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G. Lefranc · SciRah

Researcher profile · Semantic Scholar

G. Lefranc

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G. Lefranc — researcher profile on SciRah

h-index: 47
Works: 195
Citations: 10K

Most-cited papers

IMGT, the international ImMunoGeneTics information system®
M. Lefranc, V. Giudicelli, Q. Kaas, E. Duprat +6 more
2004Nucleic Acids Res.877 citations Open access
Semantic Scholar
IMGT unique numbering for immunoglobulin and T cell receptor variable domains and Ig superfamily V-like domains.
M. Lefranc, C. Pommie, M. Ruiz, V. Giudicelli +4 more
2003Developmental and Comparative Immunology740 citations Open access
Semantic Scholar
IMGT unique numbering for immunoglobulin and T cell receptor constant domains and Ig superfamily C-like domains.
M. Lefranc, C. Pommie, Q. Kaas, E. Duprat +9 more
2005Developmental and Comparative Immunology519 citations
Semantic Scholar
IMGT®, the international ImMunoGeneTics information system® 25 years on
M. Lefranc, V. Giudicelli, P. Duroux, Joumana Jabado-Michaloud +10 more
2014Nucleic Acids Res.509 citations Open access
Semantic Scholar
Deep Dermatophytosis and Inherited CARD9 Deficiency
F. Lanternier, S. Pathan, Quentin B. Vincent, Luyan Liu +29 more
2013New England Journal of Medicine365 citations Open access
Semantic Scholar
IMGT standardized criteria for statistical analysis of immunoglobulin V‐REGION amino acid properties
C. Pommie, Séverine Levadoux, R. Sabatier, G. Lefranc +1 more
2004Journal of Molecular Recognition292 citations
Semantic Scholar
The extended clinical phenotype of 64 patients with DOCK8 deficiency
K. Engelhardt, E. Gertz, S. Keleş, A. Schäffer +53 more
2015Journal of Allergy and Clinical Immunology181 citations Open access
Semantic Scholar
Evidence for balancing selection from nucleotide sequence analyses of human G6PD.
B. Verrelli, J. McDonald, G. Argyropoulos, G. Destro‐Bisol +6 more
2002American Journal of Human Genetics159 citations Open access
Semantic Scholar
Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean
S. Plaza, F. Calafell, A. Helal, N. Bouzerna +3 more
2003Annals of Human Genetics149 citations Open access
Semantic Scholar
DOCK8 functions as an adaptor that links Toll-like receptor–MyD88 signaling to B cell activation
H. Jabara, Douglas R. McDonald, E. Janssen, M. Massaad +27 more
2012Nature Immunology145 citations Open access
Semantic Scholar
A Homozygous mucosa-associated ly 1 mphoid tissue 1 (MALT1) mutation in a family with 2 combined immunodeficiency
H. Jabara, T. Ohsumi, J. Chou, M. Massaad +15 more
2013Journal of Allergy and Clinical Immunology139 citations Open access
Semantic Scholar
Update in chronic obstructive pulmonary disease: role of antioxidant and metabolizing gene polymorphisms
R. Lakhdar, S. Denden, A. Kassab, N. Leban +5 more
2011Experimental Lung Research131 citations Open access
Semantic Scholar
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2)
Pui Y. Lee, E. Kellner, Yuelong Huang, Elissa Furutani +27 more
2020Journal of Allergy and Clinical Immunology125 citations Open access
Semantic Scholar
Human Gm, Km, and Am allotypes and their molecular characterization: a remarkable demonstration of polymorphism.
M. Lefranc, G. Lefranc
2012Methods in molecular biology124 citations
Semantic Scholar
Mutations in OSTM1 (Grey Lethal) Define a Particularly Severe Form of Autosomal Recessive Osteopetrosis With Neural Involvement
A. Pangrazio, P. Poliani, A. Mégarbané, G. Lefranc +10 more
2006Journal of Bone and Mineral Research114 citations Open access
Semantic Scholar
IMGT-ONTOLOGY for Immunogenetics and Immunoinformatics
M. Lefranc, V. Giudicelli, Chantal Ginestoux, N. Bosc +16 more
2004Silico Biol.106 citations
Semantic Scholar
