Sanjay Shete
#102,431
Most Influential Person Now
American genetic epidemiologist
Sanjay Shete's AcademicInfluence.com Rankings
Sanjay Shetemedical Degrees
Medical
#2485
World Rank
#2912
Historical Rank
#469
USA Rank
Epidemiology
#451
World Rank
#473
Historical Rank
#72
USA Rank
Public Health
#572
World Rank
#591
Historical Rank
#85
USA Rank
Download Badge
Medical
Sanjay Shete's Degrees
- Bachelors Biology University of California, Berkeley
- PhD Genetic Epidemiology Stanford University
Similar Degrees You Can Earn
Why Is Sanjay Shete Influential?
(Suggest an Edit or Addition)According to Wikipedia, Sanjay Shete is a professor in statistical genetic, genetic epidemiology, behavioral genetics and biostatistics at The University of Texas MD Anderson Cancer Center. He is Barnhart Family Distinguished Professor in Targeted Therapies and section chief of behavioral and social statistics in the division of Quantitative Sciences.
Sanjay Shete's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Clinical impact of COVID-19 on patients with cancer (CCC19): a cohort study (2020) (1264)
- Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 (2008) (1262)
- Circulating Tumor Cells in Patients with Breast Cancer Dormancy (2004) (873)
- Genome-wide association study identifies five susceptibility loci for glioma (2009) (781)
- HER-2 gene amplification can be acquired as breast cancer progresses. (2004) (560)
- Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients. (2001) (519)
- Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. (2007) (459)
- Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. (2009) (436)
- Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections (2007) (434)
- A risk model for prediction of lung cancer. (2007) (389)
- Mutations in Transforming Growth Factor-&bgr; Receptor Type II Cause Familial Thoracic Aortic Aneurysms and Dissections (2005) (368)
- Exploring joint effects of genes and the clinical efficacy of morphine for cancer pain: OPRM1 and COMT gene (2007) (296)
- Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes. (2002) (270)
- p53 Genotypes and Haplotypes Associated With Lung Cancer Susceptibility and Ethnicity. (2002) (261)
- Mutations in myosin light chain kinase cause familial aortic dissections. (2010) (261)
- Genome-wide association study of glioma and meta-analysis (2012) (225)
- Familial Thoracic Aortic Aneurysms and Dissections: Genetic Heterogeneity With a Major Locus Mapping to 5q13-14 (2001) (220)
- Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors (2017) (213)
- From genotype to phenotype: correlating XRCC1 polymorphisms with mutagen sensitivity. (2003) (207)
- Ask-Advise-Connect: a new approach to smoking treatment delivery in health care settings. (2013) (193)
- Myozenin 2 Is a Novel Gene for Human Hypertrophic Cardiomyopathy (2007) (187)
- 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 (2009) (173)
- Germline mutations in shelterin complex genes are associated with familial glioma. (2015) (167)
- uPAR and HER-2 gene status in individual breast cancer cells from blood and tissues (2006) (161)
- Chromosome 7p11.2 (EGFR) variation influences glioma risk. (2011) (161)
- Mapping a Locus for Familial Thoracic Aortic Aneurysms and Dissections (TAAD2) to 3p24–25 (2003) (152)
- Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis. (2004) (151)
- Essential hypertension vs. secondary hypertension among children. (2015) (142)
- Depressive symptoms and health-related quality of life in breast cancer survivors. (2012) (141)
- Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations. (2010) (139)
- Genetic variants on 15q25.1, smoking, and lung cancer: an assessment of mediation and interaction. (2012) (137)
- Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival. (2010) (119)
- Adding Further Power to the Haseman and Elston Method for Detecting Linkage in Larger Sibships: Weighting Sums and Differences (2003) (102)
- Molecular epidemiology, cancer-related symptoms, and cytokines pathway. (2008) (101)
- Polymorphisms in TBX21 and STAT4 increase the risk of systemic sclerosis: evidence of possible gene-gene interaction and alterations in Th1/Th2 cytokines. (2009) (94)
- Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome. (2006) (91)
- Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33. (2014) (88)
- GLIOGENE—an International Consortium to Understand Familial Glioma (2007) (88)
- The role of MMP-2 and MMP-9 polymorphisms in sporadic intracranial aneurysms. (2006) (82)
- Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy. (2007) (82)
- Genetic advances in glioma: susceptibility genes and networks. (2010) (82)
- Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. (2012) (81)
- Approaching a Scientific Consensus on the Association between Allergies and Glioma Risk: A Report from the Glioma International Case-Control Study (2016) (78)
- Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (77)
- Mediating effects of smoking and chronic obstructive pulmonary disease on the relation between the CHRNA5‐A3 genetic locus and lung cancer risk (2010) (76)
- The worldwide distribution of the VHL 598C>T mutation indicates a single founding event. (2004) (75)
- Early referral to supportive care specialists for symptom burden in lung cancer patients (2012) (74)
- Genetic linkage and imprinting effects on body mass index in children and young adults (2003) (71)
- Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23. (2005) (71)
- 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 (2011) (70)
- Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women <or=55 years. (2006) (69)
- Cytokine Genes and Pain Severity in Lung Cancer: Exploring the Influence of TNF-α-308 G/A IL6-174G/C and IL8-251T/A (2007) (67)
- Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting. (2002) (65)
- The moderating role of parental smoking on their children's attitudes toward smoking among a predominantly minority sample: a cross-sectional analysis (2008) (64)
- Role of Inflammation Gene Polymorphisms on Pain Severity in Lung Cancer Patients (2009) (63)
- Survival patterns in squamous cell carcinoma of the head and neck: pain as an independent prognostic factor for survival. (2014) (61)
- Health Literacy, Smoking, and Health Indicators in African American Adults (2015) (60)
- Promoter polymorphism (−786t>C) in the endothelial nitric oxide synthase gene is associated with risk of sporadic breast cancer in non‐Hispanic white women age younger than 55 years (2006) (60)
- Association of Interleukin 23 Receptor Polymorphisms with Anti-Topoisomerase-I Positivity and Pulmonary Hypertension in Systemic Sclerosis (2009) (60)
- Genetic variations in interleukin-8 and interleukin-10 are associated with pain, depressed mood, and fatigue in lung cancer patients. (2013) (59)
- Methylenetetrahydrofolate reductase polymorphisms and risk of squamous cell carcinoma of the head and neck: A case‐control analysis (2005) (58)
- X‐Chromosome Genetic Association Test Accounting for X‐Inactivation, Skewed X‐Inactivation, and Escape from X‐Inactivation (2014) (55)
- The Ask-Advise-Connect approach for smokers in a safety net healthcare system: a group-randomized trial. (2013) (53)
- Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222 (2013) (52)
- Neuropathic pain in breast cancer survivors: using the ID pain as a screening tool. (2010) (52)
- Chemotherapy-induced peripheral neuropathy as a predictor of neuropathic pain in breast cancer patients previously treated with paclitaxel. (2009) (52)
- The Influence of Tumor Necrosis Factor-α −308 G/A and IL-6 −174 G/C on Pain and Analgesia Response in Lung Cancer Patients Receiving Supportive Care (2008) (51)
- Deciphering the 8q24.21 association for glioma. (2013) (49)
- Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes (2013) (48)
- The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium. (2015) (48)
- Testing departure from Hardy-Weinberg proportions. (2012) (48)
- Effect of Winsorization on Power and Type 1 Error of Variance Components and Related Methods of QTL Detection (2004) (48)
- Genomic imprinting and linkage test for quantitative-trait Loci in extended pedigrees. (2003) (47)
- Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms (2011) (45)
- Sensation seeking, risk behaviors, and alcohol consumption among Mexican origin youth. (2011) (45)
- Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium. (2011) (44)
- Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes. (2009) (43)
- Exposure to Smoking Imagery in the Movies and Experimenting with Cigarettes among Mexican Heritage Youth (2009) (43)
- Using the weighted area under the net benefit curve for decision curve analysis (2016) (42)
- New insights into susceptibility to glioma. (2010) (42)
- 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 (2018) (41)
- Estimation of odds ratios of genetic variants for the secondary phenotypes associated with primary diseases (2011) (40)
- A test for genetic association that incorporates information about deviation from Hardy-Weinberg proportions in cases. (2008) (40)
- Finding factors influencing risk: Comparing Bayesian stochastic search and standard variable selection methods applied to logistic regression models of cases and controls (2008) (38)
- Inherited variation in immune genes and pathways and glioblastoma risk (2010) (38)
- Complex segregation analysis reveals a multigene model for lung cancer (2004) (37)
- Familial Thoracic Aortic Aneurysms and Dissections: Identification of a Novel Locus for Stable Aneurysms With a Low Risk for Progression to Aortic Dissection (2011) (37)
- Causal relationships between body mass index, smoking and lung cancer: Univariable and multivariable Mendelian randomization (2020) (37)
- Smoking Behaviors in Survivors of Smoking-Related and Non–Smoking-Related Cancers (2020) (37)
- Description of selected characteristics of familial glioma patients - results from the Gliogene Consortium. (2013) (35)
- Systemic hypertension requiring treatment in the neonatal intensive care unit. (2013) (34)
- Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics. (2014) (33)
- Distinct Loci in the CHRNA5/CHRNA3/CHRNB4 Gene Cluster Are Associated With Onset of Regular Smoking (2013) (33)
- History of chickenpox in glioma risk: a report from the glioma international case–control study (GICC) (2016) (32)
- Improving the Power of Sib Pair Quantitative Trait Loci Detection by Phenotype Winsorization (2002) (32)
- Haplotypes of two variants in p16 (CDKN2/MTS-1/INK4a) exon 3 and risk of squamous cell carcinoma of the head and neck: a case-control study. (2002) (31)
- Investigating Multiple Candidate Genes and Nutrients in the Folate Metabolism Pathway to Detect Genetic and Nutritional Risk Factors for Lung Cancer (2013) (31)
