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Medrxiv : the Preprint Server for Health Sciences
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April 1, 2025
Identification of GGC Repeat Expansions in <i>ZFHX3</i> Among Chilean Movement Disorder Patients
Paula Saffie-Awad, Abraham Moller, Kensuke Daida, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 2, 2025
Long-read sequencing identifies <i>FGF14</i> repeat expansions in Parkinson's disease
Fulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Brain : a Journal of Neurology
|
December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's disease
Fulya Akçimen, Kensuke Daida, Lara M Lange, 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.
Movement Disorders Clinical Practice
|
January 24, 2024
Efficacy and Safety of Elobixibat in Parkinson's Disease with Chronic Constipation: CONST-PD Study
Taku Hatano, Genko Oyama, Yasushi Shimo, 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.
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.
Biorxiv : the Preprint Server for Biology
|
November 28, 2024
CNV-Finder: Streamlining Copy Number Variation Discovery
Nicole Kuznetsov, Kensuke Daida, Mary B Makarious, 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.
Neurobiology of Aging
|
August 11, 2020
PLA2G6 variants associated with the number of affected alleles in Parkinson's disease in Japan
Kensuke Daida, Kenya Nishioka, Yuanzhe Li, et al.
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of 7
Search research articles
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Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Medrxiv : the Preprint Server for Health Sciences
|
April 1, 2025
Identification of GGC Repeat Expansions in <i>ZFHX3</i> Among Chilean Movement Disorder Patients
Paula Saffie-Awad, Abraham Moller, Kensuke Daida, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 2, 2025
Long-read sequencing identifies <i>FGF14</i> repeat expansions in Parkinson's disease
Fulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Brain : a Journal of Neurology
|
December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's disease
Fulya Akçimen, Kensuke Daida, Lara M Lange, 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.
Movement Disorders Clinical Practice
|
January 24, 2024
Efficacy and Safety of Elobixibat in Parkinson's Disease with Chronic Constipation: CONST-PD Study
Taku Hatano, Genko Oyama, Yasushi Shimo, 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.
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.
Biorxiv : the Preprint Server for Biology
|
November 28, 2024
CNV-Finder: Streamlining Copy Number Variation Discovery
Nicole Kuznetsov, Kensuke Daida, Mary B Makarious, 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.
Neurobiology of Aging
|
August 11, 2020
PLA2G6 variants associated with the number of affected alleles in Parkinson's disease in Japan
Kensuke Daida, Kenya Nishioka, Yuanzhe Li, et al.
Page
of 7