M. des Georges - Concepedia

Author

M. des Georges

Also Known As

Georges M., M D Georges, M Des Georges, M Georges, M. Des Georges, M. Georges, M. des Georges, Maalouly Georges, Marie Des Georges

Publications

432

Citations

H-Index

Concepts

All Affiliations

Inserm Hôpital Arnaud de Villeneuve Hôpital Robert-Debré Hôpital Pellegrin Hôpital Cochin

About

M. des Georges is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	150
2	Pathology	3	3	124
3	Molecular Genetics	2	2	40
4	Clinical Genetics	2	2	79
5	Public Health	1	1	14

M. des Georges

Publications

377

Citations

H-Index

Page 1

	Year	Citations
The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening Christel Thauvin‐Robinet, À. Munck, Frédéric Huet, Journal of Medical Genetics	2009	126
The molecular genetic epidemiology of cystic fibrosis: Report of a joint meeting of WHO/ECFTN/ICF(M)A/ECFS Harry Cuppens, Boulyjenkov, Francesc Calafell, Molecular Genetic EpidemiologyJoint MeetingFibrosisGenetic DisorderGenetics	2004	65
Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis Isabelle Sermet‐Gaudelus, E. Girodon, Delphine Roussel, Thorax	2010	50
Sinonasal mucosal melanoma: A 44-case study and literature analysis Marine Dréno, M. des Georges, F. Espitalier, European Annals of Otorhinolaryngology Head and Neck Diseases Literature AnalysisSurgical PathologyHistopathologyMelanomaPathology	2017	45
Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10‐year experience Anne Girardet, Aliya Ishmukhametova, Marjolaine Willems, Clinical Genetics	2014	28
Structure, evolution and chromosomal localization of the human pregnancy-specific β1 glycoprotein gene family Catherine Streydio, S. Swillens, M. des Georges, Genomics Developmental BiologyGenetic DisorderGeneticsChromosome BiologyMolecular Genetics	1990	26
Variants in <i>CFTR</i> untranslated regions are associated with congenital bilateral absence of the vas deferens E. Lopez, Victoria Viart, Caroline Guittard, Journal of Medical Genetics	2010	23
Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: A large European study [3] Amaral, Paula Pacheco, Susanne Beck, Mendelian DisorderGenetic DisorderMedicineGeneticsCystic Fibrosis Patients	2001	14

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