PubRank

Sanjay Shete

Author PubWeight™ 144.92‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nat Genet 2008 16.17
2 Circulating tumor cells in patients with breast cancer dormancy. Clin Cancer Res 2004 4.48
3 A risk model for prediction of lung cancer. J Natl Cancer Inst 2007 4.25
4 Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis. Am J Hum Genet 2004 3.83
5 HER-2 gene amplification can be acquired as breast cancer progresses. Proc Natl Acad Sci U S A 2004 3.43
6 Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections. Circulation 2005 2.77
7 Mutations in myosin light chain kinase cause familial aortic dissections. Am J Hum Genet 2010 2.67
8 Genetic variants on 15q25.1, smoking, and lung cancer: an assessment of mediation and interaction. Am J Epidemiol 2012 2.16
9 Genome-wide association study of glioma and meta-analysis. Hum Genet 2012 1.96
10 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. Cancer Prev Res (Phila) 2011 1.86
11 Ask-Advise-Connect: a new approach to smoking treatment delivery in health care settings. JAMA Intern Med 2013 1.86
12 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. Ann Rheum Dis 2009 1.84
13 Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum Mol Genet 2011 1.83
14 Exploring joint effects of genes and the clinical efficacy of morphine for cancer pain: OPRM1 and COMT gene. Pain 2006 1.72
15 uPAR and HER-2 gene status in individual breast cancer cells from blood and tissues. Proc Natl Acad Sci U S A 2006 1.61
16 Estimation of odds ratios of genetic variants for the secondary phenotypes associated with primary diseases. Genet Epidemiol 2011 1.57
17 p53 Genotypes and Haplotypes Associated With Lung Cancer Susceptibility and Ethnicity. J Natl Cancer Inst 2002 1.56
18 Mediating effects of smoking and chronic obstructive pulmonary disease on the relation between the CHRNA5-A3 genetic locus and lung cancer risk. Cancer 2010 1.55
19 Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes. Carcinogenesis 2002 1.52
20 Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy. Circ Res 2007 1.51
21 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. Cancer Epidemiol Biomarkers Prev 2002 1.51
22 GLIOGENE an International Consortium to Understand Familial Glioma. Cancer Epidemiol Biomarkers Prev 2007 1.42
23 Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival. J Clin Oncol 2010 1.40
24 Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations. J Autoimmun 2009 1.38
25 Sensation seeking, risk behaviors, and alcohol consumption among Mexican origin youth. J Adolesc Health 2011 1.30
26 The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium. Am J Epidemiol 2015 1.27
27 Polymorphisms in TBX21 and STAT4 increase the risk of systemic sclerosis: evidence of possible gene-gene interaction and alterations in Th1/Th2 cytokines. Arthritis Rheum 2009 1.24
28 Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy. Hum Mol Genet 2007 1.23
29 Finding factors influencing risk: comparing Bayesian stochastic search and standard variable selection methods applied to logistic regression models of cases and controls. Stat Med 2008 1.22
30 Genetic linkage and imprinting effects on body mass index in children and young adults. Eur J Hum Genet 2003 1.21
31 Exposure to smoking imagery in the movies and experimenting with cigarettes among Mexican heritage youth. Cancer Epidemiol Biomarkers Prev 2009 1.20
32 Molecular epidemiology, cancer-related symptoms, and cytokines pathway. Lancet Oncol 2008 1.19
33 Inherited variation in immune genes and pathways and glioblastoma risk. Carcinogenesis 2010 1.17
34 Examining the effect of linkage disequilibrium on multipoint linkage analysis. BMC Genet 2005 1.14
35 Genetic advances in glioma: susceptibility genes and networks. Curr Opin Genet Dev 2010 1.14
36 Depressive symptoms and health-related quality of life in breast cancer survivors. J Womens Health (Larchmt) 2011 1.13
37 From genotype to phenotype: correlating XRCC1 polymorphisms with mutagen sensitivity. DNA Repair (Amst) 2003 1.13
38 A test for genetic association that incorporates information about deviation from Hardy-Weinberg proportions in cases. Am J Hum Genet 2008 1.12
39 Effects of population structure on genetic association studies. BMC Genet 2005 1.09
