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ARVO Annual Meeting Abstract June 2024

Identification of novel candidate genes for inherited retinal disorders in consanguineous families from Pakistan and Iran

Helen Nabiryo Frederiksen; Asad Munir; Ijaz Anwar; Sergey Oreshkov; Ainee Zafar; Ruth Choung; Abdur Rashid; Mukhtar Ullah; Asad Umar; Shumaila Zulfiqar; Humera Kausar; Fatemeh Suri; Atta Ur Rehman; Stylianos E. Antonarakis; Muhammad Ansar

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):1520.

ARVO Annual Meeting Abstract June 2023

A missense mutation in SLC6A6 impairs taurine transport and results in Leber congenital amaurosis with short cardiac atrioventricular conduction time

Mukhtar Ullah; Mathieu Quinodoz; Atta Ur Rehman; Madhur Shetty; Rosalie Grijalva; Giacomo Calzetti; Abdur Rashid; Sanaullah Jan; Alessandra Pia Porretta; L. Keith Henry; Andrea Superti-Furga; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4529.

ARVO Annual Meeting Abstract June 2020

Genetic Testing Identifies Known and Unknown Mutations in Iranian Families with Hereditary Retinal Diseases

Zeinab Ravesh; Arash Salmaninejad; Neda Sepahi; Atta Ur Rehman; Nicola Bedoni; Alireza Pasdar; Mathieu Quinodoz; Virginie Gisèle Peter; Majid Mojarrad; Ali Ghanbari Asad; Mehran Piran; Saman Ghalamkari; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2384.

ARVO Annual Meeting Abstract June 2020

Exploring the genetic landscape of inherited retinal diseases in North-Western Pakistan reveals a high degree of autozygosity and prevalent founder mutations

Atta Ur Rehman; Virginie Gisèle Peter; Mathieu Quinodoz; Abdur Rashid; Syed Akhtar Khan; Andrea Superti-Furga; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2385.

ARVO Annual Meeting Abstract July 2018

A rare chromosomal rearrangement in the X-linked opsin gene array is associated with retinal degeneration

Atta Ur Rehman; Quy Ai Ngo; Inmaculada Martin-Merida; Blanca Garcia-Sandoval; Carmen Ayuso; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5407.

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