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Juliette Faraco
Juliette Faraco
Sr Research Scientist, Stanford University
Verified email at stanford.edu
Title
Cited by
Cited by
Year
The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene
L Lin, J Faraco, R Li, H Kadotani, W Rogers, X Lin, X Qiu, PJ de Jong, ...
Cell 98 (3), 365-376, 1999
30401999
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
C Peyron, J Faraco, W Rogers, B Ripley, S Overeem, Y Charnay, ...
Nature medicine 6 (9), 991-997, 2000
23792000
Narcolepsy onset is seasonal and increased following the 2009 H1N1 pandemic in China
F Han, L Lin, SC Warby, J Faraco, J Li, SX Dong, P An, L Zhao, LH Wang, ...
Annals of neurology 70 (3), 410-417, 2011
5552011
Narcolepsy is strongly associated with the T-cell receptor alpha locus
J Hallmayer, J Faraco, L Lin, S Hesselson, J Winkelmann, M Kawashima, ...
Nature genetics 41 (6), 708-711, 2009
5452009
Characterization of sleep in zebrafish and insomnia in hypocretin receptor mutants
T Yokogawa, W Marin, J Faraco, G Pézeron, L Appelbaum, J Zhang, ...
PLoS biology 5 (10), e277, 2007
3912007
Concomitant loss of dynorphin, NARP, and orexin in narcolepsy
A Crocker, RA España, M Papadopoulou, CB Saper, J Faraco, T Sakurai, ...
Neurology 65 (8), 1184-1188, 2005
3362005
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy
J Winkelmann, L Lin, B Schormair, BR Kornum, J Faraco, G Plazzi, ...
Human molecular genetics 21 (10), 2205-2210, 2012
2622012
Common variants in P2RY11 are associated with narcolepsy
BR Kornum, M Kawashima, J Faraco, L Lin, TJ Rico, S Hesselson, ...
Nature genetics 43 (1), 66-71, 2011
2582011
Kleine–Levin syndrome: a systematic study of 108 patients
I Arnulf, L Lin, N Gadoth, J File, M Lecendreux, P Franco, J Zeitzer, B Lo, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
2582008
ImmunoChip study implicates antigen presentation to T cells in narcolepsy
J Faraco, L Lin, BR Kornum, EE Kenny, G Trynka, M Einen, TJ Rico, ...
PLoS genetics 9 (2), e1003270, 2013
2552013
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12. 1
J Winkelmann, D Czamara, B Schormair, F Knauf, EC Schulte, ...
PLoS genetics 7 (7), e1002171, 2011
2112011
Narcolepsy with hypocretin/orexin deficiency, infections and autoimmunity of the brain
BR Kornum, J Faraco, E Mignot
Current opinion in neurobiology 21 (6), 897-903, 2011
1682011
ApaI dimorphism at the human vitamin D receptor gene locus.
JH Faraco, NA Morrison, A Baker, J Shine, PM Frossard
Nucleic acids research 17 (5), 2150, 1989
1671989
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
F Han, J Faraco, XS Dong, HM Ollila, L Lin, J Li, P An, S Wang, KW Jiang, ...
PLoS genetics 9 (10), e1003880, 2013
1592013
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy
T Miyagawa, M Kawashima, N Nishida, J Ohashi, R Kimura, A Fujimoto, ...
Nature genetics 40 (11), 1324-1328, 2008
1562008
HLA-DPB1 and HLA class I confer risk of and protection from narcolepsy
HM Ollila, JM Ravel, F Han, J Faraco, L Lin, X Zheng, G Plazzi, ...
The American Journal of Human Genetics 96 (1), 136-146, 2015
1462015
Genomic and functional conservation of sedative-hypnotic targets in the zebrafish
C Renier, JH Faraco, P Bourgin, T Motley, P Bonaventure, F Rosa, ...
Pharmacogenetics and genomics 17 (4), 237-253, 2007
1352007
Regulation of hypocretin (orexin) expression in embryonic zebrafish
JH Faraco, L Appelbaum, W Marin, SE Gaus, P Mourrain, E Mignot
Journal of Biological Chemistry 281 (40), 29753-29761, 2006
1282006
Construction and characterization of an eightfold redundant dog genomic bacterial artificial chromosome library
R Li, E Mignot, J Faraco, H Kadotani, J Cantanese, B Zhao, X Lin, ...
Genomics 58 (1), 9-17, 1999
1281999
Genetic studies in the sleep disorder narcolepsy
H Kadotani, J Faraco, E Mignot
Genome research 8 (5), 427-434, 1998
1041998
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