Search Results - Andrew Singleton
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The Future of Genetic Analysis of Neurological Disorders by John Hardy, Andrew Singleton
Published in Neurobiology of Disease (2000-04-01)Get full text
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Research Protocol: A Transdisciplinary Multi-Case Study Research Design Using Mixed Methods to Evaluate the Long-Term Impact of Holocaust Museum Education in Australia by Helena Robinson, Avril Alba, Donna-Lee Frieze, Steven Cooke, Andrew Singleton
Published in International Journal of Qualitative Methods (2024-03-01)Get full text
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A simple and efficient algorithm for genome‐wide homozygosity analysis in disease by Wei Liu, Jinhui Ding, Jesse Raphael Gibbs, Sue Jane Wang, John Hardy, Andrew Singleton
Published in Molecular Systems Biology (2009-09-01)Get full text
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Family satisfaction in the trauma and surgical intensive care unit: another important quality measure by Tom Maxim, Agustin Alvarez, Yvonne Hojberg, Derek Antoku, Chioma Moneme, Andrew Singleton, Caroline Park, Kazuhide Matsushima
Published in Trauma Surgery & Acute Care Open (2019-09-01)Get full text
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Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational Study by Deborah A Hall, Josh M Shulman, Andrew Singleton, Sara Bandres Ciga, Michelle Hyczy S Tosin, Bichun Ouyang, Lisa Shulman
Published in JMIR Research Protocols (2025-04-01)Get full text
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Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging. by Heather E Wheeler, E Jeffrey Metter, Toshiko Tanaka, Devin Absher, John Higgins, Jacob M Zahn, Julie Wilhelmy, Ronald W Davis, Andrew Singleton, Richard M Myers, Luigi Ferrucci, Stuart K Kim
Published in PLoS Genetics (2009-10-01)Get full text
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A Bayesian mathematical model of motor and cognitive outcomes in Parkinson's disease. by Boris Hayete, Diane Wuest, Jason Laramie, Paul McDonagh, Bruce Church, Shirley Eberly, Anthony Lang, Kenneth Marek, Karl Runge, Ira Shoulson, Andrew Singleton, Caroline Tanner, Iya Khalil, Ajay Verma, Bernard Ravina
Published in PLoS ONE (2017-01-01)Get full text
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Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients. by Gamze Guven, Ebba Lohmann, Jose Bras, J Raphael Gibbs, Hakan Gurvit, Basar Bilgic, Hasmet Hanagasi, Patrizia Rizzu, Peter Heutink, Murat Emre, Nihan Erginel-Unaltuna, Walter Just, John Hardy, Andrew Singleton, Rita Guerreiro
Published in PLoS ONE (2016-01-01)Get full text
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Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. by James F Meschia, Andrew Singleton, Michael A Nalls, Stephen S Rich, Pankaj Sharma, Luigi Ferrucci, Mar Matarin, Dena G Hernandez, Kerra Pearce, Thomas G Brott, Robert D Brown, John Hardy, Bradford B Worrall
Published in PLoS ONE (2011-01-01)Get full text
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Genetic variability in CLU and its association with Alzheimer's disease. by Rita J Guerreiro, John Beck, J Raphael Gibbs, Isabel Santana, Martin N Rossor, Jonathan M Schott, Michael A Nalls, Helena Ribeiro, Beatriz Santiago, Nick C Fox, Catarina Oliveira, John Collinge, Simon Mead, Andrew Singleton, John Hardy
Published in PLoS ONE (2010-03-01)Get full text
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Biobank-scale genetic characterization of Alzheimer’s disease and related dementias across diverse ancestries by Marzieh Khani, Fulya Akçimen, Spencer M. Grant, Suleyman Can Akerman, Paul Suhwan Lee, Faraz Faghri, Hampton Leonard, Jonggeol Jeffrey Kim, Mary B. Makarious, Mathew J. Koretsky, Jeffrey D. Rothstein, Cornelis Blauwendraat, Mike A. Nalls, Andrew Singleton, Sara Bandres-Ciga
Published in Nature Communications (2025-08-01)Get full text
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NOTCH3 variants and risk of ischemic stroke. by Owen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, Christophe Verbeeck, Daniel J Serie, Sruti Rayaprolu, Stephen S Rich, Michael A Nalls, Andrew Singleton, Rita Guerreiro, Emma Kinsella, Zbigniew K Wszolek, Thomas G Brott, Robert D Brown, Bradford B Worrall, James F Meschia
Published in PLoS ONE (2013-01-01)Get full text
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Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24. by Caryline Agler, Dahlia M Nielsen, Ganokon Urkasemsin, Andrew Singleton, Noriko Tonomura, Snaevar Sigurdsson, Ruqi Tang, Keith Linder, Sampath Arepalli, Dena Hernandez, Kerstin Lindblad-Toh, Joyce van de Leemput, Alison Motsinger-Reif, Dennis P O'Brien, Jerold Bell, Tonya Harris, Steven Steinberg, Natasha J Olby
Published in PLoS Genetics (2014-02-01)Get full text
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