Hasil Pencarian - Nikolas Pontikos
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Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophy oleh Michalis Georgiou, Naser Ali, Elizabeth Yang, Parampal S. Grewal, Tryfon Rotsos, Nikolas Pontikos, Anthony G. Robson, Michel Michaelides
Diterbitkan 2021-03-01Dapatkan teks lengkap
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Frequency and distribution of corneal astigmatism and keratometry features in adult life: Methodology and findings of the UK Biobank study. oleh Nikolas Pontikos, Sharon Chua, Paul J Foster, Stephen J Tuft, Alexander C Day, UK Biobank Eye and Vision Consortium
Diterbitkan 2019-01-01Dapatkan teks lengkap
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The Human Salivary Microbiome Is Shaped by Shared Environment Rather than Genetics: Evidence from a Large Family of Closely Related Individuals oleh Liam Shaw, Andre L. R. Ribeiro, Adam P. Levine, Nikolas Pontikos, Francois Balloux, Anthony W. Segal, Adam P. Roberts, Andrew M. Smith
Diterbitkan 2017-11-01Dapatkan teks lengkap
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One- and two-year visual outcomes from the Moorfields age-related macular degeneration database: a retrospective cohort study and an open science resource oleh Praveen Patel, Livia Faes, Siegfried Wagner, Dun Jack Fu, Katrin Fasler, Gabriella Moraes, Karsten U Kortuem, Reena Chopra, Gabriella Preston, Nikolas Pontikos
Diterbitkan 2019-06-01Dapatkan teks lengkap
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Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques oleh Yu Fujinami-Yokokawa, Nikolas Pontikos, Lizhu Yang, Kazushige Tsunoda, Kazutoshi Yoshitake, Takeshi Iwata, Hiroaki Miyata, Kaoru Fujinami, on behalf of Japan Eye Genetics Consortium
Diterbitkan 2019-01-01Dapatkan teks lengkap
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7
Predicting sex from retinal fundus photographs using automated deep learning oleh Edward Korot, Nikolas Pontikos, Xiaoxuan Liu, Siegfried K. Wagner, Livia Faes, Josef Huemer, Konstantinos Balaskas, Alastair K. Denniston, Anthony Khawaja, Pearse A. Keane
Diterbitkan 2021-05-01Dapatkan teks lengkap
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Phenogenon: Gene to phenotype associations for rare genetic diseases. oleh Nikolas Pontikos, Cian Murphy, Ismail Moghul, Gavin Arno, Kaoru Fujinami, Yu Fujinami, Dayyanah Sumodhee, Susan Downes, Andrew Webster, Jing Yu, UK Inherited Retinal Dystrophy Consortium, Phenopolis Consortium
Diterbitkan 2020-01-01Dapatkan teks lengkap
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10
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility Study oleh Rose M Gilbert, Dayyanah Sumodhee, Nikolas Pontikos, Catherine Hollyhead, Angus Patrick, Samuel Scarles, Sabrina Van Der Smissen, Rodrigo M Young, Nick Nettleton, Andrew R Webster, Jocelyn Cammack
Diterbitkan 2022-01-01Dapatkan teks lengkap
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11
Evaluating the Effects of C3 Inhibition on Geographic Atrophy Progression from Deep-Learning OCT Quantification: A Split-Person Study oleh Dun Jack Fu, Veronika Lipkova, Bart Liefers, Sophie Glinton, Livia Faes, Alex McKeown, Lukas Scheibler, Nikolas Pontikos, Praveen J. Patel, Gongyu Zhang, Pearse A. Keane, Konstantinos Balaskas
Diterbitkan 2023-09-01Dapatkan teks lengkap
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OP-3 Personalised model to predict keratoconus progression from demographic, topographic and genetic data oleh Pirro Hysi, Stephen J Tuft, Nikolas Pontikos, Bruce D Allan, Alison J Hardcastle, Olivia Li, Howard P Maile, Mary D Fortune, Patrick J Royston, Marcello T Leucci, Daniel M Gore
