Anna Ruiz
Impact in
- Cancer Research top 10%
- MicroRNA in disease regulation
- Oncology top 10%
- Cutaneous Melanoma Detection and Management
- Cancer-related Molecular Pathways
Papers in
- Co-authors
- Susana Puig (9 shared papers)TERESA CASTEL (5 shared papers)Xavier Estivill (7 shared papers)Josep Malvehy (5 shared papers)Anna Brunet‐Vega (6 shared papers)Eugeni Saigí (2 shared papers)Carles Pericay (1 shared paper)Anna Ferrer (1 shared paper)
- Journals
- The American Journal of Human Genetics (6 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (2 papers)Genetics in Medicine (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- SpainFranceUnited States
In The Last Decade
Anna Ruiz
43 papers receiving 953 citations
Peers
Comparison fields: 5 of 35
- Cancer Research 131
- Oncology 219
- Genetics 164
- Genetics 43
- Molecular Biology 76
Countries citing papers authored by Anna Ruiz
This map shows the geographic impact of Anna Ruiz'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 Anna Ruiz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Ruiz more than expected).
Fields of papers citing papers by Anna Ruiz
This network shows the impact of papers produced by Anna Ruiz. 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 Anna Ruiz. The network helps show where Anna Ruiz may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Ruiz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 148 | |
| 2 | 2005 | 124 | |
| 3 | Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) gene. | 1995 | 75 |
| 4 | 1997 | 51 | |
| 5 | 1999 | 50 | |
| 6 | 2016 | 44 | |
| 7 | 2020 | 40 | |
| 8 | 2022 | 40 | |
| 9 | 1998 | 39 | |
| 10 | 2020 | 36 | |
| 11 | 2014 | 34 | |
| 12 | 2018 | 27 | |
| 13 | 2003 | 25 | |
| 14 | 2022 | 25 | |
| 15 | 2021 | 23 | |
| 16 | 2022 | 22 | |
| 17 | 2018 | 21 | |
| 18 | 2021 | 19 | |
| 19 | 2019 | 17 | |
| 20 | 2014 | 15 |
About Anna Ruiz
Anna Ruiz is a scholar working on Genetics, Oncology, Psychiatry and Mental health, Genetics and Cancer Research, having authored 51 papers that have together received 973 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Cutaneous Melanoma Detection and Management (8 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers), Epilepsy research and treatment (1 paper), Schizophrenia research and treatment (1 paper) and Cleft Lip and Palate Research (1 paper). The work is most often cited by research in Cancer Research (131 citations), Oncology (219 citations), Genetics (164 citations), Genetics (43 citations) and Molecular Biology (76 citations). Anna Ruiz has collaborated with scholars based in Spain, France and United States. Frequent co-authors include Susana Puig, TERESA CASTEL, Xavier Estivill, Josep Malvehy, Anna Brunet‐Vega, Eugeni Saigí, Carles Pericay, Anna Ferrer, Elisabeth Gabau and Emma Dotor. Their work appears in journals such as The American Journal of Human Genetics, Clinical Genetics, Journal of Medical Genetics, Genetics in Medicine and European Journal of Human 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.