- Developments in our understanding of the genetic basis of birth defects. (2015) (30)
- Androgen receptor polymorphisms and risk of biochemical failure among prostatectomy patients (2004) (30)
- Gene network analysis shows immune-signaling and ERK1/2 as novel genetic markers for multiple addiction phenotypes: alcohol, smoking and opioid addiction (2015) (30)
- Randomized Controlled Trial of a Sun Protection Intervention for Children of Melanoma Survivors (2013) (29)
- Recognizing spatial and temporal clustering patterns of dengue outbreaks in Taiwan (2018) (29)
- Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case–control study (2018) (28)
- Method for Evaluating Multiple Mediators: Mediating Effects of Smoking and COPD on the Association between the CHRNA5-A3 Variant and Lung Cancer Risk (2012) (28)
- Influence of subjective social status on the relationship between positive outcome expectations and experimentation with cigarettes. (2009) (27)
- MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients (2016) (27)
- Declining awareness of HPV and HPV vaccine within the general US population (2020) (27)
- Sex-specific gene and pathway modeling of inherited glioma risk (2017) (27)
- Sensation‐seeking genes and physical activity in youth (2013) (26)
- Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li–Fraumeni syndrome (2011) (26)
- Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation (2010) (25)
- Efficacy of Ask Advise Connect in a Safety Net Healthcare System (2013) (25)
- Association Between Vaginal Douching and Genital Human Papillomavirus Infection Among Women in the United States. (2016) (24)
- Identification of Small and Non-Small Cell Lung Cancer Markers in Peripheral Blood Using Cytokinesis-Blocked Micronucleus and Spectral Karyotyping Assays (2017) (24)
- Trends in HPV Vaccination Initiation and Completion Within Ages 9–12 Years: 2008–2018 (2021) (24)
- Disparities in Secondhand Smoke Exposure in the United States (2020) (23)
- Using Both Cases and Controls for Testing Hardy-Weinberg Proportions in a Genetic Association Study (2010) (23)
- MicroRNA target site polymorphisms in the VHL‐HIF1α pathway predict renal cell carcinoma risk (2014) (22)
- Comparison of Haplotype Inference Methods Using Genotypic Data from Unrelated Individuals (2004) (22)
- Effects of population structure on genetic association studies (2005) (22)
- Lack of an association between the angiotensin-converting enzyme insertion/deletion polymorphism and intracranial aneurysms in a Caucasian population in the United States. (2005) (21)
- 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 (2012) (21)
- Assessment of Trends in Cigarette Smoking Cessation After Cancer Diagnosis Among US Adults, 2000 to 2017 (2020) (21)
- Mixed‐effects Logistic Approach for Association Following Linkage Scan for Complex Disorders (2007) (21)
- Targeted Sequencing in Chromosome 17q Linkage Region Identifies Familial Glioma Candidates in the Gliogene Consortium (2015) (20)
- A call for the introduction of gender-neutral HPV vaccination to national immunisation programmes in Africa. (2019) (20)
- Informative gene network for chemotherapy-induced peripheral neuropathy (2015) (20)
- Identifying novel genes and biological processes relevant to the development of cancer therapy-induced mucositis: An informative gene network analysis (2017) (20)
- Identification of circulating tumor cells using 4-color fluorescence in situ hybridization: Validation of a noninvasive aid for ruling out lung cancer in patients with low-dose computed tomography-detected lung nodules. (2020) (19)
- Transcriptome‐wide association study reveals candidate causal genes for lung cancer (2018) (19)
- A Genome-Wide Association Study Identifies Two Novel Susceptible Regions for Squamous Cell Carcinoma of the Head and Neck (2020) (19)
- Effect of Box-Cox Transformation on Power of Haseman-Elston and Maximum-Likelihood Variance Components Tests to Detect Quantitative Trait Loci (2003) (19)
- Examining the effect of linkage disequilibrium on multipoint linkage analysis (2005) (19)
- An RCT with the combination of varenicline and bupropion for smoking cessation: clinical implications for front line use (2018) (18)
- Exposure to Court-Ordered Tobacco Industry Antismoking Advertisements Among US Adults (2019) (18)
- Practical Barriers and Ethical Challenges in Genetic Data Sharing (2014) (18)
- A Variable Age of Onset Segregation Model for Linkage Analysis, with Correction for Ascertainment, Applied to Glioma (2012) (18)
- Oral microbiome and onset of oral mucositis in patients with squamous cell carcinoma of the head and neck (2020) (18)
- The CHRNA3 rs578776 Variant is Associated with an Intrinsic Reward Sensitivity Deficit in Smokers (2013) (18)
- Differences in Breast and Colorectal Cancer Screening Adherence Among Women Residing in Urban and Rural Communities in the United States (2021) (18)
- Protein-altering germline mutations implicate novel genes related to lung cancer development (2020) (17)
- Allergy and glioma risk: Test of association by genotype (2011) (17)
- Correlates of Sun Protection and Sunburn in Children of Melanoma Survivors. (2016) (17)
- Familial thoracic aortic aneurysms and dissections: Three families with early‐onset ascending and descending aortic dissections in women (2006) (17)
- Linkage Analysis of Affected Sib Pairs Allowing for Parent‐of‐Origin Effects (2005) (17)
- Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics (2020) (17)
- Cigarette Experimentation in Mexican Origin Youth: Psychosocial and Genetic Determinants (2011) (17)
- Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer (2014) (17)
- Age‐specific genome‐wide association study in glioblastoma identifies increased proportion of ‘lower grade glioma’‐like features associated with younger age (2018) (17)
- Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility (2019) (16)
- The relationship between body-mass index and overall survival in non-small cell lung cancer by sex, smoking status, and race: A pooled analysis of 20,937 International lung Cancer consortium (ILCCO) patients. (2020) (16)
- Testing Hardy-Weinberg Proportions in a Frequency-Matched Case-Control Genetic Association Study (2011) (15)
- Cohort study of oncologic emergencies in patients with head and neck cancer (2017) (15)
- Positional Identification of Microdeletions with Genetic Markers (2003) (14)
- Familial aggregation of first degree relatives of children with essential hypertension (2018) (14)
- Distinct epidemiological profiles associated with inflammatory breast cancer (IBC): A comprehensive analysis of the IBC registry at The University of Texas MD Anderson Cancer Center (2018) (14)
- Parametric Approach to Genomic Imprinting Analysis with Applications to Angelman’s Syndrome (2005) (14)
- Effects of measured susceptibility genes on cancer risk in family studies (2009) (13)
- Determinants of patient‐reported xerostomia among long‐term oropharyngeal cancer survivors (2021) (13)
- Blood-Based Biomarker Panel for Personalized Lung Cancer Risk Assessment (2022) (13)
- Calculation of exact p-values when SNPs are tested using multiple genetic models (2014) (13)
- A Note on the Optimal Measure of Allelic Association (2003) (13)
- Cancer-Related Risk Perceptions and Beliefs in Texas: Findings from a 2018 Population-Level Survey (2019) (13)
- Comprehensive pathway‐based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer (2012) (13)
- 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 (2011) (12)
- Identifying Modifier Loci in Existing Genome Scan Data (2008) (12)
- Aspirin, NSAIDs, and Glioma Risk: Original Data from the Glioma International Case–Control Study and a Meta-analysis (2018) (12)
- A pilot study to assess tobacco use among sexual minorities in Houston, Texas. (2015) (12)
- Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk. (2010) (12)
- Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers (2021) (12)
- Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer (2018) (12)
- Joint linkage and imprinting analyses of GAW15 rheumatoid arthritis and gene expression data (2007) (12)
- Genetic determinants of immune-related adverse events in patients with melanoma receiving immune checkpoint inhibitors (2021) (11)
- Differences in Sun Protection Behaviors Between Rural and Urban Communities in Texas (2019) (11)
- A Linkage Disequilibrium–Based Approach to Selecting Disease-Associated Rare Variants (2013) (11)
- Testing Departure from Hardy-Weinberg Proportions. (2017) (10)
- Reasons for not receiving the HPV vaccine among eligible adults: Lack of knowledge and of provider recommendations contribute more than safety and insurance concerns (2020) (10)
- The null distribution of stochastic search gene suggestion: a Bayesian approach to gene mapping (2007) (10)
- Analysis of Secondary Phenotype Involving the Interactive Effect of the Secondary Phenotype and Genetic Variants on the Primary Disease (2012) (10)
- Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients (2016) (10)
- Selection of X-chromosome Inactivation Model (2017) (9)
- Genetic Determinants of Lung Cancer Prognosis in Never Smokers: A Pooled Analysis in the International Lung Cancer Consortium (2020) (9)
- Gamma-ray-induced mutagen sensitivity and risk of sporadic breast cancer in young women: a case–control study (2012) (9)
- Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies (2018) (9)
- Beliefs About HPV Vaccine’s Success at Cervical Cancer Prevention Among Adult US Women (2019) (9)
- Gaussian graphical models for phenotypes using pedigree data and exploratory analysis using networks with genetic and nongenetic factors based on Genetic Analysis Workshop 18 data (2014) (9)
- Joint Effects of GermLine p 53 Mutation and Sex on Cancer Risk in Li-Fraumeni Syndrome (2006) (9)
- Individual-specific liability groups in genetic linkage, with applications to kindreds with Li-Fraumeni syndrome. (2002) (9)
- Safety Concerns or Adverse Effects as the Main Reason for Human Papillomavirus Vaccine Refusal (2021) (8)
- Genome‐wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk (2020) (8)
- Statistical Methods for Anomalous Discrete Time Series Based on Minimum Cell Count (2008) (8)
- Detection of disease-associated deletions in case–control studies using SNP genotypes with application to rheumatoid arthritis (2009) (8)
- Demographic, psychosocial, and genetic risk associated with smokeless tobacco use among Mexican heritage youth (2015) (8)
- Partitioned glioma heritability shows subtype-specific enrichment in immune cells. (2021) (8)
- Epidemiology of Childhood Onset Essential Hypertension (2018) (8)
- Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome (2016) (8)
- Uniformly minimum variance unbiased estimation of gene diversity. (2003) (8)
- Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma (2020) (8)