DOCK8 Functions as an Adaptor that Links TLR–MyD88 Signaling to B Cell Activation
H. Jabara, Douglas R. McDonald, E. Janssen, M. Massaad +31 more
2012101 citations
Semantic Scholar
IMGT unique numbering for MHC groove G-DOMAIN and MHC superfamily (MhcSF) G-LIKE-DOMAIN.
M. Lefranc, E. Duprat, Q. Kaas, Madeleine Tranne +2 more
2005Developmental and Comparative Immunology97 citations
Semantic Scholar
DOCK8 deficient patients have a breakdown in peripheral B cell tolerance and defective regulatory T cells
E. Janssen, H. Morbach, Sumana Ullas, Jason M. Bannock +11 more
2014Journal of Allergy and Clinical Immunology94 citations Open access
Semantic Scholar
IMGT-Choreography for Immunogenetics and Immunoinformatics
M. Lefranc, Oliver Clément, Q. Kaas, E. Duprat +7 more
2005Silico Biol.91 citations
Semantic Scholar
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
H. Jiao, B. Tóth, Melinda Erdős, I. Fransson +14 more
2008Molecular Immunology87 citations Open access
Semantic Scholar
Population Structure in the Mediterranean Basin: A Y Chromosome Perspective
C. Capelli, N. Redhead, V. Romano, F. Cali +14 more
2006Annals of Human Genetics76 citations Open access
Semantic Scholar
The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape
G. Busby, G. Hellenthal, F. Montinaro, S. Tofanelli +24 more
2015Current Biology72 citations Open access
Semantic Scholar
Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects
M. Medlej‐Hashim, V. Delague, E. Chouery, N. Salem +4 more
2004BMC Medical Genetics72 citations Open access
Semantic Scholar
Immunoglobulins or Antibodies: IMGT® Bridging Genes, Structures and Functions
M. Lefranc, G. Lefranc
2020Biomedicines70 citations Open access
Semantic Scholar
[Familial Mediterranean Fever (FMF): from diagnosis to treatment].
M. Medlej‐Hashim, J. Loiselet, G. Lefranc, A. Mégarbané
2004Sante62 citations
Semantic Scholar
Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations.
M. Medlej‐Hashim, J. Serre, S. Corbani, O. Saab +7 more
2005European Journal of Medical Genetics61 citations
Semantic Scholar
NF‐NF‐κBB‐dependent expression of the antiapoptotic factor c‐FLIP is regulated by calpain 3, the protein involved in limb‐girdle muscular dystrophy type 2A
Béatrice Benayoun, S. Baghdiguian, A. Lajmanovich, M. Bartoli +9 more
2008The FASEB Journal58 citations
Semantic Scholar
A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2
E. Chouery, J. Abou-Ghoch, S. Corbani, N. El Ali +11 more
2012Clinical Genetics53 citations
Semantic Scholar
Plasmacytoid Dendritic Cell Depletion in DOCK8 Deficiency: Rescue of Severe Herpetic Infections with Interferon Alpha-2b Therapy
S. Keleş, H. Jabara, I. Reisli, Douglas R. McDonald +7 more
2014Journal of Allergy and Clinical Immunology50 citations Open access
Semantic Scholar
Clinical, molecular, and cellular immunologic findings in patients with SP110-associated veno-occlusive disease with immunodeficiency syndrome.
S. Cliffe, D. Bloch, S. Suryani, E. Kamsteeg +23 more
2012Journal of Allergy and Clinical Immunology50 citations Open access
Semantic Scholar
Hemoglobinopathies in North Africa: A Review
Amel Haj Khelil, S. Denden, N. Leban, H. Daimi +4 more
2010Hemoglobin48 citations
Semantic Scholar
A novel homozygous mutation in Recombination Activating Gene 2 in two relatives with different clinical phenotypes: Omenn syndrome and Hyper-IgM syndrome
J. Chou, Rima Hanna-Wakim, I. Tirosh, J. Kane +12 more
2012Journal of Allergy and Clinical Immunology46 citations Open access
Semantic Scholar
A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort
A. Mégarbané, S. Bizzari, A. Deepthi, S. Sabbagh +19 more
2021Journal of Neuromuscular Diseases38 citations Open access
Semantic Scholar
