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Mark T W Ebbert

Showing results (21-30 of 62) with videos related to

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Frontiers in Genetics|June 12, 2026
Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomicsPatricia Hayes Doyle, Madeline L Page, J Anthony Brandon, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Surveying the landscape of RNA isoform diversity and expression across 9 GTEx tissues using long-read sequencing dataMadeline L Page, Bernardo Aguzzoli Heberle, J Anthony Brandon, et al.
BMC Genomics|July 1, 2016
Presenilin E318G variant and Alzheimer's disease risk: the Cache County studyAriel A Hippen, Mark T W Ebbert, Maria C Norton, et al.
BMC Genomics|July 1, 2016
Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levelsMark T W Ebbert, Lyndsay A Staley, Joshua Parker, et al.
Communications Biology|September 2, 2022
The Polygenic Risk Score Knowledge Base offers a centralized online repository for calculating and contextualizing polygenic risk scoresMadeline L Page, Elizabeth L Vance, Matthew E Cloward, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 10, 2015
Interaction between variants in CLU and MS4A4E modulates Alzheimer's disease riskMark T W Ebbert, Kevin L Boehme, Mark E Wadsworth, et al.
BMC Genomics|December 4, 2025
A bioinformatic survey of RNA isoform diversity and expression across 9 GTEx tissues using long-read sequencing dataMadeline L Page, Bernardo Aguzzoli Heberle, J Anthony Brandon, et al.
NAR Genomics and Bioinformatics|June 6, 2022
The Ramp Atlas: facilitating tissue and cell-specific ramp sequence analyses through an intuitive web interfaceJustin B Miller, Taylor E Meurs, Matthew W Hodgman, et al.
The Journal of Experimental Medicine|August 8, 2018
Microglial translational profiling reveals a convergent APOE pathway from aging, amyloid, and tauSilvia S Kang, Mark T W Ebbert, Kelsey E Baker, et al.
BMC Bioinformatics|August 1, 2014
Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) filesMark T W Ebbert, Mark E Wadsworth, Kevin L Boehme, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
Frontiers in Genetics|June 12, 2026
Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomicsPatricia Hayes Doyle, Madeline L Page, J Anthony Brandon, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Surveying the landscape of RNA isoform diversity and expression across 9 GTEx tissues using long-read sequencing dataMadeline L Page, Bernardo Aguzzoli Heberle, J Anthony Brandon, et al.
BMC Genomics|July 1, 2016
Presenilin E318G variant and Alzheimer's disease risk: the Cache County studyAriel A Hippen, Mark T W Ebbert, Maria C Norton, et al.
BMC Genomics|July 1, 2016
Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levelsMark T W Ebbert, Lyndsay A Staley, Joshua Parker, et al.
Communications Biology|September 2, 2022
The Polygenic Risk Score Knowledge Base offers a centralized online repository for calculating and contextualizing polygenic risk scoresMadeline L Page, Elizabeth L Vance, Matthew E Cloward, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 10, 2015
Interaction between variants in CLU and MS4A4E modulates Alzheimer's disease riskMark T W Ebbert, Kevin L Boehme, Mark E Wadsworth, et al.
BMC Genomics|December 4, 2025
A bioinformatic survey of RNA isoform diversity and expression across 9 GTEx tissues using long-read sequencing dataMadeline L Page, Bernardo Aguzzoli Heberle, J Anthony Brandon, et al.
NAR Genomics and Bioinformatics|June 6, 2022
The Ramp Atlas: facilitating tissue and cell-specific ramp sequence analyses through an intuitive web interfaceJustin B Miller, Taylor E Meurs, Matthew W Hodgman, et al.
The Journal of Experimental Medicine|August 8, 2018
Microglial translational profiling reveals a convergent APOE pathway from aging, amyloid, and tauSilvia S Kang, Mark T W Ebbert, Kelsey E Baker, et al.
BMC Bioinformatics|August 1, 2014
Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) filesMark T W Ebbert, Mark E Wadsworth, Kevin L Boehme, et al.
Pageof 7