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Daniel Schorderet
Daniel Schorderet
Professor, faculty of Biology and Medicine, Lausanne, Switzerland
Verified email at unil.ch
Title
Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
110422021
A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia
T Borsello, PGH Clarke, L Hirt, A Vercelli, M Repici, DF Schorderet, ...
Nature medicine 9 (9), 1180-1186, 2003
8182003
Cell-permeable peptide inhibitors of JNK: novel blockers of β-cell death
C Bonny, A Oberson, S Negri, C Sauser, DF Schorderet
Diabetes 50 (1), 77-82, 2001
6992001
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
FL Munier, E Korvatska, A Djemaï, DL Paslier, L Zografos, G Pescia, ...
Nature genetics 15 (3), 247-251, 1997
6441997
Mutations of keratinocyte transglutaminase in lamellar ichthyosis
M Huber, I Rettler, K Bernasconi, E Frenk, SPM Lavrijsen, M Ponec, A Bon, ...
Science 267 (5197), 525-528, 1995
5941995
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy
EM Stone, AJ Lotery, FL Munier, E Héon, B Piguet, RH Guymer, ...
Nature genetics 22 (2), 199-202, 1999
5251999
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, P De Jonghe, A Löfgren, A Vandenberghe, ...
European Journal of Human Genetics 4 (1), 25-33, 1996
5181996
Zebrafish: Housing and husbandry recommendations
P Aleström, L D’Angelo, PJ Midtlyng, DF Schorderet, S Schulte-Merker, ...
Laboratory animals 54 (3), 213-224, 2020
4502020
Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
S Biswas, FL Munier, J Yardley, N Hart-Holden, R Perveen, P Cousin, ...
Human molecular genetics 10 (21), 2415-2423, 2001
4482001
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12. 3: the first 2,253 cases
F Rousseau, D Heitz, J Tarleton, J MacPherson, H Malmgren, N Dahl, ...
American journal of human genetics 55 (2), 225, 1994
3701994
The γ-crystallins and human cataracts: a puzzle made clearer
E Héon, M Priston, DF Schorderet, GD Billingsley, PO Girard, N Lubsen, ...
The American Journal of Human Genetics 65 (5), 1261-1267, 1999
3201999
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Z Yang, Y Chen, C Lillo, J Chien, Z Yu, M Michaelides, M Klein, ...
The Journal of clinical investigation 118 (8), 2908-2916, 2008
2892008
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2
A Li, X Jiao, FL Munier, DF Schorderet, W Yao, F Iwata, M Hayakawa, ...
The American Journal of Human Genetics 74 (5), 817-826, 2004
2792004
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness
I Audo, S Kohl, BP Leroy, FL Munier, X Guillonneau, S Mohand-Saïd, ...
The American Journal of Human Genetics 85 (5), 720-729, 2009
2732009
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter
JC Fleming, E Tartaglini, MP Steinkamp, DF Schorderet, N Cohen, ...
Nature genetics 22 (3), 305-308, 1999
2521999
Methylation silencing and mutations of the p14ARF and p16INK4a genes in colon cancer
N Burri, P Shaw, H Bouzourene, I Sordat, B Sordat, M Gillet, D Schorderet, ...
Laboratory investigation 81 (2), 217-229, 2001
2512001
BIGH3 mutation spectrum in corneal dystrophies
FL Munier, BE Frueh, P Othenin-Girard, S Uffer, P Cousin, MX Wang, ...
Investigative ophthalmology & visual science 43 (4), 949-954, 2002
2462002
Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration
LY Marmorstein, FL Munier, Y Arsenijevic, DF Schorderet, PJ McLaughlin, ...
Proceedings of the National Academy of Sciences 99 (20), 13067-13072, 2002
2352002
Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness
C Zeitz, B Kloeckener-Gruissem, U Forster, S Kohl, I Magyar, B Wissinger, ...
The American Journal of Human Genetics 79 (4), 657-667, 2006
2052006
Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis
F Macari, M Landau, P Cousin, B Mevorah, S Brenner, R Panizzon, ...
The American Journal of Human Genetics 67 (5), 1296-1301, 2000
1872000
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