Co-Authors
This is a "connection" page, showing publications co-authored by YANHONG LIU and SANJAY SHETE.
Connection Strength
1.392
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Immunogenetic Determinants of Susceptibility to Head and Neck Cancer in the Million Veteran Program Cohort. Cancer Res. 2023 02 03; 83(3):386-397.
Score: 0.223
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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 Sep; 131(9):1507-17.
Score: 0.107
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Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium. Cancer Res. 2011 Dec 15; 71(24):7568-75.
Score: 0.102
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Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk. Carcinogenesis. 2010 Oct; 31(10):1762-9.
Score: 0.093
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Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival. J Clin Oncol. 2010 May 10; 28(14):2467-74.
Score: 0.092
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Genetic advances in glioma: susceptibility genes and networks. Curr Opin Genet Dev. 2010 Jun; 20(3):239-44.
Score: 0.091
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New insights into susceptibility to glioma. Arch Neurol. 2010 Mar; 67(3):275-8.
Score: 0.091
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Genome-wide association study identifies five susceptibility loci for glioma. Nat Genet. 2009 Aug; 41(8):899-904.
Score: 0.087
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Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies. Cancer Epidemiol Biomarkers Prev. 2024 03 01; 33(3):389-399.
Score: 0.060
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Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk. Hum Mol Genet. 2022 08 23; 31(16):2831-2843.
Score: 0.054
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Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Nat Genet. 2022 08; 54(8):1167-1177.
Score: 0.054
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Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat Genet. 2017 May; 49(5):789-794.
Score: 0.037
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Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium. Sci Rep. 2015 Feb 05; 5:8278.
Score: 0.032
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Germline mutations in shelterin complex genes are associated with familial glioma. J Natl Cancer Inst. 2015 Jan; 107(1):384.
Score: 0.032
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Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer. Neuro Oncol. 2014 Oct; 16(10):1333-40.
Score: 0.030
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Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222. Br J Cancer. 2013 May 28; 108(10):2178-85.
Score: 0.028
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Deciphering the 8q24.21 association for glioma. Hum Mol Genet. 2013 Jun 01; 22(11):2293-302.
Score: 0.028
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Description of selected characteristics of familial glioma patients - results from the Gliogene Consortium. Eur J Cancer. 2013 Apr; 49(6):1335-45.
Score: 0.028
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A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma. Cancer Epidemiol Biomarkers Prev. 2012 Dec; 21(12):2242-51.
Score: 0.027
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A novel approach to exploring potential interactions among single-nucleotide polymorphisms of inflammation genes in gliomagenesis: an exploratory case-only study. Cancer Epidemiol Biomarkers Prev. 2011 Aug; 20(8):1683-1689.
Score: 0.025
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Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum Mol Genet. 2011 Jul 15; 20(14):2897-904.
Score: 0.025
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Inherited variation in immune genes and pathways and glioblastoma risk. Carcinogenesis. 2010 Oct; 31(10):1770-7.
Score: 0.023
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Allergy and glioma risk: test of association by genotype. Int J Cancer. 2011 Apr 01; 128(7):1736-40.
Score: 0.023