Eva Pipiras
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 3
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- Congenital heart defects research 3
- Retinal Development and Disorders 2
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- Prenatal Screening and Diagnostics 7
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- Chromosomal and Genetic Variations 6
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- Congenital limb and hand anomalies 3
- Co-authors
- Franck ToledoArnaud CoquelleMichelle DebatisseGérard ButtinBrigitte BenzackenCéline DupontAlain VerloèsAndrée Delahaye‐Duriez
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Eva Pipiras
26 papers receiving 675 citations
Peers
Comparison fields: 5 of 68
- Genetics 424
- Molecular Biology 475
- Cancer Research 80
- Pediatrics, Perinatology and Child Health 86
- Neurology 48
Countries citing papers authored by Eva Pipiras
This map shows the geographic impact of Eva Pipiras'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 Eva Pipiras with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Pipiras more than expected).
Fields of papers citing papers by Eva Pipiras
This network shows the impact of papers produced by Eva Pipiras. 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 Eva Pipiras. The network helps show where Eva Pipiras may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Eva Pipiras, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 2 | |
| 2 | 2020 | 9 | |
| 3 | 2019 | 7 | |
| 4 | 2018 | 19 | |
| 5 | 2018 | 25 | |
| 6 | 2017 | 15 | |
| 7 | 2012 | 37 | |
| 8 | 2011 | 2 | |
| 9 | 2010 | 20 | |
| 10 | 2009 | 41 | |
| 11 | 2007 | 3 | |
| 12 | 2007 | 3 | |
| 13 | 2006 | 6 | |
| 14 | 2006 | 16 | |
| 15 | 2006 | 18 | |
| 16 | 2004 | 8 | |
| 17 | 2004 | 15 | |
| 18 | 2003 | 18 | |
| 19 | 1998 | 96 | |
| 20 | 1997 | 330 |
About Eva Pipiras
Eva Pipiras is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 26 papers that have together received 744 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Chromosomal and Genetic Variations (6 papers), Genomics and Rare Diseases (3 papers), Congenital limb and hand anomalies (3 papers), Congenital heart defects research (3 papers) and Retinal Development and Disorders (2 papers). The work is most often cited by research in Genetics (424 citations), Molecular Biology (475 citations) and Cancer Research (80 citations). Eva Pipiras has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Franck Toledo, Arnaud Coquelle, Michelle Debatisse, Gérard Buttin, Brigitte Benzacken, Céline Dupont, Alain Verloès, Andrée Delahaye‐Duriez, Anne‐Claude Tabet and Séverine Drunat. Their work appears in journals such as Cell, The EMBO Journal and Neurology.
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.