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Jane E Ranchalis

Showing results (11-20 of 18) with videos related to

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Biorxiv : the Preprint Server for Biology|September 15, 2025
CUT&TIME captures the history of open chromatin in developing neuronsKiara C Eldred, Matthew Wooten, Derek H Janssens, et al.
Journal of Lipid Research|May 27, 2015
PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activityDaniel Seung Kim, Amber A Burt, Jane E Ranchalis, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 24, 2017
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorderDaniel Seung Kim, Amber A Burt, Jane E Ranchalis, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Genetic diversity and regulatory features of human-specific <i>NOTCH2NL</i> duplicationsTaylor D Real, Prajna Hebbar, DongAhn Yoo, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditionsYong-Han Hank Cheng, Adriana E Sedeño-Cortés, Jane E Ranchalis, et al.
Cell Genomics|March 31, 2026
Genetic diversity and regulatory features of human-specific NOTCH2NL duplicationsTaylor D Real, Prajna Hebbar, DongAhn Yoo, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
A telomere-to-telomere map of somatic mutation burden and functional impact in cancerMin-Hwan Sohn, Danilo Dubocanin, Mitchell R Vollger, et al.
American Journal of Human Genetics|February 25, 2014
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related lociVinicius Tragante, Michael R Barnes, Santhi K Ganesh, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Biorxiv : the Preprint Server for Biology|September 15, 2025
CUT&TIME captures the history of open chromatin in developing neuronsKiara C Eldred, Matthew Wooten, Derek H Janssens, et al.
Journal of Lipid Research|May 27, 2015
PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activityDaniel Seung Kim, Amber A Burt, Jane E Ranchalis, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 24, 2017
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorderDaniel Seung Kim, Amber A Burt, Jane E Ranchalis, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Genetic diversity and regulatory features of human-specific <i>NOTCH2NL</i> duplicationsTaylor D Real, Prajna Hebbar, DongAhn Yoo, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditionsYong-Han Hank Cheng, Adriana E Sedeño-Cortés, Jane E Ranchalis, et al.
Cell Genomics|March 31, 2026
Genetic diversity and regulatory features of human-specific NOTCH2NL duplicationsTaylor D Real, Prajna Hebbar, DongAhn Yoo, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
A telomere-to-telomere map of somatic mutation burden and functional impact in cancerMin-Hwan Sohn, Danilo Dubocanin, Mitchell R Vollger, et al.
American Journal of Human Genetics|February 25, 2014
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related lociVinicius Tragante, Michael R Barnes, Santhi K Ganesh, et al.
Pageof 2