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Kevin S Smith

Showing results (51-60 of 65) with videos related to

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Biorxiv : the Preprint Server for Biology|January 30, 2023
Multi-omic identification of key transcriptional regulatory programs during endurance exercise trainingGregory R Smith, Bingqing Zhao, Malene E Lindholm, et al.
Genome Research|May 9, 2015
The landscape of genomic imprinting across diverse adult human tissuesYael Baran, Meena Subramaniam, Anne Biton, et al.
Cell Genomics|May 2, 2024
Molecular adaptations in response to exercise training are associated with tissue-specific transcriptomic and epigenomic signaturesVenugopalan D Nair, Hanna Pincas, Gregory R Smith, et al.
Nature Communications|March 21, 2026
Multi-omic identification of key transcriptional regulatory programs during endurance exercise training in ratsGregory R Smith, Bingqing Zhao, Malene E Lindholm, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathiesMaggie T Arriaga, Rodrigo Mendez, Rachel A Ungar, et al.
American Journal of Human Genetics|September 20, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathiesTaylor M Arriaga, Rodrigo Mendez, Rachel A Ungar, et al.
HGG Advances|March 11, 2026
Biallelic Variants in RNU6ATAC Result in a Minor Spliceopathy Characterized by Transcriptome-Wide Minor Intron Retention Events and Short Stature with Variable Multisystem ManifestationsRodrigo Mendez, Taylor M Arriaga, Jialan Ma, et al.
Nature Genetics|April 11, 2017
Population- and individual-specific regulatory variation in SardiniaMauro Pala, Zachary Zappala, Mara Marongiu, et al.
Biorxiv : the Preprint Server for Biology|November 21, 2023
Transcriptomics and chromatin accessibility in multiple African population samplesMarianne K DeGorter, Page C Goddard, Emre Karakoc, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2024
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderJennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Biorxiv : the Preprint Server for Biology|January 30, 2023
Multi-omic identification of key transcriptional regulatory programs during endurance exercise trainingGregory R Smith, Bingqing Zhao, Malene E Lindholm, et al.
Genome Research|May 9, 2015
The landscape of genomic imprinting across diverse adult human tissuesYael Baran, Meena Subramaniam, Anne Biton, et al.
Cell Genomics|May 2, 2024
Molecular adaptations in response to exercise training are associated with tissue-specific transcriptomic and epigenomic signaturesVenugopalan D Nair, Hanna Pincas, Gregory R Smith, et al.
Nature Communications|March 21, 2026
Multi-omic identification of key transcriptional regulatory programs during endurance exercise training in ratsGregory R Smith, Bingqing Zhao, Malene E Lindholm, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathiesMaggie T Arriaga, Rodrigo Mendez, Rachel A Ungar, et al.
American Journal of Human Genetics|September 20, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathiesTaylor M Arriaga, Rodrigo Mendez, Rachel A Ungar, et al.
HGG Advances|March 11, 2026
Biallelic Variants in RNU6ATAC Result in a Minor Spliceopathy Characterized by Transcriptome-Wide Minor Intron Retention Events and Short Stature with Variable Multisystem ManifestationsRodrigo Mendez, Taylor M Arriaga, Jialan Ma, et al.
Nature Genetics|April 11, 2017
Population- and individual-specific regulatory variation in SardiniaMauro Pala, Zachary Zappala, Mara Marongiu, et al.
Biorxiv : the Preprint Server for Biology|November 21, 2023
Transcriptomics and chromatin accessibility in multiple African population samplesMarianne K DeGorter, Page C Goddard, Emre Karakoc, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2024
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderJennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Pageof 7