Alexandra Soto-Ortolaza: search on Z-Library

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1

RAB39B gene is not a common cause of Parkinson’s disease or dementia with Lewy bodies

Hodges, Kyndall, Brewer, Sheridan S., Labbé, Catherine, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Strongosky, Audrey J., Uitti, Ryan J., van Gerpen, Jay A., Ertekin-Taner, Nilüfer, Kantarci, Kej

Journal:

Neurobiology of Aging

Year:

2016

Language:

english

File:

PDF, 288 KB

english, 2016

2

LINGO1 rs9652490 is associated with essential tremor and Parkinson disease

Carles Vilariño-Güell, Owen A. Ross, Christian Wider, Barbara Jasinska-Myga, Stephanie A. Cobb, Alexandra I. Soto-Ortolaza, Jennifer M. Kachergus, Brett H. Keeling, Justus C. Dachsel, Heather L. Melro

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 113 KB

english, 2010

3

Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank

Bieniek, Kevin F., Ross, Owen A., Cormier, Kerry A., Walton, Ronald L., Soto-Ortolaza, Alexandra, Johnston, Amelia E., DeSaro, Pamela, Boylan, Kevin B., Graff-Radford, Neill R., Wszolek, Zbigniew K.,

Journal:

Acta Neuropathologica

Year:

2015

Language:

english

File:

PDF, 2.64 MB

english, 2015

4

MAPT haplotype diversity in multiple system atrophy

Labbé, Catherine, Heckman, Michael G., Lorenzo-Betancor, Oswaldo, Murray, Melissa E., Ogaki, Kotaro, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Fujioka, Shinsuke, Koga, Shunsuke, Uitti, Ryan J.,

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 282 KB

english, 2016

5

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies: Table 1.

Walton, Ronald L., Soto-Ortolaza, Alexandra I., Murray, Melissa E., Lorenzo-Betancor, Oswaldo, Ogaki, Kotaro, Heckman, Michael G., Rayaprolu, Sruti, Rademakers, Rosa, Ertekin-Taner, Nilüfer, Uitti, Ry

Journal:

Neurology: Genetics

Year:

2016

Language:

english

File:

PDF, 255 KB

english, 2016

6

Genetic Susceptibility Variants in Parkinsonism

Soto-Ortolaza, Alexandra I., Ross, Owen A.

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 660 KB

english, 2015

7

Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease

Bahareh Behrouz, Carles Vilariño-Güell, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Jan O. Aasly, Sigrid Sando, Timothy Lynch, David Craig, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross, Matthe

Journal:

Neuroscience Letters

Year:

2010

Language:

english

File:

PDF, 125 KB

english, 2010

8

Identification of genetic modifiers of age-at-onset for familial Parkinson’s disease

Hill-Burns, Erin M., Ross, Owen A., Wissemann, William T., Soto-Ortolaza, Alexandra I., Zareparsi, Sepideh, Siuda, Joanna, Lynch, Timothy, Wszolek, Zbigniew K., Silburn, Peter A., Mellick, George D.,

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 1.64 MB

english, 2016

9

LINGO1andLINGO2variants are associated with essential tremor and Parkinson disease

Carles Vilariño-Güell, Christian Wider, Owen A. Ross, Barbara Jasinska-Myga, Jennifer Kachergus, Stephanie A. Cobb, Alexandra I. Soto-Ortolaza, Bahareh Behrouz, Michael G. Heckman, Nancy N. Diehl, Cla

Journal:

Year:

2010

Language:

english

File:

PDF, 223 KB

english, 2010

10

Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa

Barbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, Christian Wider, Alexandra I. Soto-Ortolaza, Mounir Kefi, Lefkos T. Middleton, Lianna Ishihara-Paul, Rachel A. Gibson, Rim Amouri, Sam

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 113 KB

english, 2010

11

Genome-wide association study in essential tremor identifies three new loci

Müller, Stefanie H., Girard, Simon L., Hopfner, Franziska, Merner, Nancy D., Bourassa, Cynthia V., Lorenz, Delia, Clark, Lorraine N., Tittmann, Lukas, Soto-Ortolaza, Alexandra I., Klebe, Stephan, Hall

Journal:

Year:

2016

Language:

english

File:

PDF, 433 KB

english, 2016

12

Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremor

Brett H. Keeling, Carles Vilariño-Güell, Alexandra I. Soto-Ortolaza, Owen A. Ross, Ryan J. Uitti, Alex Rajput, Zbigniew K. Wszolek, Matthew J. Farrer

