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51. Characterization of the cancer spectrum in men with germline BRCA1 and BRCA2 pathogenic variants

53. EPCO-04. GENOMIC AND EPIGENOMIC HALLMARKS OF SCHWANNOMATOSIS SCHWANNOMAS

54. Correction to: Epigenomic, genomic, and transcriptomic landscape of schwannomatosis

55. Epigenomic, genomic, and transcriptomic landscape of schwannomatosis

60. Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers

61. Infrastructure in Central, Eastern, and Southeastern Europe

62. Update of NGS analysis of Italian survey of second tumors in patients with diagnosis of GIST (gastrointestinal stromal tumor).

67. The 'laissez faire' bias of managed floating

69. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

70. The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome

73. Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

74. Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers

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

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

77. Heterozygosity for loss-of-function variants in LZTR1is associated with isolated multiple café-au-laitmacules

80. Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

81. Additional file 4: Table S5. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

82. Additional file 2: Table S3. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

83. Additional file 6: Table S6. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

84. Additional file 7: Table S7. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

85. Additional file 3: Table S4. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

86. Additional file 5: Table S2. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

87. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1and BRCA2pathogenic variants

88. Birt-Hogg-Dubé Syndrome: The experience of an Italian Centre

89. Double somatic <italic>SMARCB1</italic> and <italic>NF2</italic> mutations in sporadic spinal schwannoma.

91. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

94. The rs3834129 polymorphism and breast cancer risk in mutation carriers

95. A Systematic Assessment of Accuracy in Detecting Somatic Mosaic Variants by Deep Amplicon Sequencing: Application to NF2 Gene

96. mutations in male breast cancer: a population-based study in Central Italy

97. Expanding the mutational spectrum of LZTR1 in schwannomatosis

98. Founder mutations account for the majority of -attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy

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