The intellectual disability of trisomy 21: differences in gene expression in a case series of patients with lower and higher IQ
A. Mégarbané, F. Noguier, S. Stora, L. Manchon +10 more
2013European Journal of Human Genetics38 citations Open access
Semantic Scholar
Correlation of EPHX1, GSTP1, GSTM1, and GSTT1 genetic polymorphisms with antioxidative stress markers in chronic obstructive pulmonary disease
R. Lakhdar, S. Denden, Manel Haj Mouhamed, Abdelkader Chalgoum +6 more
2011Experimental Lung Research38 citations Open access
Semantic Scholar
Flow cytometry biomarkers distinguish DOCK8 deficiency from severe atopic dermatitis
E. Janssen, E. Tsitsikov, W. Al-Herz, G. Lefranc +6 more
2013Clinical Immunology37 citations Open access
Semantic Scholar
Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency, Centromeric Instability, Facial Anomalies (ICF) Syndrome
M. Brun, E. Lana, I. Rivals, G. Lefranc +4 more
2011PLoS ONE36 citations Open access
Semantic Scholar
Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia.
A. Mégarbané, A. Pangrazio, A. Villa, E. Chouery +4 more
2013European Journal of Medical Genetics33 citations
Semantic Scholar
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: Report of a new family with additional features and review
H. Mégarbané, Cynthia Zablit, N. Waked, G. Lefranc +2 more
2004American Journal of Medical Genetics. Part A31 citations
Semantic Scholar
Molecular study of six families originating from the Middle-East and presenting with autosomal recessive osteopetrosis.
N. Souraty, P. Noun, Claudia Djambas-Khayat, E. Chouery +5 more
2007European Journal of Medical Genetics30 citations
Semantic Scholar
IMGT® and 30 Years of Immunoinformatics Insight in Antibody V and C Domain Structure and Function
M. Lefranc, G. Lefranc
2019Antibodies28 citations Open access
Semantic Scholar
Exon duplication and triplication in the human T-cell receptor gamma constant region genes and RFLP in French, Lebanese, Tunisian, and Black African populations
C. Buresi, N. Ghanem, S. Huck, G. Lefranc +1 more
2004Immunogenetics27 citations
Semantic Scholar
Association Analysis of IL10, TNF-α, and IL23R-IL12RB2 SNPs with Behçet’s Disease Risk in Western Algeria
Ouahiba Khaib Dit Naib, M. Aribi, A. Idder, A. Chiali +4 more
2013Frontiers in Immunology26 citations Open access
Semantic Scholar
DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations
E. Lana, A. Mégarbané, H. Tourrière, P. Sarda +3 more
2012European Journal of Human Genetics25 citations Open access
Semantic Scholar
Gm, Am and Km immunoglobulin allotypes of two populations in Tunisia
G. Lefranc, G. de Lange, L. Rivat, A. Langancy +5 more
2004Human Genetics24 citations
Semantic Scholar
Combined Analysis of EPHX1, GSTP1, GSTM1 and GSTT1 Gene Polymorphisms in Relation to Chronic Obstructive Pulmonary Disease Risk and Lung Function Impairment
R. Lakhdar, S. Denden, J. Knani, N. Leban +5 more
2011Disease Markers22 citations Open access
Semantic Scholar
Relationship between glutathione S-transferase P1 polymorphisms and chronic obstructive pulmonary disease in a Tunisian population.
R. Lakhdar, S. Denden, J. Knani, N. Leban +5 more
2010Genetics and Molecular Research21 citations Open access
Semantic Scholar
Transcriptomic study in women with trisomy 21 identifies a possible role of the GTPases of the immunity-associated proteins (GIMAP) in the protection of breast cancer
A. Mégarbané, D. Piquemal, A. Rebillat, S. Stora +8 more
2020Scientific Reports19 citations Open access
Semantic Scholar
Epidermodysplasia verruciformis as a manifestation of ARTEMIS deficiency in a young adult.
A. Tahiat, Y. Badran, J. Chou, Brittney Cangemi +10 more
2017Journal of Allergy and Clinical Immunology18 citations
Semantic Scholar

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