Connection

YANHONG LIU to Humans

This is a "connection" page, showing publications YANHONG LIU has written about Humans.
Connection Strength

0.272
  1. Immunogenetic Determinants of Susceptibility to Head and Neck Cancer in the Million Veteran Program Cohort. Cancer Res. 2023 02 03; 83(3):386-397.
    View in: PubMed
    Score: 0.017
  2. Genetic modulation of longitudinal change in neurocognitive function among adult glioma patients. J Neurooncol. 2022 Jan; 156(1):185-193.
    View in: PubMed
    Score: 0.016
  3. Dietary quality and the colonic mucosa-associated gut microbiome in humans. Am J Clin Nutr. 2019 09 01; 110(3):701-712.
    View in: PubMed
    Score: 0.013
  4. Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer. J Thorac Oncol. 2018 10; 13(10):1483-1495.
    View in: PubMed
    Score: 0.012
  5. Genetic epidemiology and risk factors for brain tumors. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Apr 28; 43(4):345-353.
    View in: PubMed
    Score: 0.012
  6. Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer. J Thorac Oncol. 2016 Jan; 11(1):52-61.
    View in: PubMed
    Score: 0.010
  7. Genetic Modulation of Neurocognitive Function in Glioma Patients. Clin Cancer Res. 2015 Jul 15; 21(14):3340-6.
    View in: PubMed
    Score: 0.010
  8. WNT signaling pathway gene polymorphisms and risk of hepatic fibrosis and inflammation in HCV-infected patients. PLoS One. 2013; 8(12):e84407.
    View in: PubMed
    Score: 0.009
  9. Genomic copy number imbalances associated with bone and non-bone metastasis of early-stage breast cancer. Breast Cancer Res Treat. 2014 Jan; 143(1):189-201.
    View in: PubMed
    Score: 0.009
  10. 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.
    View in: PubMed
    Score: 0.008
  11. Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk. Carcinogenesis. 2010 Oct; 31(10):1762-9.
    View in: PubMed
    Score: 0.007
  12. 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.
    View in: PubMed
    Score: 0.007
  13. Genetic advances in glioma: susceptibility genes and networks. Curr Opin Genet Dev. 2010 Jun; 20(3):239-44.
    View in: PubMed
    Score: 0.007
  14. New insights into susceptibility to glioma. Arch Neurol. 2010 Mar; 67(3):275-8.
    View in: PubMed
    Score: 0.007
  15. Association and interactions between DNA repair gene polymorphisms and adult glioma. Cancer Epidemiol Biomarkers Prev. 2009 Jan; 18(1):204-14.
    View in: PubMed
    Score: 0.006
  16. Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma. Hum Mutat. 2008 Mar; 29(3):381-9.
    View in: PubMed
    Score: 0.006
  17. Tagging SNPs in non-homologous end-joining pathway genes and risk of glioma. Carcinogenesis. 2007 Sep; 28(9):1906-13.
    View in: PubMed
    Score: 0.006
  18. PNPLA3, Obesity, and Heavy Alcohol Use in Cirrhosis Patients May Exert a Synergistic Increase Hepatocellular Carcinoma Risk. Clin Gastroenterol Hepatol. 2024 Sep; 22(9):1858-1866.e4.
    View in: PubMed
    Score: 0.005
  19. Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies. Cancer Epidemiol Biomarkers Prev. 2024 03 01; 33(3):389-399.
    View in: PubMed
    Score: 0.005
  20. Characterization of the oral microbiota among middle-aged men with and without human papillomavirus infection. Oral Oncol. 2023 07; 142:106401.
    View in: PubMed
    Score: 0.004
  21. Immune Infiltration in Tumor and Adjacent Non-Neoplastic Regions Codetermines Patient Clinical Outcomes in Early-Stage Lung Cancer. J Thorac Oncol. 2023 09; 18(9):1184-1198.
    View in: PubMed
    Score: 0.004
  22. Risk stratification for hepatocellular cancer among patients with cirrhosis using a hepatic fat polygenic risk score. PLoS One. 2023; 18(2):e0282309.
    View in: PubMed
    Score: 0.004
  23. 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.
    View in: PubMed
    Score: 0.004
  24. 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.
    View in: PubMed
    Score: 0.004
  25. Clonal Hematopoiesis Mutations in Patients with Lung Cancer Are Associated with Lung Cancer Risk Factors. Cancer Res. 2022 01 15; 82(2):199-209.
    View in: PubMed
    Score: 0.004
  26. Whole exome sequencing analysis in severe chronic obstructive pulmonary disease. Hum Mol Genet. 2018 11 01; 27(21):3801-3812.
    View in: PubMed
    Score: 0.003
  27. Ancestry and Risk of Hepatic Fibrosis and Inflammation in Patients With HCV Infection. Clin Gastroenterol Hepatol. 2019 08; 17(9):1912-1914.
    View in: PubMed
    Score: 0.003
  28. Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients. J Neurooncol. 2018 Jan; 136(1):33-39.
    View in: PubMed
    Score: 0.003
  29. Combined Proteomic-Molecular Epidemiology Approach to Identify Precision Targets in Brain Cancer. ACS Chem Neurosci. 2018 01 17; 9(1):80-84.
    View in: PubMed
    Score: 0.003
  30. 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.
    View in: PubMed
    Score: 0.003
  31. Genetic variations in the homologous recombination repair pathway genes modify risk of glioma. J Neurooncol. 2016 Jan; 126(1):11-17.
    View in: PubMed
    Score: 0.003
