Ikuti
Juliette Faraco
Juliette Faraco
Sr Research Scientist, Stanford University
Email yang diverifikasi di stanford.edu
Judul
Dikutip oleh
Dikutip oleh
Tahun
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
31431999
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
24592000
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
5682011
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
5612009
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
4192007
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
3452005
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
2802012
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
2772008
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
2682011
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
2652013
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
2182011
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
1711989
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
1682008
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
1672013
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
1662011
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
1542015
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
1402007
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
1392006
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
1291999
Genetic studies in the sleep disorder narcolepsy
H Kadotani, J Faraco, E Mignot
Genome research 8 (5), 427-434, 1998
1011998
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