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C. Ged · SciRah

Researcher profile · Semantic Scholar

C. Ged

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C. Ged — researcher profile on SciRah

h-index: 27
Works: 93
Citations: 2,630

Most-cited papers

CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations
G. Cullot, J. Boutin, J. Toutain, F. Prat +16 more
2019Nature Communications420 citations Open access
Semantic Scholar
Analysis of SPINK 5, KLK 7 and FLG genotypes in a French atopic dermatitis cohort.
T. Hubiche, C. Ged, A. Bénard, C. Léauté-Labrèze +4 more
2007Acta Dermato-Venereologica131 citations Open access
Semantic Scholar
Protective Effects of Catalase Overexpression on UVB-induced Apoptosis in Normal Human Keratinocytes*
H. Rezvani, F. Mazurier, M. Cario-André, C. Pain +3 more
2006Journal of Biological Chemistry118 citations Open access
Semantic Scholar
UGT1A1 genotype and irinotecan therapy: general review and implementation in routine practice
M. Etienne-Grimaldi, J. Boyer, F. Thomas, Sylvie Quaranta +13 more
2015Fundamental & Clinical Pharmacology116 citations
Semantic Scholar
A prevalent mutation with founder effect in xeroderma pigmentosum group C from north Africa.
N. Soufir, C. Ged, A. Bourillon, F. Austerlitz +13 more
2010Journal of Investigative Dermatology96 citations Open access
Semantic Scholar
ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria.
J. To-Figueras, S. Ducamp, J. Clayton, C. Badenas +10 more
2011Blood90 citations
Semantic Scholar
Loss of epidermal hypoxia-inducible factor-1α accelerates epidermal aging and affects re-epithelialization in human and mouse
H. Rezvani, N. Ali, Martin Serrano-Sanchez, P. Dubus +8 more
2011Journal of Cell Science88 citations Open access
Semantic Scholar
Congenital erythropoietic porphyria: a single‐observer clinical study of 29 cases
R. Katugampola, M. Badminton, A. Finlay, S. Whatley +10 more
2012British Journal of Dermatology80 citations Open access
Semantic Scholar
Correction of congenital erythropoietic porphyria by bone marrow transplantation.
Caroline Thomas, C. Ged, Y. Nordmann, H. de Verneuil +3 more
1996Jornal de Pediatria72 citations
Semantic Scholar
A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases
R. Katugampola, A. Anstey, A. Finlay, S. Whatley +10 more
2012British Journal of Dermatology71 citations
Semantic Scholar
Hypoxia-inducible factor-1α regulates the expression of nucleotide excision repair proteins in keratinocytes
H. Rezvani, W. Mahfouf, N. Ali, Cécile Chemin +6 more
2009Nucleic Acids Research66 citations Open access
Semantic Scholar
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
J. Boutin, J. Rosier, D. Cappellen, F. Prat +15 more
2021Nature Communications64 citations Open access
Semantic Scholar
Gene therapy of a mouse model of protoporphyria with a self-inactivating erythroid-specific lentiviral vector without preselection.
E. Richard, Manuel Mendez, F. Mazurier, Carine Morel +10 more
2001Molecular Therapy63 citations Open access
Semantic Scholar
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients.
I. Callebaut, R. Joubrel, S. Pissard, C. Kannengiesser +14 more
2014Human Molecular Genetics54 citations Open access
Semantic Scholar
Successful match-unrelated donor bone marrow transplantation for congenital erythropoietic porphyria (Günther disease)
S. Dupuis-Girod, V. Akkari, C. Ged, C. Galambrun +7 more
2005European Journal of Pediatrics54 citations
Semantic Scholar
A Systematic Analysis of the Mutations of the Uroporphyrinogen III Synthase Gene in Congenital Erythropoietic Porphyria
A. Fontanellas, M. Bensidhoum, R. D. de Salamanca, A. Tirado +2 more
1996European Journal of Human Genetics54 citations
Semantic Scholar
Congenital erythropoietic porphyria: mutation update and correlations between genotype and phenotype.
C. Ged, F. Moreau-Gaudry, E. Richard, Elodie Robert-Richard +1 more
2009Cellular and Molecular Biology46 citations
