Laurence Heidet - Concepedia

Author

Laurence Heidet

Hôpital Necker-Enfants Malades ORCID

Also Known As

A Ghoneimi, G. He, Heidet, L, Heidet, L., L Heidet, L. Heidet, LAURENCE HEIDET, Laurence Heidet, Sandrine Hayette

204

Publications

7.3K

Citations

H-Index

129

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Inserm Université Paris Cité Assistance Publique – Hôpitaux de Paris Délégation Paris 5

About

Laurence Heidet is an author at Hôpital Necker-Enfants Malades specializing in medicine, pathology, and renal pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	46	3.5K
2	Education	1	1	21
3	Health Sciences	1	1	120
4	Natural Sciences	1	1	55
5	Allergy	1	1	28

Laurence Heidet

Publications

6.8K

Citations

H-Index

Page 1

	Year	Citations
Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy Christoph Licht, Hans‐Joachim Anders, Bernd Höppe, Kidney International HypertensionUrologyRenal FunctionKidney FailurePhysiology	2011	350
Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group Clifford E. Kashtan, Jie Ding, Guido Garosi, Kidney International Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathology	2018	297
Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases Laurence Heidet, Stéphane Decramer, Audrey Pawtowski, Clinical Journal of the American Society of Nephrology	2010	292
Early Glomerular Filtration Defect and Severe Renal Disease in Podocin-Deficient Mice Séverine Roselli, Laurence Heidet, Mireille Sich, Molecular and Cellular Biology	2003	260
COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome Ilaria Longo, Paola Porcedda, Francesca Mari, Kidney International Mendelian DisorderGenetic DisorderMedicineGeneticsCol4a3/col4a4 Mutations	2002	229
Expression of the Nonmuscle Myosin Heavy Chain IIA in the Human Kidney and Screening for MYH9 Mutations in Epstein and Fechtner Syndromes Christelle Arrondel, Nicolas Vodovar, Bertrand Knebelmann, Journal of the American Society of Nephrology Glomerular DiseaseFechtner SyndromesGeneticsRenal PathologyImmunology	2002	216
Structure of the Human Type IV Collagen Gene COL4A3 and Mutations in Autosomal Alport Syndrome Laurence Heidet, Christelle Arrondel, Lionel Forestier, Journal of the American Society of Nephrology	2001	189
Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing Vincent Morinière, Karin Dahan, Pascale Hilbert, Journal of the American Society of Nephrology	2014	166
Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation Frank T.L. Van Der Loop, Laurence Heidet, Erika Timmer, Kidney International Developmental AnomalyMendelian DisorderGenetic DisorderGeneticsPathology	2000	163
Evidence of digenic inheritance in Alport syndrome Maria Antonietta Mencarelli, Laurence Heidet, Helen Storey, Journal of Medical Genetics	2015	159

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