40 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
41 Deciphering the 8q24.21 association for glioma. Hum Mol Genet 2013 1.08
42 The worldwide distribution of the VHL 598C>T mutation indicates a single founding event. Blood 2003 1.07
43 Cytokine genes and pain severity in lung cancer: exploring the influence of TNF-alpha-308 G/A IL6-174G/C and IL8-251T/A. Cancer Epidemiol Biomarkers Prev 2007 1.05
44 The moderating role of parental smoking on their children's attitudes toward smoking among a predominantly minority sample: a cross-sectional analysis. Subst Abuse Treat Prev Policy 2008 1.05
45 Improving the power of sib pair quantitative trait loci detection by phenotype winsorization. Hum Hered 2002 1.04
46 Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome. Cancer Res 2006 1.03
47 Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes. J Pain Symptom Manage 2009 1.02
48 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. Cancer 2006 1.02
49 Method for evaluating multiple mediators: mediating effects of smoking and COPD on the association between the CHRNA5-A3 variant and lung cancer risk. PLoS One 2012 1.00
50 Chemotherapy-induced peripheral neuropathy as a predictor of neuropathic pain in breast cancer patients previously treated with paclitaxel. J Pain 2009 1.00
51 Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women <or=55 years. Carcinogenesis 2006 1.00
52 The Ask-Advise-Connect approach for smokers in a safety net healthcare system: a group-randomized trial. Am J Prev Med 2013 1.00
53 Investigating multiple candidate genes and nutrients in the folate metabolism pathway to detect genetic and nutritional risk factors for lung cancer. PLoS One 2013 0.99
54 New insights into susceptibility to glioma. Arch Neurol 2010 0.98
55 Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms. Am J Med Genet A 2011 0.98
56 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. Genet Epidemiol 2011 0.97
57 Association of interleukin 23 receptor polymorphisms with anti-topoisomerase-I positivity and pulmonary hypertension in systemic sclerosis. J Rheumatol 2009 0.96
58 The null distribution of stochastic search gene suggestion: a Bayesian approach to gene mapping. BMC Proc 2007 0.96
59 Genetic variations in interleukin-8 and interleukin-10 are associated with pain, depressed mood, and fatigue in lung cancer patients. J Pain Symptom Manage 2012 0.96
60 The influence of tumor necrosis factor-alpha -308 G/A and IL-6 -174 G/C on pain and analgesia response in lung cancer patients receiving supportive care. Cancer Epidemiol Biomarkers Prev 2008 0.96
61 Role of inflammation gene polymorphisms on pain severity in lung cancer patients. Cancer Epidemiol Biomarkers Prev 2009 0.95
62 The role of MMP-2 and MMP-9 polymorphisms in sporadic intracranial aneurysms. J Neurosurg 2006 0.95
63 Complex segregation analysis reveals a multigene model for lung cancer. Hum Genet 2004 0.94
64 Description of selected characteristics of familial glioma patients - results from the Gliogene Consortium. Eur J Cancer 2013 0.94
65 Seeking gene relationships in gene expression data using support vector machine regression. BMC Proc 2007 0.92
66 Linkage analysis of affected sib pairs allowing for parent-of-origin effects. Ann Hum Genet 2005 0.91
67 Statistical methods for anomalous discrete time series based on minimum cell count. Biom J 2008 0.91
68 Methylenetetrahydrofolate reductase polymorphisms and risk of squamous cell carcinoma of the head and neck: a case-control analysis. Int J Cancer 2005 0.91
69 Using both cases and controls for testing hardy-weinberg proportions in a genetic association study. Hum Hered 2010 0.90
70 Analysis of secondary phenotype involving the interactive effect of the secondary phenotype and genetic variants on the primary disease. Ann Hum Genet 2012 0.89
71 Comparison of haplotype inference methods using genotypic data from unrelated individuals. Hum Hered 2004 0.89
72 Imprinting detection by extending a regression-based QTL analysis method. Hum Genet 2007 0.89
73 X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation. Genet Epidemiol 2014 0.89
74 Testing departure from Hardy-Weinberg proportions. Methods Mol Biol 2012 0.88
75 Influence of subjective social status on the relationship between positive outcome expectations and experimentation with cigarettes. J Adolesc Health 2008 0.88
