Laëtitia Lambert
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
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- Genetic Neurodegenerative Diseases
Papers in
- Genetics 40
- Genomics and Rare Diseases 15
- Genetics and Neurodevelopmental Disorders 13
- Genomic variations and chromosomal abnormalities 8
- Neurogenetic and Muscular Disorders Research 6
- Genetic Syndromes and Imprinting 5
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- Hereditary Neurological Disorders 5
- Co-authors
- Christophe Philippe (9 shared papers)Philippe Jonveaux (8 shared papers)Daniel Amsallem (3 shared papers)Christophe Némos (3 shared papers)Christine Francannet (1 shared paper)Fabienne Giuliano (3 shared papers)Julien Thévenon (2 shared papers)Lila Allou (4 shared papers)
- Journals
- Journal of Medical Genetics (10 papers)Clinical Genetics (6 papers)Human Mutation (6 papers)European Journal of Medical Genetics (4 papers)European Journal of Human Genetics (4 papers)
- Partner nations
- FranceUnited StatesCanada
In The Last Decade
Laëtitia Lambert
69 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 92
- Genetics 801
- Cellular and Molecular Neuroscience 186
- Psychiatry and Mental health 125
- Molecular Biology 593
- Neurology 102
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 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 117 | |
| 2 | 2012 | 93 | |
| 3 | 2009 | 93 | |
| 4 | 2013 | 86 | |
| 5 | 2009 | 73 | |
| 6 | 2013 | 67 | |
| 7 | 2014 | 65 | |
| 8 | 2022 | 59 | |
| 9 | 2023 | 58 | |
| 10 | 2012 | 57 | |
| 11 | 2018 | 48 | |
| 12 | 2016 | 47 | |
| 13 | 2016 | 43 | |
| 14 | 2019 | 41 | |
| 15 | 2021 | 41 | |
| 16 | 2023 | 37 | |
| 17 | 2021 | 36 | |
| 18 | 2015 | 33 | |
| 19 | 2020 | 29 | |
| 20 | 2018 | 28 |
About Laëtitia Lambert
Laëtitia Lambert is a scholar working on Genetics, Cellular and Molecular Neuroscience, Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 73 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (15 papers), Genetics and Neurodevelopmental Disorders (13 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA modifications and cancer (6 papers), Neurogenetic and Muscular Disorders Research (6 papers), Prenatal Screening and Diagnostics (6 papers), Hereditary Neurological Disorders (5 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Genetics (801 citations), Cellular and Molecular Neuroscience (186 citations), Psychiatry and Mental health (125 citations), Molecular Biology (593 citations) and Neurology (102 citations). Laëtitia Lambert has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Christophe Philippe, Philippe Jonveaux, Daniel Amsallem, Christophe Némos, Christine Francannet, Fabienne Giuliano, Julien Thévenon, Lila Allou, Mylène Valduga and Bérénice Doray. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Human Mutation, European Journal of Medical Genetics and European Journal of Human 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.