Foudil Lamari

3.2k total citations
28 papers, 582 citations indexed

About

Foudil Lamari is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Foudil Lamari has authored 28 papers receiving a total of 582 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 10 papers in Molecular Biology and 8 papers in Clinical Biochemistry. Recurrent topics in Foudil Lamari's work include Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (7 papers) and Cellular transport and secretion (7 papers). Foudil Lamari is often cited by papers focused on Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (7 papers) and Cellular transport and secretion (7 papers). Foudil Lamari collaborates with scholars based in France, United States and Spain. Foudil Lamari's co-authors include Fanny Mochel, Jean‐Marie Saudubray, F. Sedel, Yann Nadjar, Agnès Camuzat, Ángeles García‐Cazorla, Àngels García‐Cazorla, Alexis Brice, Emmanuel Roze and Fabienne Clot and has published in prestigious journals such as Analytical Biochemistry, Annals of Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Foudil Lamari

26 papers receiving 575 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Foudil Lamari France 14 257 227 109 95 80 28 582
Yann Nadjar France 16 176 0.7× 243 1.1× 124 1.1× 77 0.8× 46 0.6× 37 551
Annette Bley Germany 14 500 1.9× 349 1.5× 47 0.4× 115 1.2× 51 0.6× 29 816
Kristin N. Varhaug Norway 9 243 0.9× 81 0.4× 167 1.5× 66 0.7× 66 0.8× 15 599
Mauro Scarpelli Italy 17 535 2.1× 179 0.8× 94 0.9× 312 3.3× 85 1.1× 34 796
Johann Penzien Germany 14 268 1.0× 76 0.3× 143 1.3× 184 1.9× 106 1.3× 17 627
Hendrik Rosewich Germany 18 567 2.2× 105 0.5× 95 0.9× 137 1.4× 71 0.9× 34 857
Andrea J. Arreguin United States 8 246 1.0× 124 0.5× 138 1.3× 38 0.4× 43 0.5× 10 485
Jonathon S. Dunn United States 9 148 0.6× 130 0.6× 32 0.3× 35 0.4× 107 1.3× 10 590
Christina Ising Germany 12 284 1.1× 197 0.9× 35 0.3× 23 0.2× 62 0.8× 19 760
Maria Chiara Meschini Italy 15 461 1.8× 121 0.5× 35 0.3× 242 2.5× 91 1.1× 23 637

Countries citing papers authored by Foudil Lamari

Since Specialization
Citations

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

Fields of papers citing papers by Foudil Lamari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Foudil Lamari

