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Alex W Hewitt

Showing results (321-330 of 425) with videos related to

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Ophthalmology. Glaucoma|December 14, 2020
A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home TonometryAyub Qassim, Sean Mullany, Mona S Awadalla, et al.
Plos Genetics|May 21, 2010
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessYi Lu, David P Dimasi, Pirro G Hysi, et al.
Nature Communications|June 9, 2023
A village in a dish model system for population-scale hiPSC studiesDrew R Neavin, Angela M Steinmann, Nona Farbehi, et al.
BMC Medical Genomics|July 25, 2018
Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritisElisabeth De Smit, Samuel W Lukowski, Lisa Anderson, et al.
Developmental Cell|February 14, 2024
Wnt dose escalation during the exit from pluripotency identifies tranilast as a regulator of cardiac mesodermZhixuan Wu, Sophie Shen, Dalia Mizikovsky, et al.
Neuropsychologia|October 1, 2008
Genetic influences on handedness: data from 25,732 Australian and Dutch twin familiesSarah E Medland, David L Duffy, Margaret J Wright, et al.
Nature|December 13, 2023
The landscape of genomic structural variation in Indigenous AustraliansAndre L M Reis, Melissa Rapadas, Jillian M Hammond, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
Clinical & Experimental Ophthalmology|December 17, 2011
Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentEmmanuelle Souzeau, Ivan Goldberg, Paul R Healey, et al.
JAMA Ophthalmology|January 18, 2019
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital GlaucomaOwen M Siggs, Emmanuelle Souzeau, Francesca Pasutto, et al.
Pageof 43

Showing results (321-330 of 425) with videos related to

Sort By:
Pageof 43
Ophthalmology. Glaucoma|December 14, 2020
A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home TonometryAyub Qassim, Sean Mullany, Mona S Awadalla, et al.
Plos Genetics|May 21, 2010
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessYi Lu, David P Dimasi, Pirro G Hysi, et al.
Nature Communications|June 9, 2023
A village in a dish model system for population-scale hiPSC studiesDrew R Neavin, Angela M Steinmann, Nona Farbehi, et al.
BMC Medical Genomics|July 25, 2018
Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritisElisabeth De Smit, Samuel W Lukowski, Lisa Anderson, et al.
Developmental Cell|February 14, 2024
Wnt dose escalation during the exit from pluripotency identifies tranilast as a regulator of cardiac mesodermZhixuan Wu, Sophie Shen, Dalia Mizikovsky, et al.
Neuropsychologia|October 1, 2008
Genetic influences on handedness: data from 25,732 Australian and Dutch twin familiesSarah E Medland, David L Duffy, Margaret J Wright, et al.
Nature|December 13, 2023
The landscape of genomic structural variation in Indigenous AustraliansAndre L M Reis, Melissa Rapadas, Jillian M Hammond, et al.
JAMA Ophthalmology|September 30, 2018
Myocilin Gene Gln368Ter Variant Penetrance and Association With Glaucoma in Population-Based and Registry-Based StudiesXikun Han, Emmanuelle Souzeau, Jue-Sheng Ong, et al.
Clinical & Experimental Ophthalmology|December 17, 2011
Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitmentEmmanuelle Souzeau, Ivan Goldberg, Paul R Healey, et al.
JAMA Ophthalmology|January 18, 2019
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital GlaucomaOwen M Siggs, Emmanuelle Souzeau, Francesca Pasutto, et al.
Pageof 43