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Jamie E Craig

Showing results (181-190 of 352) with videos related to

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Human Mutation|December 21, 2012
Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian familyKate J Laurie, Alpana Dave, Tania Straga, et al.
American Journal of Medical Genetics. Part A|November 24, 2020
Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Francesca Pasutto, et al.
JAMA Ophthalmology|November 21, 2024
Predictive Power of Polygenic Risk Scores for Intraocular Pressure or Vertical Cup-Disc RatioWeixiong He, Samantha Sze-Yee Lee, Santiago Diaz Torres, et al.
Investigative Ophthalmology & Visual Science|May 8, 2009
Heritability of central corneal thickness in nuclear familiesJohn A Landers, Alex W Hewitt, David P Dimasi, et al.
International Journal of Molecular Sciences|April 12, 2022
Identifying Genetic Biomarkers Predicting Response to Anti-Vascular Endothelial Growth Factor Injections in Diabetic Macular EdemaRajya L Gurung, Liesel M FitzGerald, Ebony Liu, et al.
Clinical & Experimental Ophthalmology|November 3, 2010
Rationale, methods and baseline demographics of the Bhaktapur Glaucoma StudySuman S Thapa, Pooja P Rana, Shankhar N Twayana, et al.
The Journal of Clinical Investigation|December 1, 2022
Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucomaHaojie Fu, Owen M Siggs, Lachlan Sw Knight, et al.
BMC Ophthalmology|March 1, 2022
The effect of insulin on response to intravitreal anti-VEGF injection in diabetic macular edema in type 2 diabetes mellitusRajya L Gurung, Liesel M FitzGerald, Ebony Liu, et al.
JAMA Ophthalmology|July 15, 2021
Association of Monogenic and Polygenic Risk With the Prevalence of Open-Angle GlaucomaOwen M Siggs, Xikun Han, Ayub Qassim, et al.
Genome Research|October 6, 2009
Rapid inexpensive genome-wide association using pooled whole bloodJamie E Craig, Alex W Hewitt, Amy E McMellon, et al.
Pageof 36

Showing results (181-190 of 352) with videos related to

Sort By:
Pageof 36
Human Mutation|December 21, 2012
Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian familyKate J Laurie, Alpana Dave, Tania Straga, et al.
American Journal of Medical Genetics. Part A|November 24, 2020
Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variantsEmmanuelle Souzeau, Owen M Siggs, Francesca Pasutto, et al.
JAMA Ophthalmology|November 21, 2024
Predictive Power of Polygenic Risk Scores for Intraocular Pressure or Vertical Cup-Disc RatioWeixiong He, Samantha Sze-Yee Lee, Santiago Diaz Torres, et al.
Investigative Ophthalmology & Visual Science|May 8, 2009
Heritability of central corneal thickness in nuclear familiesJohn A Landers, Alex W Hewitt, David P Dimasi, et al.
International Journal of Molecular Sciences|April 12, 2022
Identifying Genetic Biomarkers Predicting Response to Anti-Vascular Endothelial Growth Factor Injections in Diabetic Macular EdemaRajya L Gurung, Liesel M FitzGerald, Ebony Liu, et al.
Clinical & Experimental Ophthalmology|November 3, 2010
Rationale, methods and baseline demographics of the Bhaktapur Glaucoma StudySuman S Thapa, Pooja P Rana, Shankhar N Twayana, et al.
The Journal of Clinical Investigation|December 1, 2022
Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucomaHaojie Fu, Owen M Siggs, Lachlan Sw Knight, et al.
BMC Ophthalmology|March 1, 2022
The effect of insulin on response to intravitreal anti-VEGF injection in diabetic macular edema in type 2 diabetes mellitusRajya L Gurung, Liesel M FitzGerald, Ebony Liu, et al.
JAMA Ophthalmology|July 15, 2021
Association of Monogenic and Polygenic Risk With the Prevalence of Open-Angle GlaucomaOwen M Siggs, Xikun Han, Ayub Qassim, et al.
Genome Research|October 6, 2009
Rapid inexpensive genome-wide association using pooled whole bloodJamie E Craig, Alex W Hewitt, Amy E McMellon, et al.
Pageof 36