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51. Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078)).

52. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element.

53. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.

54. Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk.

55. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

56. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.

57. Gene-environment interactions relevant to estrogen and risk of breast cancer: Can gene-environment interactions be detected only among candidate snps from genome-wide association studies?.

58. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.

59. Technological readiness and implementation of genomic-driven precision medicine for complex diseases

60. Genetic insights into biological mechanisms governing human ovarian ageing

61. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium

62. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

63. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

64. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

65. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

66. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

67. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

68. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer

69. Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

70. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

71. Gene-environment interactions relevant to estrogen and risk of breast cancer:can gene-environment interactions be detected only among candidate SNPs from genome-wide association studies?

72. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

73. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

74. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

75. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

76. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

79. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer

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

81. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

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

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

84. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

85. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

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

87. Two truncating variants in FANCC and breast cancer risk.

88. Prediction of contralateral breast cancer: external validation of risk calculators in 20 international cohorts.

89. Prediction and clinical utility of a contralateral breast cancer risk model.

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

91. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

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

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

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

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

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

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

98. The impact of alcohol consumption and physical activity on breast cancer: The role of breast cancer risk

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

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

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