Laëtitia Lambert

2.0k total citations
32 papers, 509 citations indexed

About

Laëtitia Lambert is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Laëtitia Lambert has authored 32 papers receiving a total of 509 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 17 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Laëtitia Lambert's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and RNA modifications and cancer (5 papers). Laëtitia Lambert is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and RNA modifications and cancer (5 papers). Laëtitia Lambert collaborates with scholars based in France, United States and Australia. Laëtitia Lambert's co-authors include Christophe Philippe, Philippe Jonveaux, Daniel Amsallem, Christophe Némos, Christine Francannet, Fabienne Giuliano, Julien Thévenon, Alice Goldenberg, B Delobel and Valérie Layet and has published in prestigious journals such as Neurology, Journal of Agricultural and Food Chemistry and Frontiers in Immunology.

In The Last Decade

Laëtitia Lambert

29 papers receiving 496 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Laëtitia Lambert France 11 351 235 77 61 59 32 509
Tracie C. Rosser United States 10 205 0.6× 260 1.1× 86 1.1× 24 0.4× 22 0.4× 13 444
Adriana Lo‐Castro Italy 12 212 0.6× 166 0.7× 98 1.3× 45 0.7× 77 1.3× 18 390
Tiia Reimand Estonia 13 291 0.8× 229 1.0× 21 0.3× 18 0.3× 55 0.9× 41 488
Shino Shimada Japan 15 318 0.9× 315 1.3× 35 0.5× 19 0.3× 43 0.7× 36 545
Aneek Das Bhowmik India 13 179 0.5× 179 0.8× 68 0.9× 25 0.4× 87 1.5× 36 428
Elisabeth Gabau Spain 16 463 1.3× 336 1.4× 103 1.3× 12 0.2× 20 0.3× 36 675
Julie Lauzon Canada 10 228 0.6× 196 0.8× 38 0.5× 23 0.4× 13 0.2× 23 430
Shinji Ono Japan 11 130 0.4× 153 0.7× 38 0.5× 26 0.4× 22 0.4× 26 383
Naohiro Kurotaki Japan 12 312 0.9× 223 0.9× 35 0.5× 32 0.5× 14 0.2× 20 446

Countries citing papers authored by Laëtitia Lambert

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Laëtitia Lambert

This figure shows the co-authorship network connecting the top 25 collaborators of Laëtitia Lambert. A scholar is included among the top collaborators of Laëtitia Lambert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laëtitia Lambert. Laëtitia Lambert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ravel, Jean‐Marie, Emmanuelle Schmitt, Lucie Hopes, et al.. (2025). Mild cognitive dysfunction in hereditary spastic paraplegia 4 disease related to fluorodesoxyglucose cerebral positron emission tomography. Brain Communications. 7(6). fcaf382–fcaf382.
2.
Pellerin, David, Matt C. Danzi, Céline Bonnet, et al.. (2024). Oculomotor Findings in Spinocerebellar Ataxia 27B: A Case Series. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 52(5). 868–870. 1 indexed citations
3.
Bonnet, Céline, et al.. (2024). Megalencephaly secondary to a novel germline missense variant p.Asp322Tyr in AKT3 associated with growth hormone deficiency and central hypothyroidism: A case report. American Journal of Medical Genetics Part A. 194(7). e63585–e63585. 1 indexed citations
4.
Bonnet, Céline, Virginie Roth, Yannis Duffourd, et al.. (2024). Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 194(9). e63642–e63642. 1 indexed citations
5.
Gençpınar, Pınar, Ange‐Line Bruel, Christophe Philippe, et al.. (2024). Patients with complex and very-early-onset ATL1-related spastic paraplegia offer insights on genotype/phenotype correlations and support for autosomal recessive forms of SPG3A. Journal of Neurology. 271(9). 6343–6348. 1 indexed citations
6.
Kaoma, Tony, François Bernardin, Laurent Vallar, et al.. (2023). Cross‐Talk between miRNAs from the Dlk1‐Dio3 Locus and Histone Methylation to Protect Male Cerebellum from Methyl Donor Deficiency. Molecular Nutrition & Food Research. 67(21). e2300040–e2300040.
7.
Bronner, Myriam, et al.. (2023). ENPP1 homozygous stop-loss variant causing generalized arterial calcifications of infancy: About a severe neonatal clinical case. European Journal of Medical Genetics. 66(8). 104803–104803.
8.
Ravel, Jean‐Marie, M. Renaud, Jean Muller, et al.. (2023). Clinical utility of periodic reinterpretation of CNVs of uncertain significance: an 8-year retrospective study. Genome Medicine. 15(1). 39–39. 7 indexed citations
9.
Lambert, Laëtitia, Céline Bonnet, Bruno Leheup, et al.. (2023). MAST1-related mega-corpus-callosum syndrome with central hypogonadism. European Journal of Medical Genetics. 66(11). 104853–104853. 1 indexed citations
10.
Lambert, Laëtitia, Ange‐Line Bruel, Frédéric Tran Mau‐Them, et al.. (2022). Atypical phenotype of a patient with Bardet–Biedl syndrome type 4. Molecular Genetics & Genomic Medicine. 10(5). e1869–e1869. 1 indexed citations
11.
Ravel, Jean‐Marie, Laëtitia Lambert, Céline Bonnet, et al.. (2022). Reduced penetrance of an eastern French mutation in ATL1 autosomal-dominant inheritance (SPG3A): extended phenotypic spectrum coupled with brain 18F-FDG PET. Neurogenetics. 23(4). 241–255. 4 indexed citations
12.
Vuillaume, Marie‐Laure, Marie‐Pierre Moizard, Jean‐Luc Alessandri, et al.. (2018). Mutation update for theGPC3gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. Human Mutation. 39(6). 790–805. 22 indexed citations
13.
Wiedemann, Arnaud, et al.. (2018). Annual Injection of Zoledronic Acid Improves Bone Status in Children with Cerebral Palsy and Rett Syndrome. Calcified Tissue International. 104(4). 355–363. 13 indexed citations
14.
Valduga, Mylène, et al.. (2015). WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period. Journal of Human Genetics. 60(5). 267–271. 26 indexed citations
15.
Caumes, Roseline, Odile Boespflug‐Tanguy, Nathalie Villeneuve, et al.. (2014). Late onset epileptic spasms is frequent in MECP2 gene duplication: Electroclinical features and long-term follow-up of 8 epilepsy patients. European Journal of Paediatric Neurology. 18(4). 475–481. 18 indexed citations
16.
Vincent, Marie, Corinne Collet, Alain Verloès, et al.. (2013). Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability. European Journal of Human Genetics. 22(1). 52–56. 15 indexed citations
17.
Allou, Lila, Laëtitia Lambert, Daniel Amsallem, et al.. (2012). 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements. European Journal of Human Genetics. 20(12). 1216–1223. 50 indexed citations
18.
Lambert, Laëtitia, et al.. (2012). Down syndrome with partial trisomy of chromosome 21 because of a de-novo unbalanced translocation t(13;21)(q10;q22). Clinical Dysmorphology. 21(4). 200–203. 2 indexed citations
19.
Philippe, Christophe, et al.. (2009). Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females. Journal of Medical Genetics. 47(1). 59–65. 64 indexed citations
20.
Némos, Christophe, Laëtitia Lambert, Fabienne Giuliano, et al.. (2009). Mutational spectrum of CDKL5 in early‐onset encephalopathies: a study of a large collection of French patients and review of the literature. Clinical Genetics. 76(4). 357–371. 83 indexed citations

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.

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