- A Novel Approach to Detect Parent‐of‐Origin Effects from Pedigree Data with Application to Beckwith‐Wiedemann Syndrome (2007) (7)
- A Risk Prediction Model for Smoking Experimentation in Mexican American Youth (2014) (7)
- Imprinting detection by extending a regression-based QTL analysis method (2007) (7)
- Association of dual and poly tobacco use with depressive symptoms and use of antidepressants. (2020) (7)
- Prevalence of and Risk Factors for Oral Human Papillomavirus Infection With Multiple Genotypes in the United States (2017) (7)
- Capitalizing on Admixture in Genome-Wide Association Studies: A Two-Stage Testing Procedure and Application to Height in African-Americans (2011) (7)
- A Large-Scale Genome-Wide Gene-Gene Interaction Study of Lung Cancer Susceptibility in Europeans With a Trans-Ethnic Validation in Asians (2022) (7)
- A Novel Approach to Exploring Potential Interactions among Single-Nucleotide Polymorphisms of Inflammation Genes in Gliomagenesis: An Exploratory Case-Only Study (2011) (7)
- Chronic obstructive pulmonary disease among lung cancer-free smokers: The importance of healthy controls. (2018) (6)
- Characteristics of us adults attempting tobacco use cessation using e-cigarettes. (2020) (6)
- Anamorelin combined with physical activity, and nutritional counseling for cancer-related fatigue: a preliminary study (2021) (6)
- Adding power to Haseman and Elston’s (1972) method (2000) (6)
- Genetic imprinting analysis for alcoholism genes using variance components approach (2005) (6)
- Childhood‐Onset Essential Hypertension and the Family Structure (2016) (6)
- 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 (Annals of the Rheumatic Diseases (2010) 69, (822-827) DOI:10.1136/ard.2 (2011) (6)
- Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer (2022) (6)
- Smoking cessation (SC) and lung cancer (LC) outcomes: A survival benefit for recent-quitters? A pooled analysis of 34,649 International Lung Cancer Consortium (ILCCO) patients. (2020) (6)
- Genetic, psychosocial, and demographic factors associated with social disinhibition in Mexican-origin youth (2014) (6)
- Variance Components Analysis for Genetic Linkage of Time to Onset for Disease (2001) (6)
- Estimation of indirect effect when the mediator is a censored variable (2018) (6)
- Physician‐office vs home uptake of colorectal cancer screening using FOBT/FIT among screening‐eligible US adults (2019) (6)
- Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis. (2013) (5)
- Exact Statistical Tests for Heterogeneity of Frequencies Based on Extreme Values (2010) (5)
- Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study (2019) (5)
- Trends in the rates of health-care providers’ recommendation for HPV vaccine from 2012 to 2018: a multi-round cross-sectional analysis of the health information national trends survey (2021) (5)
- Response to Zang et al. and Han et al. (2009) (5)
- A Robust and Powerful Set-Valued Approach to Rare Variant Association Analyses of Secondary Traits in Case-Control Sequencing Studies (2016) (5)
- A New Approach to Smoking Treatment Delivery in Health Care Settings (2015) (5)
- A powerful hybrid approach to select top single-nucleotide polymorphisms for genome-wide association study (2011) (5)
- Using mobile and sensor technology to identify early dehydration risk in head and neck cancer patients undergoing radiation treatment: Impact on symptoms. (2018) (5)
- Comparison of genome-wide single-nucleotide polymorphism linkage analyses in Caucasian and Hispanic NARAC families (2007) (4)
- Awareness of Heated Tobacco Products among Us Adults – Health Information National Trends Survey, 2020 (2022) (4)
- Corrigendum: Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections (2008) (4)
- Examining lung cancer screening utilization with public-use data: Opportunities and challenges. (2021) (4)
- Modeling Age×Major Gene Interaction by a Variance Component Approach (2001) (4)
- Association of Risk Factors With Patient-Reported Voice and Speech Symptoms Among Long-term Survivors of Oropharyngeal Cancer (2021) (4)
- Real-world patient-reported and clinical outcomes of BNT162b2 mRNA COVID-19 vaccine in patients with cancer. (2021) (4)
- Processing and Analyzing Human Microbiome Data. (2017) (4)
- Empirical estimation of sequencing error rates using smoothing splines (2016) (4)
- Analysis of alcoholism data using support vector machines (2005) (4)
- Genetic variants in CYP2B6 and HSD17B12 associated with risk of squamous cell carcinoma of the head and neck (2022) (3)
- Are beliefs about the importance of genetics for cancer prevention and early detection associated with high risk cancer genetic testing in the U.S. Population? (2022) (3)
- Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (3)
- Prevalence and determinants of cervical cancer screening with a combination of cytology and human papillomavirus testing. (2019) (3)
- Erratum: Mutations in myosin light chain kinase cause familial aortic dissections (American Journal of Human Genetics (2010) 87 (701-707)) (2011) (3)
- Imprinting detection by extending a regression-based QTL analysis method (2007) (3)
- TLINKAGE-IMPRINT: A Model-Based Approach to Performing Two-Locus Genetic Imprinting Analysis (2006) (3)
- Mediation analysis in a case‐control study when the mediator is a censored variable (2018) (3)
