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Movement Disorders : Official Journal of the Movement Disorder Society
|
June 23, 2025
Screening of Hidden Pathogenic Structural Variants in PRKN
Kensuke Daida, Guillaume Cogan, Christelle Tesson, et al.
Annals of Clinical and Translational Neurology
|
February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural Variants
André Fienemann, Theresa Lüth, Susen Schaake, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 4, 2023
Long-read sequencing resolves a complex structural variant in <i>PRKN</i> Parkinson's disease
Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 6, 2023
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease
Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Journal of Human Genetics
|
May 14, 2020
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan
Yuanzhe Li, Aya Ikeda, Hiroyo Yoshino, et al.
Cell Reports
|
March 15, 2026
Single-nucleus multiome analysis in the human prefrontal cortex identifies gene expression and cis-regulatory elements associated with aging
Adam Catching, Cory A Weller, Fangle Hu, et al.
NPJ Parkinson'S Disease
|
May 24, 2024
Profiling complex repeat expansions in RFC1 in Parkinson's disease
Pilar Alvarez Jerez, Kensuke Daida, Abigail Miano-Burkhardt, et al.
Biorxiv : the Preprint Server for Biology
|
July 9, 2025
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, Abraham Moller, et al.
NPJ Parkinson'S Disease
|
July 26, 2024
Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing
Pilar Alvarez Jerez, Kensuke Daida, Francis P Grenn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 3, 2025
Identification of GGC Repeat Expansions in ZFHX3 among Chilean Movement Disorder Patients
Paula Saffie-Awad, Abraham Moller, Kensuke Daida, et al.
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Search research articles
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Showing results (31-40 of 61) with videos related to
Sort By:
Page
of 7
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 23, 2025
Screening of Hidden Pathogenic Structural Variants in PRKN
Kensuke Daida, Guillaume Cogan, Christelle Tesson, et al.
Annals of Clinical and Translational Neurology
|
February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural Variants
André Fienemann, Theresa Lüth, Susen Schaake, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 4, 2023
Long-read sequencing resolves a complex structural variant in <i>PRKN</i> Parkinson's disease
Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 6, 2023
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease
Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Journal of Human Genetics
|
May 14, 2020
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan
Yuanzhe Li, Aya Ikeda, Hiroyo Yoshino, et al.
Cell Reports
|
March 15, 2026
Single-nucleus multiome analysis in the human prefrontal cortex identifies gene expression and cis-regulatory elements associated with aging
Adam Catching, Cory A Weller, Fangle Hu, et al.
NPJ Parkinson'S Disease
|
May 24, 2024
Profiling complex repeat expansions in RFC1 in Parkinson's disease
Pilar Alvarez Jerez, Kensuke Daida, Abigail Miano-Burkhardt, et al.
Biorxiv : the Preprint Server for Biology
|
July 9, 2025
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, Abraham Moller, et al.
NPJ Parkinson'S Disease
|
July 26, 2024
Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing
Pilar Alvarez Jerez, Kensuke Daida, Francis P Grenn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 3, 2025
Identification of GGC Repeat Expansions in ZFHX3 among Chilean Movement Disorder Patients
Paula Saffie-Awad, Abraham Moller, Kensuke Daida, et al.
Page
of 7