| 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 | 3127 | 1999 |
| 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 | 2457 | 2000 |
| 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 | 578 | 2011 |
| 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 | 565 | 2009 |
| 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 | 422 | 2007 |
| 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 | 345 | 2005 |
| 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 | 277 | 2012 |
| 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 | 274 | 2011 |
| 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 | 271 | 2008 |
| 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 | 267 | 2013 |
| 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 | 219 | 2011 |
| 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 | 174 | 1989 |
| 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 | 170 | 2013 |
| 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 | 169 | 2011 |
| 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 | 169 | 2008 |
| 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 | 153 | 2015 |
| 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 | 141 | 2007 |
| 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 | 133 | 2006 |
| 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 | 130 | 1999 |
| Genetic studies in the sleep disorder narcolepsy H Kadotani, J Faraco, E Mignot Genome research 8 (5), 427-434, 1998 | 101 | 1998 |