- Association of Exposure to Court-Ordered Tobacco Industry Antismoking Advertisements With Intentions and Attempts to Quit Smoking Among US Adults (2020) (3)
- Association Analysis of Driver Gene–Related Genetic Variants Identified Novel Lung Cancer Susceptibility Loci with 20,871 Lung Cancer Cases and 15,971 Controls (2020) (3)
- Effect of dexamethasone on dyspnoea in patients with cancer (ABCD): a parallel-group, double-blind, randomised, controlled trial. (2022) (3)
- Examining Rural–Urban Differences in Fatalism and Information Overload: Data from 12 NCI-Designated Cancer Centers (2022) (3)
- Seeking gene relationships in gene expression data using support vector machine regression (2007) (3)
- Analysis of genes for alcoholism using two-disease-locus models (2005) (3)
- Factors Influencing Discussion of Cancer Genetic Testing with Health-Care Providers in a Population-Based Survey (2021) (3)
- An Approach to Analyze Longitudinal Zero-Inflated Microbiome Count Data Using Two-Stage Mixed Effects Models (2020) (2)
- Active surveillance of chemotherapy-related symptom burden in ambulatory cancer patients via the implementation of electronic patient-reported outcomes and sensor-enabled vital signs capture: protocol for a decentralised feasibility pilot study (2022) (2)
- Prevalence of abnormal cervical cancer screening outcomes among screening-compliant women in the United States. (2019) (2)
- An Open-Source Web App for Creating and Scoring Qualtrics-based Implicit Association Test (2021) (2)
- New Editor and New Directions for Genetic Epidemiology (2012) (2)
- Association of provider HPV vaccination training with provider assessment of HPV vaccination status and recommendation of HPV vaccination (2022) (2)
- Time-varying SMART design and data analysis methods for evaluating adaptive intervention effects (2016) (2)
- Risk factors associated with patient‐reported fatigue among long‐term oropharyngeal carcinoma survivors (2022) (2)
- Genetic Factors associated with Pain Severity, Daily Opioid Dose Requirement, and Pain Response among Advanced Cancer Patients receiving Supportive Care. (2021) (2)
- Evaluating Methods for Modeling Epistasis Networks with Application to Head and Neck Cancer (2015) (2)
- False-Negative-Rate Based Approach for Selecting Top Single-Nucleotide Polymorphisms in the First Stage of a Two-Stage Genome-Wide Association Study. (2011) (2)
- Genetic determinants of adverse events in cancer patients receiving immune checkpoint inhibitors. (2019) (2)
- Sex-specific genome-wide association study in glioma identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21 (2017) (2)
- Small sample properties of rare variant analysis methods (2014) (2)
- Adaptations of Linkage and Association Methods for the Study of Asthma, A Complex Trait (2001) (2)
- Healthcare Provider Recommendations and Observed Changes in HPV Vaccination Acceptance during the COVID-19 Pandemic (2022) (2)
- Genetic susceptibility to patient-reported xerostomia among long-term oropharyngeal cancer survivors (2022) (2)
- HPV Vaccination Training of Healthcare Providers and Perceived Self-Efficacy in HPV Vaccine-Hesitancy Counseling (2022) (2)
- An approach to estimate bidirectional mediation effects with application to body mass index and fasting glucose (2018) (2)
- Development, Implementation, and Evaluation of a Distance Learning and Telementoring Program for Cervical Cancer Prevention in Cameroon (2022) (2)
- The influence of parent–child gender on intentions to refuse HPV vaccination due to safety concerns/side effects, National Immunization Survey – Teen, 2010–2019 (2022) (2)
- Accurate detection of circulating tumor cells (CTCs) in patients with metastatic papillary thyroid cancer (MPTC) via an interphase fluorescence in situ hybridization (IFISH) assay. (2016) (2)
- Correction: Association of Interleukin 23 Receptor Polymorphisms with Anti-topoisomerase-I Positivity and Pulmonary Hypertension in Systemic Sclerosis (2010) (2)
- Cross-sectional survey for assessing cancer care providers’ characteristics and attitudes on smoking cessation in Colombia and Mexico (2021) (1)
- Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility (2020) (1)
- ABSTRACTS 32nd Annual Meeting • American Society of Preventive Oncology, Bethesda, Maryland • March 16-18, 2008 (2008) (1)
- Healthcare Provider’s Perceived Self-Efficacy in HPV Vaccination Hesitancy Counseling and HPV Vaccination Acceptance (2023) (1)
- Genetic, Psychological, and Personal Network Factors Associated With Changes in Binge Drinking Over 2 Years Among Mexican Heritage Adolescents in the USA. (2019) (1)
- Association of hearing loss and tinnitus symptoms with health‐related quality of life among long‐term oropharyngeal cancer survivors (2022) (1)
- Advances in Statistical Bioinformatics: Bayesian Model Averaging for Genetic Association Studies (2013) (1)
- Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk (2021) (1)
- Erratum to: Survey of familial glioma and role of germline p16/p14 and p53 mutation (2010) (1)
- ATOPIC CONDITIONS, ANTIHISTAMINE USE, AND GLIOMA RISK : PRELIMINARY RESULTS FROM THE GLIOMA INTERNATIONAL CASE-CONTROL STUDY (2013) (1)
- Clinical Characteristics and Cause of Death Among Hospitalized Decedents With Cancer and COVID-19 (2022) (1)
- 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 (2018) (1)
- Mediation model with a categorical exposure and a censored mediator with application to a genetic study (2021) (1)