76 Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23. Cancer Res 2005 0.88
77 Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol 2013 0.87
78 Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience. Genet Epidemiol 2007 0.87
79 Neuropathic pain in breast cancer survivors: using the ID pain as a screening tool. J Pain Symptom Manage 2010 0.87
80 Early referral to supportive care specialists for symptom burden in lung cancer patients: a comparison of non-Hispanic whites, Hispanics, and non-Hispanic blacks. Cancer 2011 0.86
81 Capitalizing on admixture in genome-wide association studies: a two-stage testing procedure and application to height in African-Americans. Front Genet 2011 0.86
82 Familial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in women. Am J Med Genet A 2006 0.86
83 Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes. Support Care Cancer 2013 0.85
84 Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome. Hum Genet 2011 0.85
85 Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk. Carcinogenesis 2010 0.85
86 Androgen receptor polymorphisms and risk of biochemical failure among prostatectomy patients. Prostate 2004 0.84
87 Positional identification of microdeletions with genetic markers. Hum Hered 2003 0.84
88 A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma. Cancer Epidemiol Biomarkers Prev 2012 0.83
89 Allergy and glioma risk: test of association by genotype. Int J Cancer 2010 0.83
90 Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis. Hum Genet 2009 0.83
91 Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis. Hum Mol Genet 2012 0.82
92 A linkage disequilibrium-based approach to selecting disease-associated rare variants. PLoS One 2013 0.82
93 Joint linkage and imprinting analyses of GAW15 rheumatoid arthritis and gene expression data. BMC Proc 2007 0.82
94 Cigarette experimentation in Mexican origin youth: psychosocial and genetic determinants. Cancer Epidemiol Biomarkers Prev 2011 0.82
95 Testing Hardy-Weinberg proportions in a frequency-matched case-control genetic association study. PLoS One 2011 0.82
96 Comprehensive pathway-based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer. Cancer 2011 0.81
97 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. Hum Genet 2012 0.81
98 Gamma-ray-induced mutagen sensitivity and risk of sporadic breast cancer in young women: a case-control study. Breast Cancer Res Treat 2012 0.81
99 Systemic hypertension requiring treatment in the neonatal intensive care unit. J Pediatr 2013 0.81
100 Lack of an association between the angiotensin-converting enzyme insertion/deletion polymorphism and intracranial aneurysms in a Caucasian population in the United States. J Neurosurg 2005 0.80
101 Effects of measured susceptibility genes on cancer risk in family studies. Hum Genet 2009 0.80
102 MicroRNA target site polymorphisms in the VHL-HIF1α pathway predict renal cell carcinoma risk. Mol Carcinog 2012 0.80
103 A powerful hybrid approach to select top single-nucleotide polymorphisms for genome-wide association study. BMC Genet 2011 0.79
104 Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation. Fam Cancer 2010 0.78
105 Comparison of genome-wide single-nucleotide polymorphism linkage analyses in Caucasian and Hispanic NARAC families. BMC Proc 2007 0.77
106 Cigarette experimentation and the population attributable fraction for associated genetic and non-genetic risk factors. PLoS One 2013 0.76
107 False-Negative-Rate Based Approach for Selecting Top Single-Nucleotide Polymorphisms in the First Stage of a Two-Stage Genome-Wide Association Study. Stat Interface 2011 0.76
108 Analysis of alcoholism data using support vector machines. BMC Genet 2005 0.75
109 Analysis of genes for alcoholism using two-disease-locus models. BMC Genet 2005 0.75
110 Identification of Small and Non-Small Cell Lung Cancer Markers in Peripheral Blood Using Cytokinesis-Blocked Micronucleus and Spectral Karyotyping Assays. Cytogenet Genome Res 2017 0.75
111 New editor and new directions for genetic epidemiology. Genet Epidemiol 2012 0.75
112 Data mining of RNA expression and DNA genotype data: presentation group 5 contributions to Genetic Analysis Workshop 15. Genet Epidemiol 2007 0.75