Alexandre Reymond
Impact in
- Cancer Research top 0.05%
- Cancer-related molecular mechanisms research
- Molecular Biology top 0.05%
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- Genomics and Phylogenetic Studies
Papers in
- Genetics 85
- Genomic variations and chromosomal abnormalities 54
- Genomics and Rare Diseases 27
- Genetics and Neurodevelopmental Disorders 20
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- Genomics and Chromatin Dynamics 30
- RNA modifications and cancer 24
- Congenital heart defects research 23
- RNA and protein synthesis mechanisms 17
- Co-authors
- Stylianos E. Antonarakis (30 shared papers)Emmanouil T. Dermitzakis (12 shared papers)Giuseppe Merla (18 shared papers)Robert Lyle (13 shared papers)Charlotte Neergaard Henrichsen (7 shared papers)Samuel Deutsch (9 shared papers)Catherine Ucla (9 shared papers)Andrea Ballabio (8 shared papers)
- Journals
- The American Journal of Human Genetics (18 papers)Nature (13 papers)Human Molecular Genetics (7 papers)European Journal of Human Genetics (7 papers)Nature Communications (6 papers)
- Partner nations
- SwitzerlandUnited StatesUnited Kingdom
In The Last Decade
Alexandre Reymond
177 papers receiving 46.4k citations
Alexandre Reymond's Hit Papers
Peers
Comparison fields: 5 of 203
- Cancer Research 9.7k
- Molecular Biology 32.4k
- Genetics 11.8k
- Aging 326
- Immunology 3.1k
Countries citing papers authored by Alexandre Reymond
This map shows the geographic impact of Alexandre Reymond'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 Alexandre Reymond with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandre Reymond more than expected).
Fields of papers citing papers by Alexandre Reymond
This network shows the impact of papers produced by Alexandre Reymond. 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 Alexandre Reymond. The network helps show where Alexandre Reymond may publish in the future.
Co-authors
The 25 scholars most cited alongside Alexandre Reymond, 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 184 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | An integrated encyclopedia of DNA elements in the human genome Hit paper breakdown → | 2012 | 13299 |
| 2 | Initial sequencing and comparative analysis of the mouse genome Hit paper breakdown → | 2002 | 5361 |
| 3 | Landscape of transcription in human cells Hit paper breakdown → | 2012 | 4122 |
| 4 | Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project Hit paper breakdown → | 2007 | 4022 |
| 5 | An integrated encyclopedia of DNA elements in the human genome Hit paper breakdown → | 2012 | 2353 |
| 6 | GENCODE reference annotation for the human and mouse genomes Hit paper breakdown → | 2018 | 2086 |
| 7 | Expanded encyclopaedias of DNA elements in the human and mouse genomes Hit paper breakdown → | 2020 | 1387 |
| 8 | The tripartite motif family identifies cell compartments Hit paper breakdown → | 2001 | 1146 |
| 9 | The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution Hit paper breakdown → | 2009 | 973 |
| 10 | 2004 | 539 | |
| 11 | 2011 | 525 | |
| 12 | GENCODE: producing a reference annotation for ENCODE Hit paper breakdown → | 2006 | 483 |
| 13 | 2010 | 420 | |
| 14 | 2011 | 372 | |
| 15 | 2009 | 346 | |
| 16 | 2012 | 326 | |
| 17 | 2012 | 269 | |
| 18 | 2013 | 267 | |
| 19 | 2009 | 252 | |
| 20 | 2012 | 240 |
About Alexandre Reymond
Alexandre Reymond is a scholar working on Genetics, Molecular Biology, Developmental Neuroscience, Plant Science and Pediatrics, Perinatology and Child Health, having authored 184 papers that have together received 47.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (54 papers), Genomics and Chromatin Dynamics (30 papers), Genomics and Rare Diseases (27 papers), RNA modifications and cancer (24 papers), Congenital heart defects research (23 papers), Chromosomal and Genetic Variations (21 papers), Genetics and Neurodevelopmental Disorders (20 papers) and RNA and protein synthesis mechanisms (17 papers). The work is most often cited by research in Cancer Research (9.7k citations), Molecular Biology (32.4k citations), Genetics (11.8k citations), Aging (326 citations) and Immunology (3.1k citations). Alexandre Reymond has collaborated with scholars based in Switzerland, United States and United Kingdom. Frequent co-authors include Stylianos E. Antonarakis, Emmanouil T. Dermitzakis, Giuseppe Merla, Robert Lyle, Charlotte Neergaard Henrichsen, Samuel Deutsch, Catherine Ucla, Andrea Ballabio, Germana Meroni and Viesturs Simanis. Their work appears in journals such as The American Journal of Human Genetics, Nature, Human Molecular Genetics, European Journal of Human Genetics and Nature Communications.
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.