1. Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8. Issue 3 (20th June 2018) Authors: Fujinami, Kaoru; Strauss, Rupert W; Chiang, John (Pei-Wen); Audo, Isabelle S; Bernstein, Paul S; Birch, David G; Bomotti, Samantha M; Cideciyan, Artur V; Ervin, Ann-Margret; Marino, Meghan J; Sahel, José-Alain; Mohand-Said, Saddek; Sunness, Janet S; Traboulsi, Elias I; West, Sheila; Wojciechowski... Other Names: author non-byline.; Scholl Hendrik PN author non-byline.; Strauss Rupert W author non-byline.; Wolfson Yulia author non-byline.; Bittencourt Millena author non-byline.; Shah Syed Mahmood author non-byline.; Ahmed Mohamed author non-byline.; Schönbach Etienne author non-byline.; Fujinami Kaoru au... Journal: British journal of ophthalmology Issue: Volume 103:Issue 3(2019) Page Start: 390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutation. Issue 5 (19th April 2007) Authors: Jacobson, Samuel G; Sumaroka, Alexander; Aleman, Tomas S; Cideciyan, Artur V; Danciger, Michael; Farber, Debora B Journal: British journal of ophthalmology Issue: Volume 91:Issue 5(2007) Page Start: 699 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Improvement in vision: a new goal for treatment of hereditary retinal degenerations. (May 2015) Authors: Jacobson, Samuel G; Cideciyan, Artur V; Aguirre, Gustavo D; Roman, Alejandro J; Sumaroka, Alexander; Hauswirth, William W; Palczewski, Krzysztof Journal: Expert opinion on orphan drugs Issue: Volume 3:Number 5(2015:May) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP). (23rd December 2020) Authors: Moreno-Leon, Laura; West, Emma L; O'Hara-Wright, Michelle; Li, Linjing; Nair, Rohini; He, Jie; Anand, Manisha; Sahu, Bhubanananda; Chavali, Venkat Ramana Murthy; Smith, Alexander J; Ali, Robin R; Jacobson, Samuel G; Cideciyan, Artur V; Khanna, Hemant Journal: Human molecular genetics Issue: Volume 29:Number 22(2020) Page Start: 3706 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration. (25th October 2016) Authors: Charng, Jason; Cideciyan, Artur V; Jacobson, Samuel G; Sumaroka, Alexander; Schwartz, Sharon B; Swider, Malgorzata; Roman, Alejandro J; Sheplock, Rebecca; Anand, Manisha; Peden, Marc C; Khanna, Hemant; Heon, Elise; Wright, Alan F; Swaroop, Anand Journal: Human molecular genetics Issue: Volume 25:Number 24(2016:Dec. 15) Page Start: 5444 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