1. Adherence and satisfaction in Argus II prosthesis users: a self determination theory model. (4th July 2022) Authors: Khan, Mariam; Branham, Kari; Jayasundera, Kanishka T.; Khan, Naheed W. Journal: Ophthalmic genetics Issue: Volume 43:Number 4(2022) Page Start: 462 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical trial design for neuroprotection in RHO autosomal dominant retinitis pigmentosa; outcome measure considerations. (4th March 2021) Authors: Otte, Benjamin; Andrews, Chris; Lacy, Gabrielle; Branham, Kari; Musch, David C.; Jayasundera, Kanishka T. Journal: Ophthalmic genetics Issue: Volume 42:Number 2(2021) Page Start: 170 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Issue 7 (14th April 2022) Authors: Solaki, Maria; Baumann, Britta; Reuter, Peggy; Andreasson, Sten; Audo, Isabelle; Ayuso, Carmen; Balousha, Ghassan; Benedicenti, Francesco; Birch, David; Bitoun, Pierre; Blain, Delphine; Bocquet, Beatrice; Branham, Kari; Català‐Mora, Jaume; De Baere, Elfride; Dollfus, Helene; Falana, Mohammed; Gio... Journal: Human mutation Issue: Volume 43:Issue 7(2022) Page Start: 832 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy. (3rd September 2017) Authors: Qian, Cynthia X.; Branham, Kari; Khan, Naheed; Lundy, Steven K.; Heckenlively, John R.; Jayasundera, Thiran Journal: Ophthalmic genetics Issue: Volume 38:Number 5(2017) Page Start: 467 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation. Issue 1 (30th September 2019) Authors: Weisschuh, Nicole; Sturm, Marc; Baumann, Britta; Audo, Isabelle; Ayuso, Carmen; Bocquet, Beatrice; Branham, Kari; Brooks, Brian P.; Catalá‐Mora, Jaume; Giorda, Roberto; Heckenlively, John R.; Hufnagel, Robert B.; Jacobson, Samuel G.; Kellner, Ulrich; Kitsiou‐Tzeli, Sofia; Matet, Alexandre; Martor... Journal: Human mutation Issue: Volume 41:Issue 1(2020) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Double hyperautofluorescent ring on fundus autofluorescence in ABCA4. (2nd January 2018) Authors: Abalem, Maria Fernanda; Qian, Cynthia X.; Branham, Kari; Schlegel, Dana; Fahim, Abigail T.; Khan, Naheed W.; Heckenlively, John R.; Jayasundera, K. Thiran Journal: Ophthalmic genetics Issue: Volume 39:Number 1(2018) Page Start: 87 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Erratum to: Worldwide Argus II implantation: recommendations to optimize patient outcomes. Issue 1 (December 2016) Authors: Ghodasra, Devon; Chen, Adrienne; Arevalo, J.; Birch, David; Branham, Kari; Coley, Brian; Dagnelie, Gislin; de Juan, Eugene; Devenyi, Robert; Dorn, Jessy; Fisher, Andy; Geruschat, Duane; Gregori, Ninel; Greenberg, Robert; Hahn, Paul; Ho, Allen; Howson, Ashley; Huang, Suber; Iezzi, Raymond; Khan, N... Journal: BMC ophthalmology Issue: Volume 16:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. (3rd April 2020) Authors: Ratnapriya, Rinki; Acar, İlhan E; Geerlings, Maartje J; Branham, Kari; Kwong, Alan; Saksens, Nicole T M; Pauper, Marc; Corominas, Jordi; Kwicklis, Madeline; Zipprer, David; Starostik, Margaret R; Othman, Mohammad; Yashar, Beverly; Abecasis, Goncalo R; Chew, Emily Y; Ferrington, Deborah A; Hoyng, ... Journal: Human molecular genetics Issue: Volume 29:Number 12(2020) Page Start: 2022 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic testing for inherited retinal degenerations: Triumphs and tribulations. Issue 3 (31st August 2020) Authors: Branham, Kari; Schlegel, Dana; Fahim, Abigail T.; Jayasundera, K. Thiran Other Names: Hufnagel Robert guestEditor.; Walter Michael guestEditor.; Arno Gavin guestEditor. Journal: American journal of medical genetics Issue: Volume 184:Issue 3(2020) Page Start: 571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsia. Issue 10 (22nd August 2018) Authors: Weisschuh, Nicole; Stingl, Katarina; Audo, Isabelle; Biskup, Saskia; Bocquet, Béatrice; Branham, Kari; Burstedt, Marie S; De Baere, Elfride; De Vries, Meindert J; Golovleva, Irina; Green, Andrew; Heckenlively, John; Leroy, Bart P; Meunier, Isabelle; Traboulsi, Elias; Wissinger, Bernd; Kohl, Susanne Journal: Human mutation Issue: Volume 39:Issue 10(2018) Page Start: 1366 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