Florence Fellmann
Impact in
Papers in
-
- RNA regulation and disease 4
- Sexual Differentiation and Disorders 4
- Genetics 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genomics and Rare Diseases 5
- BRCA gene mutations in cancer 3
- Co-authors
- Carla van El (6 shared papers)Martina C. Cornel (5 shared papers)Ros Hastings (4 shared papers)Wybo Dondorp (3 shared papers)Heidi Howard (3 shared papers)Pascal Borry (4 shared papers)Anne Cambon‐Thomsen (2 shared papers)Hans Scheffer (2 shared papers)
- Journals
- European Journal of Human Genetics (4 papers)Cytogenetic and Genome Research (2 papers)Heart Rhythm (2 papers)Human Mutation (2 papers)Nature Communications (1 paper)
- Partner nations
- SwitzerlandFranceUnited Kingdom
In The Last Decade
Florence Fellmann
48 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 102
- Genetics 691
- Neurology 96
- Pediatrics, Perinatology and Child Health 188
- Cancer Research 133
- Cardiology and Cardiovascular Medicine 193
Countries citing papers authored by Florence Fellmann
This map shows the geographic impact of Florence Fellmann'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 Florence Fellmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florence Fellmann more than expected).
Fields of papers citing papers by Florence Fellmann
This network shows the impact of papers produced by Florence Fellmann. 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 Florence Fellmann. The network helps show where Florence Fellmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Florence Fellmann, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. | 2013 | 270 |
| 2 | 2013 | 256 | |
| 3 | 2020 | 82 | |
| 4 | 2006 | 80 | |
| 5 | 2005 | 61 | |
| 6 | 2015 | 60 | |
| 7 | 2006 | 51 | |
| 8 | 2015 | 50 | |
| 9 | 2016 | 43 | |
| 10 | 2008 | 38 | |
| 11 | 2015 | 31 | |
| 12 | 1997 | 30 | |
| 13 | 2001 | 27 | |
| 14 | 2011 | 25 | |
| 15 | 2012 | 23 | |
| 16 | 2015 | 23 | |
| 17 | 2019 | 22 | |
| 18 | 2019 | 19 | |
| 19 | 1996 | 16 | |
| 20 | 2012 | 16 |
About Florence Fellmann
Florence Fellmann is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Surgery and Genetics, having authored 54 papers that have together received 1.4k indexed citations. Recurring topics across this work include Cardiac electrophysiology and arrhythmias (6 papers), Cardiovascular Effects of Exercise (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genomics and Rare Diseases (5 papers), RNA regulation and disease (4 papers), Sexual Differentiation and Disorders (4 papers), BRCA gene mutations in cancer (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). The work is most often cited by research in Genetics (691 citations), Neurology (96 citations), Pediatrics, Perinatology and Child Health (188 citations), Cancer Research (133 citations) and Cardiology and Cardiovascular Medicine (193 citations). Florence Fellmann has collaborated with scholars based in Switzerland, France and United Kingdom. Frequent co-authors include Carla van El, Martina C. Cornel, Ros Hastings, Wybo Dondorp, Heidi Howard, Pascal Borry, Anne Cambon‐Thomsen, Hans Scheffer, Bartha Maria Knoppers and Hanne Meijers‐Heijboer. Their work appears in journals such as European Journal of Human Genetics, Cytogenetic and Genome Research, Heart Rhythm, Human Mutation 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.