Cécile Ged - Concepedia

Author

Cécile Ged

Inserm ORCID

Also Known As

A. Moruno Tirado, C GED, C Ged, C. GED, C. Ged, C. M. Ged, Cecile GED, Cecile Ged, Cécile Ged, CÉCILE GED

123

Publications

3.8K

Citations

H-Index

111

Concepts

All Affiliations

Inserm Université de Bordeaux Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancers Bordeaux Population Health Centre Hospitalier Universitaire de Bordeaux

About

Cécile Ged is an author at Inserm specializing in medicine, genetics, and porphyrias.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	29	1.6K
2	Health Sciences	4	4	460
3	Natural Sciences	3	3	143
4	Public Health	1	1	44
5	Allergy	1	1	132

Cécile Ged

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations Grégoire Cullot, Julian Boutin, Jérôme Toutain, Nature Communications	2019	458
The increase in urinary excretion of 6 beta‐hydroxycortisol as a marker of human hepatic cytochrome P450IIIA induction. Cécile Ged, JM Rouillon, Lydiane Pichard, British Journal of Clinical Pharmacology Urinary ExcretionCortisol 6PharmacotherapyDaily ExcretionExperimental Pharmacology	1989	331
Analysis of SPINK 5, KLK 7 and FLG Genotypes in a French Atopic Dermatitis Cohort Thomas Hubiche, Cécile Ged, Antoine Bénard, Acta Dermato Venereologica AsthmaKlk 7AllergyAutoimmune DiseaseSpink 5	2007	132
Protective Effects of Catalase Overexpression on UVB-induced Apoptosis in Normal Human Keratinocytes Hamid Rezvani, Frédéric Mazurier, Muriel Cario, Journal of Biological Chemistry	2006	114
Characterization of cDNAs, mRNAs, and proteins related to human liver microsomal cytochrome P-450 S-mephenytoin 4-hydroxylase Cécile Ged, Diane R. Umbenhauer, Teresa M. Bellew, Biochemistry	1988	109
<i><scp>UGT</scp>1A1</i> genotype and irinotecan therapy: general review and implementation in routine practice Marie-Christine Étienne-Grimaldi, Jean‐Christophe Boyer, Fabienne Thomas, Fundamental and Clinical Pharmacology PathologyPharmacotherapyAdvanced Colorectal CancerClinical GeneticsSystems Pharmacology	2015	108
Separation of human liver microsomal tolbutamide hydroxylase and (S)-mephenytoin 4'-hydroxylase cytochrome P-450 enzymes. Pramod K. Srivastava, Chul‐Ho Yun, Philippe Beaune, Molecular Pharmacology	1991	100
A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa Nadem Soufir, Cécile Ged, Agnès Bourillon, Journal of Investigative Dermatology BiologyAllelic VariantPrevalent MutationMedicineGenetics	2010	98
Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases Ruwani Katugampola, Michael N. Badminton, A.Y. Finlay, British Journal of Dermatology	2012	93
ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria Jordi To‐Figueras, Sarah Ducamp, Jerome Clayton, Blood	2011	91

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