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SHETE, SANJAY
One or more keywords matched the following items that are connected to SHETE, SANJAY
Item TypeName
Academic Article Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes.
Academic Article Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women
Academic Article Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.
Academic Article Major histocompatibility complex (MHC) class II alleles, haplotypes and epitopes which confer susceptibility or protection in systemic sclerosis: analyses in 1300 Caucasian, African-American and Hispanic cases and 1000 controls.
Academic Article Polymorphisms in TBX21 and STAT4 increase the risk of systemic sclerosis: evidence of possible gene-gene interaction and alterations in Th1/Th2 cytokines.
Academic Article New insights into susceptibility to glioma.
Academic Article Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival.
Academic Article Methylenetetrahydrofolate reductase polymorphisms and risk of squamous cell carcinoma of the head and neck: a case-control analysis.
Academic Article Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222.
Academic Article Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
Academic Article Genome-wide association study identifies five susceptibility loci for glioma.
Academic Article Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations.
Academic Article Association of interleukin 23 receptor polymorphisms with anti-topoisomerase-I positivity and pulmonary hypertension in systemic sclerosis.
Academic Article Genetic advances in glioma: susceptibility genes and networks.
Academic Article Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation.
Academic Article Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers.
Academic Article Investigating multiple candidate genes and nutrients in the folate metabolism pathway to detect genetic and nutritional risk factors for lung cancer.
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 Complex segregation analysis reveals a multigene model for lung cancer.
Academic Article GLIOGENE an International Consortium to Understand Familial Glioma.
Academic Article Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
Academic Article Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium.
Concept Genetic Predisposition to Disease
Academic Article Genetic variations in interleukin-8 and interleukin-10 are associated with pain, depressed mood, and fatigue in lung cancer patients.
Academic Article Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking.
Academic Article Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms.
Academic Article Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer.
Academic Article Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
Academic Article Germline mutations in shelterin complex genes are associated with familial glioma.
Academic Article Improving the power of sib pair quantitative trait loci detection by phenotype winsorization.
Academic Article Molecular epidemiology, cancer-related symptoms, and cytokines pathway.
Academic Article A linkage disequilibrium-based approach to selecting disease-associated rare variants.
Academic Article Modeling age x major gene interaction by a variance component approach.
Academic Article Linkage analysis of affected sib pairs allowing for parent-of-origin effects.
Academic Article Familial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in women.
Academic Article Mixed-effects logistic approach for association following linkage scan for complex disorders.
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 Gene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank report.
Academic Article Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics.
Academic Article Variance components analysis for genetic linkage of time to onset for disease.
Academic Article Adaptations of linkage and association methods for the study of asthma, a complex trait.
Academic Article Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23.
Academic Article A test for genetic association that incorporates information about deviation from Hardy-Weinberg proportions in cases.
Academic Article Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection.
Academic Article Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome.
Academic Article Comprehensive pathway-based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer.
Academic Article Effects of measured susceptibility genes on cancer risk in family studies.
Academic Article Power and type I error results for a bias-correction approach recently shown to provide accurate odds ratios of genetic variants for the secondary phenotypes associated with primary diseases.
Academic Article Mutations in myosin light chain kinase cause familial aortic dissections.
Academic Article MicroRNA target site polymorphisms in the VHL-HIF1a pathway predict renal cell carcinoma risk.
Academic Article Developments in our understanding of the genetic basis of birth defects.
Academic Article Gene network analysis shows immune-signaling and ERK1/2 as novel genetic markers for multiple addiction phenotypes: alcohol, smoking and opioid addiction.
Academic Article Demographic, psychosocial, and genetic risk associated with smokeless tobacco use among Mexican heritage youth.
Academic Article The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium.
Academic Article Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Academic Article Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.
Academic Article MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients.
Academic Article A Robust and Powerful Set-Valued Approach to Rare Variant Association Analyses of Secondary Traits in Case-Control Sequencing Studies.
Academic Article Identifying novel genes and biological processes relevant to the development of cancer therapy-induced mucositis: An informative gene network analysis.
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 Sex-specific gene and pathway modeling of inherited glioma risk.
Academic Article Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer.
Academic Article Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics.
Academic Article Genome-wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk.
Academic Article Transcriptome-wide association study reveals candidate causal genes for lung cancer.
Academic Article Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility.
Academic Article A Genome-Wide Association Study Identifies Two Novel Susceptible Regions for Squamous Cell Carcinoma of the Head and Neck.
Academic Article Association Analysis of Driver Gene-Related Genetic Variants Identified Novel Lung Cancer Susceptibility Loci with 20,871 Lung Cancer Cases and 15,971 Controls.
Academic Article Protein-altering germline mutations implicate novel genes related to lung cancer development.
Academic Article Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma.
Academic Article Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers.
Academic Article Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk.
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 Genetic susceptibility to patient-reported xerostomia among long-term oropharyngeal cancer survivors.
Academic Article A Large-Scale Genome-Wide Gene-Gene Interaction Study of Lung Cancer Susceptibility in Europeans With a Trans-Ethnic Validation in Asians.
Academic Article A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genes.
Academic Article Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.
Academic Article Use of breast surveillance between women with pathogenic variants and variants of uncertain significance in breast cancer susceptibility genes.
Academic Article The genomic landscape of familial glioma.
Academic Article Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.
Academic Article Impact of individual level uncertainty of lung cancer polygenic risk score (PRS) on risk stratification.
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  • Genetic Predisposition to Disease