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Plos One
|
June 13, 2017
A Bayesian mathematical model of motor and cognitive outcomes in Parkinson's disease
Boris Hayete, Diane Wuest, Jason Laramie, et al.
Plos Genetics
|
October 17, 2009
Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging
Heather E Wheeler, E Jeffrey Metter, Toshiko Tanaka, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 24, 2023
omicSynth: an Open Multi-omic Community Resource for Identifying Druggable Targets across Neurodegenerative Diseases
Chelsea X Alvarado, Mary B Makarious, Cory A Weller, et al.
American Journal of Human Genetics
|
January 5, 2024
omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases
Chelsea X Alvarado, Mary B Makarious, Cory A Weller, et al.
American Journal of Human Genetics
|
August 13, 2025
omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases
Chelsea X Alvarado, Mary B Makarious, Cory A Weller, et al.
Neurobiology of Aging
|
November 7, 2017
Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease
Sultan Chaudhury, Tulsi Patel, Imelda S Barber, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 20, 2008
WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia
Margaret M Timmons, James Garbern, Pamela G Robey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 10, 2011
Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred)
Katrina Gwinn, Michael J Devine, Lee-Way Jin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 10, 2009
The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasm
Giovanni Defazio, Mar Matarin, Elizabeth L Peckham, et al.
Plos One
|
September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
Gamze Guven, Ebba Lohmann, Jose Bras, et al.
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of 29
Search research articles
Search
Showing results (121-130 of 286) with videos related to
Sort By:
Page
of 29
Plos One
|
June 13, 2017
A Bayesian mathematical model of motor and cognitive outcomes in Parkinson's disease
Boris Hayete, Diane Wuest, Jason Laramie, et al.
Plos Genetics
|
October 17, 2009
Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging
Heather E Wheeler, E Jeffrey Metter, Toshiko Tanaka, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 24, 2023
omicSynth: an Open Multi-omic Community Resource for Identifying Druggable Targets across Neurodegenerative Diseases
Chelsea X Alvarado, Mary B Makarious, Cory A Weller, et al.
American Journal of Human Genetics
|
January 5, 2024
omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases
Chelsea X Alvarado, Mary B Makarious, Cory A Weller, et al.
American Journal of Human Genetics
|
August 13, 2025
omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases
Chelsea X Alvarado, Mary B Makarious, Cory A Weller, et al.
Neurobiology of Aging
|
November 7, 2017
Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease
Sultan Chaudhury, Tulsi Patel, Imelda S Barber, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 20, 2008
WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia
Margaret M Timmons, James Garbern, Pamela G Robey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 10, 2011
Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred)
Katrina Gwinn, Michael J Devine, Lee-Way Jin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 10, 2009
The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasm
Giovanni Defazio, Mar Matarin, Elizabeth L Peckham, et al.
Plos One
|
September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
Gamze Guven, Ebba Lohmann, Jose Bras, et al.
Page
of 29