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Items: 35

1.

Analysis of Hypoxic and Hypercapnic Ventilatory Response in Healthy Volunteers.

Goldberg S, Ollila HM, Lin L, Sharifi H, Rico T, Andlauer O, Aran A, Bloomrosen E, Faraco J, Fang H, Mignot E.

PLoS One. 2017 Jan 3;12(1):e0168930. doi: 10.1371/journal.pone.0168930. eCollection 2017.

2.

EIF3G is associated with narcolepsy across ethnicities.

Holm A, Lin L, Faraco J, Mostafavi S, Battle A, Zhu X, Levinson DF, Han F, Gammeltoft S, Jennum P, Mignot E, Kornum BR.

Eur J Hum Genet. 2015 Nov;23(11):1573-80. doi: 10.1038/ejhg.2015.4. Epub 2015 Feb 11.

3.

HLA-DPB1 and HLA class I confer risk of and protection from narcolepsy.

Ollila HM, Ravel JM, Han F, Faraco J, Lin L, Zheng X, Plazzi G, Dauvilliers Y, Pizza F, Hong SC, Jennum P, Knudsen S, Kornum BR, Dong XS, Yan H, Hong H, Coquillard C, Mahlios J, Jolanki O, Einen M, Arnulf I, Högl B, Frauscher B, Crowe C, Partinen M, Huang YS, Bourgin P, Vaarala O, Désautels A, Montplaisir J, Mack SJ, Mindrinos M, Fernandez-Vina M, Mignot E.

Am J Hum Genet. 2015 Jan 8;96(1):136-46. doi: 10.1016/j.ajhg.2014.12.010. Erratum in: Am J Hum Genet. 2015 May 7;96(5):852. Lavault, Sophie [removed]; Arnulf, Isabelle [added].

4.

Dual cases of type 1 narcolepsy with schizophrenia and other psychotic disorders.

Canellas F, Lin L, Julià MR, Clemente A, Vives-Bauza C, Ollila HM, Hong SC, Arboleya SM, Einen MA, Faraco J, Fernandez-Vina M, Mignot E.

J Clin Sleep Med. 2014 Sep 15;10(9):1011-8. doi: 10.5664/jcsm.4040.

5.

Heterotopic pancreas complicated by pseudocyst in the gastric wall diagnosed by endoscopic ultrasound-guided fine needle aspiration.

Rocha HL, Bueno FK, Faraco J, Assef MS, Araki OM, Nakao F, Rossini LG.

Endosc Ultrasound. 2013 Jul;2(3):159-61. doi: 10.7178/eus.06.009.

6.

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.

Han F, Faraco J, Dong XS, Ollila HM, Lin L, Li J, An P, Wang S, Jiang KW, Gao ZC, Zhao L, Yan H, Liu YN, Li QH, Zhang XZ, Hu Y, Wang JY, Lu YH, Lu CJ, Zhou W, Hallmayer J, Huang YS, Strohl KP, Pollmächer T, Mignot E.

PLoS Genet. 2013 Oct;9(10):e1003880. doi: 10.1371/journal.pgen.1003880. Epub 2013 Oct 31.

7.

Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia.

Khor SS, Miyagawa T, Toyoda H, Yamasaki M, Kawamura Y, Tanii H, Okazaki Y, Sasaki T, Lin L, Faraco J, Rico T, Honda Y, Honda M, Mignot E, Tokunaga K.

PeerJ. 2013 Apr 16;1:e66. doi: 10.7717/peerj.66. Print 2013.

8.

ImmunoChip study implicates antigen presentation to T cells in narcolepsy.

Faraco J, Lin L, Kornum BR, Kenny EE, Trynka G, Einen M, Rico TJ, Lichtner P, Dauvilliers Y, Arnulf I, Lecendreux M, Javidi S, Geisler P, Mayer G, Pizza F, Poli F, Plazzi G, Overeem S, Lammers GJ, Kemlink D, Sonka K, Nevsimalova S, Rouleau G, Desautels A, Montplaisir J, Frauscher B, Ehrmann L, Högl B, Jennum P, Bourgin P, Peraita-Adrados R, Iranzo A, Bassetti C, Chen WM, Concannon P, Thompson SD, Damotte V, Fontaine B, Breban M, Gieger C, Klopp N, Deloukas P, Wijmenga C, Hallmayer J, Onengut-Gumuscu S, Rich SS, Winkelmann J, Mignot E.

PLoS Genet. 2013;9(2):e1003270. doi: 10.1371/journal.pgen.1003270. Epub 2013 Feb 14.

9.

HLA-DQ association and allele competition in Chinese narcolepsy.

Han F, Lin L, Li J, Dong SX, An P, Zhao L, Liu NY, Li QY, Yan H, Gao ZC, Faraco J, Strohl KP, Liu X, Miyadera H, Mignot E.

Tissue Antigens. 2012 Oct;80(4):328-35. doi: 10.1111/j.1399-0039.2012.01948.x. Epub 2012 Aug 4.

