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Page 1
Kleine-Levin syndrome is associated with LMOD3 variants.
Al Shareef SM, Basit S, Li S, Pfister C, Pradervand S, Lecendreux M, Mayer G, Dauvilliers Y, Salpietro V, Houlden H, BaHammam AS, Tafti M. Al Shareef SM, et al. Among authors: pradervand s. J Sleep Res. 2019 Jun;28(3):e12718. doi: 10.1111/jsr.12718. Epub 2018 Jun 19. J Sleep Res. 2019. PMID: 29923248
DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe.
Tafti M, Hor H, Dauvilliers Y, Lammers GJ, Overeem S, Mayer G, Javidi S, Iranzo A, Santamaria J, Peraita-Adrados R, Vicario JL, Arnulf I, Plazzi G, Bayard S, Poli F, Pizza F, Geisler P, Wierzbicka A, Bassetti CL, Mathis J, Lecendreux M, Donjacour CE, van der Heide A, Heinzer R, Haba-Rubio J, Feketeova E, Högl B, Frauscher B, Benetó A, Khatami R, Cañellas F, Pfister C, Scholz S, Billiard M, Baumann CR, Ercilla G, Verduijn W, Claas FH, Dubois V, Nowak J, Eberhard HP, Pradervand S, Hor CN, Testi M, Tiercy JM, Kutalik Z. Tafti M, et al. Among authors: pradervand s. Sleep. 2014 Jan 1;37(1):19-25. doi: 10.5665/sleep.3300. Sleep. 2014. PMID: 24381371 Free PMC article.
Rare missense mutations in P2RY11 in narcolepsy with cataplexy.
Degn M, Dauvilliers Y, Dreisig K, Lopez R, Pfister C, Pradervand S, Rahbek Kornum B, Tafti M. Degn M, et al. Among authors: pradervand s. Brain. 2017 Jun 1;140(6):1657-1668. doi: 10.1093/brain/awx093. Brain. 2017. PMID: 28460015
Homer1a is a core brain molecular correlate of sleep loss.
Maret S, Dorsaz S, Gurcel L, Pradervand S, Petit B, Pfister C, Hagenbuchle O, O'Hara BF, Franken P, Tafti M. Maret S, et al. Among authors: pradervand s. Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):20090-5. doi: 10.1073/pnas.0710131104. Epub 2007 Dec 6. Proc Natl Acad Sci U S A. 2007. PMID: 18077435 Free PMC article.
Elevated Tribbles homolog 2-specific antibody levels in narcolepsy patients.
Cvetkovic-Lopes V, Bayer L, Dorsaz S, Maret S, Pradervand S, Dauvilliers Y, Lecendreux M, Lammers GJ, Donjacour CE, Du Pasquier RA, Pfister C, Petit B, Hor H, Mühlethaler M, Tafti M. Cvetkovic-Lopes V, et al. Among authors: pradervand s. J Clin Invest. 2010 Mar;120(3):713-9. doi: 10.1172/JCI41366. Epub 2010 Feb 15. J Clin Invest. 2010. PMID: 20160349 Free PMC article.
KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis.
Gueneau L, Fish RJ, Shamseldin HE, Voisin N, Tran Mau-Them F, Preiksaitiene E, Monroe GR, Lai A, Putoux A, Allias F, Ambusaidi Q, Ambrozaityte L, Cimbalistienė L, Delafontaine J, Guex N, Hashem M, Kurdi W, Jamuar SS, Ying LJ, Bonnard C, Pippucci T, Pradervand S, Roechert B, van Hasselt PM, Wiederkehr M, Wright CF; DDD Study; Xenarios I, van Haaften G, Shaw-Smith C, Schindewolf EM, Neerman-Arbez M, Sanlaville D, Lesca G, Guibaud L, Reversade B, Chelly J, Kučinskas V, Alkuraya FS, Reymond A. Gueneau L, et al. Among authors: pradervand s. Am J Hum Genet. 2018 Jan 4;102(1):116-132. doi: 10.1016/j.ajhg.2017.12.002. Epub 2017 Dec 28. Am J Hum Genet. 2018. PMID: 29290337 Free PMC article.
97 results