Functional consequences of a CKIδ mutation causing familial advanced sleep phase syndrome von Fu, Ying-Hui, Padiath, Quasar S, Saigoh, Noriko, Xu, Ying, Saigoh, Kazumasa, Wu, Susan C, Jones, Christopher R, Shapiro, Robert E, Ptá ek, Louis J

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Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus von Padiath, Quasar Saleem, Srivastava, Achal Kumar, Roy, Sanghmitra, Jain, Satish, Brahmachari, Samir Kumar

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Glycogen Synthase Kinase 3β as a Likely Target for the Action of Lithium on Circadian Clocks von Padiath, Quasar Saleem, Paranjpe, Dhanashree, Jain, Sanjeev, Sharma, Vijay Kumar

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Chance in our strands? von Padiath, Quasar Saleem, Rao, B Jagadeeshwara

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Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study von Balestrini, S, Mikati, MA, Garcia-Roves, RA, Carboni, M, Hunanyan, AS, Kherallah, B, McLean, M, Prange, L, De Grandis, E, Gagliardi, A, Pisciotta, L, Stagnaro, M, Veneselli, E, Campistol, J, Fons, C, Pias-Peleteiro, L, Brashear, A, Miller, C, Samoes, R, Brankovic, V, Padiath, QS, Potic, A, Pilch, J, Vezyroglou, K, Bye, AME, Davis, AM, Ryan, MM, Semsarian, C, Hollingsworth, G, Scheffer, IE, Granata, T, Nardocci, N, Ragona, F, Arzimanoglou, A, Panagiotakaki, E, Carrilho, I, Zucca, C, Novy, J, Dzieżyc, K, Parowicz, M, Mazurkiewicz-Bełdzińska, M, Weckhuysen, S, Pons, R, Groppa, S, Sinden, DS, Pitt, GS, Tinker, A, Ashworth, M, Michalak, Z, Thom, M, Cross, JH, Vavassori, R, Kaski, JP, Sisodiya, SM

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