Item Type | Name |
Academic Article
|
Higher lung cancer risk for younger African-Americans with the Pro/Pro p53 genotype.
|
Academic Article
|
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
|
Academic Article
|
Power of a simplified multivariate test for genetic linkage.
|
Academic Article
|
Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients.
|
Academic Article
|
p53 Genotypes and Haplotypes Associated With Lung Cancer Susceptibility and Ethnicity.
|
Academic Article
|
Genetic susceptibility to lung cancer: the role of DNA damage and repair.
|
Academic Article
|
XPA polymorphism associated with reduced lung cancer risk and a modulating effect on nucleotide excision repair capacity.
|
Academic Article
|
An evolutionary perspective on single-nucleotide polymorphism screening in molecular cancer epidemiology.
|
Academic Article
|
Admixture mapping of lung cancer in 1812 African-Americans.
|
Academic Article
|
Novel genetic variants in the chromosome 5p15.33 region associate with lung cancer risk.
|
Academic Article
|
A case-control study of a sex-specific association between a 15q25 variant and lung cancer risk.
|
Academic Article
|
Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.
|
Academic Article
|
Characterization of BRCA1 and BRCA2 mutations in a large United States sample.
|
Academic Article
|
Validity of models for predicting BRCA1 and BRCA2 mutations.
|
Academic Article
|
Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation.
|
Academic Article
|
Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer.
|
Academic Article
|
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
|
Academic Article
|
Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium.
|
Academic Article
|
An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs.
|
Academic Article
|
Variants in inflammation genes are implicated in risk of lung cancer in never smokers exposed to second-hand smoke.
|
Academic Article
|
Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy.
|
Academic Article
|
Multistage analysis of variants in the inflammation pathway and lung cancer risk in smokers.
|
Academic Article
|
Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma.
|
Academic Article
|
Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.
|
Academic Article
|
Pilot study of CYP2B6 genetic variation to explore the contribution of nitrosamine activation to lung carcinogenesis.
|
Academic Article
|
Deletion in poly(ADP-ribose)polymerase pseudogene and lung cancer risk.
|
Academic Article
|
Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males.
|
Academic Article
|
Dietary intake of isothiocyanates: evidence of a joint effect with glutathione S-transferase polymorphisms in lung cancer risk.
|
Academic Article
|
Association of a p73 exon 2 G4C14-to-A4T14 polymorphism with risk of squamous cell carcinoma of the head and neck.
|
Academic Article
|
Relationship between CYP2A6 and CHRNA5-CHRNA3-CHRNB4 variation and smoking behaviors and lung cancer risk.
|
Academic Article
|
Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans.
|
Concept
|
Genotype
|
Academic Article
|
Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients.
|
Academic Article
|
Characterization of large structural genetic mosaicism in human autosomes.
|
Academic Article
|
Genetic variations in radiation and chemotherapy drug action pathways predict clinical outcomes in esophageal cancer.
|
Academic Article
|
Aurora-A and p16 polymorphisms contribute to an earlier age at diagnosis of pancreatic cancer in Caucasians.
|
Academic Article
|
Genetic variants in the cell cycle control pathways contribute to early onset colorectal cancer in Lynch syndrome.
|
Academic Article
|
A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.
|
Academic Article
|
Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.
|
Academic Article
|
Identification of the NF-?B activating protein-like locus as a risk locus for rheumatoid arthritis.
|
Academic Article
|
Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders.
|
Academic Article
|
Modeling age x major gene interaction by a variance component approach.
|
Academic Article
|
p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population.
|
Academic Article
|
DNMT3b polymorphism and hereditary nonpolyposis colorectal cancer age of onset.
|
Academic Article
|
Forward-time simulations of human populations with complex diseases.
|
Academic Article
|
Interactions between cigarette smoking and selected polymorphisms in xenobiotic metabolizing enzymes in risk for colorectal cancer: A case-only analysis.
|
Academic Article
|
A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.
|
Academic Article
|
Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk.
|
Academic Article
|
A variant in FTO shows association with melanoma risk not due to BMI.
|
Academic Article
|
Variance components analysis for genetic linkage of time to onset for disease.
|
Academic Article
|
ATM polymorphism and hereditary nonpolyposis colorectal cancer (HNPCC) age of onset (United States).
|
Academic Article
|
Genetic variation in genes for the xenobiotic-metabolizing enzymes CYP1A1, EPHX1, GSTM1, GSTT1, and GSTP1 and susceptibility to colorectal cancer in Lynch syndrome.
