Follow
pulst sm
pulst sm
Unknown affiliation
Verified email at hsc.utah.edu
Title
Cited by
Cited by
Year
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2
GA Rouleau, P Merel, M Lutchman, M Sanson, J Zucman, C Marineau, ...
Nature 363 (6429), 515-521, 1993
16561993
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
SM Pulst, A Nechiporuk, T Nechiporuk, S Gispert, XN Chen, ...
Nature genetics 14 (3), 269-276, 1996
13001996
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
9872015
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
T Matsuura, T Yamagata, DL Burgess, A Rasmussen, RP Grewal, ...
Nature genetics 26 (2), 191-194, 2000
6192000
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice
LA Becker, B Huang, G Bieri, R Ma, DA Knowles, P Jafar-Nejad, ...
Nature 544 (7650), 367-371, 2017
5152017
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region
K Kamino, HT Orr, H Payami, EM Wijsman, ME Alonso, SM Pulst, ...
American journal of human genetics 51 (5), 998, 1992
3781992
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human
DP Huynh, K Figueroa, N Hoang, SM Pulst
Nature genetics 26 (1), 44-50, 2000
3702000
The neuroimaging and clinical spectrum of neurofibromatosis 2
VF Mautner, M Lindenau, ME Baser, W Hazim, M Tatagiba, W Haase, ...
Neurosurgery 38 (5), 880-886, 1996
3511996
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype
JR Korenberg, H Kawashima, SM Pulst, T Ikeuchi, N Ogasawara, ...
American journal of human genetics 47 (2), 236, 1990
3451990
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes
MF Waters, NA Minassian, G Stevanin, KP Figueroa, JPA Bannister, ...
Nature genetics 38 (4), 447-451, 2006
3412006
Antisense oligonucleotide therapy for spinocerebellar ataxia type 2
DR Scoles, P Meera, MD Schneider, S Paul, W Dansithong, KP Figueroa, ...
Nature 544 (7650), 362-366, 2017
3122017
Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2
J Liu, TS Tang, H Tu, O Nelson, E Herndon, DP Huynh, SM Pulst, ...
Journal of Neuroscience 29 (29), 9148-9162, 2009
3112009
The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
DH Geschwind, S Perlman, CP Figueroa, LJ Treiman, SM Pulst
American journal of human genetics 60 (4), 842, 1997
3001997
A novel protein with RNA-binding motifs interacts with ataxin-2
H Shibata, DP Huynh, SM Pulst
Human molecular genetics 9 (9), 1303-1313, 2000
2782000
The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI
DP Huynh, DR Scoles, D Nguyen, SM Pulst
Human molecular genetics 12 (20), 2587-2597, 2003
2732003
Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1
RM Costa, T Yang, DP Huynh, SM Pulst, DH Viskochil, AJ Silva, ...
Nature genetics 27 (4), 399-405, 2001
2342001
Spinal tumors in patients with neurofibromatosis type 2: MR imaging study of frequency, multiplicity, and variety.
VF Mautner, M Tatagiba, M Lindenau, C Fünsterer, SM Pulst, ME Baser, ...
AJR. American journal of roentgenology 165 (4), 951-955, 1995
2341995
Expression of ataxin‐2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2
DP Huynh, MR Del Bigio, DH Ho, SM Pulst
Annals of Neurology: Official Journal of the American Neurological …, 1999
2321999
Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease
TT Nguyen, SS Oh, D Weaver, A Lewandowska, D Maxfield, MH Schuler, ...
Proceedings of the National Academy of Sciences 111 (35), E3631-E3640, 2014
2232014
The system can't perform the operation now. Try again later.
Articles 1–20