Delphine S. Ally
- Oncology top 5%
- Cutaneous Melanoma Detection and Management 1
- Cancer Research top 10%
- Cancer Genomics and Diagnostics 1
- Cell Biology top 10%
-
- RNA modifications and cancer 1
- Mitochondrial Function and Pathology 1
- Dermatology top 10%
-
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
- Genomic variations and chromosomal abnormalities 1
-
- Prenatal Screening and Diagnostics 1
- Co-authors
- Paul HigginsNicholas C. DracopoliM. A. TuckerChristopher J. HussussianJeffery P. StruewingAnirban MaitraPeter E. BarkerJohn P. Jakupciak
- Cited by
- OncologyCancer ResearchCell Biology
- Journals
- Nature Genetics (1 paper)Diabetologia (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesFinland
In The Last Decade
Delphine S. Ally
4 papers receiving 1.0k citations
Hit Papers
Peers
Comparison fields: 5 of 71
- Oncology 683
- Cancer Research 301
- Cell Biology 157
- Molecular Biology 634
- Dermatology 70
Countries citing papers authored by Delphine S. Ally
This map shows the geographic impact of Delphine S. Ally'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 Delphine S. Ally with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Delphine S. Ally more than expected).
Fields of papers citing papers by Delphine S. Ally
This network shows the impact of papers produced by Delphine S. Ally. 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 Delphine S. Ally. The network helps show where Delphine S. Ally may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Delphine S. Ally, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 73 | |
| 2 | 2000 | 18 | |
| 3 | 1999 | 32 | |
| 4 | Germline p16 mutations in familial melanomabreakdown → | 1994 | 939 |
About Delphine S. Ally
Delphine S. Ally is a scholar working on Genetics, Cancer Research and Endocrinology, Diabetes and Metabolism, having authored 4 papers that have together received 1.1k indexed citations. Recurring topics across this work include RNA modifications and cancer (1 paper), Genomics and Rare Diseases (1 paper), Genetic Syndromes and Imprinting (1 paper), Cutaneous Melanoma Detection and Management (1 paper), Prenatal Screening and Diagnostics (1 paper), Mitochondrial Function and Pathology (1 paper), Cancer Genomics and Diagnostics (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Oncology (683 citations), Cancer Research (301 citations) and Cell Biology (157 citations). Delphine S. Ally has collaborated with scholars based in United States and Finland. Frequent co-authors include Paul Higgins, Nicholas C. Dracopoli, M. A. Tucker, Christopher J. Hussussian, Jeffery P. Struewing, Anirban Maitra, Peter E. Barker, John P. Jakupciak, Michael D. Coble and Catherine D. O’Connell. Their work appears in journals such as Nature Genetics, Diabetologia and American 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.