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Andrew B Singleton

Showing results (41-50 of 397) with videos related to

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Neuroscience Letters|April 9, 2008
Association between AKT1 gene and Parkinson's disease: a protective haplotypeGeorgia Xiromerisiou, Georgios M Hadjigeorgiou, Alexandros Papadimitriou, et al.
BMC Neurology|December 26, 2006
A common genetic factor for Parkinson disease in ethnic Chinese population in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Neuroscience Letters|November 20, 2003
Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's diseaseChristopher M Morris, Kirsty K O'Brien, Alison M Gibson, et al.
Neuron|April 8, 2021
Tackling neurodegenerative diseases with genomic engineering: A new stem cell initiative from the NIHDaniel M Ramos, William C Skarnes, Andrew B Singleton, et al.
The Lancet. Neurology|September 15, 2025
The temporal order of genetic, environmental, and pathological risk factors in Parkinson's disease: paving the way to preventionCornelis Blauwendraat, Huw R Morris, Kendall Van Keuren-Jensen, et al.
Neurobiology of Aging|June 23, 2012
Large C9orf72 repeat expansions are not a common cause of Parkinson's diseaseElisa Majounie, Yevgeniya Abramzon, Alan E Renton, et al.
Parkinsonism & Related Disorders|January 22, 2015
Head injury, potential interaction with genes, and risk for Parkinson's diseaseJianjun Gao, Rui Liu, Edward Zhao, et al.
Frontiers in Aging|May 11, 2023
Variant biomarker discovery using mass spectrometry-based proteogenomicsLuke Reilly, Sahba Seddighi, Andrew B Singleton, et al.
Annals of Neurology|April 1, 2024
Towards a Global View of Parkinson's Disease GeneticsMarzieh Khani, Catalina Cerquera-Cleves, Mariam Kekenadze, et al.
American Journal of Human Genetics|February 14, 2009
Genotype-imputation accuracy across worldwide human populationsLucy Huang, Yun Li, Andrew B Singleton, et al.
Pageof 40

Showing results (41-50 of 397) with videos related to

Sort By:
Pageof 40
Neuroscience Letters|April 9, 2008
Association between AKT1 gene and Parkinson's disease: a protective haplotypeGeorgia Xiromerisiou, Georgios M Hadjigeorgiou, Alexandros Papadimitriou, et al.
BMC Neurology|December 26, 2006
A common genetic factor for Parkinson disease in ethnic Chinese population in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Neuroscience Letters|November 20, 2003
Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's diseaseChristopher M Morris, Kirsty K O'Brien, Alison M Gibson, et al.
Neuron|April 8, 2021
Tackling neurodegenerative diseases with genomic engineering: A new stem cell initiative from the NIHDaniel M Ramos, William C Skarnes, Andrew B Singleton, et al.
The Lancet. Neurology|September 15, 2025
The temporal order of genetic, environmental, and pathological risk factors in Parkinson's disease: paving the way to preventionCornelis Blauwendraat, Huw R Morris, Kendall Van Keuren-Jensen, et al.
Neurobiology of Aging|June 23, 2012
Large C9orf72 repeat expansions are not a common cause of Parkinson's diseaseElisa Majounie, Yevgeniya Abramzon, Alan E Renton, et al.
Parkinsonism & Related Disorders|January 22, 2015
Head injury, potential interaction with genes, and risk for Parkinson's diseaseJianjun Gao, Rui Liu, Edward Zhao, et al.
Frontiers in Aging|May 11, 2023
Variant biomarker discovery using mass spectrometry-based proteogenomicsLuke Reilly, Sahba Seddighi, Andrew B Singleton, et al.
Annals of Neurology|April 1, 2024
Towards a Global View of Parkinson's Disease GeneticsMarzieh Khani, Catalina Cerquera-Cleves, Mariam Kekenadze, et al.
American Journal of Human Genetics|February 14, 2009
Genotype-imputation accuracy across worldwide human populationsLucy Huang, Yun Li, Andrew B Singleton, et al.
Pageof 40