- Inflammation genes and pain severity in lung cancer patients. (2009) (1)
- Differentiating anomalous disease intensity with confounding variables in space (2020) (1)
- Short-form adaptive measure of financial toxicity from the Economic Strain and Resilience in Cancer (ENRICh) study: Derivation using modern psychometric techniques (2022) (1)
- Approaching a Scienti fi c Consensus on the Association between Allergies and Glioma Risk : A Report from the Glioma International Case-Control Study (2016) (1)
- Erratum: Familial thoracic aortic aneurysms and dissections: Three families with early-onset ascending and descending aortic dissections in women (American Journal of Medical Genetics DOI: 10.1002/ajmg.a.31236) (2006) (1)
- Calculation of exact p-values when SNPs are tested using multiple genetic models (2014) (1)
- Aspirin, Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), and Glioma Risk: Original Data from the Glioma International Case-Control Study and a Meta-Analysis (2018) (1)
- Cigarette Experimentation and the Population Attributable Fraction for Associated Genetic and Non-Genetic Risk Factors (2013) (1)
- Iam hiQ—a novel pair of accuracy indices for imputed genotypes (2022) (1)
- Comparing smoking behavior between female-to-male and male-to-female transgender adults (2020) (1)
- HPV Vaccination Uptake, Hesitancy, and Refusal: Observations of Health-Care Professionals During the COVID-19 Pandemic (2022) (1)
- Comparison of multilevel modeling and the family-based association test for identifying genetic variants associated with systolic and diastolic blood pressure using Genetic Analysis Workshop 18 simulated data (2014) (1)
- Financial Toxicities Persist for Cancer Survivors Irrespective of Current Cancer Status: An Analysis of Medical Expenditure Panel Survey (2022) (1)
- Abstract LB-424: A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility to bladder cancer (2011) (1)
- A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genes (2022) (1)
- The C598T VHL mutation arose in an ancestor common to Asian and Caucasian populations (2004) (0)
- Abstract 3446: Aspirin, non-steroidal anti-inflammatory drugs (NSAIDs) and the risk of glioma: Results from the Glioma International Case Control Study (2016) (0)
- Risk Factors of Patient-Reported Xerostomia Among Oropharyngeal Cancer Survivors Treated with Definitive Radiotherapy. (2021) (0)
- Abstract 716: Trends in Medicare reimbursements within the first year of cervical cancer diagnosis, 2007-2015 (2023) (0)
- Abstract B21: Depression and quality of life in breast cancer survivors: 6–13 years postchemotherapy (2010) (0)
- Immune-related adverse events and symptom burden in patients with melanoma receiving adjuvant immune checkpoint inhibitor. (2022) (0)
- Abstract 1140: Declining awareness of HPV and HPV vaccination within the general US population (2020) (0)
- Statistical Methods for Analyzing X-Chromosome Data (2015) (0)
- THE FREQUENCY OF THE RS55705857 RISK ALLELE IS ELEVATED AND SIMILAR IN FAMILIAL AND SPORADIC GLIOMA PATIENTS (2013) (0)
- Precision Medicine and Associated Challenges (2018) (0)
- Use of breast surveillance between women with pathogenic variants and variants of uncertain significance in breast cancer susceptibility genes (2022) (0)
- Accounting for EGFR mutations in epidemiological analyses of non-small cell lung cancers: Examples based on the International Lung Cancer Consortium data. (2022) (0)
- A reply to "Lung cancer outcomes: Are BMI and race clinically relevant?" (2021) (0)
- Implementation of an e-learning model to build capacity of providers within a cervical cancer prevention programme in Africa: a successful experience in Cameroon (2020) (0)
- Implementation of electronic patient-reported outcomes and biometrics surveillance for the management of chemotherapy-related symptom burden: Results from a decentralized feasibility pilot study. (2022) (0)
- MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients (2016) (0)
- Iam hiQ—a novel pair of accuracy indices for imputed genotypes (2022) (0)
- Abstract 2209: HPV non-vaccination due to safety concerns/side effects: Variations in vaccination intentions by Parent-Child Gender, National Immunization Survey - Teen, 2010 - 2019 (2022) (0)
- Abstract 435: COVID-19 & cancer prevention in Texas: Reasons cited for HPV vaccination hesitancy and refusal during the pandemic (2022) (0)
- Clinical Cancer and Direct-to-Consumer Genetic Test Result-Sharing Behavior: Findings from HINTS 2020 (2022) (0)
- Empirical estimation of sequencing error rates using smoothing splines (2016) (0)
- Acknowledgement to the Reviewers (2009) (0)
- Cytokine gene polymorphisms and cancer-related symptoms in lung cancer patients (2007) (0)
- Abstract 22: Screening and Treatment of Female Sex Workers for Cervical Precancers in Cameroon (2021) (0)
- Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer (2018) (0)
- I’am hiQ – A Novel Accuracy Index for Imputed Genotypes (2021) (0)
- The influence of polymorphisms in cytokine genes on pain and response to analgesia in lung cancer patients receiving palliative treatment (2008) (0)
- 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 (2012) (0)
- POT1 GERMLINE MUTATIONS MAY EXPLAIN A SUBSET OF FAMILIAL GLIOMA : A REPORT FROM THE GLIOGENE CONSORTIUM (2013) (0)
- GENE-23. PREVIOUSLY IDENTIFIED COMMON GLIOMA RISK SNPs ARE ASSOCIATED WITH FAMILIAL GLIOMA (2018) (0)
