1. A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia. (7th November 2020) Authors: Mahmood, Tariq; El-Asrag, Mohammed E; Poulter, James A; Cardno, Alastair G; Tomlinson, Anneka; Ahmed, Sophia; Al-Amri, Ahmed; Nazari, Jamshid; Neill, Joanna; Chamali, Rifka S; Kiwan, Nancy; Ghuloum, Suhaila; Alhaj, Hamid A; Randerson Moor, Juliette; Khan, Shabana; Al-Amin, Hassen; Johnson, Colin ... Journal: Schizophrenia bulletin Issue: Volume 47:Number 3(2021) Page Start: 796 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CFH, VEGF and HTRA1 promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration. Issue 2 (10th May 2011) Authors: McKibbin, Martin; Ali, Manir; Bansal, Shveta; Baxter, Paul D; West, Kumi; Williams, Grange; Cassidy, Frances; Inglehearn, Chris F Journal: British journal of ophthalmology Issue: Volume 96:Issue 2(2012) Page Start: 208 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Changing the status quo bias. Issue 7 (17th January 2011) Authors: Khan, Kamron N; Ali, Manir; Toomes, Carmel; Inglehearn, Chris F; Bradbury, John Journal: British journal of ophthalmology Issue: Volume 95:Issue 7(2011) Page Start: 1034 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021) Authors: Poulter, James A.; Gravett, Molly S. C.; Taylor, Rachel L.; Fujinami, Kaoru; De Zaeytijd, Julie; Bellingham, James; Rehman, Atta Ur; Hayashi, Takaaki; Kondo, Mineo; Rehman, Abdur; Ansar, Muhammad; Donnelly, Dan; Toomes, Carmel; Ali, Manir; De Baere, Elfride; Leroy, Bart P.; Davies, Nigel P.; Hend... Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: ii Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISM. Issue 3 (March 2018) Authors: Khan, Kamron N.; Lord, Emma C.; Arno, Gavin; Islam, Farrah; Carss, Keren J.; Raymond, FLucy; Toomes, Carmel; Ali, Manir; Inglehearn, Chris F.; Webster, Andrew R.; Moore, Anthony T.; Poulter, James A.; Michaelides, Michel Journal: Retina Issue: Volume 38:Issue 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. Issue 7 (5th May 2016) Authors: Al‐Amri, Ahmed; Saegh, Abeer Al; Al‐Mamari, Watfa; El‐Asrag, Mohammed E.; Ivorra, Jose L.; Cardno, Alastair G.; Inglehearn, Chris F.; Clapcote, Steven J.; Ali, Manir Journal: American journal of medical genetics Issue: Volume 170:Issue 7(2016) Page Start: 1826 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Matrix metalloproteinases in keratoconus – Too much of a good thing?. (May 2019) Authors: di Martino, Erica; Ali, Manir; Inglehearn, Chris F. Journal: Experimental eye research Issue: Volume 182(2019) Page Start: 137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene. Issue 8 (6th May 2019) Authors: Felden, Julia; Baumann, Britta; Ali, Manir; Audo, Isabelle; Ayuso, Carmen; Bocquet, Beatrice; Casteels, Ingele; Garcia‐Sandoval, Blanca; Jacobson, Samuel G.; Jurklies, Bernhard; Kellner, Ulrich; Kessel, Line; Lorenz, Birgit; McKibbin, Martin; Meunier, Isabelle; de Ravel, Thomy; Rosenberg, Thomas;... Journal: Human mutation Issue: Volume 40:Issue 8(2019) Page Start: 1145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. New variants and in silico analyses in GRK1 associated Oguchi disease. Issue 2 (30th November 2020) Authors: Poulter, James A.; Gravett, Molly S. C.; Taylor, Rachel L.; Fujinami, Kaoru; De Zaeytijd, Julie; Bellingham, James; Rehman, Atta Ur; Hayashi, Takaaki; Kondo, Mineo; Rehman, Abdur; Ansar, Muhammad; Donnelly, Dan; Toomes, Carmel; Ali, Manir; De Baere, Elfride; Leroy, Bart P.; Davies, Nigel P.; Hend... Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 164 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. New variants and in silico analyses in GRK1 associated Oguchi disease. Issue 2 (30th November 2020) Authors: Poulter, James A.; Gravett, Molly S. C.; Taylor, Rachel L.; Fujinami, Kaoru; De Zaeytijd, Julie; Bellingham, James; Rehman, Atta Ur; Hayashi, Takaaki; Kondo, Mineo; Rehman, Abdur; Ansar, Muhammad; Donnelly, Dan; Toomes, Carmel; Ali, Manir; De Baere, Elfride; Leroy, Bart P.; Davies, Nigel P.; Hend... Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 164 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