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849 results on '"Cybulski C."'

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51. Impact of BRCA1 mutation on survival after early onset breast cancer

52. Screening with Magnetic Resonance Imaging in women at low and intermediate risk of breast Cancer

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

58. The CHEK2 variant C.349A>G is associated with prostate cancer risk and carriers share a common ancestor

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

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

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

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

63. The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor

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

65. 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)

68. Breast cancer predisposing alleles in Poland

69. CHEK2 is a multiorgan cancer susceptibility gene

72. Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study

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

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

81. 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)

82. Germline variation at 8q24 and prostate cancer risk in men of European ancestry (vol 9, 4616, 2018)

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

86. Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

87. A common variant of CDKN2A (p16) predisposes to breast cancer

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

89. 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).

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

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

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

93. 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).

94. 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).

95. Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.

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

97. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (vol 9, 1340, 2018)

98. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (vol 9, 3707, 2018)

99. Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (vol 9, 4079, 2018)

100. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (vol 8, 1892, 2017)

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