Daniel F. Schorderet

Overview

Best Publications

• Guidelines for the use and interpretation of assays for monitoring autophagy

  Daniel J. Klionsky;Fabio C. Abdalla;Hagai Abeliovich;Robert T. Abraham

  8665
  Citations

• Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

  Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  8488
  Citations

• Cell-Permeable Peptide Inhibitors of JNK: Novel Blockers of β-Cell Death

  Christophe Bonny;Anne Oberson;Stéphanie Negri;Christelle Sauser

  917
  Citations

• Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

  Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  895
  Citations

• A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia.

  Tiziana Borsello;Peter G H Clarke;Lorenz Hirt;Alessandro Vercelli

  824
  Citations

• Mutations of keratinocyte transglutaminase in lamellar ichthyosis.

  Marcel Huber;Irmingard Rettler;Katja Bernasconi;Edgar Frenk

  657
  Citations

• Kerato-epithelin mutations in four 5q31-linked corneal dystrophies.

  F L Munier;E Korvatska;A Djemaï;D Le Paslier

  648
  Citations

• A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.

  Edwin M. Stone;Andrew J. Lotery;Francis L. Munier;Elise Héon

  527
  Citations

• Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study

  E. Nelis;C. van Broeckhoven;E.C.M. Mariman;A.A.W.M. Gabreëls-Festen

  515
  Citations

• Zebrafish: Housing and husbandry recommendations:

  Peter Aleström;Livia D'Angelo;Paul J Midtlyng;Daniel F Schorderet

  502
  Citations

• Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy

  Susmito Biswas;Francis L. Munier;Jill Yardley;Niki Hart-Holden

  424
  Citations

• The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer

  Elise Héon;Megan Priston;Daniel F. Schorderet;Gail D. Billingsley

  350
  Citations

• Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice

  Zhenglin Yang;Yali Chen;Concepcion Lillo;Jeremy Chien

  291
  Citations

• Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

  Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  287
  Citations

• Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.

  Anren Li;Xiaodong Jiao;Francis L. Munier;Daniel F. Schorderet

  279
  Citations

• TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

  Isabelle Audo;Susanne Kohl;Bart P. Leroy;Francis L. Munier

  270
  Citations

• The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.

  Judith C. Fleming;Elena Tartaglini;Mara P. Steinkamp;Daniel F. Schorderet

  255
  Citations

• BIGH3 mutation spectrum in corneal dystrophies.

  Francis L. Munier;Beatrice E. Frueh;Philippe Othenin-Girard;Sylvie Uffer

  246
  Citations

• Methylation silencing and mutations of the p14ARF and p16INK4a genes in colon cancer.

  Nathalie Burri;Phillip Shaw;Hanifa Bouzourene;Isabelle Sordat

  235
  Citations

• Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.

  Christina Zeitz;Barbara Kloeckener-Gruissem;Ursula Forster;Susanne Kohl

  232
  Citations