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Neuro-Degenerative Diseases
|
November 30, 2011
Using DNA methylation to understand biological consequences of genetic variability
Dena G Hernandez, Andrew B Singleton
Journal of Neurochemistry
|
April 20, 2016
Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance
Dena G Hernandez, Xylena Reed, Andrew B Singleton
Neuroscience Letters
|
July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cells
Casey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 14, 2015
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
Mike A Nalls, Margaux F Keller, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2018
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus
Cornelis Blauwendraat, Jose M Bras, Mike A Nalls, et al.
Neurobiology of Aging
|
May 30, 2015
EIF4G1 mutations do not cause Parkinson's disease
Noah Nichols, Jose M Bras, Dena G Hernandez, et al.
Plos One
|
August 23, 2012
Genome wide assessment of young onset Parkinson's disease from Finland
Dena G Hernandez, Michael A Nalls, Pauli Ylikotila, et al.
Epigenetics
|
November 20, 2019
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
Kumaraswamy Naidu Chitrala, Dena G Hernandez, Michael A Nalls, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|
September 11, 2015
Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study
Ann Zenobia Moore, Dena G Hernandez, Toshiko Tanaka, et al.
Scientific Reports
|
December 13, 2019
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis
Ari Siitonen, Laura Kytövuori, Mike A Nalls, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 148) with videos related to
Sort By:
Page
of 15
Neuro-Degenerative Diseases
|
November 30, 2011
Using DNA methylation to understand biological consequences of genetic variability
Dena G Hernandez, Andrew B Singleton
Journal of Neurochemistry
|
April 20, 2016
Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance
Dena G Hernandez, Xylena Reed, Andrew B Singleton
Neuroscience Letters
|
July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cells
Casey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 14, 2015
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
Mike A Nalls, Margaux F Keller, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2018
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus
Cornelis Blauwendraat, Jose M Bras, Mike A Nalls, et al.
Neurobiology of Aging
|
May 30, 2015
EIF4G1 mutations do not cause Parkinson's disease
Noah Nichols, Jose M Bras, Dena G Hernandez, et al.
Plos One
|
August 23, 2012
Genome wide assessment of young onset Parkinson's disease from Finland
Dena G Hernandez, Michael A Nalls, Pauli Ylikotila, et al.
Epigenetics
|
November 20, 2019
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
Kumaraswamy Naidu Chitrala, Dena G Hernandez, Michael A Nalls, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|
September 11, 2015
Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study
Ann Zenobia Moore, Dena G Hernandez, Toshiko Tanaka, et al.
Scientific Reports
|
December 13, 2019
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis
Ari Siitonen, Laura Kytövuori, Mike A Nalls, et al.
Page
of 15