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314 results on '"Chanock S.J."'

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51. Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers.

52. Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance.

53. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.

54. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.

55. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.

56. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

57. An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk

58. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

59. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

60. Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

61. Genetically Determined Height and Risk of Non-hodgkin Lymphoma

62. Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways

63. Lipid trait variants and the risk of non-hodgkin lymphoma subtypes: a mendelian randomization study

64. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

66. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

68. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

69. Two truncating variants in FANCC and breast cancer risk

70. Genome-wide association study of germline variants and breast cancer-specific mortality

71. Discovery of common and rare genetic risk variants for colorectal cancer

74. Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes

75. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

76. Correction to: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (Nature Genetics, (2018), 50, 7, (928-936), 10.1038/s41588-018-0142-8).

77. Germline variation at 8q24 and prostate cancer risk in men of European ancestry.

78. Shared heritability and functional enrichment across six solid cancers.

79. Genome-wide association study of germline variants and breast cancer-specific mortality.

80. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4).

81. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.

82. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.

83. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1).

84. Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (Nature Genetics, (2018), 50, 7, (928-936), 10.1038/s41588-018-0142-8).

85. Associations of autozygosity with a broad range of human phenotypes

86. Erratum: Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature communications (2019) 10 1 (431))

87. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)

88. Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients

89. Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility

90. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.

91. Identification of nine new susceptibility loci for endometrial cancer.

92. Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

93. Germline variation at 8q24 and prostate cancer risk in men of European ancestry

94. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

95. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

96. Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor

97. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

98. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

99. Body mass index and breast cancer survival

100. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

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