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 106 KB

english, 2010

13

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

Nicola J. Rutherford, Michael G. Heckman, Mariely DeJesus-Hernandez, Matt C. Baker, Alexandra I. Soto-Ortolaza, Sruti Rayaprolu, Heather Stewart, Elizabeth Finger, Kathryn Volkening, William W. Seeley

Journal:

Neurobiology of Aging

Year:

2012

Language:

english

File:

PDF, 344 KB

english, 2012

14

Human leukocyte antigen variation and Parkinson’s disease

Andreas Puschmann, Christophe Verbeeck, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Timothy Lynch, Barbara Jasinska-Myga, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Ryan J. Uitti, Zbi

Journal:

Parkinsonism & Related Disorders

Year:

2011

Language:

english

File:

PDF, 119 KB

english, 2011

15

Angiogenin variation and Parkinson disease

Sruti Rayaprolu, Alexandra Soto-Ortolaza, Rosa Rademakers, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross

Journal:

Annals of Neurology

Year:

2012

Language:

english

File:

PDF, 710 KB

english, 2012

16

VPS35 Mutations in Parkinson Disease

Carles Vilariño-Güell, Christian Wider, Owen A. Ross, Justus C. Dachsel, Jennifer M. Kachergus, Sarah J. Lincoln, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Greggory J. Wilhoite, Justin A. Bacon,

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 580 KB

english, 2011

17

Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration

Sanchez-Contreras, Monica, Heckman, Michael G., Tacik, Pawel, Diehl, Nancy, Brown, Patricia H., Soto-Ortolaza, Alexandra I., Christopher, Elizabeth A., Walton, Ronald L., Ross, Owen A., Golbe, Lawrenc

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 653 KB

english, 2016

18

LRRK2 variation and Parkinson's disease in African Americans

Owen A. Ross, Greggory J. Wilhoite, Justin A. Bacon, Alexandra Soto-Ortolaza, Jennifer Kachergus, Stephanie A. Cobb, Andreas Puschmann, Carles Vilariño-Güell, Matthew J. Farrer, Neill Graff-Radford, J

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 639 KB

english, 2010

19

Heterodimerization of Lrrk1–Lrrk2: Implications for LRRK2-associated Parkinson disease

Justus C. Dachsel, Kenya Nishioka, Carles Vilariño-Güell, Sarah J. Lincoln, Alexandra I. Soto-Ortolaza, Jennifer Kachergus, Kelly M. Hinkle, Michael G. Heckman, Barbara Jasinska-Myga, Julie P. Taylor,

Journal:

Mechanisms of Ageing and Development

Year:

2010

Language:

english

File:

PDF, 384 KB

english, 2010

20

Association of α-, β-, and γ-Synuclein With Diffuse Lewy Body Disease

Nishioka, Kenya, Wider, Christian, Vilariño-Güell, Carles, Soto-Ortolaza, Alexandra I., Lincoln, Sarah J., Kachergus, Jennifer M., Jasinska-Myga, Barbara, Ross, Owen A., Rajput, Alex, Robinson, Christ

Journal:

Archives of Neurology

Year:

2010

Language:

english

File:

PDF, 266 KB

english, 2010

21

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

Kouri, Naomi, Ross, Owen A., Dombroski, Beth, Younkin, Curtis S., Serie, Daniel J., Soto-Ortolaza, Alexandra, Baker, Matthew, Finch, Ni Cole A., Yoon, Hyejin, Kim, Jungsu, Fujioka, Shinsuke, McLean, C

Journal:

Nature Communications

Year:

2015

Language:

english

File:

PDF, 712 KB

english, 2015

22

Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome

DeJesus-Hernandez, Mariely, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I., Rutherford, Nicola J., Heckman, Michael G., Traynor, Sharleen, Strongosky, Audrey, Graff-Radford, Neill, Van Gerpen, Jay, Uit

Journal:

Parkinsonism & Related Disorders

Year:

2013

Language:

english

File:

PDF, 156 KB

english, 2013

23

SLC1A2 rs3794087 does not associate with essential tremor

Ross, Jay P., Rayaprolu, Sruti, Bernales, Cecily Q., Soto-Ortolaza, Alexandra I., van Gerpen, Jay, Uitti, Ryan J., Wszolek, Zbigniew K., Rajput, Alex, Rajput, Ali H., Rajput, Michele L., Ross, Owen A.