Diterbitkan 2022-05-01Artikel -
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Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus oleh Valentina Cipriani, Raquel S. Silva, Gavin Arno, Nikolas Pontikos, Ambreen Kalhoro, Sandra Valeina, Inna Inashkina, Mareta Audere, Katrina Rutka, Bernard Puech, Michel Michaelides, Veronica van Heyningen, Baiba Lace, Andrew R. Webster, Anthony T. Moore
Diterbitkan 2017-08-01Dapatkan teks lengkap
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14
Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review oleh Howard Maile, Ji-Peng Olivia Li, Daniel Gore, Marcello Leucci, Padraig Mulholland, Scott Hau, Anita Szabo, Ismail Moghul, Konstantinos Balaskas, Kaoru Fujinami, Pirro Hysi, Alice Davidson, Petra Liskova, Alison Hardcastle, Stephen Tuft, Nikolas Pontikos
Diterbitkan 2021-12-01Dapatkan teks lengkap
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Author Correction: Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder oleh Roberto Bonelli, Victoria E. Jackson, Aravind Prasad, Jacob E. Munro, Samaneh Farashi, Tjebo F. C. Heeren, Nikolas Pontikos, Lea Scheppke, Martin Friedlander, MacTel Consortium, Catherine A. Egan, Rando Allikmets, Brendan R. E. Ansell, Melanie Bahlo
Diterbitkan 2021-04-01Dapatkan teks lengkap
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Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder oleh Roberto Bonelli, Victoria E. Jackson, Aravind Prasad, Jacob E. Munro, Samaneh Farashi, Tjebo F. C. Heeren, Nikolas Pontikos, Lea Scheppke, Martin Friedlander, MacTel Consortium, Catherine A. Egan, Rando Allikmets, Brendan R. E. Ansell, Melanie Bahlo
Diterbitkan 2021-03-01Dapatkan teks lengkap
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AlzEye: longitudinal record-level linkage of ophthalmic imaging and hospital admissions of 353 157 patients in London, UK oleh Mario Cortina-Borja, Axel Petzold, Pearse A Keane, Steffen Erhard Petersen, Jugnoo S Rahi, Alastair K Denniston, Daniel C Alexander, Konstantinos Balaskas, Xiaoxuan Liu, Nikolas Pontikos, Hugh Montgomery, Robbert Struyven, Siegfried Karl Wagner, Fintan Hughes, Eric Topol, Jack Hindley
Diterbitkan 2022-03-01Dapatkan teks lengkap
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Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies oleh Shirleny R. Cardoso, Alicia C.M. Ellison, Amanda J. Walne, David Cassiman, Manoj Raghavan, Bhuvan Kishore, Philip Ancliff, Carmen Rodríguez-Vigil, Bieke Dobbels, Ana Rio-Machin, Ahad F.H. Al Seraihi, Nikolas Pontikos, Hemanth Tummala, Tom Vulliamy, Inderjeet Dokal
Diterbitkan 2017-08-01Dapatkan teks lengkap
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Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping. oleh Chris Wallace, Antony J Cutler, Nikolas Pontikos, Marcin L Pekalski, Oliver S Burren, Jason D Cooper, Arcadio Rubio García, Ricardo C Ferreira, Hui Guo, Neil M Walker, Deborah J Smyth, Stephen S Rich, Suna Onengut-Gumuscu, Stephen J Sawcer, Maria Ban, Sylvia Richardson, John A Todd, Linda S Wicker
Diterbitkan 2015-06-01Dapatkan teks lengkap
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Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease. oleh Nihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, Amanda N Sadan, Anita Szabo, Christina Zarouchlioti, Jana Jedlickova, Szi Kay Leung, Tianyi Liao, Lubica Dudakova, Pavlina Skalicka, Mohit Parekh, Ismail Moghul, Aaron R Jeffries, Michael E Cheetham, Kirithika Muthusamy, Alison J Hardcastle, Nikolas Pontikos, Petra Liskova, Stephen J Tuft, Alice E Davidson
Diterbitkan 2024-05-01Dapatkan teks lengkap
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