Xavier Estivill
Impact in
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics
- Cancer-related molecular mechanisms research
- Sensory Systems top 0.05%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 177
- Genomic variations and chromosomal abnormalities 53
- Genetics and Neurodevelopmental Disorders 51
- Genomics and Rare Diseases 36
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- RNA modifications and cancer 37
- Mitochondrial Function and Pathology 33
- Co-authors
- Raquel Rabionet (40 shared papers)Lluı́s Armengol (33 shared papers)Paolo Gasparini (40 shared papers)Mónica Gratacòs (56 shared papers)Eulàlia Martı́ (22 shared papers)Virginia Nunes (64 shared papers)Teresa Casals (61 shared papers)Juan Ramon González Ruiz (26 shared papers)
- Journals
- Human Genetics (60 papers)Human Mutation (45 papers)Human Molecular Genetics (26 papers)Nature Genetics (25 papers)Nature (17 papers)
- Partner nations
- SpainUnited KingdomUnited States
In The Last Decade
Xavier Estivill
645 papers receiving 59.4k citations
Xavier Estivill's Hit Papers
Peers
Comparison fields: 5 of 214
- Cancer Research 9.8k
- Sensory Systems 3.1k
- Genetics 13.9k
- Molecular Biology 27.0k
- Genetics 3.4k
Countries citing papers authored by Xavier Estivill
This map shows the geographic impact of Xavier Estivill'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 Xavier Estivill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xavier Estivill more than expected).
Fields of papers citing papers by Xavier Estivill
This network shows the impact of papers produced by Xavier Estivill. 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 Xavier Estivill. The network helps show where Xavier Estivill may publish in the future.
Co-authors
The 25 scholars most cited alongside Xavier Estivill, 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 651 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project Hit paper breakdown → | 2007 | 4022 |
| 2 | Global variation in copy number in the human genome Hit paper breakdown → | 2006 | 3352 |
| 3 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 4 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 5 | International network of cancer genome projects Hit paper breakdown → | 2010 | 1836 |
| 6 | Transcriptome and genome sequencing uncovers functional variation in humans Hit paper breakdown → | 2013 | 1399 |
| 7 | Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia Hit paper breakdown → | 2011 | 1265 |
| 8 | A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 Hit paper breakdown → | 2010 | 884 |
| 9 | Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity Hit paper breakdown → | 2012 | 836 |
| 10 | Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia Hit paper breakdown → | 2011 | 821 |
| 11 | Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa Hit paper breakdown → | 2019 | 730 |
| 12 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 13 | Non-coding recurrent mutations in chronic lymphocytic leukaemia Hit paper breakdown → | 2015 | 695 |
| 14 | SNPassoc: an R package to perform whole genome association studies Hit paper breakdown → | 2007 | 687 |
| 15 | Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Hit paper breakdown → | 2008 | 629 |
| 16 | 1998 | 557 | |
| 17 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 18 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 19 | 1998 | 454 | |
| 20 | 2011 | 436 |
About Xavier Estivill
Xavier Estivill is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Sensory Systems and Cancer Research, having authored 651 papers that have together received 61.2k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (99 papers), Genomic variations and chromosomal abnormalities (53 papers), Genetics and Neurodevelopmental Disorders (51 papers), Neonatal Respiratory Health Research (41 papers), Hearing, Cochlea, Tinnitus, Genetics (38 papers), RNA modifications and cancer (37 papers), Genomics and Rare Diseases (36 papers) and Mitochondrial Function and Pathology (33 papers). The work is most often cited by research in Cancer Research (9.8k citations), Sensory Systems (3.1k citations), Genetics (13.9k citations), Molecular Biology (27.0k citations) and Genetics (3.4k citations). Xavier Estivill has collaborated with scholars based in Spain, United Kingdom and United States. Frequent co-authors include Raquel Rabionet, Lluı́s Armengol, Paolo Gasparini, Mónica Gratacòs, Eulàlia Martı́, Virginia Nunes, Teresa Casals, Juan Ramon González Ruiz, Maria Lourdes Arbonés and Josep Maria Mercader. Their work appears in journals such as Human Genetics, Human Mutation, Human Molecular Genetics, Nature Genetics and Nature.
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.