Silvia Casadei
About
In The Last Decade
Silvia Casadei
31 papers receiving 3.3k citations
Hit Papers
Peers
Comparison fields: 5 of 85
- Genetics 2.1k
- Molecular Biology 1.6k
- Oncology 1.3k
- Reproductive Medicine 1.0k
- Cancer Research 905
Countries citing papers authored by Silvia Casadei
This map shows the geographic impact of Silvia Casadei's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Silvia Casadei with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Silvia Casadei more than expected).
Fields of papers citing papers by Silvia Casadei
This network shows the impact of papers produced by Silvia Casadei. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Silvia Casadei. The network helps show where Silvia Casadei may publish in the future.
Co-authorship network of co-authors of Silvia Casadei
This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Casadei. A scholar is included among the top collaborators of Silvia Casadei based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Silvia Casadei. Silvia Casadei is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Title | Journal | Authors | Indexed citations |
|---|---|---|---|---|
| 1 | Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management | Journal of Allergy and Clinical Immunology | Sarah K. Baxter, Tom Walsh et al. | 21 |
| 2 | Genomic analysis of inherited hearing loss in the Palestinian population | Proceedings of the National Academy of Sciences | Amal Abu Rayyan, Silvia Casadei et al. | 38 |
| 3 | CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes | Journal of Medical Genetics | Tom Walsh, Silvia Casadei et al. | 18 |
| 4 | Amplification of the Mutation-Carrying BRCA2 Allele Promotes RAD51 Loading and PARP Inhibitor Resistance in the Absence of Reversion Mutations | Molecular Cancer Therapeutics | Pyoung Hwa Park, Tomomi M. Yamamoto et al. | 20 |
| 5 | Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance | Genetics in Medicine | John Michael O. Rañola, Christina Smith et al. | 42 |
| 6 | Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2 | Breast Cancer Research and Treatment | Irene Catucci, Silvia Casadei et al. | 8 |
| 7 | Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis | Genetics in Medicine | Brian H. Shirts, Stephen J. Salipante et al. | 13 |
| 8 | Inherited predisposition to breast cancer among African American women | Breast Cancer Research and Treatment | Jane Churpek, Tom Walsh et al. | 114 |
| 9 | Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas breakdown → | Clinical Cancer Research | Kathryn P. Pennington, Tom Walsh et al. | 712 |
| 10 | Inherited mutations in breast cancer genes in African American breast cancer patients revealed by targeted genomic capture and next generation sequencing. | Journal of Clinical Oncology | Jane Churpek, Tom Walsh et al. | 5 |
| 11 | Characteristics of women with ovarian carcinoma who have BRCA1 and BRCA2 mutations not identified by clinical testing | Gynecologic Oncology | Barbara M. Norquist, Kathryn P. Pennington et al. | 21 |
| 12 | Loss of function germline mutations in RAD51D in women with ovarian carcinoma | Gynecologic Oncology | Christopher C. Pennil, Silvia Casadei et al. | 28 |
| 13 | Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer | Cancer Research | Silvia Casadei, Barbara M. Norquist et al. | 182 |
| 14 | Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing breakdown → | Proceedings of the National Academy of Sciences | Tom Walsh, Silvia Casadei et al. | 662 |
| 15 | Disease family history and modification of breast cancer risk in common BRCA2 variants | Oncology Reports | Ian Seymour, Silvia Casadei et al. | 12 |
| 16 | 655Val and 1170Pro ERBB2 SNPs in Familial Breast Cancer Risk and BRCA1 Alterations | Analytical Cellular Pathology | Stefania Tommasi, Vita Fedele et al. | 19 |
| 17 | Results of a population-based screening for hereditary breast cancer in a region of North-Central Italy: contribution of BRCA1/2 germ-line mutations | Breast Cancer Research and Treatment | Ian Seymour, Silvia Casadei et al. | 5 |
| 18 | Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer | JAMA | Tom Walsh, Silvia Casadei et al. | 469 |
| 19 | Analysis of single nucleotide polymorphisms in coding and non-coding regions of human BRCA1 and BRCA2 genes | Cancer Research | Silvia Casadei, Ian Seymour et al. | 1 |
| 20 | Detection of germline BRCA1 mutations by Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method | British Journal of Cancer | Silvia Casadei, Laura Cortesi et al. | 3 |
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.