Silvia Casadei

8.9k total citations · 3 hit papers
33 papers, 3.4k citations indexed

About

Silvia Casadei is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Silvia Casadei has authored 33 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 18 papers in Molecular Biology and 11 papers in Cancer Research. Recurrent topics in Silvia Casadei's work include BRCA gene mutations in cancer (28 papers), DNA Repair Mechanisms (12 papers) and Cancer Genomics and Diagnostics (11 papers). Silvia Casadei is often cited by papers focused on BRCA gene mutations in cancer (28 papers), DNA Repair Mechanisms (12 papers) and Cancer Genomics and Diagnostics (11 papers). Silvia Casadei collaborates with scholars based in United States, Italy and Israel. Silvia Casadei's co-authors include Tom Walsh, Mary‐Claire King, Ming K. Lee, Elizabeth M. Swisher, Barbara M. Norquist, Sunday M. Stray, Anne Thornton, Christopher C. Pennil, Alex S. Nord and Jessica B. Mandell and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JAMA and Journal of Clinical Oncology.

In The Last Decade

Silvia Casadei

31 papers receiving 3.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas

2013 712 citations Kathryn P. Pennington, Tom Walsh et al. Clinical Cancer Research profile →
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

2011 662 citations Tom Walsh, Silvia Casadei et al. Proceedings of the National Academy of Sciences profile →
Inherited Mutations in Women With Ovarian Carcinoma

2015 503 citations Barbara M. Norquist, Maria I. Harrell et al. profile →

Peers

Silvia Casadei

GENET

ONCOL

Siranoush Manoukian Italy

Susan Shanley United Kingdom

B A Ponder United Kingdom

Sheila Seal United Kingdom

Sunday M. Stray United States

Nadine Collins United Kingdom

Olivier Caron France

Jolanta Kupryjańczyk Poland

Rósa B. Barkardóttir Iceland

Johanna Tapper Finland

Siranoush Manoukian Italy

Silvia Casadei

1.3k ×0.6

GENET

992 ×0.6

637 ×0.5

ONCOL

444 ×0.4

798 ×0.9

Citations per year, relative to Silvia Casadei Silvia Casadei (= 1×) peers Siranoush Manoukian

Countries citing papers authored by Silvia Casadei

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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20 of 20 papers shown

Baxter, Sarah K., Tom Walsh, Silvia Casadei, et al.. (2021). Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management. Journal of Allergy and Clinical Immunology. 149(1). 327–339. 21 indexed citations

Rayyan, Amal Abu, Silvia Casadei, Zippora Brownstein, et al.. (2020). Genomic analysis of inherited hearing loss in the Palestinian population. Proceedings of the National Academy of Sciences. 117(33). 20070–20076. 38 indexed citations

Walsh, Tom, Silvia Casadei, Katherine M. Munson, et al.. (2020). CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes. Journal of Medical Genetics. 58(12). 850–852. 18 indexed citations

Park, Pyoung Hwa, Tomomi M. Yamamoto, Hua Li, et al.. (2019). Amplification of the Mutation-Carrying BRCA2 Allele Promotes RAD51 Loading and PARP Inhibitor Resistance in the Absence of Reversion Mutations. Molecular Cancer Therapeutics. 19(2). 602–613. 20 indexed citations

Rañola, John Michael O., Christina Smith, Timothy Bergquist, et al.. (2018). Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance. Genetics in Medicine. 21(6). 1435–1442. 42 indexed citations

Catucci, Irene, Silvia Casadei, Yuan Chun Ding, et al.. (2016). 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. 160(1). 121–129. 8 indexed citations

Shirts, Brian H., Stephen J. Salipante, Silvia Casadei, et al.. (2014). Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis. Genetics in Medicine. 16(10). 783–786. 13 indexed citations

Churpek, Jane, Tom Walsh, Yonglan Zheng, et al.. (2014). Inherited predisposition to breast cancer among African American women. Breast Cancer Research and Treatment. 149(1). 31–39. 114 indexed citations

Pennington, Kathryn P., Tom Walsh, Maria I. Harrell, et al.. (2013). Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas. Clinical Cancer Research. 20(3). 764–775. 712 indexed citations breakdown →

10.

Churpek, Jane, Tom Walsh, Yonglan Zheng, et al.. (2013). 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. 31(15_suppl). CRA1501–CRA1501. 5 indexed citations

11.

Norquist, Barbara M., Kathryn P. Pennington, Kathy Agnew, et al.. (2012). Characteristics of women with ovarian carcinoma who have BRCA1 and BRCA2 mutations not identified by clinical testing. Gynecologic Oncology. 128(3). 483–487. 21 indexed citations

12.

Pennil, Christopher C., Silvia Casadei, Kathy Agnew, et al.. (2012). Loss of function germline mutations in RAD51D in women with ovarian carcinoma. Gynecologic Oncology. 127(3). 552–555. 28 indexed citations

13.

Casadei, Silvia, Barbara M. Norquist, Tom Walsh, et al.. (2011). Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer. Cancer Research. 71(6). 2222–2229. 182 indexed citations

14.

Walsh, Tom, Silvia Casadei, Ming K. Lee, et al.. (2011). Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proceedings of the National Academy of Sciences. 108(44). 18032–18037. 662 indexed citations breakdown →

15.

Seymour, Ian, Silvia Casadei, Valentina Zampiga, et al.. (2008). Disease family history and modification of breast cancer risk in common BRCA2 variants. Oncology Reports. 19(3). 783–6. 12 indexed citations

16.

Tommasi, Stefania, Vita Fedele, Rosanna Lacalamita, et al.. (2007). 655Val and 1170Pro ERBB2 SNPs in Familial Breast Cancer Risk and BRCA1 Alterations. Analytical Cellular Pathology. 29(3). 241–248. 19 indexed citations

17.

Seymour, Ian, Silvia Casadei, Valentina Zampiga, et al.. (2007). 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. 112(2). 343–349. 5 indexed citations

18.

Walsh, Tom, Silvia Casadei, Elizabeth M. Swisher, et al.. (2006). Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer. JAMA. 295(12). 1379–1379. 469 indexed citations

19.

Casadei, Silvia, Ian Seymour, Simonetta Rosato, et al.. (2004). Analysis of single nucleotide polymorphisms in coding and non-coding regions of human BRCA1 and BRCA2 genes. Cancer Research. 64. 301–301. 1 indexed citations

20.

Casadei, Silvia, Laura Cortesi, Valeria Pensotti, et al.. (2001). Detection of germline BRCA1 mutations by Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method. British Journal of Cancer. 85(6). 845–849. 3 indexed citations

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.

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