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 143 KB

english, 2014

24

Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease

Shannon, Barbara, Soto-Ortolaza, Alexandra, Rayaprolu, Sruti, Cannon, Heather D., Labbé, Catherine, Benitez, Bruno A., Choi, Jiyoon, Lynch, Timothy, Boczarska-Jedynak, Magdalena, Opala, Grzegorz, Kryg

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 167 KB

english, 2014

25

VPS35 Mutations in Parkinson Disease

Carles Vilariño-Güell, Christian Wider, Owen A. Ross, Justus C. Dachsel, Jennifer M. Kachergus, Sarah J. Lincoln, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Greggory J. Wilhoite, Justin A. Bacon,

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 29 KB

english, 2011

26

Investigating FUS variation in Parkinson's disease

Labbé, Catherine, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra, Ogaki, Kotaro, Uitti, Ryan J., Wszolek, Zbigniew K., Ross, Owen A.

Journal:

Parkinsonism & Related Disorders

Year:

2014

Language:

english

File:

PDF, 414 KB

english, 2014

27

MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies

Labbé, Catherine, Heckman, Michael G., Lorenzo-Betancor, Oswaldo, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Murray, Melissa E., Allen, Mariet, Uitti, Ryan J., Wszolek, Zbigniew K., Smith, Glenn

Journal:

Alzheimer's & Dementia

Year:

2016

Language:

english

File:

PDF, 469 KB

english, 2016

28

Investigating the role of FUS exonic variants in Essential Tremor

Labbé, Catherine, Soto-Ortolaza, Alexandra I., Rayaprolu, Sruti, Harriott, Andrea M., Strongosky, Audrey J., Uitti, Ryan J., Van Gerpen, Jay A., Wszolek, Zbigniew K., Ross, Owen A.

Journal:

Parkinsonism & Related Disorders

Year:

2013

Language:

english

File:

PDF, 179 KB

english, 2013

29

Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium

Heckman, Michael G., Soto-Ortolaza, Alexandra I., Aasly, Jan O., Abahuni, Nadine, Annesi, Grazia, Bacon, Justin A., Bardien, Soraya, Bozi, Maria, Brice, Alexis, Brighina, Laura, Carr, Jonathan, Charti

Journal:

Movement Disorders

Year:

2013

Language:

english

File:

PDF, 231 KB

english, 2013

30

Evaluation of the Role of SNCA Variants in Survival without Neurological Disease

Heckman, Michael G., Soto-Ortolaza, Alexandra I., Diehl, Nancy N., Carrasquillo, Minerva M., Uitti, Ryan J., Wszolek, Zbigniew K., Graff-Radford, Neill R., Ross, Owen A., Toft, Mathias

Journal:

Year:

2012

Language:

english

File:

PDF, 344 KB

english, 2012

31

VPS35 and DNAJC13 disease-causing variants in essential tremor

Rajput, Alex, Ross, Jay P, Bernales, Cecily Q, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Ross, Owen A, van Gerpen, Jay, Uitti, Ryan J, Wszolek, Zbigniew K, Rajput, Ali H, Vilariño-Güell, Carles

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 127 KB

english, 2015

32

Analysis ofCOQ2gene in multiple system atrophy

Ogaki, Kotaro, Fujioka, Shinsuke, Heckman, Michael G, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Labbé, Catherine, Walton, Ronald L, Lorenzo-Betancor, Oswaldo, Wang, Xue, Asmann, Yan, Rademakers, R

Journal:

Molecular Neurodegeneration

Year:

2014

Language:

english

File:

PDF, 2.33 MB

english, 2014

33

Genetic variants of α-synuclein are not associated with essential tremor

Owen A. Ross, Karen N. Conneely, Tao Wang, Carles Vilarino-Guell, Alexandra I. Soto-Ortolaza, Alex Rajput, Zbigniew K. Wszolek, Ryan J. Uitti, Elan D. Louis, Lorraine N. Clark, Matthew J. Farrer, Clau

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 264 KB

english, 2011

34

The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants

Heckman, Michael G., Elbaz, Alexis, Soto-Ortolaza, Alexandra I., Serie, Daniel J., Aasly, Jan O., Annesi, Grazia, Auburger, Georg, Bacon, Justin A., Boczarska-Jedynak, Magdalena, Bozi, Maria, Brighina

