Search research articles
Contact Us
Filters
Showing results (31-40 of 47) with videos related to
Page
of 5
Sort By:
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
June 26, 2024
An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndrome
Allison Snyder, Veronica H Ryan, James Hawrot, et al.
NPJ Dementia
|
June 22, 2026
Haplotype-resolved DNA methylation at the <i>APOE</i> locus identifies allele-specific epigenetic signatures relevant to Alzheimer's disease risk
Rylee M Genner, Melissa Meredith, Kensuke Daida, et al.
American Journal of Human Genetics
|
December 4, 2018
Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons
Sarah A McClymont, Paul W Hook, Alexandra I Soto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 1, 2020
The Parkinson's Disease Genome-Wide Association Study Locus Browser
Francis P Grenn, Jonggeol J Kim, Mary B Makarious, et al.
Biorxiv : the Preprint Server for Biology
|
July 10, 2026
Long-read sequencing maps transposable element variation and its regulatory and epigenetic effects in the human brain
Alexis Ayuketah, Melissa Meredith, Cristian Groza, et al.
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.
Nature Methods
|
September 14, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.
JAMA Neurology
|
July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
Cornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Biorxiv : the Preprint Server for Biology
|
April 29, 2026
The complete genome of the KOLF2.1J reference iPSC line
Pilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>
Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 47) with videos related to
Sort By:
Page
of 5
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
June 26, 2024
An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndrome
Allison Snyder, Veronica H Ryan, James Hawrot, et al.
NPJ Dementia
|
June 22, 2026
Haplotype-resolved DNA methylation at the <i>APOE</i> locus identifies allele-specific epigenetic signatures relevant to Alzheimer's disease risk
Rylee M Genner, Melissa Meredith, Kensuke Daida, et al.
American Journal of Human Genetics
|
December 4, 2018
Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons
Sarah A McClymont, Paul W Hook, Alexandra I Soto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 1, 2020
The Parkinson's Disease Genome-Wide Association Study Locus Browser
Francis P Grenn, Jonggeol J Kim, Mary B Makarious, et al.
Biorxiv : the Preprint Server for Biology
|
July 10, 2026
Long-read sequencing maps transposable element variation and its regulatory and epigenetic effects in the human brain
Alexis Ayuketah, Melissa Meredith, Cristian Groza, et al.
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.
Nature Methods
|
September 14, 2023
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation
Mikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.
JAMA Neurology
|
July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
Cornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Biorxiv : the Preprint Server for Biology
|
April 29, 2026
The complete genome of the KOLF2.1J reference iPSC line
Pilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>
Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Page
of 5