Laëtitia Lambert
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
-
- Autoimmune Neurological Disorders and Treatments
Papers in
- Genetics 23
- Genetics and Neurodevelopmental Disorders 8
- Genomic variations and chromosomal abnormalities 8
- Genetic Syndromes and Imprinting 4
- Neurogenetic and Muscular Disorders Research 4
- Connective tissue disorders research 3
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- RNA modifications and cancer 5
- Hedgehog Signaling Pathway Studies 3
- Co-authors
- Christophe Philippe (8 shared papers)Philippe Jonveaux (7 shared papers)Daniel Amsallem (3 shared papers)Christine Francannet (1 shared paper)Christophe Némos (3 shared papers)Fabienne Giuliano (2 shared papers)Julien Thévenon (2 shared papers)B Delobel (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)European Journal of Medical Genetics (2 papers)Journal of Medical Genetics (2 papers)Clinical Genetics (2 papers)Brain Communications (1 paper)
- Partner nations
- FranceUnited StatesAustralia
In The Last Decade
Laëtitia Lambert
29 papers receiving 496 citations
Peers
Comparison fields: 5 of 62
- Genetics 351
- Neurology 61
- Cognitive Neuroscience 77
- Psychiatry and Mental health 59
- Molecular Biology 235
Countries citing papers authored by Laëtitia Lambert
This map shows the geographic impact of Laëtitia Lambert'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 Laëtitia Lambert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laëtitia Lambert more than expected).
Fields of papers citing papers by Laëtitia Lambert
This network shows the impact of papers produced by Laëtitia Lambert. 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 Laëtitia Lambert. The network helps show where Laëtitia Lambert may publish in the future.
Co-authors
The 25 scholars most cited alongside Laëtitia Lambert, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 83 | |
| 2 | 2012 | 80 | |
| 3 | 2009 | 64 | |
| 4 | 2013 | 52 | |
| 5 | 2012 | 50 | |
| 6 | 2016 | 33 | |
| 7 | 2015 | 26 | |
| 8 | 2018 | 22 | |
| 9 | 2014 | 18 | |
| 10 | 2013 | 15 | |
| 11 | 2018 | 13 | |
| 12 | 2021 | 10 | |
| 13 | 2023 | 7 | |
| 14 | 2022 | 5 | |
| 15 | 2017 | 5 | |
| 16 | 2022 | 4 | |
| 17 | 2019 | 4 | |
| 18 | 2018 | 4 | |
| 19 | 2022 | 3 | |
| 20 | 2012 | 2 |
About Laëtitia Lambert
Laëtitia Lambert is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 32 papers that have together received 509 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA modifications and cancer (5 papers), Genetic Syndromes and Imprinting (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Hereditary Neurological Disorders (3 papers), Connective tissue disorders research (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). The work is most often cited by research in Genetics (351 citations), Neurology (61 citations), Cognitive Neuroscience (77 citations), Psychiatry and Mental health (59 citations) and Molecular Biology (235 citations). Laëtitia Lambert has collaborated with scholars based in France, United States and Australia. Frequent co-authors include Christophe Philippe, Philippe Jonveaux, Daniel Amsallem, Christine Francannet, Christophe Némos, Fabienne Giuliano, Julien Thévenon, B Delobel, Bérénice Doray and Alice Goldenberg. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Journal of Medical Genetics, Clinical Genetics and Brain 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.