Émilie Cornec-Le Gall

Author

Also Known As

Cornec-Le Gall, E., Cornec-Le Gall, Emilie, E Cornec-Le Gall, E Gall, E. Cornec le Gall, E. Cornec-Le Gall, E. Gall, Emilie Cornec Le Gall, Emilie Cornec-Le Gall, Gall, Emilie Cornec-Le

153

Publications

5.3K

Citations

H-Index

Concepts

All Affiliations

Inserm Centre Hospitalier Régional Universitaire de Brest Université de Bretagne Occidentale Mayo Clinic Génétique, Génomique Fonctionnelle et Biotechnologies

ÉC

About

Émilie Cornec-Le Gall is an author at Inserm specializing in medicine, chronic kidney disease, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	16	2.3K
2	Public Health	3	3	584
3	Engineering	1	1	21
4	Health Sciences	1	1	21
5	Epidemiology	1	1	19

Émilie Cornec-Le Gall

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Type of PKD1 Mutation Influences Renal Outcome in ADPKD Émilie Cornec-Le Gall, Marie‐Pierre Audrézet, Jian‐Min Chen, Journal of the American Society of Nephrology Glomerular DiseaseUrologyRenal DiseaseRenal FunctionMedicine	2013	493
Mutations in GANAB , Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease Binu Porath, Vladimir G. Gainullin, Émilie Cornec-Le Gall, The American Journal of Human Genetics HepatologyDisease MechanismMedicineLiver PhysiologyInherited Metabolic Disease	2016	448
The PROPKD Score Émilie Cornec-Le Gall, Marie‐Pierre Audrézet, Annick Rousseau, Journal of the American Society of Nephrology	2015	337
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease Émilie Cornec-Le Gall, Rory J. Olson, Whitney Besse, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsRenal Pathology	2018	302
Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients Marie‐Pierre Audrézet, Émilie Cornec-Le Gall, Jian‐Min Chen, Human Mutation Adpkd Pathogenic MutationsUrologyRenal DiseaseUnrelated PatientsMedicine	2012	175
Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference Anna Köttgen, Émilie Cornec-Le Gall, Jan Halbritter, Kidney International	2022	169
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype Sarah R. Senum, Ying Li, Katherine A. Benson, The American Journal of Human Genetics UrologyAutoimmune DiseaseMedicineRenal PathologyGenetic Epidemiology	2021	151
Use of Highly Individualized Complement Blockade Has Revolutionized Clinical Outcomes after Kidney Transplantation and Renal Epidemiology of Atypical Hemolytic Uremic Syndrome Julien Zuber, Marie Frimat, Sophie Caillard, Journal of the American Society of Nephrology	2019	122
An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International Roman‐Ulrich Müller, A. Lianne Messchendorp, Henrik Birn, Nephrology Dialysis Transplantation HypertensionPatient SelectionRenal PathologyGenetic EpidemiologyRenal Inflammation	2021	122
Polycystic Kidney Disease without an Apparent Family History Ioan-Andrei Iliuta, Vinusha Kalatharan, Kairong Wang, Journal of the American Society of Nephrology	2017	97

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