Suchergebnisse - Andrew Singleton

Querying “No Religion”: State, Society, and Spirituality in Australia von Anna Halafoff, Andrew Singleton, Elenie Poulos

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On the configuration of a regional Arctic Numerical Weather Prediction system to maximize predictive capacity von Morten KØltzow, Rafael Grote, Andrew Singleton

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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 von Helena Robinson, Avril Alba, Donna-Lee Frieze, Steven Cooke, Andrew Singleton

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A simple and efficient algorithm for genome‐wide homozygosity analysis in disease von Wei Liu, Jinhui Ding, Jesse Raphael Gibbs, Sue Jane Wang, John Hardy, Andrew Singleton

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Complex, Critical and Caring: Young People’s Diverse Religious, Spiritual and Non-Religious Worldviews in Australia and Canada von Anna Halafoff, Heather Shipley, Pamela D. Young, Andrew Singleton, Mary Lou Rasmussen, Gary Bouma

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Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3. von Njideka Okubadejo, Angela Britton, Cynthia Crews, Rufus Akinyemi, John Hardy, Andrew Singleton, Jose Bras

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TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis. von Rita J Guerreiro, Jennifer C Schymick, Cynthia Crews, Andrew Singleton, John Hardy, Bryan J Traynor

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Family satisfaction in the trauma and surgical intensive care unit: another important quality measure von Tom Maxim, Agustin Alvarez, Yvonne Hojberg, Derek Antoku, Chioma Moneme, Andrew Singleton, Caroline Park, Kazuhide Matsushima

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Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational Study von Deborah A Hall, Josh M Shulman, Andrew Singleton, Sara Bandres Ciga, Michelle Hyczy S Tosin, Bichun Ouyang, Lisa Shulman

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A Bayesian mathematical model of motor and cognitive outcomes in Parkinson's disease. von 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

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Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients. von 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

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Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. von 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

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Genetic variability in CLU and its association with Alzheimer's disease. von 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

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Biobank-scale genetic characterization of Alzheimer’s disease and related dementias across diverse ancestries von 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

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NOTCH3 variants and risk of ischemic stroke. von 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

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LRRK2 and GBA1 variant carriers have higher urinary bis(monacylglycerol) phosphate concentrations in PPMI cohorts von Kalpana M. Merchant, Tanya Simuni, Janel Fedler, Chelsea Caspell-Garcia, Michael Brumm, Kelly N. H. Nudelman, Elizabeth Tengstrandt, Frank Hsieh, Roy N. Alcalay, Christopher Coffey, Lana Chahine, Tatiana Foroud, Andrew Singleton, Daniel Weintraub, Samantha Hutten, Todd Sherer, Brit Mollenhauer, Andrew Siderowf, Caroline Tanner, Ken Marek, the Parkinson’s Progression Markers Initiative

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Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. von Alastair J Noyce, Demis A Kia, Gibran Hemani, Aude Nicolas, T Ryan Price, Eduardo De Pablo-Fernandez, Philip C Haycock, Patrick A Lewis, Thomas Foltynie, George Davey Smith, International Parkinson Disease Genomics Consortium, Anette Schrag, Andrew J Lees, John Hardy, Andrew Singleton, Mike A Nalls, Neil Pearce, Debbie A Lawlor, Nicholas W Wood

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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lara M. Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio J. Keller Sarmiento, Ai-Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih-Hua Fang, Peter Heutink, Kishore R. Kumar, Shen-Yang Lim, Enza Maria Valente, Mike Nalls, Cornelis Blauwendraat, Andrew Singleton, Niccolo Mencacci, Katja Lohmann, Christine Klein, the Global Parkinson’s Genetic Program (GP2)

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A proteogenomic view of Parkinson’s disease causality and heterogeneity von Sergio Kaiser, Luqing Zhang, Brit Mollenhauer, Jaison Jacob, Simonne Longerich, Jorge Del-Aguila, Jacob Marcus, Neha Raghavan, David Stone, Olumide Fagboyegun, Douglas Galasko, Mohammed Dakna, Bilada Bilican, Mary Dovlatyan, Anna Kostikova, Jingyao Li, Brant Peterson, Michael Rotte, Vinicius Sanz, Tatiana Foroud, Samantha J. Hutten, Mark Frasier, Hirotaka Iwaki, Andrew Singleton, Ken Marek, Karen Crawford, Fiona Elwood, Mirko Messa, Pablo Serrano-Fernandez

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Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lara M. Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio J. Keller Sarmiento, Ai-Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih-Hua Fang, Peter Heutink, Kishore R. Kumar, Shen-Yang Lim, Enza Maria Valente, Mike Nalls, Cornelis Blauwendraat, Andrew Singleton, Niccolo Mencacci, Katja Lohmann, Christine Klein, the Global Parkinson’s Genetic Program (GP2)

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