Search

Your search keyword '"Papi, Laura"' showing total 528 results

Search Constraints

Start Over You searched for: Author "Papi, Laura" Remove constraint Author: "Papi, Laura"
528 results on '"Papi, Laura"'

Search Results

51. Germline mutations in MSH2 and ATM gene in patients with GIST (gastrointestinal stromal tumor) and second epitelial tumors.

52. Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

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

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

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

56. The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

57. Characterization of the Cancer Spectrum in Men with Germline BRCA1 and BRCA2 Pathogenic Variants:Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

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

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

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

66. Epigenomic, genomic, and transcriptomic landscape of schwannomatosis

67. Infrastructure in Central, Eastern, and Southeastern Europe

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

73. The 'laissez faire' bias of managed floating

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

76. Trade Tensions, Global Value Chains, and Spillovers

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

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

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

81. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

82. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

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

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

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

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

90. Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression

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

92. High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

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

94. 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

95. 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

96. 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

97. 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

98. 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

99. 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

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

Catalog

Books, media, physical & digital resources