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R Chao

Showing results (281-290 of 316) with videos related to

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Implementation Science : IS|May 12, 2025
A pragmatic randomized trial to compare strategies for implementing primary HPV testing for routine cervical cancer screening in a large healthcare systemChun R Chao, Nancy Cannizzaro, Erin E Hahn, et al.
Pediatric Blood & Cancer|October 29, 2022
"The simple life experiences that every other human gets": Desire for normalcy among adolescents and young adults with advanced cancerPuja J Umaretiya, Lauren Fisher, Andrea Altschuler, et al.
Ophthalmology. Retina|April 25, 2019
Thomas A. Swift's Electric Rifle Injuries to the Eye and Ocular Adnexa: The Management of Complex TraumaStavros N Moysidis, Nicole Koulisis, Damien C Rodger, et al.
Genome Research|May 15, 2024
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
International Journal of Cancer|February 24, 2025
Pregnancy and pregnancy outcomes after adolescent and young adult cancer in the AYA horizon studyHazel B Nichols, Chelsea Anderson, Christopher D Baggett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
HGG Advances|March 24, 2022
Biallelic variants in <i>TAMM41</i> are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial diseaseKyle Thompson, Lucas Bianchi, Francesca Rastelli, et al.
Human Mutation|March 10, 2022
seqr: A web-based analysis and collaboration tool for rare disease genomicsLynn S Pais, Hana Snow, Ben Weisburd, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 2, 2023
Recurrent de novo <i>SPTLC2</i> variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesisSafoora B Syeda, Museer A Lone, Payam Mohassel, et al.
Pageof 32

Showing results (281-290 of 316) with videos related to

Sort By:
Pageof 32
Implementation Science : IS|May 12, 2025
A pragmatic randomized trial to compare strategies for implementing primary HPV testing for routine cervical cancer screening in a large healthcare systemChun R Chao, Nancy Cannizzaro, Erin E Hahn, et al.
Pediatric Blood & Cancer|October 29, 2022
"The simple life experiences that every other human gets": Desire for normalcy among adolescents and young adults with advanced cancerPuja J Umaretiya, Lauren Fisher, Andrea Altschuler, et al.
Ophthalmology. Retina|April 25, 2019
Thomas A. Swift's Electric Rifle Injuries to the Eye and Ocular Adnexa: The Management of Complex TraumaStavros N Moysidis, Nicole Koulisis, Damien C Rodger, et al.
Genome Research|May 15, 2024
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
International Journal of Cancer|February 24, 2025
Pregnancy and pregnancy outcomes after adolescent and young adult cancer in the AYA horizon studyHazel B Nichols, Chelsea Anderson, Christopher D Baggett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
HGG Advances|March 24, 2022
Biallelic variants in <i>TAMM41</i> are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial diseaseKyle Thompson, Lucas Bianchi, Francesca Rastelli, et al.
Human Mutation|March 10, 2022
seqr: A web-based analysis and collaboration tool for rare disease genomicsLynn S Pais, Hana Snow, Ben Weisburd, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 2, 2023
Recurrent de novo <i>SPTLC2</i> variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesisSafoora B Syeda, Museer A Lone, Payam Mohassel, et al.
Pageof 32