredity, vol. 56, no. 1-3, pp. 73–82, 2003
Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions
Bioinformatics, vol. 19, no. 3, pp. 376–382, 2003
Effect of cardiopulmonary bypass on urea cycle intermediates and nitric oxide levels after congenital heart surgery
The Journal of Pediatrics, vol. 142, no. 1, pp. 26–30, 2003
Proteomic patterns of tumour subsets in non-small-cell lung cancer
The Lancet, vol. 362, no. 9382, pp. 433–439, 2003
Petri net modeling of high-order genetic systems using grammatical evolution
Biosystems, vol. 72, no. 1-2, pp. 177–186, 2003
MnSOD polymorphism and breast cancer in a population-based case–control study
Cancer Letters, vol. 199, no. 1, pp. 27–33, 2003
Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity
Genetic Epidemiology, vol. 24, no. 2, pp. 150–157, 2003
Symbolic discriminant analysis of microarray data in autoimmune disease
Genetic Epidemiology, vol. 23, no. 1, pp. 57–69, 2002
New strategies for identifying gene-gene interactions in hypertension
Annals of Medicine, vol. 34, no. 2, pp. 88–95, 2002
The relationship between plasma t-PA and PAI-1 levels is dependent on epistatic effects of the ACE I/D and PAI-1 4G/5G polymorphisms
Clinical Genetics, vol. 62, no. 1, pp. 53–59, 2002
A comparison of combinatorial partitioning and linear regression for the detection of epistatic effects of the ACE I/D and PAI-1 4G/5G polymorphisms on plasma PAI-1 levels
Clinical Genetics, vol. 62, no. 1, pp. 74–79, 2002
ß2-Adrenergic receptor genotype and preterm delivery
American Journal of Obstetrics and Gynecology, vol. 187, no. 5, pp. 1294–1298, 2002
Nature, vol. 409, no. 6820, pp. 565–565, 2001
Multifactor-Dimensionality Reduction Reveals High-Order Interactions among Estrogen-Metabolism Genes in Sporadic Breast Cancer
The American Journal of Human Genetics, vol. 69, no. 1, pp. 138–147, 2001
Improved Power of Sib-Pair Linkage Analysis Using Measures of Complex Trait Dynamics
Human Heredity, vol. 52, no. 2, pp. 113–115, 2001
Effect of time of day on intraindividual variability in ambulatory blood pressure
American Journal of Hypertension, vol. 13, no. 11, pp. 1203–1209, 2000
Predictors of interindividual variation in ambulatory blood pressure and their time or activity dependence
American Journal of Hypertension, vol. 13, no. 1, pp. 52–60, 2000
Detection of linear and nonlinear dependencies in time series using the method of surrogate data in S-PLUS
Computer Methods and Programs in Biomedicine, vol. 63, no. 2, pp. 117–121, 2000
Physics in Medicine and Biology, vol. 44, no. 6, pp. L11–L12, 1999
Artificial intelligence programming with LabVIEW: genetic algorithms for instrumentation control and optimization
Computer Methods and Programs in Biomedicine, vol. 47, no. 1, pp. 73–79, 1995