Daniel F. Schorderet

Author

Also Known As

D F Schorderet, D SCHORDERET, D Schorderet, D. F. Schorderet, D. Schorderet, D.F. Schorderet, DANIEL F. SCHORDERET, Daniel F Schorderet, Daniel F. Schorderet, Daniel F. Schorderet, MD, PhD

410

Publications

23.4K

Citations

H-Index

179

Concepts

All Affiliations

University of Lausanne Institut de Recherche en Opthalmologie Hôpital Ophtalmique Jules-Gonin École Polytechnique Fédérale de Lausanne University Hospital of Lausanne

About

Daniel F. Schorderet is an author at University of Lausanne specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	42	89	11.4K
2	Natural Sciences	6	6	4.3K
3	Public Health	6	6	287
4	Health Sciences	2	2	114
5	Social Sciences	2	2	59

Daniel F. Schorderet

178

Publications

22.6K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) Daniel J. Klionsky, Kotb Abdelmohsen, Akihisa Abe, Autophagy	2016	5.9K
Guidelines for the use and interpretation of assays for monitoring autophagy Daniel J. Klionsky, Fábio Camargo Abdalla, Hagai Abeliovich, Autophagy MitophagyParticular Autophagy AssaysImmunologyCytoskeletonMultiple Assays	2012	4K
Zebrafish: Housing and husbandry recommendations Peter Aleström, Livia D’Angelo, Paul J. Midtlyng, Laboratory Animals	2019	671
A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia Tiziana Borsello, Lorenz Hirt, Alessandro Vercelli, Nature Medicine Cerebral IschemiaCerebral Vascular RegulationMedicineApoptosisCell Death	2003	656
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies Francis L. Munier, Elena Korvatska, Assia Djemaï, Nature Genetics Kerato-epithelin MutationsOcular PathologyOphthalmologyCorneal Dystrophy	1997	608
Cell-Permeable Peptide Inhibitors of JNK Christophe Bonny, Anne Oberson, Stéphanie Negri, Diabetes Peptide EngineeringImmunologyImmune RegulationCell DeathImmunologic Mechanism	2001	570
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy Edwin M. Stone, Andrew Lotery, Francis L. Munier, Nature Genetics Ocular DiseaseRetinal DystrophyOphthalmologyGenetic DisorderMedicine	1999	491
Mutations of Keratinocyte Transglutaminase in Lamellar Ichthyosis Marcel Huber, Irmingard Rettler, Katja Bernasconi, Science Tgk GeneDevelopmental BiologyAutoimmune DiseaseGeneticsHistopathology	1995	484
Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2 Anren Li, Xiaodong Jiao, Francis L. Munier, The American Journal of Human Genetics Mendelian DisorderOphthalmologyCorneal DystrophyGenetic DisorderGenetics	2004	280
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice Zhenglin Yang, Yali Chen, Concepción Lillo, Journal of Clinical Investigation Ocular DiseaseSignal TransductionDevelopmental BiologyOphthalmologyRetina	2008	271

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