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 754 KB

english, 2014

35

Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population

Alex Rajput, Carles Vilariño-Güell, Michele L. Rajput, Owen A. Ross, Alexandra I. Soto-Ortolaza, Sarah J. Lincoln, Stephanie A. Cobb, Michael G. Heckman, Matthew J. Farrer, Ali Rajput

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 369 KB

english, 2009

36

Neuropathologically defined subtypes of Alzheimer’s disease differ significantly from neurofibrillary tangle-predominant dementia

Nicholas J. Janocko, Kevin A. Brodersen, Alexandra I. Soto-Ortolaza, Owen A. Ross, Amanda M. Liesinger, Ranjan Duara, Neill R. Graff-Radford, Dennis W. Dickson, Melissa E. Murray

Journal:

Acta Neuropathologica

Year:

2012

Language:

english

File:

PDF, 2.22 MB

english, 2012

37

TARDBP mutations in Parkinson's disease

Rayaprolu, Sruti, Fujioka, Shinsuke, Traynor, Sharleen, Soto-Ortolaza, Alexandra I., Petrucelli, Leonard, Dickson, Dennis W., Rademakers, Rosa, Boylan, Kevin B., Graff-Radford, Neill R., Uitti, Ryan J

Journal:

Parkinsonism & Related Disorders

Year:

2013

Language:

english

File:

PDF, 147 KB

english, 2013

38

Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease

Hoffman-Zacharska, Dorota, Koziorowski, Dariusz, Ross, Owen A., Milewski, Michał, Poznański, Jarosław, Jurek, Marta, Wszolek, Zbigniew K., Soto-Ortolaza, Alexandra, Sławek, Jarosław, Janik, Piotr, Jam

Journal:

Parkinsonism & Related Disorders

Year:

2013

Language:

english

File:

PDF, 468 KB

english, 2013

39

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Rademakers, Rosa, Baker, Matt, Nicholson, Alexandra M, Rutherford, Nicola J, Finch, NiCole, Soto-Ortolaza, Alexandra, Lash, Jennifer, Wider, Christian, Wojtas, Aleksandra, DeJesus-Hernandez, Mariely,

Journal:

Nature Genetics

Year:

2011

Language:

english

File:

PDF, 1020 KB

english, 2011

40

Analysis of Nuclear Export Sequence Regions of FUS-Related RNA-Binding Proteins in Essential Tremor

Lorenzo-Betancor, Oswaldo, Ogaki, Kotaro, Soto-Ortolaza, Alexandra, Labbé, Catherine, Vilariño-Güell, Carles, Rajput, Alex, Rajput, Ali H., Pastor, Pau, Ortega, Sara, Lorenzo, Elena, Strongosky, Audre

Journal:

Year:

2014

Language:

english

File:

PDF, 658 KB

english, 2014

41

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

Alexis Elbaz, Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto-Ortolaza, Frédéric Moisan, Jan Aasly, Grazia Annesi, Maria Bozi, Laura Brighina, Marie-Christine Chartier-Harlin, Alain Destée, Carl

Journal:

Annals of Neurology

Year:

2011

Language:

english

File:

PDF, 639 KB

english, 2011

42

LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation

Oswaldo Lorenzo-Betancor, Lluís Samaranch, Mario Ezquerra, Eduardo Tolosa, Elena Lorenzo, Jaione Irigoyen, Carles Gaig, María A. Pastor, Alexandra I. Soto-Ortolaza, Owen A. Ross, María C. Rodríguez-Or

Journal:

Movement Disorders

Year:

2012

Language:

english

File:

PDF, 1006 KB

english, 2012

43

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Owen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, Jan O Aasly, Nadine Abahuni, Grazia Annesi, Justin A Bacon, Soraya Bardien, Maria Bozi, Alexis Brice, Laura Brighina, Christine Van Broeckhov

Journal:

The Lancet Neurology

Year:

2011

Language:

english

File:

PDF, 271 KB

english, 2011

44

LRRK2 variation and dementia with Lewy bodies

Heckman, Michael G., Soto-Ortolaza, Alexandra I., Sanchez Contreras, Monica Y., Murray, Melissa E., Pedraza, Otto, Diehl, Nancy N., Walton, Ronald, Labbé, Catherine, Lorenzo-Betancor, Oswaldo, Uitti,

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 299 KB

english, 2016

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