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Kensuke Daida

Showing results (41-50 of 61) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 1, 2025
Identification of GGC Repeat Expansions in <i>ZFHX3</i> Among Chilean Movement Disorder PatientsPaula 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 diseaseFulya 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 diseaseFulya 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 riskRylee 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 StudyTaku 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 methylationMikhail 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 methylationMikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole 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 linePilar 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 JapanKensuke Daida, Kenya Nishioka, Yuanzhe Li, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Medrxiv : the Preprint Server for Health Sciences|April 1, 2025
Identification of GGC Repeat Expansions in <i>ZFHX3</i> Among Chilean Movement Disorder PatientsPaula 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 diseaseFulya 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 diseaseFulya 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 riskRylee 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 StudyTaku 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 methylationMikhail 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 methylationMikhail Kolmogorov, Kimberley J Billingsley, Mira Mastoras, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole 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 linePilar 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 JapanKensuke Daida, Kenya Nishioka, Yuanzhe Li, et al.
Pageof 7