Silvia Casadei

8.9k citations

33 papers · 3.4k indexed · 3 hit papers · h-index 19

Co-authors: Tom Walsh Mary‐Claire King Ming K. Lee Elizabeth M. Swisher Barbara M. Norquist Sunday M. Stray Anne Thornton Christopher C. Pennil
Topics: BRCA gene mutations in cancer (28 papers)DNA Repair Mechanisms (12 papers)Cancer Genomics and Diagnostics (11 papers)
Cited by: Reproductive Medicine Genetics Cancer Research
Journals: Proceedings of the National Academy of Sciences JAMA Journal of Clinical Oncology
Partner nations: United States Italy Israel

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

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

#	Work	Indexed citations
1	Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management 2021 ·Journal of Allergy and Clinical Immunology ·Sarah K. Baxter,Tom Walsh,Silvia Casadei,(unknown),Eric J. Allenspach,David Hagin,Gesmar Rodrigues Silva Segundo,Ming K. Lee,Süleyman Gülsüner,Brian H. Shirts,Kathleen E. Sullivan,Michael D. Keller,Troy R. Torgerson,Mary‐Claire King	21
2	Genomic analysis of inherited hearing loss in the Palestinian population 2020 ·Proceedings of the National Academy of Sciences ·Amal Abu Rayyan,(unknown),Silvia Casadei,Zippora Brownstein,(unknown),Hashem Shahin,Christina Canavati,(unknown),(unknown),(unknown),Ryan J. Carlson,Süleyman Gülsüner,Ming K. Lee,Karen B. Avraham,Tom Walsh,Mary‐Claire King,Moien Kanaan	38
3	CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes 2020 ·Journal of Medical Genetics ·Tom Walsh,Silvia Casadei,Katherine M. Munson,Mary Eng,Jessica B. Mandell,Süleyman Gülsüner,Mary‐Claire King	18
4	Amplification of the Mutation-Carrying BRCA2 Allele Promotes RAD51 Loading and PARP Inhibitor Resistance in the Absence of Reversion Mutations 2019 ·Molecular Cancer Therapeutics ·Pyoung Hwa Park,Tomomi M. Yamamoto,Hua Li,Allen L. Alcivar,Bing Xia,Yifan Wang,Andrea J. Bernhardy,Kristen M. Turner,Andrew V. Kossenkov,Zachary L. Watson,Kian Behbakht,Silvia Casadei,Elizabeth M. Swisher,Paul S. Mischel,Neil Johnson,Benjamin G. Bitler	20
5	Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance 2018 ·Genetics in Medicine ·(unknown),John Michael O. Rañola,Christina Smith,(unknown),Timothy Bergquist,Silvia Casadei,Deborah J. Bowen,Brian H. Shirts	42
6	Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2 2016 ·Breast Cancer Research and Treatment ·Irene Catucci,Silvia Casadei,Yuan Chun Ding,Sara Volorio,Filomena Ficarazzi,Anna Falanga,Marina Marchetti,Carlo Tondini,Michela Franchi,Aaron W. Adamson,Jessica B. Mandell,Tom Walsh,Olufunmilayo I. Olopade,Siranoush Manoukian,Paolo Radice,Charité Ricker,Jeffrey N. Weitzel,Mary‐Claire King,Paolo Peterlongo,Susan L. Neuhausen	8
7	Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis 2014 ·Genetics in Medicine ·Brian H. Shirts,Stephen J. Salipante,Silvia Casadei,(unknown),Judith A. Martin,Angela Jacobson,(unknown),Karen M. Koehler,Robert Livingston,Mary‐Claire King,Tom Walsh,Colin C. Pritchard	13
8	Inherited predisposition to breast cancer among African American women 2014 ·Breast Cancer Research and Treatment ·Jane Churpek,Tom Walsh,Yonglan Zheng,(unknown),Anne Thornton,Ming K. Lee,Silvia Casadei,(unknown),Barbara Neistadt,Matthew M. Churpek,Dezheng Huo,Cecilia Zvosec,Fang Liu,Qun Niu,Rafael Márquez,Jing Zhang,James D. Fackenthal,Mary‐Claire King,Olufunmilayo I. Olopade	114
9	Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomasbreakdown → 2013 ·Clinical Cancer Research ·Kathryn P. Pennington,Tom Walsh,Maria I. Harrell,Ming K. Lee,Christopher C. Pennil,Mara H. Rendi,Anne Thornton,Barbara M. Norquist,Silvia Casadei,Alex S. Nord,Kathy Agnew,Colin C. Pritchard,Sheena Scroggins,Rochelle L. Garcia,Mary‐Claire King,Elizabeth M. Swisher	712