PMID:
22862152
10.

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.

Winkelmann J, Lin L, Schormair B, Kornum BR, Faraco J, Plazzi G, Melberg A, Cornelio F, Urban AE, Pizza F, Poli F, Grubert F, Wieland T, Graf E, Hallmayer J, Strom TM, Mignot E.

Hum Mol Genet. 2012 May 15;21(10):2205-10. doi: 10.1093/hmg/dds035. Epub 2012 Feb 9.

11.

Narcolepsy with hypocretin/orexin deficiency, infections and autoimmunity of the brain.

Kornum BR, Faraco J, Mignot E.

Curr Opin Neurobiol. 2011 Dec;21(6):897-903. doi: 10.1016/j.conb.2011.09.003. Epub 2011 Sep 30. Review.

PMID:
21963829
12.

Narcolepsy onset is seasonal and increased following the 2009 H1N1 pandemic in China.

Han F, Lin L, Warby SC, Faraco J, Li J, Dong SX, An P, Zhao L, Wang LH, Li QY, Yan H, Gao ZC, Yuan Y, Strohl KP, Mignot E.

Ann Neurol. 2011 Sep;70(3):410-7. doi: 10.1002/ana.22587. Epub 2011 Aug 22.

PMID:
21866560
13.

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.

Winkelmann J, Czamara D, Schormair B, Knauf F, Schulte EC, Trenkwalder C, Dauvilliers Y, Polo O, Högl B, Berger K, Fuhs A, Gross N, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Xiong L, Montplaisir J, Rouleau GA, Fietze I, Vávrová J, Kemlink D, Sonka K, Nevsimalova S, Lin SC, Wszolek Z, Vilariño-Güell C, Farrer MJ, Gschliesser V, Frauscher B, Falkenstetter T, Poewe W, Allen RP, Earley CJ, Ondo WG, Le WD, Spieler D, Kaffe M, Zimprich A, Kettunen J, Perola M, Silander K, Cournu-Rebeix I, Francavilla M, Fontenille C, Fontaine B, Vodicka P, Prokisch H, Lichtner P, Peppard P, Faraco J, Mignot E, Gieger C, Illig T, Wichmann HE, Müller-Myhsok B, Meitinger T.

PLoS Genet. 2011 Jul;7(7):e1002171. doi: 10.1371/journal.pgen.1002171. Epub 2011 Jul 14. Erratum in: PLoS Genet. 2011 Aug;7(8). doi: 10.1371/annotation/393ad2d3-df4f-4770-87bc-00bfabf79362.

14.

β2 adrenergic receptor polymorphisms and nocturnal blood pressure dipping status in the Wisconsin Sleep Cohort Study.

Vardeny O, Peppard PE, Finn LA, Faraco JH, Mignot E, Hla KM.

J Am Soc Hypertens. 2011 Mar-Apr;5(2):114-22. doi: 10.1016/j.jash.2011.01.005. Erratum in: J Am Soc Hypertens. 2011 May-Jun;5(3):193.

15.

Common variants in P2RY11 are associated with narcolepsy.

Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, Winkelmann J, Plazzi G, Nevsimalova S, Hong SC, Honda Y, Honda M, Högl B, Ton TG, Montplaisir J, Bourgin P, Kemlink D, Huang YS, Warby S, Einen M, Eshragh JL, Miyagawa T, Desautels A, Ruppert E, Hesla PE, Poli F, Pizza F, Frauscher B, Jeong JH, Lee SP, Strohl KP, Longstreth WT Jr, Kvale M, Dobrovolna M, Ohayon MM, Nepom GT, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Peppard P, Young T, Jennum P, Steinman L, Tokunaga K, Kwok PY, Risch N, Hallmayer J, Mignot E.

Nat Genet. 2011 Jan;43(1):66-71. doi: 10.1038/ng.734. Epub 2010 Dec 19. Erratum in: Nat Genet. 2011 Oct;43(10):1040.

16.

Narcolepsy is strongly associated with the T-cell receptor alpha locus.

Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Honda Y, Honda M, Högl B, Longstreth WT Jr, Montplaisir J, Kemlink D, Einen M, Chen J, Musone SL, Akana M, Miyagawa T, Duan J, Desautels A, Erhardt C, Hesla PE, Poli F, Frauscher B, Jeong JH, Lee SP, Ton TG, Kvale M, Kolesar L, Dobrovolná M, Nepom GT, Salomon D, Wichmann HE, Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Young T, Peppard P, Tokunaga K, Kwok PY, Risch N, Mignot E.

Nat Genet. 2009 Jun;41(6):708-11. doi: 10.1038/ng.372. Epub 2009 May 3. Erratum in: Nat Genet. 2009 Jul;41(7):859. Hong, Sheng Seung-Chul [corrected to Hong, Seung-Chul].

17.

Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.

