Ignacio Blanco
Impact in
- Pathology and Forensic Medicine top 0.1%
- Genetic factors in colorectal cancer
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Papers in
-
- Genetic factors in colorectal cancer 56
- Genetics 59
- BRCA gene mutations in cancer 48
- Genomic variations and chromosomal abnormalities 11
- Co-authors
- Gabriel Capellá (46 shared papers)Conxi Lázaro (48 shared papers)Enric C. Sumalla (5 shared papers)Cristian Ochoa (4 shared papers)Sara González (19 shared papers)Marta Pineda (19 shared papers)Joan Brunet (18 shared papers)Eduard Serra (26 shared papers)
- Journals
- Breast Cancer Research and Treatment (10 papers)European Journal of Human Genetics (9 papers)Gut (7 papers)PLoS ONE (7 papers)Human Mutation (7 papers)
- Partner nations
- SpainUnited KingdomUnited States
In The Last Decade
Ignacio Blanco
231 papers receiving 17.2k citations
Ignacio Blanco's Hit Papers
Peers
Comparison fields: 5 of 181
- Pathology and Forensic Medicine 4.7k
- Cancer Research 2.4k
- Infectious Diseases 3.0k
- Genetics 3.8k
- Neurology 1.9k
Countries citing papers authored by Ignacio Blanco
This map shows the geographic impact of Ignacio Blanco'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 Ignacio Blanco with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ignacio Blanco more than expected).
Fields of papers citing papers by Ignacio Blanco
This network shows the impact of papers produced by Ignacio Blanco. 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 Ignacio Blanco. The network helps show where Ignacio Blanco may publish in the future.
Co-authors
The 25 scholars most cited alongside Ignacio Blanco, 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 238 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autoantibodies against type I IFNs in patients with life-threatening COVID-19 Hit paper breakdown → | 2020 | 2063 |
| 2 | Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 Hit paper breakdown → | 2020 | 1718 |
| 3 | Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts Hit paper breakdown → | 2013 | 580 |
| 4 | Peutz–Jeghers syndrome: a systematic review and recommendations for management Hit paper breakdown → | 2010 | 536 |
| 5 | Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1 / 2 (CIMBA) Hit paper breakdown → | 2012 | 529 |
| 6 | Guidelines for the clinical management of familial adenomatous polyposis (FAP) Hit paper breakdown → | 2008 | 526 |
| 7 | Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database Hit paper breakdown → | 2019 | 481 |
| 8 | 2013 | 463 | |
| 9 | Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Hit paper breakdown → | 2021 | 459 |
| 10 | Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database Hit paper breakdown → | 2017 | 450 |
| 11 | Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database Hit paper breakdown → | 2015 | 446 |
| 12 | 2007 | 423 | |
| 13 | Association of Type and Location ofBRCA1andBRCA2Mutations With Risk of Breast and Ovarian Cancer Hit paper breakdown → | 2015 | 397 |
| 14 | 2013 | 328 | |
| 15 | 2010 | 276 | |
| 16 | 2003 | 274 | |
| 17 | 2006 | 226 | |
| 18 | 2008 | 222 | |
| 19 | 2015 | 209 | |
| 20 | 2014 | 198 |
About Ignacio Blanco
Ignacio Blanco is a scholar working on Pathology and Forensic Medicine, Genetics, Neurology, Cancer Research and Infectious Diseases, having authored 238 papers that have together received 17.6k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (56 papers), BRCA gene mutations in cancer (48 papers), Neurofibromatosis and Schwannoma Cases (32 papers), Cancer Genomics and Diagnostics (24 papers), SARS-CoV-2 and COVID-19 Research (20 papers), Colorectal Cancer Screening and Detection (18 papers), DNA Repair Mechanisms (14 papers) and Genomic variations and chromosomal abnormalities (11 papers). The work is most often cited by research in Pathology and Forensic Medicine (4.7k citations), Cancer Research (2.4k citations), Infectious Diseases (3.0k citations), Genetics (3.8k citations) and Neurology (1.9k citations). Ignacio Blanco has collaborated with scholars based in Spain, United Kingdom and United States. Frequent co-authors include Gabriel Capellá, Conxi Lázaro, Enric C. Sumalla, Cristian Ochoa, Sara González, Marta Pineda, Joan Brunet, Eduard Serra, Víctor Manuel Landassuri Moreno and Elisabet Guinó. Their work appears in journals such as Breast Cancer Research and Treatment, European Journal of Human Genetics, Gut, PLoS ONE and Human Mutation.
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.