Semantic Scholar
Human cell engraftment after busulfan or irradiation conditioning of NOD/SCID mice.
Elodie Robert-Richard, C. Ged, J. Ortet, X. Santarelli +3 more
2006Haematologica42 citations
Semantic Scholar
Effective gene therapy of mice with congenital erythropoietic porphyria is facilitated by a survival advantage of corrected erythroid cells.
Elodie Robert-Richard, F. Moreau-Gaudry, Magalie Lalanne, I. Lamrissi‐Garcia +5 more
2008American Journal of Human Genetics40 citations Open access
Semantic Scholar
Therapeutic potential of proteasome inhibitors in congenital erythropoietic porphyria
J. Blouin, Yann Duchartre, P. Costet, Magalie Lalanne +5 more
2013Proceedings of the National Academy of Sciences of the United States of America36 citations Open access
Semantic Scholar
Metabolic correction of congenital erythropoietic porphyria by retrovirus-mediated gene transfer into Epstein-Barr virus-transformed B-cell lines.
FranGois Moreau-Gaudry, Frédéric Mazurier, M. Bensidhoum, C. Ged +1 more
1995Blood32 citations
Semantic Scholar
Murine retroviral but not human cellular promoters induce in vivo erythroid-specific deregulation that can be partially prevented by insulators.
Elodie Robert-Richard, E. Richard, P. Malik, C. Ged +2 more
2007Molecular Therapy31 citations Open access
Semantic Scholar
Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage
N. Fayyad, F. Kobaisi, D. Beal, W. Mahfouf +7 more
2020Frontiers in Genetics29 citations Open access
Semantic Scholar
Erythropoietic porphyrias: animal models and update in gene-based therapies.
E. Richard, Elodie Robert-Richard, C. Ged, F. Moreau-Gaudry +1 more
2008Current Gene Therapy29 citations
Semantic Scholar
Correction of the Enzyme Defect in Cultured Congenital Erythropoietic Porphyria Disease Cells by Retrovirus-Mediated Gene Transfer
F. Moreau-Gaudry, C. Ged, C. Barbot, F. Mazurier +4 more
1995Human Gene Therapy29 citations
Semantic Scholar
A knock-in mouse model of congenital erythropoietic porphyria.
C. Ged, Manuel Mendez, E. Robert, Magalie Lalanne +7 more
2006Genomics28 citations Open access
Semantic Scholar
Congenital erythropoietic porphyria: report of a novel mutation with absence of clinical manifestations in a homozygous mutant sibling.
C. Ged, H. Mégarbané, E. Chouery, Magalie Lalanne +2 more
2004Journal of Investigative Dermatology28 citations Open access
Semantic Scholar
[Allogeneic bone marrow transplantation in congenital erythropoietic porphyria. Gunther's disease].
C. Lagarde, D. Hamel-Teillac, Y. de Prost, S. Blanche +5 more
1998Annales de dermatologie et de vénéréologie26 citations
Semantic Scholar
The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism
C. Ka, Julie Guellec, X. Pepermans, C. Kannengiesser +12 more
2018Haematologica25 citations Open access
Semantic Scholar
Missense UROS mutations causing congenital erythropoietic porphyria reduce UROS homeostasis that can be rescued by proteasome inhibition
J. Blouin, G. Bernardo-Seisdedos, Emma Sasso, J. Estève +7 more
2017Human Molecular Genetics25 citations Open access
Semantic Scholar
Impact of high-flux/high-efficiency dialysis on folate and homocysteine metabolism.
C. Lasseur, F. Parrot, Y. Delmas, C. Level +5 more
2001JN. Journal of Nephrology (Milano. 1992)25 citations
Semantic Scholar
Description of a new mutation in hepatoerythropoietic porphyria and prenatal exclusion of a homozygous fetus.
C. Ged, Dolores Ozalla, Carmen Herrero, Mario Lecha +3 more
2002Archives of Dermatology24 citations Open access
Semantic Scholar
Metabolic correction of congenital erythropoietic porphyria with iPSCs free of reprogramming factors.
A. Bedel, Miguel Taillepierre, V. Guyonnet-Duperat, E. Lippert +12 more
2012American Journal of Human Genetics23 citations Open access
Semantic Scholar
Highly Efficient Lentiviral Gene Transfer in CD34+ and CD34+/38−/lin− Cells from Mobilized Peripheral Blood after Cytokine Prestimulation
