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Cécile Ged

Observed names: C GED, C Ged, C. GED, C. Ged, C. M. Ged, Cecile GED, Cecile Ged, Cécile Ged, CÉCILE GED, GED, Cécile, Ged Cécile
Observed institutions: Hôpital Necker-Enfants Malades, Université de Bordeaux, Inserm, Vanderbilt University, Centre Hospitalier Universitaire de Bordeaux, Institut Necker Enfants Malades, Laboratory of Excellence GR-Ex, Hôpital Saint-André, Hôpital Pellegrin, Centre Hospitalier Régional Universitaire de Brest, Centre Hospitalier Universitaire Pointe-à-Pitre, Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancers, Institut des Maladies Génétiques Imagine, Université Paris Diderot, Université Bordeaux Segalen, BoRdeaux Institute of onCology, Columbia University, Vanderbilt University Medical Center
ORCID: 0000-0001-7257-8264
Observed ORCID: 0000-0001-7257-8264
OpenAlex ID: A5067779999
CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations
2019 · Grégoire Cullot, Julian Boutin, et al. · Nature Communications · 484
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The increase in urinary excretion of 6 beta‐hydroxycortisol as a marker of human hepatic cytochrome P450IIIA induction.
1989 · C Ged, JM Rouillon, et al. · British Journal of Clinical Pharmacology · 332
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Analysis of SPINK 5, KLK 7 and FLG Genotypes in a French Atopic Dermatitis Cohort
2007 · T Hubiche, C Ged, et al. · Acta Dermato Venereologica · 133
Protective Effects of Catalase Overexpression on UVB-induced Apoptosis in Normal Human Keratinocytes
2006 · Hamid Reza Rezvani, Frédéric Mazurier, et al. · Journal of Biological Chemistry · 125
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UGT 1A1 genotype and irinotecan therapy: general review and implementation in routine practice
2015 · Marie‐Christine Etienne‐Grimaldi, Jean‐Christophe Boyer, et al. · Fundamental and Clinical Pharmacology · 117
A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa
2010 · Nadem Soufir, Cecile Ged, et al. · Journal of Investigative Dermatology · 110
Characterization of cDNAs, mRNAs, and proteins related to human liver microsomal cytochrome P-450 S-mephenytoin 4-hydroxylase
1988 · Cecile Ged, Diane R. Umbenhauer, et al. · Biochemistry · 108
Separation of human liver microsomal tolbutamide hydroxylase and (S)-mephenytoin 4'-hydroxylase cytochrome P-450 enzymes.
1991 · P K Srivastava, C H Yun, et al. · Molecular Pharmacology · 100
Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases
2012 · R.P. Katugampola, M.N. Badminton, et al. · British Journal of Dermatology · 95
Loss of epidermal hypoxia-inducible factor-1α accelerates epidermal aging and affects re-epithelialization in human and mouse
2011 · Hamid Reza Rezvani, Nsrein Ali, et al. · Journal of Cell Science · 94
ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria
2011 · Jordi To-Figueras, Sarah Ducamp, et al. · Blood · 90
A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases
2012 · R.P. Katugampola, A.V. Anstey, et al. · British Journal of Dermatology · 85
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
2021 · J. Boutin, J. Rosier, et al. · Nature Communications · 82
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Hypoxia-inducible factor-1α regulates the expression of nucleotide excision repair proteins in keratinocytes
2009 · Hamid Reza Rezvani, Walid Mahfouf, et al. · Nucleic Acids Research · 73
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Uroporphyrinogen decarboxylase: complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyria.
1996 · M J Moran-Jimenez, C Ged, et al. · PubMed · 72
Successful match-unrelated donor bone marrow transplantation for congenital erythropoietic porphyria (Günther disease)
2004 · Sophie Dupuis-Girod, Véronique Akkari, et al. · European Journal of Pediatrics · 71
Correction of congenital erythropoietic porphyria by bone marrow transplantation
1996 · Caroline Thomas, Cecile Ged, et al. · The Journal of Pediatrics · 69
Gene Therapy of a Mouse Model of Protoporphyria with a Self-Inactivating Erythroid-Specific Lentiviral Vector without Preselection
2001 · Emmanuel Richard, Manuel Mendez, et al. · Molecular Therapy · 63
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Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients
2014 · I. Callebaut, R. Joubrel, et al. · Human Molecular Genetics · 60
A Systematic Analysis of the Mutations of the Uroporphyrinogen III Synthase Gene in Congenital Erythropoietic Porphyria
1996 · H. de Verneuil, C. Ged, et al. · European Journal of Human Genetics · 55
Effective Gene Therapy of Mice with Congenital Erythropoietic Porphyria Is Facilitated by a Survival Advantage of Corrected Erythroid Cells
2008 · Elodie Robert-Richard, François Moreau-Gaudry, et al. · The American Journal of Human Genetics · 51
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Human cell engraftment after busulfan or irradiation conditioning of NOD/SCID mice.
2006 · Elodie Robert-Richard, Cécile Ged, et al. · PubMed · 51
Hematopoietic stem cell gene therapy of murine protoporphyria by methylguanine-DNA-methyltransferase-mediated in vivo drug selection
2004 · E Richard, E Robert, et al. · Gene Therapy · 46
Protection of normal human reconstructed epidermis from UV by catalase overexpression
2006 · H R Rezvani, M Cario-André, et al. · Cancer Gene Therapy · 45
Congenital erythropoietic porphyria: mutation update and correlations between genotype and phenotype.
2009 · C Ged, F Moreau-Gaudry, et al. · PubMed · 44
Works count: 125
Citation count: 3,971
H-index: 33
I10-index: 74
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