- “A combined Test for Genetic Association that Incorporates Information about Hardy Weinberg Disequilibrium in Cases” (2008) (0)
- Mosaic chromosomal alterations is associated with increased lung cancer risk: insight from the INTEGRAL-ILCCO cohort analysis (2023) (0)
- Gene-gene Interaction of AhR With and Within the Wnt Cascade Affects Susceptibility to Lung Cancer (2021) (0)
- Abstract 1315: Estimating sex-specific effects of genetic loci associated with glioma risk (2017) (0)
- Additional file 1: of Using the weighted area under the net benefit curve for decision curve analysis (2016) (0)
- Lower respiratory tract disease (LRTD) in patients with cancer and COVID-19: A COVID-19 and Cancer Consortium (CCC19) study. (2021) (0)
- Abstract 2421: Factors associated with abnormal cervical cancer screening results among screening compliant women in the United States (2019) (0)
- Prevalence of Abnormal Cervical Cancer Screening Outcomes among Women in the United States: Results from the National Health Interview Survey, 2018. (2020) (0)
- Sclerosis Anti-Topoisomerase-I Positivity and Pulmonary Hypertension in Systemic Association of Interleukin 23 Receptor Polymorphisms with MAYES and (2009) (0)
- Protein-altering germline mutations implicate novel genes related to lung cancer development (2020) (0)
- Chromosome 7p11.2(EGFR) and 7q36.1(XRCC2) variants influence glioma risk (2011) (0)
- Informative gene network for chemotherapy-induced peripheral neuropathy (2015) (0)
- Gene–gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer (2022) (0)
- Abstract 233: Evaluating glioma risk associated with extent of European admixture in African-Americans and Latinos (2018) (0)
- Erratum to: Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation (2010) (0)
- Corrections (1994) (0)
- Gender-neutral HPV vaccination in Africa - Authors' reply. (2019) (0)
- A new test for linkage in affected sib pairs (2000) (0)
- Genome-wide association study of glioma and meta-analysis (2012) (0)
- Industry-sponsored antismoking advertisements in low-income countries. (2020) (0)
- DEMOGRAPHICS AND LIFESTYLE FACTORS IN GLIOMA RISK : A REPORT FROM THE GLIOMA INTERNATIONAL CASE-CONTROL STUDY (2016) (0)
- Using Ascertainment for Targeted Resequencing to Increase Power to Identify Causal Variants. (2011) (0)
- Identifying dehydration risk in head and neck cancer patients undergoing radiation therapy using remote, sensor-based monitoring: A randomized controlled trial. (2016) (0)
- EPID-01CHICKEN POX AND GLIOMA RISK: PRELIMINARY RESULTS FROM THE GLIOGENE INTERNATIONAL CASE-CONTROL STUDY. (2015) (0)
- GENE-47. EVALUATING GLIOMA RISK ASSOCIATED WITH EXTENT OF EUROPEAN ADMIXTURE IN AFRICAN-AMERICANS AND LATINOS (2017) (0)
- The genomic landscape of familial glioma (2023) (0)
- Spatially varying effects of measured confounding variables on disease risk (2021) (0)
- Erratum: Survey of familial glioma and role of germline p16 INK4A/p14ARF and p53 mutation (Familial Cancer DOI: 10.1007/s10689-010-9346-5) (2010) (0)
- Abstract 2782: Risk loci for a breast-colon cancer phenotype: results from a genome-wide association study (2015) (0)
- Chronic obstructive pulmonary disease among lung cancer free smokers: The importance of health controls (2016) (0)
- Political Ideology and the Support or Opposition to United States Tobacco Control Policies (2021) (0)
- 31st Annual Meeting • American Society of Preventive Oncology, Houston, Texas • March 2–4, 2007 (2007) (0)
- Title: Trans-ethnic genome-wide meta-analysis of 35,732 cases and 34,424 controls identifies novel genomic cross-ancestry loci contributing to lung cancer susceptibility (2020) (0)
- Correction to: Processing and Analyzing Human Microbiome Data. (2017) (0)
- Immunogenetic Determinants of Susceptibility to Head and Neck Cancer in the Million Veteran Program Cohort (2022) (0)
- Abstract P6-02-04: Use of breast surveillance between women with pathogenic variants and variants of uncertain significance in breast cancer susceptibility genes (2023) (0)
- Abstract 04: Using family-based genome-wide data to evaluate imprinting and maternal genetic effects: A pilot study of glioma risk. (2012) (0)
- Abstract 3055: ACTA2 Mutations Cause Diverse And Diffuse Vascular Diseases, Including Aortic Aneurysms, Premature Coronary Artery Disease And Moyamoya Disease (2007) (0)
- Respiratory and cardiometabolic comorbidities and Stage I-III non-small cell lung cancer (NSCLC) survival: A pooled analysis from the International Lung Cancer Consortium (ILCCO). (2022) (0)
- Erratum: Imprinting detection by extending a regression-based QTL analysis method (Human Genetics 10.1007/s00439-007-0387-2) (2007) (0)
- Neuropathic pain prevalence and risk factors in head and neck cancer survivors (2022) (0)
- Abstract 4173: Previously identified common glioma risk SNPs are associated with familial glioma (2019) (0)
- Pain and survival in patients with squamous cell cancer of the head and neck (HNSCC): analysis of 2,622 newly diagnosed HNSCC patients (2013) (0)
- Impact of U.S. Preventive Services Task Force lung cancer screening update on drivers of disparities in screening eligibility (2022) (0)
- Assessing current temporal and space-time anomalies of disease incidence (2017) (0)
This paper list is powered by the following services:
Other Resources About Sanjay Shete
What Schools Are Affiliated With Sanjay Shete?
Sanjay Shete is affiliated with the following schools:
