Laurent Vallat

968 total citations
27 papers, 632 citations indexed

About

Laurent Vallat is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Laurent Vallat has authored 27 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 11 papers in Pathology and Forensic Medicine. Recurrent topics in Laurent Vallat's work include Chronic Lymphocytic Leukemia Research (12 papers), Lymphoma Diagnosis and Treatment (9 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Laurent Vallat is often cited by papers focused on Chronic Lymphocytic Leukemia Research (12 papers), Lymphoma Diagnosis and Treatment (9 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Laurent Vallat collaborates with scholars based in France, United States and Germany. Laurent Vallat's co-authors include John G. Gribben, Hélène Merle‐Béral, Valérie Rimelen, Michèle Beau‐Faller, Éric Guérin, Céline Mascaux, Anne‐Claire Voegeli, Erwan Pencreach, Christine Dierks and Meike Burger and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Bioinformatics.

In The Last Decade

Laurent Vallat

26 papers receiving 621 citations

Peers

Laurent Vallat
Fernando Pardal Portugal
Y. Terui Japan
Laurence Cooke United States
Giuseppe Dastoli Italy
Esther A. Beuling Netherlands
Christopher Riley United States
Linda W. Horton United States
Simona Tavolaro Italy
B. Markman Australia
Davide Torti Italy
Fernando Pardal Portugal
Laurent Vallat
Citations per year, relative to Laurent Vallat Laurent Vallat (= 1×) peers Fernando Pardal

Countries citing papers authored by Laurent Vallat

Since Specialization
Citations

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

Fields of papers citing papers by Laurent Vallat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurent Vallat

This figure shows the co-authorship network connecting the top 25 collaborators of Laurent Vallat. A scholar is included among the top collaborators of Laurent Vallat 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 Laurent Vallat. Laurent Vallat 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.
Champagnat, Nicolas, et al.. (2024). MultiRNAflow: integrated analysis of temporal RNA-seq data with multiple biological conditions. Bioinformatics. 40(5). 2 indexed citations
2.
Kawka, Lou, Nicolás Meyer, Tao Ye, et al.. (2023). Association Between Bruton's Tyrosine Kinase Gene Overexpression and Risk of Lymphoma in Primary Sjögren's Syndrome. Arthritis & Rheumatology. 75(10). 1798–1811. 3 indexed citations
3.
4.
Martin, M., Anne‐Marie Knapp, Sophie Jung, et al.. (2023). Normal B cells express ZAP70 in chronic lymphocytic leukemia: A link between autoimmunity and lymphoproliferation?. American Journal of Hematology. 99(1). 48–56.
5.
Fournier, Élise, Maël Heiblig, Pascale Flandrin‐Gresta, et al.. (2022). Molecular heterogeneity and measurable residual disease of rare NPM1 mutations in acute myeloid leukemia: a nationwide experience from the GBMHM study group. Leukemia. 36(5). 1390–1400. 2 indexed citations
6.
Pencreach, Erwan, Éric Guérin, Valérie Rimelen, et al.. (2022). Direct Targeting KRAS Mutation in Non-Small Cell Lung Cancer: Focus on Resistance. Cancers. 14(5). 1321–1321. 58 indexed citations
7.
Carapito, Raphaël, Luc‐Matthieu Fornecker, Nicodème Paul, et al.. (2021). Temporal multiomic modeling reveals a B-cell receptor proliferative program in chronic lymphocytic leukemia. Leukemia. 35(5). 1463–1474. 7 indexed citations
8.
Bertrand, Frédèric, et al.. (2020). selectBoost: a general algorithm to enhance the performance of variable selection methods. Bioinformatics. 37(5). 659–668. 2 indexed citations
9.
Ilias, W., Laurent Miguet, Caroline Mayeur‐Rousse, et al.. (2019). BCR-associated factors driving chronic lymphocytic leukemia cells proliferation ex vivo. Scientific Reports. 9(1). 701–701. 26 indexed citations
10.
Fornecker, Luc‐Matthieu, Frédèric Bertrand, Nicodème Paul, et al.. (2019). Multi-omics dataset to decipher the complexity of drug resistance in diffuse large B-cell lymphoma. Scientific Reports. 9(1). 895–895. 26 indexed citations
11.
Reix, Nathalie, Arnaud Agin, Seiamak Bahram, et al.. (2015). Clinical laboratory medicine: continuous amelioration with a book of objectives and satisfaction survey. Annales de biologie clinique. 73(3). 359–368. 1 indexed citations
12.
Loarer, François Le, Stéphane Barète, Laurent Vallat, et al.. (2014). Primary Cutaneous CD8+ T-cell Lymphoma Masquerading as Acral Vascular Syndrome. Acta Dermato Venereologica. 94(3). 317–319. 2 indexed citations
13.
Bertrand, Frédèric, et al.. (2013). Cascade: a R package to study, predict and simulate the diffusion of a signal through a temporal gene network. Bioinformatics. 30(4). 571–573. 6 indexed citations
14.
Perrot, Aurore, Cédric Pionneau, Nabih Azar, et al.. (2012). Waldenström’s macroglobulinemia harbors a unique proteome where Ku70 is severely underexpressed as compared with other B-lymphoproliferative disorders. Blood Cancer Journal. 2(9). e88–e88. 5 indexed citations
15.
Grassin‐Delyle, Stanislas, Amparo Buenestado, Laurent Vallat, et al.. (2011). Expression and proliferative effect of hemokinin-1 in human B-cells. Peptides. 32(5). 1027–1034. 13 indexed citations
16.
Marteau, Jean‐Brice, O. Rigaud, Thibaut Brugat, et al.. (2010). Concomitant heterochromatinisation and down-regulation of gene expression unveils epigenetic silencing of RELBin an aggressive subset of chronic lymphocytic leukemia in males. BMC Medical Genomics. 3(1). 53–53. 11 indexed citations
17.
Rigolet, Aude, P. Cacoub, Aurélie Schnuriger, et al.. (2005). Genetic heterogeneity of the hypervariable region I of Hepatitis C virus and lymphoproliferative disorders. Leukemia. 19(6). 1070–1076. 4 indexed citations
18.
Vallat, Laurent, Yves Benhamou, Maya Gutierrez, et al.. (2004). Clonal B cell populations in the blood and liver of patients with chronic hepatitis C virus infection. Arthritis & Rheumatism. 50(11). 3668–3678. 86 indexed citations
19.
Vallat, Laurent. (2003). The resistance of B-CLL cells to DNA damage-induced apoptosis defined by DNA microarrays. Blood. 101(11). 4598–4606. 74 indexed citations
20.
Guipaud, Olivier, Ludovic Deriano, Laurent Vallat, et al.. (2003). B-cell chronic lymphocytic leukaemia: a polymorphic family unified by genomic features. The Lancet Oncology. 4(8). 506–514. 26 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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