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Nature Medicine
|
July 18, 2023
Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region
Christa Caggiano, Arya Boudaie, Ruhollah Shemirani, et al.
Cell
|
January 22, 2022
Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration
Tara E Tracy, Jesus Madero-Pérez, Danielle L Swaney, et al.
Nature Genetics
|
August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2025
Diverse Genomes, Shared Health: Insights from a Health System Biobank
Roni Haas, Michael P Margolis, Angela Wei, et al.
Cell
|
March 28, 2026
Advancing precision health discovery in a genetically diverse health system
Roni Haas, Michael P Margolis, Angela Wei, et al.
Molecular Neurodegeneration
|
August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Molecular Neurodegeneration
|
October 14, 2024
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypes
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
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Search research articles
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Showing results (31-40 of 40) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 40 results.
Nature Medicine
|
July 18, 2023
Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region
Christa Caggiano, Arya Boudaie, Ruhollah Shemirani, et al.
Cell
|
January 22, 2022
Tau interactome maps synaptic and mitochondrial processes associated with neurodegeneration
Tara E Tracy, Jesus Madero-Pérez, Danielle L Swaney, et al.
Nature Genetics
|
August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2025
Diverse Genomes, Shared Health: Insights from a Health System Biobank
Roni Haas, Michael P Margolis, Angela Wei, et al.
Cell
|
March 28, 2026
Advancing precision health discovery in a genetically diverse health system
Roni Haas, Michael P Margolis, Angela Wei, et al.
Molecular Neurodegeneration
|
August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Molecular Neurodegeneration
|
October 14, 2024
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and <i>MAPT</i> Sub-haplotypes
Hui Wang, Timothy S Chang, Beth A Dombroski, et al.
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