|
Figueroa, Karla P; Gan, Shi-Rui; Perlman, Susan et al. (2018) C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias. Mov Disord 33:497-498
|
|
Scoles, Daniel R; Pulst, Stefan M (2018) Spinocerebellar Ataxia Type 2. Adv Exp Med Biol 1049:175-195
|
|
Scoles, Daniel R; Meera, Pratap; Schneider, Matthew D et al. (2017) Antisense oligonucleotide therapy for spinocerebellar ataxia type 2. Nature 544:362-366
|
|
Meera, Pratap; Pulst, Stefan; Otis, Thomas (2017) A positive feedback loop linking enhanced mGluR function and basal calcium in spinocerebellar ataxia type 2. Elife 6:
|
|
Pflieger, Lance T; Dansithong, Warunee; Paul, Sharan et al. (2017) Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2. Hum Mol Genet 26:3069-3080
|
|
Graf, Julia; Hellenbroich, Yorck; Veelken, Norbert et al. (2016) Two different genetic diseases in the same patient: Coincident, concomitant, or causally related? Mov Disord 31:491-2
|
|
Scoles, Daniel R; Ho, Mi H T; Dansithong, Warunee et al. (2015) Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat. PLoS One 10:e0128769
|
|
Dansithong, Warunee; Paul, Sharan; Figueroa, Karla P et al. (2015) Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model. PLoS Genet 11:e1005182
|
|
Matilla-Dueñas, A; Ashizawa, T; Brice, A et al. (2014) Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias. Cerebellum 13:269-302
|
|
Neuenschwander, Annalese G; Thai, Khanh K; Figueroa, Karla P et al. (2014) Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysis. JAMA Neurol 71:1529-34
|
Showing the most recent 10 out of 43 publications