F. Géronimi, E. Richard, I. Redonnet-Vernhet, I. Lamrissi‐Garcia +4 more
2003Stem Cells23 citations
Semantic Scholar
Porphyrias: Animal models and prospects for cellular and gene therapy
H. de Verneuil, C. Ged, S. Boulechfar, F. Moreau-Gaudry
1995Journal of Bioenergetics and Biomembranes23 citations
Semantic Scholar
A bicistronic SIN‐lentiviral vector containing G156A MGMT allows selection and metabolic correction of hematopoietic protoporphyric cell lines
E. Richard, F. Géronimi, Magalie Lalanne, C. Ged +5 more
2003Journal of Gene Medicine22 citations
Semantic Scholar
Correction of deficient CD34+ cells from peripheral blood after mobilization in a patient with congenital erythropoietic porphyria.
F. Mazurier, F. Géronimi, I. Lamrissi‐Garcia, Carine Morel +6 more
2001Molecular Therapy22 citations Open access
Semantic Scholar
Iron chelation rescues hemolytic anemia and skin photosensitivity in congenital erythropoietic porphyria.
J. Blouin, C. Ged, Magalie Lalanne, I. Lamrissi‐Garcia +9 more
2020Blood21 citations
Semantic Scholar
Identification of Two New Mutations in Congenital Erythropoietic Porphyria
M. Bensidhoum, C. Ged, Isabelle Hombrados, F. Moreau-Gaudry +4 more
1995European Journal of Human Genetics21 citations
Semantic Scholar
Phlebotomy as an efficient long-term treatment of congenital erythropoietic porphyria
A. Mirmiran, A. Poli, C. Ged, C. Schmitt +12 more
2020Haematologica20 citations Open access
Semantic Scholar
Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model
S. Millot, C. Delaby, Boualem Moulouel, T. Lefèbvre +12 more
2017Haematologica20 citations Open access
Semantic Scholar
Lentivirus-mediated gene transfer of uroporphyrinogen III synthase fully corrects the porphyric phenotype in human cells
F. Géronimi, E. Richard, I. Lamrissi‐Garcia, Magalie Lalanne +4 more
2003Journal of molecular medicine20 citations
Semantic Scholar
Usefulness of a global clinical ichthyosis vulgaris scoring system for predicting common FLG null mutations in an adult caucasian population
K. Ezzedine, C. Droitcourt, C. Ged, A. Diallo +4 more
2012British Journal of Dermatology17 citations
Semantic Scholar
Bone marrow transplantation in congenital erythropoietic porphyria: Sustained efficacy but unexpected liver dysfunction.
C. Besnard, C. Schmitt, L. Galmiche-Rolland, D. Debray +11 more
2019Biology of Blood and Marrow Transplantation16 citations Open access
Semantic Scholar
Rapid analysis and efficient selection of human transduced primitive hematopoietic cells using the humanized S65T green fluorescent protein
F. Mazurier, F. Moreau-Gaudry, V. Maguer-Satta, S. Salesse +7 more
1998Gene Therapy16 citations
Semantic Scholar
[Successful gene therapy of mice with congenital erythropoietic porphyria].
H. de Verneuil, Elodie Robert-Richard, C. Ged, F. Mazurier +2 more
2008Medecine sciences : M/S15 citations Open access
Semantic Scholar
Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomy
J. Blouin, C. Ged, G. Bernardo-Seisdedos, Txomin Cabantous +7 more
2021Molecular Genetics and Metabolism Reports13 citations Open access
Semantic Scholar
[Congenital erythropoeietic porphyria treated by haematopoietic stem cell allograft].
I. Lebreuilly-Sohyer, A. Morice, A. Acher, A. Dompmartin +5 more
2010Annales de dermatologie et de vénéréologie13 citations
Semantic Scholar
Gene transfer of the uroporphyrinogen III synthase cDNA into haematopoietic progenitor cells in view of a future gene therapy in congenital erythropoietic porphyria
F. Mazurier, F. Moreau-Gaudry, S. Salesse, C. Barbot +3 more
1997Journal of Inherited Metabolic Disease13 citations
Semantic Scholar
Xeroderma pigmentosum in South Africa: Evidence for a prevalent founder effect
M. Kgokolo, F. Morice-Picard, H. Rezvani, F. Austerlitz +5 more
2019British Journal of Dermatology12 citations Open access
Semantic Scholar

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I. Lamrissi‐Garcia

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