|
Academic Article
|
Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis.
|
Academic Article
|
Genetic variants of p21 and p27 and pancreatic cancer risk in non-Hispanic Whites: a case-control study.
|
Academic Article
|
Power analysis for case-control association studies of samples with known family histories.
|
Academic Article
|
Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.
|
Academic Article
|
A single-nucleotide polymorphism in tumor suppressor gene SEL1L as a predictive and prognostic marker for pancreatic ductal adenocarcinoma in Caucasians.
|
Academic Article
|
Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers.
|
Academic Article
|
Polymorphisms of nucleotide excision repair genes predict melanoma survival.
|
Academic Article
|
Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.
|
Academic Article
|
A chromosome 15 quantitative trait locus controls levels of radiation-induced jejunal crypt cell apoptosis in mice.
|
Academic Article
|
Cyclin D1 polymorphism and increased risk of colorectal cancer at young age.
|
Academic Article
|
Genotype-phenotype correlations in Peutz-Jeghers syndrome.
|
Academic Article
|
Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
|
Academic Article
|
Twins, tissue, and time: an assessment of SNPs and CNVs.
|
Academic Article
|
GSTM1 polymorphism does not affect hereditary nonpolyposis colorectal cancer age of onset.
|
Academic Article
|
Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene.
|
Academic Article
|
Genetic variants in CYP2R1, CYP24A1, and VDR modify the efficacy of vitamin D3 supplementation for increasing serum 25-hydroxyvitamin D levels in a randomized controlled trial.
|
Academic Article
|
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.
|
Academic Article
|
Genetic variants in Hippo pathway genes YAP1, TEAD1 and TEAD4 are associated with melanoma-specific survival.
|
Academic Article
|
Association of Common Genetic Polymorphisms with Melanoma Patient IL-12p40 Blood Levels, Risk, and Outcomes.
|
Academic Article
|
Functional Variants in Notch Pathway Genes NCOR2, NCSTN, and MAML2 Predict Survival of Patients with Cutaneous Melanoma.
|
Academic Article
|
Genetic Risk Can Be Decreased: Quitting Smoking Decreases and Delays Lung Cancer for Smokers With High and Low CHRNA5 Risk Genotypes - A Meta-Analysis.
|
Academic Article
|
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
|
Academic Article
|
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
|
Academic Article
|
Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.
|
Academic Article
|
Can a susceptibility locus for schizophrenia be excluded from chromosome 5q11-13?
|
Academic Article
|
The probabilistic determination of identity-by-descent sharing for pairs of relatives from pedigrees.
|
Academic Article
|
Estimating the power of linkage analysis in hereditary breast cancer.
|
Academic Article
|
A more powerful robust sib-pair test of linkage for quantitative traits.
|
Academic Article
|
Linkage between the APOB gene and serum ApoB levels in a large pedigree from the Bogalusa Heart Study.
|
Academic Article
|
Genetic contributions to quantitative lipoprotein traits associated with coronary artery disease: analysis of a large pedigree from the Bogalusa Heart Study.
|
Academic Article
|
Genetic variability in the tumor necrosis factor-lymphotoxin region influences susceptibility to rheumatoid arthritis.
|
Academic Article
|
Association and linkage with quantitative traits.
|
Academic Article
|
Familial clustering of rheumatoid arthritis with other autoimmune diseases.
|
Academic Article
|
Testing for linkage under robust genetic models.
|
Academic Article
|
Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families.
|
Academic Article
|
Missense mutations in hMLH1 and hMSH2 are associated with exonic splicing enhancers.
|
Academic Article
|
CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease.
|
Academic Article
|
Functional variants of OCTN cation transporter genes are associated with Crohn disease.
|
Academic Article
|
New joint covariance- and marginal-based tests for association and linkage for quantitative traits for random and non-random sampling.
|
Academic Article
|
A major lung cancer susceptibility locus maps to chromosome 6q23-25.
|
Academic Article
|
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.
|
Academic Article
|
Support for previously identified alcoholism susceptibility Loci in a cohort selected for smoking behavior.
|
Academic Article
|
DLG5 variants contribute to Crohn disease risk in a Canadian population.
|
Academic Article
|
Ascertainment correction for Markov chain Monte Carlo segregation and linkage analysis of a quantitative trait.
|
Academic Article
|
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
|
Academic Article
|
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus.
|
Academic Article
|
Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.