This figure shows the co-authorship network connecting the top 25 collaborators of Foudil Lamari. A scholar is included among the top collaborators of Foudil Lamari 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 Foudil Lamari. Foudil Lamari 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.
Rossignol, Francis, Foudil Lamari, & Grant A. Mitchell. (2025). Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders. Journal of Inherited Metabolic Disease. 48(2). e70008–e70008. 4 indexed citations
2.
Van, K. Dang, Foudil Lamari, Susana Boluda, et al.. (2025). Mass spectrometric identification of novel truncated α-synuclein species following optimized immunoprecipitation from human brain tissue. Analytical Biochemistry. 706. 115942–115942.
3.
Lamari, Foudil, Francis Rossignol, & Grant A. Mitchell. (2025). Glycerophospholipids: Roles in Cell Trafficking and Associated Inborn Errors. Journal of Inherited Metabolic Disease. 48(2). e70019–e70019. 6 indexed citations
4.
Mauhin, Wladimir, Javier I. Ottaviani, Olivier Lidove, et al.. (2024). Lysosphingolipid Quantitation in Plasma and Dried‐Blood Spots Using Targeted High‐Resolution Mass Spectrometry. Journal of Clinical Laboratory Analysis. 39(1). e25131–e25131.
5.
Fernández‐Eulate, Gorka, Jean‐François Benoist, Foudil Lamari, et al.. (2022). Diagnostic approach in adult-onset neurometabolic diseases. Journal of Neurology Neurosurgery & Psychiatry. 93(4). 413–421. 13 indexed citations
6.
Kraoua, Ichraf, Dimitri Schlemmer, Catherine Caillaud, et al.. (2022). Plasma GM2 ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-Gangliosidosis. Molecular Genetics and Metabolism. 138(2). 106983–106983. 5 indexed citations
7.
Richard, Laurence, Foudil Lamari, Karima Ghorab, et al.. (2022). GM2 gangliosidosis AB variant: first case of late onset and review of the literature. Neurological Sciences. 43(11). 6517–6527. 5 indexed citations
8.
Mauhin, Wladimir, Abdellah Tebani, Damien Amelin, et al.. (2022). Sphingosine-1-Phosphate Levels Are Higher in Male Patients with Non-Classic Fabry Disease. Journal of Clinical Medicine. 11(5). 1233–1233. 3 indexed citations
9.
Masingue, Marion, Timothée Lenglet, Cyril Goizet, et al.. (2020). Natural History of Adult Patients with GM2 Gangliosidosis. Annals of Neurology. 87(4). 609–617. 41 indexed citations
10.
Tebani, Abdellah, Wladimir Mauhin, Lénaïg Abily-Donval, et al.. (2020). A Proteomics-Based Analysis Reveals Predictive Biological Patterns in Fabry Disease. Journal of Clinical Medicine. 9(5). 1325–1325. 32 indexed citations
11.
Saracino, Dario, Leila Sellami, Fabienne Clot, et al.. (2019). The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiency. Neurobiology of Aging. 85. 154.e9–154.e11. 4 indexed citations
12.
Saudubray, Jean‐Marie, Fanny Mochel, Foudil Lamari, & Ángeles García‐Cazorla. (2019). Proposal for a simplified classification of IMD based on a pathophysiological approach: A practical guide for clinicians. Journal of Inherited Metabolic Disease. 42(4). 706–727. 32 indexed citations
13.
Viodé, Arthur, Clémence Fournier, Agnès Camuzat, et al.. (2018). New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers. Frontiers in Neuroscience. 12. 589–589. 23 indexed citations
14.
Nadjar, Yann, Philippe Latour, Xavier Ayrignac, et al.. (2018). Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect. Orphanet Journal of Rare Diseases. 13(1). 175–175. 33 indexed citations
15.
Dard, Rodolphe, Valérie Touitou, Giovanni Stévanin, et al.. (2017). Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation. European Journal of Medical Genetics. 60(12). 639–642. 23 indexed citations
16.
Monneret, Denis, Véronique Fressart, Foudil Lamari, et al.. (2015). Hemolysis indexes for biochemical tests and immunoassays on Roche analyzers: Determination of allowable interference limits according to different calculation methods. Scandinavian Journal of Clinical and Laboratory Investigation. 75(2). 162–169. 34 indexed citations
17.
Clot, Fabienne, Anne Rovelet‐Lecrux, Foudil Lamari, et al.. (2014). Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics. 15(2). 95–100. 7 indexed citations
18.
Lamari, Foudil, Fanny Mochel, & Jean‐Marie Saudubray. (2014). An overview of inborn errors of complex lipid biosynthesis and remodelling. Journal of Inherited Metabolic Disease. 38(1). 3–18. 40 indexed citations
19.
Caroppo, Paola, Cathérine Belin, David Grabli, et al.. (2014). Posterior Cortical Atrophy as an Extreme Phenotype ofGRNMutations. JAMA Neurology. 72(2). 224–224. 12 indexed citations
20.
García‐Cazorla, Àngels, Fanny Mochel, Foudil Lamari, & Jean‐Marie Saudubray. (2014). The clinical spectrum of inherited diseases involved in the synthesis and remodeling of complex lipids. A tentative overview. Journal of Inherited Metabolic Disease. 38(1). 19–40. 32 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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