  32. BRCA2-branching out too? J Natl Cancer Inst. 2015 May; 107(5).
    View in: PubMed
    Score: 0.002
  33. Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium. Sci Rep. 2015 Feb 05; 5:8278.
    View in: PubMed
    Score: 0.002
  34. A recurrent mutation in PARK2 is associated with familial lung cancer. Am J Hum Genet. 2015 Feb 05; 96(2):301-8.
    View in: PubMed
    Score: 0.002
  35. Germline mutations in shelterin complex genes are associated with familial glioma. J Natl Cancer Inst. 2015 Jan; 107(1):384.
    View in: PubMed
    Score: 0.002
  36. 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.
    View in: PubMed
    Score: 0.002
  37. Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222. Br J Cancer. 2013 May 28; 108(10):2178-85.
    View in: PubMed
    Score: 0.002
  38. Prognostic value of single nucleotide polymorphisms of candidate genes associated with inflammation in early stage breast cancer. Breast Cancer Res Treat. 2013 Apr; 138(3):917-24.
    View in: PubMed
    Score: 0.002
  39. Deciphering the 8q24.21 association for glioma. Hum Mol Genet. 2013 Jun 01; 22(11):2293-302.
    View in: PubMed
    Score: 0.002
  40. Description of selected characteristics of familial glioma patients - results from the Gliogene Consortium. Eur J Cancer. 2013 Apr; 49(6):1335-45.
    View in: PubMed
    Score: 0.002
  41. 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.
    View in: PubMed
    Score: 0.002
  42. Association of BRCA1 functional single nucleotide polymorphisms with risk of differentiated thyroid carcinoma. Thyroid. 2012 Jan; 22(1):35-43.
    View in: PubMed
    Score: 0.002
  43. 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.
    View in: PubMed
    Score: 0.002
  44. Copy number imbalances between screen- and symptom-detected breast cancers and impact on disease-free survival. Cancer Prev Res (Phila). 2011 Oct; 4(10):1609-16.
    View in: PubMed
    Score: 0.002
  45. 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.
    View in: PubMed
    Score: 0.002
  46. Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum Mol Genet. 2011 Jul 15; 20(14):2897-904.
    View in: PubMed
    Score: 0.002
  47. Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population. Am J Epidemiol. 2011 Apr 15; 173(8):915-22.
    View in: PubMed
    Score: 0.002
  48. Genetic polymorphisms in DNA double-strand break repair genes XRCC5, XRCC6 and susceptibility to hepatocellular carcinoma. Carcinogenesis. 2011 Apr; 32(4):530-6.
    View in: PubMed
    Score: 0.002
  49. Possible association between polymorphisms of human vascular endothelial growth factor A gene and susceptibility to glioma in a Chinese population. Int J Cancer. 2011 Jan 01; 128(1):166-75.
    View in: PubMed
    Score: 0.002
  50. A comprehensive study of the association between the EGFR and ERBB2 genes and glioma risk. Acta Oncol. 2010 Aug; 49(6):767-75.
    View in: PubMed
    Score: 0.002
  51. Inherited variation in immune genes and pathways and glioblastoma risk. Carcinogenesis. 2010 Oct; 31(10):1770-7.
    View in: PubMed
    Score: 0.002
  52. Allergy and glioma risk: test of association by genotype. Int J Cancer. 2011 Apr 01; 128(7):1736-40.
    View in: PubMed
    Score: 0.002
  53. Genetic variations in EGF and EGFR and glioblastoma outcome. Neuro Oncol. 2010 Aug; 12(8):815-21.
    View in: PubMed
    Score: 0.002
  54. Genetic variants in inflammation pathway genes and asthma in glioma susceptibility. Neuro Oncol. 2010 May; 12(5):444-52.
    View in: PubMed
    Score: 0.002
  55. Genome-wide association study identifies five susceptibility loci for glioma. Nat Genet. 2009 Aug; 41(8):899-904.
    View in: PubMed
    Score: 0.002
  56. Molecular epidemiology of primary brain tumors. Neurotherapeutics. 2009 Jul; 6(3):427-35.
    View in: PubMed
    Score: 0.002
  57. XRCC3 haplotypes and risk of gliomas in a Chinese population: a hospital-based case-control study. Int J Cancer. 2009 Jun 15; 124(12):2948-53.
    View in: PubMed
    Score: 0.002
  58. Association of human aryl hydrocarbon receptor gene polymorphisms with risk of lung cancer among cigarette smokers in a Chinese population. Pharmacogenet Genomics. 2009 Jan; 19(1):25-34.
    View in: PubMed
    Score: 0.002
  59. Methyl-CpG binding domain 1 gene polymorphisms and lung cancer risk in a Chinese population. Biomarkers. 2008 Sep; 13(6):607-17.
    View in: PubMed
    Score: 0.002
  60. Association of polymorphisms in one-carbon metabolizing genes and lung cancer risk: a case-control study in Chinese population. Lung Cancer. 2008 Jul; 61(1):21-9.
    View in: PubMed
    Score: 0.001
  61. Genetic variants in peroxisome proliferator-activated receptor-gamma gene are associated with risk of lung cancer in a Chinese population. Carcinogenesis. 2008 Feb; 29(2):342-50.
    View in: PubMed
    Score: 0.001
  62. The influence of metabolic gene polymorphisms on urinary 1-hydroxypyrene concentrations in Chinese coke oven workers. Sci Total Environ. 2007 Aug 01; 381(1-3):38-46.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.