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Soto-Ortolaza, A. I.
96  results:
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1

MAPTH1 haplotype is a risk factor for essential tremor and ..:

Vilariño-Güell, C. ; Soto-Ortolaza, A.I. ; Rajput, A....
Neurology.  76 (2011)  7 - p. 670-672 , 2011
Link: https://doi.org/10.1212/..
 
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2

Ataxin-2 repeat-length variation and neurodegeneration:

Ross, O. A. ; Rutherford, N. J. ; Baker, M....
Human Molecular Genetics.  20 (2011)  16 - p. 3207-3212 , 2011
Link: https://doi.org/10.1093/..
 
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3

Characterization ofDCTN1genetic variability in neurodegener..:

Vilariño-Güell, C. ; Wider, C. ; Soto-Ortolaza, A. I....
Neurology.  72 (2009)  23 - p. 2024-2028 , 2009
Link: https://doi.org/10.1212/..
 
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4

Genome-wide association study in essential tremor identifie..:

Müller, Stefanie H. ; Girard, Simon L. ; Hopfner, Franziska...
Brain.  139 (2016)  12 - p. 3163-3169 , 2016
Link: https://doi.org/10.1093/..
 
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5

LRRK2 variation and dementia with Lewy bodies:

Heckman, Michael G. ; Soto-Ortolaza, Alexandra I. ; Sanchez Contreras, Monica Y....
Parkinsonism & Related Disorders.  31 (2016)  - p. 98-103 , 2016
Link: https://doi.org/10.1016/..
 
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6

Genetic susceptibility variants in parkinsonism:

Soto-Ortolaza, Alexandra I. ; Ross, Owen A.
Parkinsonism & Related Disorders.  22 (2016)  - p. S7-S11 , 2016
Link: https://doi.org/10.1016/..
 
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7

MAPT haplotype diversity in multiple system atrophy:

Labbé, Catherine ; Heckman, Michael G. ; Lorenzo-Betancor, Oswaldo...
Parkinsonism & Related Disorders.  30 (2016)  - p. 40-45 , 2016
Link: https://doi.org/10.1016/..
 
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8

RAB39B gene mutations are not a common cause of Parkinson's..:

Hodges, Kyndall ; Brewer, Sheridan S. ; Labbé, Catherine...
Neurobiology of Aging.  45 (2016)  - p. 107-108 , 2016
Link: https://doi.org/10.1016/..
 
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9

Identification of genetic modifiers of age-at-onset for fam..:

Hill-Burns, Erin M. ; Ross, Owen A. ; Wissemann, William T....
Human Molecular Genetics.  25 (2016)  17 - p. 3849-3862 , 2016
Link: https://doi.org/10.1093/..
 
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10

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's D..:

Labbé, Catherine ; Ogaki, Kotaro ; Lorenzo-Betancor, Oswaldo...
PLOS ONE.  10 (2015)  6 - p. e0128586 , 2015
Link: https://doi.org/10.1371/..
 
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11

Role for the microtubule-associated protein tau variant p.A..:

Labbé, Catherine ; Ogaki, Kotaro ; Lorenzo-Betancor, Oswaldo...
Neurology.  85 (2015)  19 - p. 1680-1686 , 2015
Link: https://doi.org/10.1212/..
 
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12

Mitochondrial targeting sequence variants of theCHCHD2gene ..:

Ogaki, Kotaro ; Koga, Shunsuke ; Heckman, Michael G....
Neurology.  85 (2015)  23 - p. 2016-2025 , 2015
Link: https://doi.org/10.1212/..
 
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13

LRRK2exonic variants and risk of multiple system atrophy:

Heckman, Michael G. ; Schottlaender, Lucia ; Soto-Ortolaza, Alexandra I....
Neurology.  83 (2014)  24 - p. 2256-2261 , 2014
Link: https://doi.org/10.1212/..
 
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14

The protective effect of LRRK2 p.R1398H on risk of Parkinso..:

Heckman, Michael G. ; Elbaz, Alexis ; Soto-Ortolaza, Alexandra I....
Neurobiology of Aging.  35 (2014)  1 - p. 266.e5-266.e14 , 2014
Link: https://doi.org/10.1016/..
 
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15

Analysis of COQ2gene in multiple system atrophy:

Ogaki, Kotaro ; Fujioka, Shinsuke ; Heckman, Michael G...
Molecular Neurodegeneration.  9 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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