10	Inherited mutations in breast cancer genes in African American breast cancer patients revealed by targeted genomic capture and next generation sequencing. 2013 ·Journal of Clinical Oncology ·Jane Churpek,Tom Walsh,Yonglan Zheng,Silvia Casadei,Anne Thornton,Ming K. Lee,Matthew M. Churpek,Dezheng Huo,Cecilia Zvosec,Fang Liu,Qun Niu,Jing Zhang,James D. Fackenthal,Mary‐Claire King,Olufunmilayo I. Olopade	5
11	Characteristics of women with ovarian carcinoma who have BRCA1 and BRCA2 mutations not identified by clinical testing 2012 ·Gynecologic Oncology ·Barbara M. Norquist,Kathryn P. Pennington,Kathy Agnew,Maria I. Harrell,Christopher C. Pennil,Ming K. Lee,Silvia Casadei,Anne Thornton,Rochelle L. Garcia,Tom Walsh,Elizabeth M. Swisher	21
12	Loss of function germline mutations in RAD51D in women with ovarian carcinoma 2012 ·Gynecologic Oncology ·(unknown),(unknown),Christopher C. Pennil,Silvia Casadei,Kathy Agnew,Sunday M. Stray,Jessica B. Mandell,Rochelle L. Garcia,Tom Walsh,Mary‐Claire King,Elizabeth M. Swisher	28
13	Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer 2011 ·Cancer Research ·Silvia Casadei,Barbara M. Norquist,Tom Walsh,Sunday M. Stray,Jessica B. Mandell,Ming K. Lee,J Stamatoyannopoulos,Mary‐Claire King	182
14	Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencingbreakdown → 2011 ·Proceedings of the National Academy of Sciences ·Tom Walsh,Silvia Casadei,Ming K. Lee,Christopher C. Pennil,Alex S. Nord,Anne Thornton,Wendy Roeb,Kathy Agnew,Sunday M. Stray,Anneka Wickramanayake,Barbara M. Norquist,Kathryn P. Pennington,Rochelle L. Garcia,Mary‐Claire King,Elizabeth M. Swisher	662
15	Disease family history and modification of breast cancer risk in common BRCA2 variants 2008 ·Oncology Reports ·Ian Seymour,Silvia Casadei,Valentina Zampiga,Simonetta Rosato,Rita Danesi,Fabio Falcini,(unknown),(unknown),Carlo Naldoni,Angelo Paradiso,Stefania Tommasi,Francesco Schittulli,Dino Amadori,Daniele Calistri	12
16	655Val and 1170Pro ERBB2 SNPs in Familial Breast Cancer Risk and BRCA1 Alterations 2007 ·Analytical Cellular Pathology ·Stefania Tommasi,Vita Fedele,Rosanna Lacalamita,(unknown),Francesco Schittulli,David G. Ginzinger,(unknown),Serenella Eppenberger‐Castori,Daniele Calistri,Silvia Casadei,Ian Seymour,Salvatore Longo,Gianluigi Giannelli,Brunella Pilato,Giovanni de Simone,Christopher C. Benz,Angelo Paradiso	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 2007 ·Breast Cancer Research and Treatment ·Ian Seymour,Silvia Casadei,Valentina Zampiga,Simonetta Rosato,Rita Danesi,Emanuela Scarpi,Fabio Falcini,(unknown),(unknown),Carlo Naldoni,Dino Amadori,Daniele Calistri	5
18	Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer 2006 ·JAMA ·Tom Walsh,Silvia Casadei,(unknown),Elizabeth M. Swisher,Sunday M. Stray,Jake Higgins,Kevin Roach,Jessica B. Mandell,Ming K. Lee,Soňa Čierniková,Lenka Foretová,Pavel Souček,Mary‐Claire King	469
19	Analysis of single nucleotide polymorphisms in coding and non-coding regions of human BRCA1 and BRCA2 genes 2004 ·Cancer Research ·Silvia Casadei,Ian Seymour,Simonetta Rosato,Elena Lucchi,Fabio Falcini,Dino Amadori,Daniele Calistri	1
20	Detection of germline BRCA1 mutations by Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method 2001 ·British Journal of Cancer ·Silvia Casadei,Laura Cortesi,Valeria Pensotti,Paolo Radice,Marco A. Pierotti,D. Amadori,Daniele Calistri	3

About Silvia Casadei

Silvia Casadei is a scholar working on Genetics, Reproductive Medicine and Cancer Research, having authored 33 papers that have together received 3.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (28 papers), DNA Repair Mechanisms (12 papers) and Cancer Genomics and Diagnostics (11 papers). The work is most often cited by research in Reproductive Medicine (1.0k citations), Genetics (2.1k citations) and Cancer Research (905 citations). Silvia Casadei has collaborated with scholars based in United States, Italy and Israel. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, JAMA and Journal of Clinical Oncology.

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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