Annick Toutain
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Molecular Biology top 2%
- Muscle Physiology and Disorders
- RNA modifications and cancer
- RNA Research and Splicing
Papers in
-
- RNA modifications and cancer 11
- Muscle Physiology and Disorders 8
- Genetics 61
- Genetics and Neurodevelopmental Disorders 26
- Genomic variations and chromosomal abnormalities 16
- Genetic Syndromes and Imprinting 11
- Genomics and Rare Diseases 9
- Neurogenetic and Muscular Disorders Research 8
- Co-authors
- Claude Moraine (19 shared papers)Arnold Münnich (6 shared papers)Valérie Cormier‐Daire (4 shared papers)Michel Vekemans (5 shared papers)Marie‐Pierre Moizard (11 shared papers)Martine Le Merrer (4 shared papers)A. Gélot (3 shared papers)Alain Verloès (13 shared papers)
- Journals
- European Journal of Human Genetics (10 papers)The American Journal of Human Genetics (7 papers)European Journal of Medical Genetics (6 papers)Human Mutation (6 papers)Clinical Genetics (6 papers)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
Annick Toutain
136 papers receiving 4.3k citations
Peers
Comparison fields: 5 of 116
- Genetics 1.5k
- Genetics 435
- Molecular Biology 2.5k
- Developmental Biology 67
- Cellular and Molecular Neuroscience 491
Countries citing papers authored by Annick Toutain
This map shows the geographic impact of Annick Toutain'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 Annick Toutain with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annick Toutain more than expected).
Fields of papers citing papers by Annick Toutain
This network shows the impact of papers produced by Annick Toutain. 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 Annick Toutain. The network helps show where Annick Toutain may publish in the future.
Co-authors
The 25 scholars most cited alongside Annick Toutain, 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 141 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 280 | |
| 2 | 2007 | 252 | |
| 3 | 2007 | 198 | |
| 4 | 2007 | 181 | |
| 5 | 2005 | 168 | |
| 6 | 2011 | 163 | |
| 7 | 2002 | 129 | |
| 8 | 2006 | 109 | |
| 9 | 2008 | 102 | |
| 10 | 1998 | 101 | |
| 11 | 2009 | 99 | |
| 12 | 2009 | 95 | |
| 13 | 2000 | 94 | |
| 14 | 2000 | 88 | |
| 15 | 2008 | 86 | |
| 16 | 2001 | 80 | |
| 17 | 2005 | 66 | |
| 18 | 2019 | 59 | |
| 19 | 2005 | 59 | |
| 20 | 2012 | 58 |
About Annick Toutain
Annick Toutain is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 141 papers that have together received 4.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (26 papers), Genomic variations and chromosomal abnormalities (16 papers), Genetic Syndromes and Imprinting (11 papers), RNA modifications and cancer (11 papers), Genomics and Rare Diseases (9 papers), Prenatal Screening and Diagnostics (9 papers), Muscle Physiology and Disorders (8 papers) and Neurogenetic and Muscular Disorders Research (8 papers). The work is most often cited by research in Genetics (1.5k citations), Genetics (435 citations), Molecular Biology (2.5k citations), Developmental Biology (67 citations) and Cellular and Molecular Neuroscience (491 citations). Annick Toutain has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Claude Moraine, Arnold Münnich, Valérie Cormier‐Daire, Michel Vekemans, Marie‐Pierre Moizard, Martine Le Merrer, A. Gélot, Alain Verloès, Renaud Touraine and Véronica Cusin. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics, Human Mutation and Clinical Genetics.
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.