The Birth of the Modern Era of Parkinson’s Disease Genetics

Por Singleton, Andrew B., Hardy, John A., Gasser, Thomas
Publicado no J Parkinsons Dis (2017)

Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21

Por Matarin, Mar, Brown, W. Mark, Singleton, Andrew, Hardy, John A., Meschia, James F.
Publicado em 2008

Genotype-Imputation Accuracy across Worldwide Human Populations

Por Huang, Lucy, Li, Yun, Singleton, Andrew B., Hardy, John A., Abecasis, Gonçalo, Rosenberg, Noah A., Scheet, Paul
Publicado em 2009

Genome Wide Assessment of Young Onset Parkinson’s Disease from Finland

Por Hernandez, Dena G., Nalls, Michael A., Ylikotila, Pauli, Keller, Margaux, Hardy, John A., Majamaa, Kari, Singleton, Andrew B.
Publicado em 2012

A blood-based gene expression and signaling pathway analysis to differentiate between high and low grade gliomas

Por Ponnampalam, Stephen N., Kamaluddin, Nor Rizan, Zakaria, Zubaidah, Matheneswaran, Vickneswaran, Ganesan, Dharmendra, Haspani, Mohammed Saffari, Ryten, Mina, Hardy, John A.
Publicado no Oncol Rep (2017)

Comparing Spatial Maps of Human Population-Genetic Variation Using Procrustes Analysis

Por Wang, Chaolong, Szpiech, Zachary A., Degnan, James H., Jakobsson, Mattias, Pemberton, Trevor J., Hardy, John A., Singleton, Andrew B., Rosenberg, Noah A.
Publicado em 2010

Identification of Stk25 as a Genetic Modifier of Tau Phosphorylation in Dab1-Mutant Mice

Por Matsuki, Tohru, Zaka, Mariam, Guerreiro, Rita, van der Brug, Marcel P., Cooper, Jonathan A., Cookson, Mark R., Hardy, John A., Howell, Brian W.
Publicado em 2012

Reelin and Stk25 Have Opposing Roles in Neuronal Polarization and Dendritic Golgi Deployment

Por Matsuki, Tohru, Matthews, Russell T., Cooper, Jonathan A., van der Brug, Marcel P., Cookson, Mark R., Hardy, John A., Olson, Eric C., Howell, Brian W.
Publicado em 2010

Association of integrin α2 gene variants with ischemic stroke

Por Matarin, Mar, Brown, W Mark, Hardy, John A, Rich, Stephen S, Singleton, Andrew B, Brown, Robert D, Brott, Thomas G, Worrall, Bradford B, Meschia, James F
Publicado em 2007

Locus Homogeneity Between Syndactyly Type 1A and Craniosynostosis Philadelphia Type?

Por Jain, Mahim, Wallis, Deeann, Robin, Nathaniel H., De Vrieze, Fabienne Wavrant, Hardy, John A., Ghadami, Mohsen, Bosse, Kristin, Betz, Regina C., Nöthen, Markus M., Arcos-Burgos, Mauricio, Muenke, Maximilian
Publicado em 2008

First effects of rising amyloid-β in transgenic mouse brain: synaptic transmission and gene expression

Por Cummings, Damian M., Liu, Wenfei, Portelius, Erik, Bayram, Sevinç, Yasvoina, Marina, Ho, Sui-Hin, Smits, Hélène, Ali, Shabinah S., Steinberg, Rivka, Pegasiou, Chrysia-Maria, James, Owain T., Matarin, Mar, Richardson, Jill C., Zetterberg, Henrik, Blennow, Kaj, Hardy, John A., Salih, Dervis A., Edwards, Frances A.
Publicado no Brain (2015)

Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies

Por Geiger, Joshua T., Ding, Jinhui, Crain, Barbara, Pletnikova, Olga, Letson, Christopher, Dawson, Ted M., Rosenthal, Liana S., Pantelyat, Alexander, Gibbs, J. Raphael, Albert, Marilyn S., Hernandez, Dena G., Hillis, Argye E., Stone, David J., Singleton, Andrew B., Hardy, John A., Troncoso, Juan C., Scholz, Sonja W.
Publicado no Neurobiol Dis (2016)

Candidate Gene Polymorphisms for Ischemic Stroke

Por Matarin, Mar, Brown, W. Mark, Dena, Hernandez, Britton, Angela, De Vrieze, Fabienne Wavrant, Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Case, L. Douglas, Chanock, Stephen J., Metter, E. Jeffrey, Ferruci, Luigi, Gamble, Dale, Hardy, John A., Rich, Stephen S., Singleton, Andrew, Meschia, James F.
Publicado em 2009

Structural genomic variation in ischemic stroke

Por Matarin, Mar, Simon-Sanchez, Javier, Fung, Hon-Chung, Scholz, Sonja, Gibbs, J. Raphael, Hernandez, Dena G., Crews, Cynthia, Britton, Angela, Wavrant De Vrieze, Fabienne, Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Silliman, Scott, Case, L. Douglas, Hardy, John A., Rich, Stephen S., Meschia, James F., Singleton, Andrew B.
Publicado em 2008

