J. Lamoril - Concepedia

Author

J. Lamoril

Also Known As

Fanny Laffargue, J LAMORIL, J Lamoril, J. Lamoril, Jerome Lamoril, Jerôme Lamoril, Jerôme Lamoril, JÉROME LAMORIL, Jérome Lamoril, Jérôme Lamoril

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Hôpital Louis-Mourier Inserm Assistance Publique – Hôpitaux de Paris Université Paris Cité Délégation Paris 7

About

J. Lamoril is an author at Hôpital Louis-Mourier specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	1.1K
2	Natural Sciences	2	2	141
3	Public Health	1	1	11
4	Allergy	1	1	19
5	Biochemistry	1	1	71

J. Lamoril

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH Laurent Gouya, Hervé Puy, Anne-Marie Robréau, Nature Genetics BiologyDominant Erythropoietic ProtoporphyriaGeneticsWildtype FechGenetic Variation	2001	260
Inheritance in Erythropoietic Protoporphyria: A Common Wild-Type Ferrochelatase Allelic Variant With Low Expression Accounts for Clinical Manifestation Laurent Gouya, Hervé Puy, J. Lamoril, Blood	1999	156
Molecular Epidemiology and Diagnosis of PBG Deaminase Gene Defects in Acute Intermittent Porphyria Hervé Puy, Jean‐Charles Deybach, J. Lamoril, The American Journal of Human Genetics Molecular EpidemiologyGeneticsPathogenesisPathologyMolecular Genetics	1997	149
Hepatitis C virus genotypes in France: relationship with epidemiology, pathogenicity and response to interferon therapy Michelle Martinot-Peignoux, F Roudot-Thoraval, Isabelle Mendel, Journal of Viral Hepatitis Hepatitis DHcv GenotypeDiagnostic VirologyHepatologyHepatitis C	1999	120
Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene J. Lamoril, Samia Boulechfar, Hubert de Verneuil, Biochemical and Biophysical Research Communications BiologyHuman Erythropoietic ProtoporphyriaIron MetabolismGeneticsMolecular Genetics	1991	118
Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase allele. Laurent Gouya, Jean‐Charles Deybach, J. Lamoril, PubMed	1996	102
From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria Hugo Lenglet, Caroline Schmitt, Thomas Grange, Human Molecular Genetics	2018	101
Trypsinogen Copy Number Mutations in Patients With Idiopathic Chronic Pancreatitis Emmanuelle Masson, Cédric Le Maréchal, Giriraj R. Chandak, Clinical Gastroenterology and Hepatology Pancreatic Fluid CollectionGeneticsPathogenesisGastroenterologyPathology	2007	81
Ferrochelatase Structural Mutant (Fechm1Pas) in the House Mouse Samia Boulechfar, J. Lamoril, Xavier Montagutelli, Genomics BiochemistryNatural SciencesBiochemical GeneticsMolecular BiologyCellular Biochemistry	1993	71
Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria J. Lamoril, Hervé Puy, Sharon D. Whatley, The American Journal of Human Genetics BiologyGenetic DisorderNatural SciencesGeneticsCpo Gene	2001	70

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