Miyagawa T, Kawashima M, Nishida N, Ohashi J, Kimura R, Fujimoto A, Shimada M, Morishita S, Shigeta T, Lin L, Hong SC, Faraco J, Shin YK, Jeong JH, Okazaki Y, Tsuji S, Honda M, Honda Y, Mignot E, Tokunaga K.

Nat Genet. 2008 Nov;40(11):1324-8. doi: 10.1038/ng.231. Epub 2008 Sep 28.

PMID:
18820697
18.

Kleine-Levin syndrome: a systematic study of 108 patients.

Arnulf I, Lin L, Gadoth N, File J, Lecendreux M, Franco P, Zeitzer J, Lo B, Faraco JH, Mignot E.

Ann Neurol. 2008 Apr;63(4):482-93. doi: 10.1002/ana.21333.

PMID:
18438947
19.

Characterization of sleep in zebrafish and insomnia in hypocretin receptor mutants.

Yokogawa T, Marin W, Faraco J, Pézeron G, Appelbaum L, Zhang J, Rosa F, Mourrain P, Mignot E.

PLoS Biol. 2007 Oct 16;5(10):e277.

20.

Genomic and functional conservation of sedative-hypnotic targets in the zebrafish.

Renier C, Faraco JH, Bourgin P, Motley T, Bonaventure P, Rosa F, Mignot E.

Pharmacogenet Genomics. 2007 Apr;17(4):237-53.

PMID:
17496723
21.

Regulation of hypocretin (orexin) expression in embryonic zebrafish.

Faraco JH, Appelbaum L, Marin W, Gaus SE, Mourrain P, Mignot E.

J Biol Chem. 2006 Oct 6;281(40):29753-61. Epub 2006 Jul 25.

22.

Concomitant loss of dynorphin, NARP, and orexin in narcolepsy.

Crocker A, España RA, Papadopoulou M, Saper CB, Faraco J, Sakurai T, Honda M, Mignot E, Scammell TE.

Neurology. 2005 Oct 25;65(8):1184-8. Epub 2005 Sep 14.

23.

Sequence of the canine major histocompatibility complex region containing non-classical class I genes.

Wagner JL, Palti Y, DiDario D, Faraco J.

Tissue Antigens. 2005 Jun;65(6):549-55.

PMID:
15896203
24.

First Report of Stolbur Phytoplasma in Avocado in Spain.

Laviña A, Batlle A, Faraco JG, Herrera CJL.

Plant Dis. 2002 Jun;86(6):692. doi: 10.1094/PDIS.2002.86.6.692A.

PMID:
30823247
25.

[Hypocretin (orexin) deficiency in narcolepsy-cataplexy].

Nevsímalová S, Vanková J, Sonka K, Faraco J, Rogers W, Overeem S, Mignot E.

Sb Lek. 2000;101(4):381-6. Czech.

PMID:
11702580
26.

Physical and radiation hybrid mapping of canine chromosome 12, in a region corresponding to human chromosome 6p12-q12.

Li R, Faraco JH, Lin L, Lin X, Hinton L, Rogers W, Lowe JK, Ostrander EA, Mignot E.

Genomics. 2001 May 1;73(3):299-315.

PMID:
11350122
27.

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains.

Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, Nevsimalova S, Aldrich M, Reynolds D, Albin R, Li R, Hungs M, Pedrazzoli M, Padigaru M, Kucherlapati M, Fan J, Maki R, Lammers GJ, Bouras C, Kucherlapati R, Nishino S, Mignot E.

Nat Med. 2000 Sep;6(9):991-7.

PMID:
10973318
28.

The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene.

Lin L, Faraco J, Li R, Kadotani H, Rogers W, Lin X, Qiu X, de Jong PJ, Nishino S, Mignot E.

Cell. 1999 Aug 6;98(3):365-76.

29.

Construction and characterization of an eightfold redundant dog genomic bacterial artificial chromosome library.

Li R, Mignot E, Faraco J, Kadotani H, Cantanese J, Zhao B, Lin X, Hinton L, Ostrander EA, Patterson DF, de Jong PJ.

Genomics. 1999 May 15;58(1):9-17.

PMID:
10331940
30.

Genetic studies in narcolepsy, a disorder affecting REM sleep.

Faraco J, Lin X, Li R, Hinton L, Lin L, Mignot E.

J Hered. 1999 Jan-Feb;90(1):129-32. Review.

PMID:
9987919
31.

Genetic studies in the sleep disorder narcolepsy.

Kadotani H, Faraco J, Mignot E.

Genome Res. 1998 May;8(5):427-34. Review.

32.
33.
34.

Structure, chromosomal localization, and expression pattern of the murine Magp gene.

Chen Y, Faraco J, Yin W, Germiller J, Francke U, Bonadio J.

J Biol Chem. 1993 Dec 25;268(36):27381-9.

35.

ApaI dimorphism at the human vitamin D receptor gene locus.

Faraco JH, Morrison NA, Baker A, Shine J, Frossard PM.

Nucleic Acids Res. 1989 Mar 11;17(5):2150. No abstract available.

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