Search | IOVS | ARVO Journals

iovs

Issues
Topics
For Authors
About
- Editorial Board

Journals Home

MANAGE ALERTS

Access Provided By:
MIT Libraries

Forgot password?

Create an Account

To View More...

Purchase this article with an account.

or

Subscribe Now

Issues
Topics
For Authors
About
- Editorial Board

Narrow View

NARROW

Content Type

Meeting Abstract (4)
Journal Articles (2)

Journal

Investigative Ophthalmology & Visual Science (6)

Article Type

ARVO Annual Meeting Abstract (4)
Genetics (2)

Topics

Cornea (2)
Eye Anatomy and Disorders (2)
Genetics (2)
Lens (1)
Visual Psychophysics and Physiological Optics (1)

Tags

congenital cataract (1)
corneal opacity (1)
family (1)
genetic heterogeneity (1)
keratoconus (1)
microcornea (1)
mutation (1)
mutation analysis (1)
myopia (1)

Specify Date Range

From: To: Apply

Showing 1 – 6 of 6

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract June 2024

Using long-read Nanopore sequencing to study the genetic basis of Fuchs Endothelial Corneal Dystrophy

Bushra Alayed; Christopher M Watson; Seema Anand; Salina Siddiqui; Chris F. Inglehearn; Manir Ali

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5785.

ARVO Annual Meeting Abstract June 2021

Myocilin mutations account for 5% of POAG in a West Yorkshire clinic

Danah Albuainain; Salina Siddiqui; Charlotte Onsiong; Mohammed El-Asrag; Peter Galloway; Chris Inglehearn; Manir Ali

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1502.

ARVO Annual Meeting Abstract June 2015

The role of genetic variants in TCF4 and LOXHD1 in Fuchs Endothelial Dystrophy in a UK Cohort

Chris Inglehearn; Salina Siddiqui; Aine Rice; Jose Ivorra; James Poulter; James Ball; Andrew Morrell; Nigel James; Carmel Toomes; Manir Ali

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2517.

ARVO Annual Meeting Abstract April 2014

Determining the genetic basis of familial Keratoconus by autozygosity mapping and whole exome sequencing

Layal Abi Farraj; Salina Siddiqui; Aine Rice; Gretta Abi-Sleymane; Carmel Toomes; Chris F Inglehearn; Manir Ali

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6410.

Genetics August 2013

Mutational Analysis of MIR184 in Sporadic Keratoconus and Myopia

PDF

Judith Lechner; Ha Ae Bae; Jasenka Guduric-Fuchs; Aine Rice; Gowthaman Govindarajan; Salina Siddiqui; Layal Abi Farraj; Shea Ping Yip; Maurice Yap; Manoranjan Das; Emmanuelle Souzeau; Doug Coster; Richard A. Mills; Richard Lindsay; Tony Phillips; Paul Mitchell; Manir Ali; Chris F. Inglehearn; Periasamy Sundaresan; Jamie E. Craig; David A. Simpson; Kathryn P. Burdon; Colin E. Willoughby
TAGS: keratoconus, mutation, mutation analysis, myopia
Invest. Ophthalmol. Vis. Sci.. 2013; 54(8):5266-5272. https://doi.org/10.1167/iovs.13-12035

Genetics June 2011

Genetic Heterogeneity for Recessively Inherited Congenital Cataract Microcornea with Corneal Opacity

PDF

Kamron Khan; Ahmed Al-Maskari; Martin McKibbin; Ian M. Carr; Adam Booth; Moin Mohamed; Salina Siddiqui; James A. Poulter; David A. Parry; Clara V. Logan; Anwar Hashmi; Tehseen Sahi; Hussain Jafri; Yasmin Raashid; Colin A. Johnson; Alex F. Markham; Carmel Toomes; Aine Rice; Eamonn Sheridan; Chris F. Inglehearn; Manir Ali
TAGS: congenital cataract, corneal opacity, genetic heterogeneity, microcornea, family
Invest. Ophthalmol. Vis. Sci.. 2011; 52(7):4294-4299. https://doi.org/10.1167/iovs.10-6776

Includes: Supplemental Content

« Previous

Advertisement

Follow @ARVOiovs

IOVS Home
Issues
Topics
For Authors
About
- Editorial Board

Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

JOURNALS HOME
TOPICS
ABOUT ARVO JOURNALS

Copyright © 2025 Association for Research in Vision and Ophthalmology.

Access Provided By:
MIT Libraries

Forgot password?

To View More...

Purchase this article with an account.

Create an Account

or

Subscribe Now

×

×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×

This site uses cookies. By continuing to use our website, you are agreeing to our privacy policy.Accept