Application of Genome-Wide Single Nucleotide Polymorphism Typing: Simple Association and Beyond

por Gibbs, J. Raphael, Singleton, Andrew
Publicado 2006

Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

por Guerreiro, Rita, Brás, José, Hardy, John, Singleton, Andrew
Publicado 2014

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

por Singleton, Andrew B., Hardy, John A., Gasser, Thomas
Publicado 2017

LRRK2: Cause, Risk, and Mechanism

por Paisán-Ruiz, Coro, Lewis, Patrick A., Singleton, Andrew B.
Publicado 2013

Genetic players in multiple system atrophy: unfolding the nature of the beast

por Stemberger, Sylvia, Scholz, Sonja W., Singleton, Andrew B., Wenning, Gregor K.
Publicado 2011

Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to l-DOPA treatment

por Bettencourt, Conceição, Morris, Huw R., Singleton, Andrew B., Hardy, John, Houlden, Henry
Publicado 2013

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan

por Fung, Hon-Chung, Chen, Chiung-Mei, Hardy, John, Singleton, Andrew B, Wu, Yih-Ru
Publicado 2006

Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3

por Okubadejo, Njideka, Britton, Angela, Crews, Cynthia, Akinyemi, Rufus, Hardy, John, Singleton, Andrew, Bras, Jose
Publicado 2008

A simple and efficient algorithm for genome-wide homozygosity analysis in disease

por Liu, Wei, Ding, Jinhui, Gibbs, Jesse Raphael, Wang, Sue Jane, Hardy, John, Singleton, Andrew
Publicado 2009

Cell population-specific expression analysis of human cerebellum

por Kuhn, Alexandre, Kumar, Azad, Beilina, Alexandra, Dillman, Allissa, Cookson, Mark R, Singleton, Andrew B
Publicado 2012

Multimodal Neuroimaging Predictors of Gait Decline

por Sargent, Lana, Tian, Qu, Nalls, Mike, Singleton, Andrew, Studenski, Stephanie, Resnick, Susan, Ferrucci, Luigi
Publicado 2020

TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis

por Guerreiro, Rita J., Schymick, Jennifer C., Crews, Cynthia, Singleton, Andrew, Hardy, John, Traynor, Bryan J.
Publicado 2008

Variant biomarker discovery using mass spectrometry-based proteogenomics

por Reilly, Luke, Seddighi, Sahba, Singleton, Andrew B., Cookson, Mark R., Ward, Michael E., Qi, Yue A.
Publicado 2023

Family satisfaction in the trauma and surgical intensive care unit: another important quality measure

por Maxim, Tom, Alvarez, Agustin, Hojberg, Yvonne, Antoku, Derek, Moneme, Chioma, Singleton, Andrew, Park, Caroline, Matsushima, Kazuhide
Publicado 2019

Analysis of rare Parkinson’s disease variants in millions of people

por Pitz, Vanessa, Makarious, Mary, Bandrés-Ciga, Sara, Iwaki, Hirotaka, Singleton, Andrew, Nalls, Mike, Heilbron, Karl, Blauwendraat, Cornelis
Publicado 2023

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 2012

Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people

por Murray, Anna, Cluett, Christie, Bandinelli, Stefania, Corsi, Anna Maria, Ferrucci, Luigi, Guralnik, Jack, Singleton, Andrew, Frayling, Timothy, Melzer, David
Publicado 2009

Human brain single nucleus cell type enrichments in neurodegenerative diseases

por Alvarado, Chelsea X, Weller, Cory A., Johnson, Nicholas, Leonard, Hampton L., Singleton, Andrew B., Reed, Xylena, Blauewendraat, Cornelis, Nalls, Mike A
Publicado 2023

A Novel DYT-5 Mutation with Phenotypic Variability within a Colombian Family

por Bernal-Pacheco, Oscar, Oyama, Genko, Briton, Angela, Singleton, Andrew B., Fernandez, Hubert H., Rodriguez, Ramon L., Malaty, Irene A., Okun, Michael S.
Publicado 2013

Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis

por Siitonen, Ari, Kytövuori, Laura, Nalls, Mike A., Gibbs, Raphael, Hernandez, Dena G., Ylikotila, Pauli, Peltonen, Markku, Singleton, Andrew B., Majamaa, Kari
Publicado 2019