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Author/Creator Pontikos, Nikolas

2. A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract. (4th March 2018)

Authors:
Berry, Vanita; Pontikos, Nikolas; Albarca-Aguilera, Monica; Plagnol, Vincent; Massouras, Andreas; Prescott, DeQuincy; Moore, Anthony T.; Arno, Gavin; Cheetham, Michael E.; Michaelides, Michel
Journal:
Ophthalmic genetics
Issue:
Volume 39:Number 2(2018)
Page Start:
236
Record Type:
Journal Article
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4. Automated deep learning design for medical image classification by health-care professionals with no coding experience: a feasibility study. Issue 5 (September 2019)

Authors:
Faes, Livia; Wagner, Siegfried K; Fu, Dun Jack; Liu, Xiaoxuan; Korot, Edward; Ledsam, Joseph R; Back, Trevor; Chopra, Reena; Pontikos, Nikolas; Kern, Christoph; Moraes, Gabriella; Schmid, Martin K; Sim, Dawn; Balaskas, Konstantinos; Bachmann, Lucas M; Denniston, Alastair K; Keane, Pearse A
Journal:
Lancet
Issue:
Volume 1:Issue 5(2019)
Page Start:
e232
Record Type:
Journal Article
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5. Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). Issue 3 (20th March 2023)

Authors:
Nguyen, Quang; Woof, William; Kabiri, Nathaniel; Sen, Sagnik; Daich Varela, Malena; Cabral De Guimaraes, Thales Antonio; Shah, Mital; Sumodhee, Dayyanah; Moghul, Ismail; Al-Khuzaei, Saoud; Liu, Yichen; Hollyhead, Catherine; Tailor, Bhavna; Lobo, Loy; Veal, Carl; Archer, Stephen; Furman, Jennifer;...
Other Names:
author non-byline.; Hollyhead Catherine author non-byline.; Tailor Bhavna author non-byline.; Lobo Loy author non-byline.; Veal Carl author non-byline.; Archer Stephen author non-byline.
Journal:
BMJ open
Issue:
Volume 13:Issue 3(2023)
Page Start:
Record Type:
Journal Article
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6. Clinical and genetic characteristics of 10 Japanese patients with PROM1‐associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population. Issue 3 (20th August 2020)

Authors:
Fujinami, Kaoru; Oishi, Akio; Yang, Lizhu; Arno, Gavin; Pontikos, Nikolas; Yoshitake, Kazutoshi; Fujinami‐Yokokawa, Yu; Liu, Xiao; Hayashi, Takaaki; Katagiri, Satoshi; Mizobuchi, Kei; Mizota, Atsushi; Shinoda, Kei; Nakamura, Natsuko; Kurihara, Toshihide; Tsubota, Kazuo; Miyake, Yozo; Iwata, Takes...
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:
656
Record Type:
Journal Article
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7. Clinically relevant deep learning for detection and quantification of geographic atrophy from optical coherence tomography: a model development and external validation study. Issue 10 (October 2021)

Authors:
Zhang, Gongyu; Fu, Dun Jack; Liefers, Bart; Faes, Livia; Glinton, Sophie; Wagner, Siegfried; Struyven, Robbert; Pontikos, Nikolas; Keane, Pearse A; Balaskas, Konstantinos
Journal:
Lancet
Issue:
Volume 3:Issue 10(2021)
Page Start:
e665
Record Type:
Journal Article
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8. Elevation in Cell Cycle and Protein Metabolism Gene Transcription in Inactive Colonic Tissue From Icelandic Patients With Ulcerative Colitis. Issue 2 (10th January 2019)

Authors:
Vinayaga-Pavan, Mathena; Frampton, Matthew; Pontikos, Nikolas; Levine, Adam P; Smith, Phillip J; Jonasson, Jon G; Björnsson, Einar S; Segal, Anthony W; Smith, Andrew M
Journal:
Inflammatory bowel diseases
Issue:
Volume 25:Issue 2(2019)
Page Start:
Record Type:
Journal Article
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9. Elevation in Cell Cycle and Protein Metabolism Gene Transcription in Inactive Colonic Tissue From Icelandic Patients With Ulcerative Colitis. Issue 2 (19th November 2018)

Authors:
Vinayaga-Pavan, Mathena; Frampton, Matthew; Pontikos, Nikolas; Levine, Adam P; Smith, Phillip J; Jonasson, Jon G; Björnsson, Einar S; Segal, Anthony W; Smith, Andrew M
Journal:
Inflammatory bowel diseases
Issue:
Volume 25:Issue 2(2019)
Page Start:
317
Record Type:
Journal Article
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10. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities. (2nd November 2017)

Authors:
Cipriani, Valentina; Kalhoro, Ambreen; Arno, Gavin; Silva, Raquel S.; Pontikos, Nikolas; Puech, Virginie; McClements, Michelle E.; Hunt, David M.; van Heyningen, Veronica; Michaelides, Michel; Webster, Andrew R.; Moore, Anthony T.; Puech, Bernard
Journal:
Ophthalmic genetics
Issue:
Volume 38:Number 6(2017)
Page Start:
511
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