J. Lamoril

2.1k total citations
54 papers, 1.5k citations indexed

About

J. Lamoril is a scholar working on Molecular Biology, Rheumatology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J. Lamoril has authored 54 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 16 papers in Rheumatology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J. Lamoril's work include Porphyrin Metabolism and Disorders (29 papers), Heme Oxygenase-1 and Carbon Monoxide (19 papers) and Folate and B Vitamins Research (15 papers). J. Lamoril is often cited by papers focused on Porphyrin Metabolism and Disorders (29 papers), Heme Oxygenase-1 and Carbon Monoxide (19 papers) and Folate and B Vitamins Research (15 papers). J. Lamoril collaborates with scholars based in France, United States and Germany. J. Lamoril's co-authors include Jean‐Charles Deybach, Bernard Grandchamp, Hervé Puy, Y Nordmann, Laurent Gouya, Vasco Da Silva, Anne-Marie Robréau, Hubert de Verneuil, Monique Bourgeois and V. Da Silva and has published in prestigious journals such as Nature Genetics, Blood and Hepatology.

In The Last Decade

J. Lamoril

45 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Lamoril France 21 1.1k 383 380 204 153 54 1.5k
Dulcinéia Martins de Albuquerque Brazil 16 238 0.2× 83 0.2× 144 0.4× 177 0.9× 47 0.3× 91 992
P Fryer United Kingdom 14 364 0.3× 97 0.3× 77 0.2× 45 0.2× 239 1.6× 16 1.2k
Jonatan Leffler Australia 17 363 0.3× 373 1.0× 13 0.0× 83 0.4× 223 1.5× 34 1.4k
M S Pollack United States 16 477 0.4× 29 0.1× 289 0.8× 110 0.5× 50 0.3× 36 1.2k
Benjamin Rauwel France 13 353 0.3× 95 0.2× 47 0.1× 218 1.1× 23 0.2× 21 807
Herbert B. Lindsley United States 14 143 0.1× 264 0.7× 13 0.0× 98 0.5× 35 0.2× 23 861
Lisa Rice United States 15 346 0.3× 101 0.3× 11 0.0× 125 0.6× 185 1.2× 24 912
Denise Bonney United Kingdom 18 165 0.2× 67 0.2× 58 0.2× 155 0.8× 32 0.2× 41 881
H Perrot France 15 266 0.2× 86 0.2× 56 0.1× 112 0.5× 48 0.3× 81 634
Sylvie François France 21 234 0.2× 55 0.1× 61 0.2× 107 0.5× 77 0.5× 67 1.3k

Countries citing papers authored by J. Lamoril

Since Specialization
Citations

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

Fields of papers citing papers by J. Lamoril

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Lamoril

This figure shows the co-authorship network connecting the top 25 collaborators of J. Lamoril. A scholar is included among the top collaborators of J. Lamoril 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 J. Lamoril. J. Lamoril 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.
Lefèbvre, Thibaud, Caroline Schmitt, J. Lamoril, et al.. (2024). 04194 In-depth biochemical investigations in a new case of ALAD deficiency: better understanding for better treatment. A48.2–A49.
2.
3.
Lamoril, J., et al.. (2019). Mutations and polymorphisms associated with iron overload in a series of 91 non-HFE haemochromatosis patients. Clinics and Research in Hepatology and Gastroenterology. 44(2). 239–241. 3 indexed citations
4.
Tchernitchko, Dimitri, et al.. (2011). Comprehensive cytochrome P450 CYP1A2 gene analysis in French caucasian patients with familial and sporadic porphyria cutanea tarda. British Journal of Dermatology. 166(2). 425–429. 8 indexed citations
5.
Masson, Emmanuelle, Cédric Le Maréchal, Giriraj R. Chandak, et al.. (2007). Trypsinogen Copy Number Mutations in Patients With Idiopathic Chronic Pancreatitis. Clinical Gastroenterology and Hepatology. 6(1). 82–88. 54 indexed citations
6.
Schmitt, Caroline, Laurent Gouya, J. Lamoril, et al.. (2005). Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria. Human Molecular Genetics. 14(20). 3089–3098. 31 indexed citations
7.
Gouya, Laurent, Hervé Puy, Anne-Marie Robréau, et al.. (2003). Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. Human Genetics. 114(3). 256–262. 34 indexed citations
8.
9.
Groß, U., Hervé Puy, J. Lamoril, et al.. (2002). A molecular, enzymatic and clinical study in a family with hereditary coproporphyria. Journal of Inherited Metabolic Disease. 25(4). 279–286. 15 indexed citations
10.
Gouya, Laurent, Hervé Puy, Anne-Marie Robréau, et al.. (2001). The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH. Nature Genetics. 30(1). 27–28. 168 indexed citations
11.
Lamoril, J., Hervé Puy, Sharon D. Whatley, et al.. (2001). Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria. The American Journal of Human Genetics. 68(5). 1130–1138. 38 indexed citations
12.
Lamoril, J., Hervé Puy, V. Da Silva, et al.. (1999). Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update. Human Mutation. 13(1). 44–53. 26 indexed citations
13.
Martinot-Peignoux, Michelle, F Roudot-Thoraval, Isabelle Mendel, et al.. (1999). Hepatitis C virus genotypes in France: relationship with epidemiology, pathogenicity and response to interferon therapy. Journal of Viral Hepatitis. 6(6). 435–443. 102 indexed citations
14.
Lamoril, J., C Andant, Catherine Bogard, et al.. (1998). Epidemiology of hepatitis C and G in sporadic and familial porphyria cutanea tarda. Hepatology. 27(3). 848–852. 40 indexed citations
15.
Puy, Hervé, et al.. (1997). Molecular analysis of porphobilinogen (PBG) deaminase gene mutations in acute intermittent porphyria: first study in patients of Slavic origin. Scandinavian Journal of Clinical and Laboratory Investigation. 57(3). 217–224. 17 indexed citations
16.
17.
Grandchamp, Bernard, et al.. (1996). Review: Molecular pathogenesis of hepatic acute porphyrias. Journal of Gastroenterology and Hepatology. 11(11). 1046–1052. 25 indexed citations
18.
Grandchamp, Bernard, J. Lamoril, & Hervé Puy. (1995). Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria. Journal of Bioenergetics and Biomembranes. 27(2). 215–219. 16 indexed citations
19.
Lamoril, J., Xavier Montagutelli, Jean‐Louis Guénet, et al.. (1993). Ferrochelatase Structural Mutant (Fechm1Pas) in the House Mouse. Genomics. 16(3). 645–648. 58 indexed citations
20.
Lamoril, J., et al.. (1991). Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene. Biochemical and Biophysical Research Communications. 181(2). 594–599. 102 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Dulcinéia Martins de Albuquerque Breakdown of academic impact, for papers by P Fryer Breakdown of academic impact, for papers by Jonatan Leffler Breakdown of academic impact, for papers by M S Pollack Breakdown of academic impact, for papers by Benjamin Rauwel Breakdown of academic impact, for papers by Herbert B. Lindsley Breakdown of academic impact, for papers by Lisa Rice Breakdown of academic impact, for papers by Denise Bonney Breakdown of academic impact, for papers by H Perrot Breakdown of academic impact, for papers by Sylvie François
Rankless by CCL
2026