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Bhooma Thiruvahindrapuram

Showing results (1-10 of 95) with videos related to

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G3 (Bethesda, Md.)|January 10, 2019
Using Next-Generation Sequencing Transcriptomics To Determine Markers of Post-traumatic Symptoms: Preliminary Findings from a Post-deployment Cohort of SoldiersCathy Boscarino, Thomas Nalpathamkalam, Giovanna Pellecchia, et al.
Journal of the Endocrine Society|July 31, 2025
Influence of Polygenic Risk on Height and BMI in Adults With a 22q11.2 MicrodeletionShengjie Ying, Tracy Heung, Bernice E Morrow, et al.
Viruses|April 26, 2025
Genomic and Epidemiological Investigations Reveal Chromosomal Integration of the Acipenserid Herpesvirus 3 Genome in Lake Sturgeon <i>Acipenser fulvescens</i>Sharon Clouthier, Umberto Rosani, Arfa Khan, et al.
European Journal of Human Genetics : EJHG|November 27, 2023
Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescueBushra Haque, David Cheerie, Saba Birkadze, et al.
Pathogens (Basel, Switzerland)|September 28, 2023
A New Sturgeon Herpesvirus from Juvenile Lake Sturgeon <i>Acipenser fulvescens</i> Displaying Epithelial Skin LesionsSharon Clouthier, Marek Tomczyk, Tamara Schroeder, et al.
Plos One|June 24, 2014
Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular MalaysiaSiti Shuhada Mokhtar, Christian R Marshall, Maude E Phipps, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndromeErika Tavares, Chen Yu Tang, Anjali Vig, et al.
Neurology. Genetics|May 31, 2018
Chorea-acanthocytosis: Homozygous 1-kb deletion in <i>VPS13A</i> detected by whole-genome sequencingSusan Walker, Rubina Dad, Bhooma Thiruvahindrapuram, et al.
Neurobiology of Disease|April 18, 2020
Expanding the search for genetic biomarkers of Parkinson's disease into the living brainSimon M Benoit, Hu Xu, Susanne Schmid, et al.
Plos One|June 12, 2019
Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel diseaseSvetlana Frenkel, Charles N Bernstein, Michael Sargent, et al.
Pageof 10

Showing results (1-10 of 95) with videos related to

Sort By:
Pageof 10
G3 (Bethesda, Md.)|January 10, 2019
Using Next-Generation Sequencing Transcriptomics To Determine Markers of Post-traumatic Symptoms: Preliminary Findings from a Post-deployment Cohort of SoldiersCathy Boscarino, Thomas Nalpathamkalam, Giovanna Pellecchia, et al.
Journal of the Endocrine Society|July 31, 2025
Influence of Polygenic Risk on Height and BMI in Adults With a 22q11.2 MicrodeletionShengjie Ying, Tracy Heung, Bernice E Morrow, et al.
Viruses|April 26, 2025
Genomic and Epidemiological Investigations Reveal Chromosomal Integration of the Acipenserid Herpesvirus 3 Genome in Lake Sturgeon <i>Acipenser fulvescens</i>Sharon Clouthier, Umberto Rosani, Arfa Khan, et al.
European Journal of Human Genetics : EJHG|November 27, 2023
Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescueBushra Haque, David Cheerie, Saba Birkadze, et al.
Pathogens (Basel, Switzerland)|September 28, 2023
A New Sturgeon Herpesvirus from Juvenile Lake Sturgeon <i>Acipenser fulvescens</i> Displaying Epithelial Skin LesionsSharon Clouthier, Marek Tomczyk, Tamara Schroeder, et al.
Plos One|June 24, 2014
Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular MalaysiaSiti Shuhada Mokhtar, Christian R Marshall, Maude E Phipps, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndromeErika Tavares, Chen Yu Tang, Anjali Vig, et al.
Neurology. Genetics|May 31, 2018
Chorea-acanthocytosis: Homozygous 1-kb deletion in <i>VPS13A</i> detected by whole-genome sequencingSusan Walker, Rubina Dad, Bhooma Thiruvahindrapuram, et al.
Neurobiology of Disease|April 18, 2020
Expanding the search for genetic biomarkers of Parkinson's disease into the living brainSimon M Benoit, Hu Xu, Susanne Schmid, et al.
Plos One|June 12, 2019
Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel diseaseSvetlana Frenkel, Charles N Bernstein, Michael Sargent, et al.
Pageof 10