Copy number variation in Parkinson's disease

by Toft, Mathias, Ross, Owen A
Published 2010

Association Studies of Sporadic Parkinson’s Disease in the Genomic Era

by Labbé, Catherine, Ross, Owen A
Published 2014

Mitochondrial J haplogroup is associated with lower blood pressure and anti-oxidant status: findings in octo/nonagenarians from the BELFAST Study

by Rea, Irene Maeve, McNerlan, Susan E., Archbold, G. Pooler, Middleton, Derek, Curran, Martin D., Young, Ian S., Ross, Owen A.
Published 2012

Association of the APOE, MTHFR and ACE Genes Polymorphisms and Stroke in Zambian Patients

by Atadzhanov, Masharip, Mwaba, Mwila H., Mukomena, Patrice N., Lakhi, Shabir, Rayaprolu, Sruti, Ross, Owen A., Meschia, James F.
Published 2013

Alpha-synuclein and tau: teammates in neurodegeneration?

by Moussaud, Simon, Jones, Daryl R, Moussaud-Lamodière, Elisabeth L, Delenclos, Marion, Ross, Owen A, McLean, Pamela J
Published 2014

Frequency of APOE, MTHFR and ACE polymorphisms in the Zambian population

by Atadzhanov, Masharip, Mwaba, Mwila H, Mukomena, Patrice N, Lakhi, Shabir, Mwaba, Peter, Rayaprolu, Sruti, Meschia, James F, Ross, Owen A
Published 2014

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

by 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.
Published 2012

Killer Immunoglobulin-like Receptors (KIR) haplogroups A and B track with Natural Killer Cells and Cytokine Profile in Aged Subjects: Observations from Octo/Nonagenarians in the Be...

by Rea, Irene Maeve, Maxwell, Lynn D, McNerlan, Susan E, Alexander, H Denis, Curran, Martin D, Middleton, Derek, Ross, Owen A
Published 2013

Polymorphic genes of detoxification and mitochondrial enzymes and risk for progressive supranuclear palsy: a case control study

by Potts, Lisa F, Cambon, Alex C, Ross, Owen A, Rademakers, Rosa, Dickson, Dennis W, Uitti, Ryan J, Wszolek, Zbigniew K, Rai, Shesh N, Farrer, Matthew J, Hein, David W, Litvan, Irene
Published 2012

A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor tics

by Blackburn, Patrick R., Zimmermann, Michael T., Gass, Jennifer M., Harris, Kimberly G., Cousin, Margot A., Boczek, Nicole J., Ross, Owen A., Klee, Eric W., Brazis, Paul W., Van Gerpen, Jay A., Atwal, Paldeep S.
Published 2016

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

by 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, Audrey J., van Gerpen, Jay A., Uitti, Ryan J., Wszolek, Zbigniew K., Ross, Owen A.
Published 2014

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

by Guerreiro, Rita, Ross, Owen A., Kun-Rodrigues, Celia, Hernandez, Dena, Orme, Tatiana, Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Ansorge, Olaf, Clarimon, Jordi, Barber, Imelda S., Braae, Anne, Brown, Kristelle, Morgan, Kevin
Published 2018

NOTCH3 Variants and Risk of Ischemic Stroke

by Ross, Owen A., Soto-Ortolaza, Alexandra I., Heckman, Michael G., Verbeeck, Christophe, Serie, Daniel J., Rayaprolu, Sruti, Rich, Stephen S., Nalls, Michael A., Singleton, Andrew, Guerreiro, Rita, Kinsella, Emma, Wszolek, Zbigniew K., Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Meschia, James F.
Published 2013

ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer’s disease

by Medway, Christopher W, Abdul-Hay, Samer, Mims, Tynickwa, Ma, Li, Bisceglio, Gina, Zou, Fanggeng, Pankratz, Shane, Sando, Sigrid B, Aasly, Jan O, Barcikowska, Maria, Siuda, Joanna, Wszolek, Zbigniew K, Ross, Owen A, Carrasquillo, Minerva, Dickson, Dennis W, Graff-Radford, Neill, Petersen, Ronald C, Ertekin-Taner, Nilüfer, Morgan, Kevin, Bu, Guojun, Younkin, Steven G
Published 2014

Clinicopathologic and 11C-Pittsburgh compound B implications of Thal amyloid phase across the Alzheimer’s disease spectrum

by Murray, Melissa E., Lowe, Val J., Graff-Radford, Neill R., Liesinger, Amanda M., Cannon, Ashley, Przybelski, Scott A., Rawal, Bhupendra, Parisi, Joseph E., Petersen, Ronald C., Kantarci, Kejal, Ross, Owen A., Duara, Ranjan, Knopman, David S., Jack, Clifford R., Dickson, Dennis W.
Published 2015

Frontotemporal dementia-associated N279K tau mutant disrupts subcellular vesicle trafficking and induces cellular stress in iPSC-derived neural stem cells

by Wren, Melissa C., Zhao, Jing, Liu, Chia-Chen, Murray, Melissa E., Atagi, Yuka, Davis, Mary D., Fu, Yuan, Okano, Hirotaka J., Ogaki, Kotaro, Strongosky, Audrey J., Tacik, Pawel, Rademakers, Rosa, Ross, Owen A., Dickson, Dennis W., Wszolek, Zbigniew K., Kanekiyo, Takahisa, Bu, Guojun
Published 2015

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson’s Disease Locus

by Labbé, Catherine, Ogaki, Kotaro, Lorenzo-Betancor, Oswaldo, Carrasquillo, Minerva M., Heckman, Michael G., McCarthy, Allan, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Lynch, Timothy, Siuda, Joanna, Opala, Grzegorz, Krygowska-Wajs, Anna, Barcikowska, Maria, Czyzewski, Krzysztof, Dickson, Dennis W., Uitti, Ryan J., Wszolek, Zbigniew K., Ross, Owen A.
Published 2015

Analysis of COQ2 gene in multiple system atrophy

by 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, Rosa, Graff-Radford, Neill, Uitti, Ryan, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A
Published 2014

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

by 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, Ryan J., van Gerpen, Jay A., Wszolek, Zbigniew K., Smith, Glenn E., Kantarci, Kejal, Lowe, Val J., Parisi, Joseph E., Jones, David T., Savica, Rodolfo, Graff-Radford, Jonathan, Knopman, David S., Petersen, Ronald C., Graff-Radford, Neill R., Ferman, Tanis J., Dickson, Dennis W., Boeve, Bradley F., Ross, Owen A., Labbé, Catherine
Published 2016

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

by Rademakers, Rosa, Baker, Matt, Nicholson, Alexandra M., Rutherford, Nicola J., Finch, NiCole, Soto-Ortolaza, Alexandra, Lash, Jennifer, Wider, Christian, Wojtas, Aleksandra, DeJesus-Hernandez, Mariely, Adamson, Jennifer, Kouri, Naomi, Sundal, Christina, Shuster, Elizabeth A., Aasly, Jan, MacKenzie, James, Roeber, Sigrun, Kretzschmar, Hans A., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Cairns, Nigel J., Ghetti, Bernardino, Spina, Salvatore, Garbern, James, Tselis, Alexandros C., Uitti, Ryan, Das, Pritam, Van Gerpen, Jay A., Meschia, James F., Levy, Shawn, Broderick, Daniel F., Graff-Radford, Neill, Ross, Owen A., Miller, Bradley B., Swerdlow, Russell H., Dickson, Dennis W., Wszolek, Zbigniew K.
Published 2011