|
Academic Article
|
Design considerations in a sib-pair study of linkage for susceptibility loci in cancer.
|
Academic Article
|
A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.
|
Academic Article
|
The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series.
|
Academic Article
|
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.
|
Academic Article
|
International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants.
|
Academic Article
|
Navigating the road to personalized medicine: can we believe?
|
Academic Article
|
Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases.
|
Academic Article
|
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.
|
Academic Article
|
Genetic association analysis of complex diseases incorporating intermediate phenotype information.
|
Academic Article
|
Genetic variation in SIRT1 affects susceptibility of lung squamous cell carcinomas in former uranium miners from the Colorado plateau.
|
Academic Article
|
Pathway-based analysis of primary biliary cirrhosis genome-wide association studies.
|
Academic Article
|
Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis.
|
Academic Article
|
SNP characteristics predict replication success in association studies.
|
Academic Article
|
Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations.
|
Academic Article
|
15q12 variants, sputum gene promoter hypermethylation, and lung cancer risk: a GWAS in smokers.
|
Academic Article
|
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.
|
Academic Article
|
Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases.
|
Academic Article
|
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
|
Academic Article
|
Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls.
|
Academic Article
|
A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.
|
Academic Article
|
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.
|
Academic Article
|
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
|
Academic Article
|
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
|
Academic Article
|
Genetic Variants in WNT2B and BTRC Predict Melanoma Survival.
|
Academic Article
|
Genetic variants in the integrin signaling pathway genes predict cutaneous melanoma survival.
|
Academic Article
|
A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.
|
Academic Article
|
seXY: a tool for sex inference from genotype arrays.
|
Academic Article
|
Pathway-analysis of published genome-wide association studies of lung cancer: A potential role for the CYP4F3 locus.
|
Academic Article
|
Somatic mutation analysis in melanoma using targeted next generation sequencing.
|
Academic Article
|
Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population.
|
Academic Article
|
Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival.
|
Academic Article
|
Common TDP1 Polymorphisms in Relation to Survival among Small Cell Lung Cancer Patients: A Multicenter Study from the International Lung Cancer Consortium.
|
Academic Article
|
Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer.
|
Academic Article
|
Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival.
|
Academic Article
|
Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.
|
Academic Article
|
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21.
|
Academic Article
|
Novel Common Genetic Susceptibility Loci for Colorectal Cancer.
|
Academic Article
|
Sex-specific gene and pathway modeling of inherited glioma risk.
|
Academic Article
|
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity.
|
Academic Article
|
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
|
Academic Article
|
Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners.
|
Academic Article
|
Genetic variants in the calcium signaling pathway genes are associated with cutaneous melanoma-specific survival.
|
Academic Article
|
Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics.
|
Academic Article
|
Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.
|
Academic Article
|
Functional annotation of melanoma risk loci identifies novel susceptibility genes.
|
Academic Article
|
Genetic variants in the folate metabolic pathway genes predict cutaneous melanoma-specific survival.
|
Academic Article
|
Genetic variants in PDSS1 and SLC16A6 of the ketone body metabolic pathway predict cutaneous melanoma-specific survival.
|
Academic Article
|
Joint modeling of eQTLs and parent-of-origin effects using an orthogonal framework with RNA-seq data.
|
Academic Article
|
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
|
Academic Article
|
Genetic variants in TKT and DERA in the nicotinamide adenine dinucleotide phosphate pathway predict melanoma survival.
|
Academic Article
|
A new efficient method to detect genetic interactions for lung cancer GWAS.
|
Grant
|
Genetic analysis of lung cancer susceptibility
|
Grant
|
Sequencing Familial Lung Cancer
|
Grant
|
Precision approaches to refining TP53-associated cancer risk
|
Academic Article
|
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers.
|
Academic Article
|
False positive findings during genome-wide association studies with imputation: influence of allele frequency and imputation accuracy.
|
Academic Article
|
Gene-gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer.
|
Academic Article
|
Genetic variants in CYP2B6 and HSD17B12 associated with risk of squamous cell carcinoma of the head and neck.
|
Academic Article
|
Admixture Mapping in African Americans Identifies New Risk Loci for HCV-Related Cirrhosis.
|
Academic Article
|
BMI-CNV: a Bayesian framework for multiple genotyping platforms detection of copy number variants.
|
Academic Article
|
Candidate pathway analysis of surfactant proteins identifies CTSH and SFTA2 that influences lung cancer risk.
|