Laetitia Boutrand

832 total citations
13 papers, 598 citations indexed

About

Laetitia Boutrand is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Laetitia Boutrand has authored 13 papers receiving a total of 598 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Laetitia Boutrand's work include Hereditary Neurological Disorders (4 papers), Molecular Biology Techniques and Applications (3 papers) and Forensic and Genetic Research (3 papers). Laetitia Boutrand is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Molecular Biology Techniques and Applications (3 papers) and Forensic and Genetic Research (3 papers). Laetitia Boutrand collaborates with scholars based in France, United States and Hungary. Laetitia Boutrand's co-authors include Stanislas Lyonnet, Jeanne Amiel, Anna Pelet, Tania Attié‐Bitach, Patrick Edery, Bruce A.J. Ponder, Claire Nihoul‐Feketé, Charis Eng, Arnold Munnich and Lois M. Mulligan and has published in prestigious journals such as FEBS Letters, Human Molecular Genetics and International Journal of Cancer.

In The Last Decade

Laetitia Boutrand

12 papers receiving 582 citations

Peers

Laetitia Boutrand
Doris B. Wilson United States
Lanying Song United States
Marion Gérard France
Tanya Bardakjian United States
Angus Dobbie United Kingdom
Pagon Ra United States
Joëlle Augé France
Wayne Lam United Kingdom
Bellinda van den Helm Netherlands
Alex Magee United Kingdom
Doris B. Wilson United States
Laetitia Boutrand
Citations per year, relative to Laetitia Boutrand Laetitia Boutrand (= 1×) peers Doris B. Wilson

Countries citing papers authored by Laetitia Boutrand

Since Specialization
Citations

This map shows the geographic impact of Laetitia Boutrand'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 Laetitia Boutrand with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laetitia Boutrand more than expected).

Fields of papers citing papers by Laetitia Boutrand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laetitia Boutrand. 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 Laetitia Boutrand. The network helps show where Laetitia Boutrand may publish in the future.

Co-authorship network of co-authors of Laetitia Boutrand

This figure shows the co-authorship network connecting the top 25 collaborators of Laetitia Boutrand. A scholar is included among the top collaborators of Laetitia Boutrand 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 Laetitia Boutrand. Laetitia Boutrand is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Mertens, Gerhard, et al.. (2003). Use of STRs in paternity testing in the Flemish population. International Congress Series. 1239. 943–946. 1 indexed citations
2.
Mertens, Gerhard, et al.. (2001). Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090. International Journal of Legal Medicine. 115(1). 40–44. 9 indexed citations
3.
Besançon, Roger, Philippe Latour, Lara Konecny, et al.. (2001). Exonic SNPs at positions 220 (A/G) and 445 (C/T) of the peripheral myelin protein 2 (PMP2). Human Mutation. 17(3). 237–237.
4.
Boutrand, Laetitia, et al.. (2001). Variations in primer sequences are the origin of allele drop-out at loci D13S317 and CD4. International Journal of Legal Medicine. 114(4-5). 295–297. 25 indexed citations
5.
Latour, Philippe, Laetitia Boutrand, Nicolas Lévy, et al.. (2001). Polymorphic Short Tandem Repeats for Diagnosis of the Charcot-Marie-Tooth 1A Duplication. Clinical Chemistry. 47(5). 829–837. 55 indexed citations
6.
Egyed, Balázs, et al.. (2000). Analysis of eight STR loci in two Hungarian populations. Forensic Science International. 113(1-3). 25–27. 18 indexed citations
7.
Bissar‐Tadmouri, Nisrine, Yeşim Parman, Laetitia Boutrand, et al.. (2000). Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients. Clinical Genetics. 58(5). 396–402. 24 indexed citations
8.
Egyed, Balázs, et al.. (2000). Analysis of eight STR loci in two Hungarian populations. International Journal of Legal Medicine. 113(5). 272–275. 19 indexed citations
9.
Egan, Kathleen M., Laetitia Boutrand, Gilbert Lenoir, et al.. (1999). Germlinebrca2 sequence variants in patients with ocular melanoma. International Journal of Cancer. 82(3). 325–328. 46 indexed citations
10.
Besançon, Roger, Philippe Latour, P. Petiot, et al.. (1999). Alternative exon 3 splicing of the human major protein zero gene in white blood cells and peripheral nerve tissue. FEBS Letters. 457(3). 339–342. 7 indexed citations
11.
Sinilnikova, Olga M., Kathleen M. Egan, Laetitia Boutrand, et al.. (1999). Germline brca2 sequence variants in patients with ocular melanoma. International Journal of Cancer. 82(3). 325–328. 1 indexed citations
12.
Attié‐Bitach, Tania, Anna Pelet, Patrick Edery, et al.. (1995). Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease. Human Molecular Genetics. 4(8). 1381–1386. 242 indexed citations
13.
Attié‐Bitach, Tania, Marianne Till, Anna Pelet, et al.. (1995). Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease. Human Molecular Genetics. 4(12). 2407–2409. 151 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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