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Brian P Brooks

Showing results (21-30 of 157) with videos related to

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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 9, 2006
Increased corneal thickness in patients with ocular colobomaJohnny Tang, Parag A Gokhale, Steven E Brooks, et al.
Ophthalmic Genetics|November 25, 2020
Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome"Julia Chertkof, Robert B Hufnagel, Delphine Blain, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
Loss of Hippo signaling causes transdifferentiation of neural retina between the optic fissure edges causing colobomaUma M Neelathi, Daniel Sanchez-Mendoza, Sydney Steele, et al.
European Journal of Human Genetics : EJHG|January 28, 2021
Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)-an updateAbdullah Aamir, Helen J Kuht, Karen Grønskov, et al.
Ophthalmic Genetics|August 14, 2020
Retinoschisis associated with Kearns-Sayre syndromeJulia Chertkof, Robert B Hufnagel, Delphine Blain, et al.
Ophthalmic Genetics|March 23, 2022
<i>De novo</i> frameshift mutation in <i>YAP1</i> associated with bilateral uveal coloboma and microphthalmiaCharles DeYoung, Bin Guan, Ehsan Ullah, et al.
Developmental Biology|September 2, 2015
nlz1 is required for cilia formation in zebrafish embryogenesisSunit Dutta, Shahila Sriskanda, Elangovan Boobalan, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 18, 2007
Optic nerve axon number in mouse is regulated by PAX2Ramakrishna P Alur, Terry A Cox, Mary Alice Crawford, et al.
BMC Ophthalmology|June 26, 2004
Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case reportBrian P Brooks, Robert Kleta, Rafael C Caruso, et al.
International Ophthalmology|July 23, 2025
Advances in machine learning for ABCA4-related retinopathy: segmentation and phenotypingYousif J Shwetar, Brian P Brooks, Brett G Jeffrey, et al.
Pageof 16

Showing results (21-30 of 157) with videos related to

Sort By:
Pageof 16
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 9, 2006
Increased corneal thickness in patients with ocular colobomaJohnny Tang, Parag A Gokhale, Steven E Brooks, et al.
Ophthalmic Genetics|November 25, 2020
Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome"Julia Chertkof, Robert B Hufnagel, Delphine Blain, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
Loss of Hippo signaling causes transdifferentiation of neural retina between the optic fissure edges causing colobomaUma M Neelathi, Daniel Sanchez-Mendoza, Sydney Steele, et al.
European Journal of Human Genetics : EJHG|January 28, 2021
Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)-an updateAbdullah Aamir, Helen J Kuht, Karen Grønskov, et al.
Ophthalmic Genetics|August 14, 2020
Retinoschisis associated with Kearns-Sayre syndromeJulia Chertkof, Robert B Hufnagel, Delphine Blain, et al.
Ophthalmic Genetics|March 23, 2022
<i>De novo</i> frameshift mutation in <i>YAP1</i> associated with bilateral uveal coloboma and microphthalmiaCharles DeYoung, Bin Guan, Ehsan Ullah, et al.
Developmental Biology|September 2, 2015
nlz1 is required for cilia formation in zebrafish embryogenesisSunit Dutta, Shahila Sriskanda, Elangovan Boobalan, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 18, 2007
Optic nerve axon number in mouse is regulated by PAX2Ramakrishna P Alur, Terry A Cox, Mary Alice Crawford, et al.
BMC Ophthalmology|June 26, 2004
Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case reportBrian P Brooks, Robert Kleta, Rafael C Caruso, et al.
International Ophthalmology|July 23, 2025
Advances in machine learning for ABCA4-related retinopathy: segmentation and phenotypingYousif J Shwetar, Brian P Brooks, Brett G Jeffrey, et al.
Pageof 16