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Kerry Goetz

Showing results (1-10 of 16) with videos related to

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Investigative Ophthalmology & Visual Science|August 2, 2014
Molecular diagnostic testing by eyeGENE: analysis of patients with hereditary retinal dystrophy phenotypes involving central vision lossAkhila Alapati, Kerry Goetz, John Suk, et al.
Scientific Reports|December 16, 2015
NGS-based Molecular diagnosis of 105 eyeGENE(®) probands with Retinitis PigmentosaZhongqi Ge, Kristen Bowles, Kerry Goetz, et al.
Investigative Ophthalmology & Visual Science|August 17, 2013
Prevalence of mutations in eyeGENE probands with a diagnosis of autosomal dominant retinitis pigmentosaLori S Sullivan, Sara J Bowne, Melissa J Reeves, et al.
Frontiers in Cell and Developmental Biology|January 11, 2021
Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal DystrophyShunbin Xu, Ardian Coku, Chithra K Muraleedharan, et al.
Clinical Trials (London, England)|June 18, 2016
Improving the value of clinical research through the use of Common Data ElementsJerry Sheehan, Steven Hirschfeld, Erin Foster, et al.
BMC Public Health|June 24, 2022
Correction: Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analysesCharisse Madlock-Brown, Ken Wilkens, Nicole Weiskopf, et al.
BMC Public Health|April 15, 2022
Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analysesCharisse Madlock-Brown, Ken Wilkens, Nicole Weiskopf, et al.
Plos Genetics|March 30, 2022
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 diseaseJana Zernant, Winston Lee, Jun Wang, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
The qMini assay identifies an overlooked class of splice variantsBin Guan, Chelsea Bender, Madhulatha Pantrangi, et al.
Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Investigative Ophthalmology & Visual Science|August 2, 2014
Molecular diagnostic testing by eyeGENE: analysis of patients with hereditary retinal dystrophy phenotypes involving central vision lossAkhila Alapati, Kerry Goetz, John Suk, et al.
Scientific Reports|December 16, 2015
NGS-based Molecular diagnosis of 105 eyeGENE(®) probands with Retinitis PigmentosaZhongqi Ge, Kristen Bowles, Kerry Goetz, et al.
Investigative Ophthalmology & Visual Science|August 17, 2013
Prevalence of mutations in eyeGENE probands with a diagnosis of autosomal dominant retinitis pigmentosaLori S Sullivan, Sara J Bowne, Melissa J Reeves, et al.
Frontiers in Cell and Developmental Biology|January 11, 2021
Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal DystrophyShunbin Xu, Ardian Coku, Chithra K Muraleedharan, et al.
Clinical Trials (London, England)|June 18, 2016
Improving the value of clinical research through the use of Common Data ElementsJerry Sheehan, Steven Hirschfeld, Erin Foster, et al.
BMC Public Health|June 24, 2022
Correction: Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analysesCharisse Madlock-Brown, Ken Wilkens, Nicole Weiskopf, et al.
BMC Public Health|April 15, 2022
Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analysesCharisse Madlock-Brown, Ken Wilkens, Nicole Weiskopf, et al.
Plos Genetics|March 30, 2022
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 diseaseJana Zernant, Winston Lee, Jun Wang, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
The qMini assay identifies an overlooked class of splice variantsBin Guan, Chelsea Bender, Madhulatha Pantrangi, et al.
Biorxiv : the Preprint Server for Biology|February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseasesShu Wen, Meng Wang, Xinye Qian, et al.
Pageof 2