CR1 is associated with amyloid plaque burden and age-related cognitive decline

Por Chibnik, Lori B., Shulman, Joshua M., Leurgans, Sue E., Schneider, Julie A., Wilson, Robert S., Tran, Dong, Aubin, Cristin, Buchman, Aron S., Heward, Christopher B., Myers, Amanda J., Hardy, John A., Huentelman, Matthew J., Corneveaux, Jason J., Reiman, Eric M., Evans, Denis A., Bennett, David A., De Jager, Philip L.
Publicado em 2011

A coding variant in CR1 interacts with APOE-ɛ4 to influence cognitive decline

Por Keenan, Brendan T., Shulman, Joshua M., Chibnik, Lori B., Raj, Towfique, Tran, Dong, Sabuncu, Mert R., Allen, April N., Corneveaux, Jason J., Hardy, John A., Huentelman, Matthew J., Lemere, Cynthia A., Myers, Amanda J., Nicholson-Weller, Anne, Reiman, Eric M., Evans, Denis A., Bennett, David A., De Jager, Philip L.
Publicado em 2012

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Por Matarín, Mar, Brown, W Mark, Scholz, Sonja, Simón-Sánchez, Javier, Fung, Hon-Chung, Hernandez, Dena, Gibbs, J Raphael, De Vrieze, Fabienne Wavrant, Crews, Cynthia, Britton, Angela, Langefeld, Carl D, Brott, Thomas G, Brown, Robert D, Worrall, Bradford B, Frankel, Michael, Silliman, Scott, Case, L Douglas, Singleton, Andrew, Hardy, John A, Rich, Stephen S, Meschia, James F
Publicado em 2007

SNCA Variants Are Associated with Increased Risk for Multiple System Atrophy

Por Scholz, Sonja W., Houlden, Henry, Schulte, Claudia, Sharma, Manu, Li, Abi, Berg, Daniela, Melchers, Anna, Paudel, Reema, Gibbs, J. Raphael, Simon-Sanchez, Javier, Paisan-Ruiz, Coro, Bras, Jose, Ding, Jinhui, Chen, Honglei, Traynor, Bryan J., Arepalli, Sampath, Zonozi, Ryan R., Revesz, Tamas, Holton, Janice, Wood, Nick, Lees, Andrew, Oertel, Wolfgang, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Illig, Thomas, Riess, Olaf, Fernandez, Hubert H., Rodriguez, Ramon L., Okun, Michael S., Poewe, Werner, Wenning, Gregor K., Hardy, John A., Singleton, Andrew B., Gasser, Thomas
Publicado em 2009

Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease

Por Simon-Sanchez, Javier, Schulte, Claudia, Bras, Jose M, Sharma, Manu, Gibbs, J Raphael, Berg, Daniela, Paisan-Ruiz, Coro, Lichtner, Peter, Scholz, Sonja W, Hernandez, Dena G, Kruger, Rejko, Federoff, Monica, Klein, Christine, Goate, Alison, Perlmutter, Joel, Bonin, Michael, Nalls, Michael A, Illig, Thomas, Gieger, Christian, Houlden, Henry, Steffens, Michael, Okun, Michael S., Cookson, Mark, Foote, Kelly D, Fernandez, Hubert H, Traynor, Bryan J., Schreiber, Stefan, Arepalli, Sampath, Zonozi, Ryan, Gwinn, Katrina, van der Brug, Marcel, Lopez, Grisel, Chanock, Stephen J, Schatzkin, Arthur, Park, Yikyung, Hollenbeck, Albert, Gao, Jianjun, Huang, Xuemei, Wood, Nick W, Lorenz, Delia, Deuschl, Gunther, Chen, Honglei, Riess, Olaf, Hardy, John A, Singleton, Andrew B, Gasser, Thomas
Publicado em 2009

A genome-wide association study in multiple system atrophy

Por Sailer, Anna, Scholz, Sonja W., Nalls, Michael A., Schulte, Claudia, Federoff, Monica, Price, T. Ryan, Lees, Andrew, Ross, Owen A., Dickson, Dennis W., Mok, Kin, Mencacci, Niccolo E., Schottlaender, Lucia, Chelban, Viorica, Ling, Helen, O'Sullivan, Sean S., Wood, Nicholas W., Traynor, Bryan J., Ferrucci, Luigi, Federoff, Howard J., Mhyre, Timothy R., Morris, Huw R., Deuschl, Günther, Quinn, Niall, Widner, Hakan, Albanese, Alberto, Infante, Jon, Bhatia, Kailash P., Poewe, Werner, Oertel, Wolfgang, Höglinger, Günter U., Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Ferreira, Joaquim, Tolosa, Eduardo, Bloem, Bastiaan R., Rascol, Olivier, Meissner, Wassilios G., Hardy, John A., Revesz, Tamas, Holton, Janice L., Gasser, Thomas, Wenning, Gregor K., Singleton, Andrew B., Houlden, Henry
Publicado no Neurology (2016)