Daniela Turchetti

2.9k citations
94 papers · 1.2k · h-index 21

Impact in

  • Genetics top 5%
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Cancer Genomics and Diagnostics

Papers in

    • BRCA gene mutations in cancer 49
    • Genomics and Rare Diseases 14
    • Genomic variations and chromosomal abnormalities 7

Daniela Turchetti

86 papers receiving 1.1k citations

Peers

Daniela Turchetti
Comparison fields: 5 of 88
  • Genetics 589
  • Cancer Research 293
  • Reproductive Medicine 152
  • Pathology and Forensic Medicine 219
  • Oncology 250
Replace Hanne Meijers-Heijboer with:
Hanne Meijers-Heijboer Netherlands
Victoria Murday United Kingdom
Aliza Amiel Israel
Shiuh‐Wen Luoh United States
Kristen M. Shannon United States
C. Marleen Kets Netherlands
Pamela Minicozzi Italy
Vijayachitra Modhukur Estonia
C. Snyder United States
Myra Wick United States
Daniela Turchetti relative to Hanne Meijers-Heijboer Netherlands Hanne Meijers-Heijboer's profile →
Citations per field
00.5×4.6×
Hanne Meijers-Heijboer · 1×
Citations per year

Countries citing papers authored by Daniela Turchetti

Since Specialization
Citations

This map shows the geographic impact of Daniela Turchetti'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 Daniela Turchetti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Turchetti more than expected).

Fields of papers citing papers by Daniela Turchetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniela Turchetti. 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 Daniela Turchetti. The network helps show where Daniela Turchetti may publish in the future.

Co-authors

The 25 scholars most cited alongside Daniela Turchetti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Daniela Turchetti Line = papers co-authored together Daniela Turchetti links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 94 papers — load more, or switch the sort, to bring in the rest.

#Work
1 202174
2 201655
3 201454
4 201552
5 200750
6 202140
7 200639
8 201732
9 201032
10 201232
11 200030
12 200026
13 201825
14 200725
15 199925
16 202025
17 200425
18 201624
19 201422
20 201821

About Daniela Turchetti

Daniela Turchetti is a scholar working on Genetics, Molecular Biology, Oncology, Cancer Research and Pathology and Forensic Medicine, having authored 94 papers that have together received 1.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (49 papers), Cancer Genomics and Diagnostics (19 papers), Genetic factors in colorectal cancer (17 papers), Genomics and Rare Diseases (14 papers), Prenatal Screening and Diagnostics (8 papers), PARP inhibition in cancer therapy (8 papers), Ovarian cancer diagnosis and treatment (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (589 citations), Cancer Research (293 citations), Reproductive Medicine (152 citations), Pathology and Forensic Medicine (219 citations) and Oncology (250 citations). Daniela Turchetti has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Lea Godino, Heather Skirton, Leigh Jackson, Laura Cortesi, Catherine Hagan Hennessy, Massimo Federico, Donatella Santini, Claudio Ceccarelli, Simona Ferrari and Pierandrea De Iaco. Their work appears in journals such as European Journal of Human Genetics, BMC Cancer, Cancers, International Journal of Molecular Sciences and Journal of Medical Genetics.

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.

Explore authors with similar magnitude of impact