Michel Michaelides

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 20

Top Topics

Heat Shock Protein

Artificial Intelligence

Top Venues

Ophthalmic genetics

The British journal of ophthalmology

Expert opinion on emerging drugs

This page only lists publications with an associated author ORCID identifier.

Publications

William Woof, Thales Antonio Cabral de Guimaraes, Saoud Al-Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga, Bernardo Mendes, Mital Shah, Paula Burke, David Parry, Siying Lin, Gunjan Naik, Biraja Ghoshal, Bart Liefers, Dun Jack Fu, Michalis Georgiou, Quang Nguyen, Alan Sousa da Silva, Yichen Liu, Yu Fujinami-Yokokawa, Nathaniel Kabiri, Dayyanah Sumodhee, Praveen J Patel, Jennifer Furman, Ismail Moghul, Juliana Maria Ferraz Sallum, Samantha Roshani De Silva, Birgit Lorenz, Frank G Holz, Kaoru Fujinami, Andrew R Webster, Omar A Mahroo, Susan M Downes, Savita Madhusudhan, Konstantinos Balaskas, Michel Michaelides, Nikolas Pontikos
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3000 Inherited Retinal Disease Patients from the United Kingdom. medRxiv : the preprint server for health sciences (2024)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Gernot Schließleder, Angelos Kalitzeos, Melissa Kasilian, Navjit Singh, Ziyuan Wang, Zhihong Jewel Hu, Manuel Großpötzl, SriniVas R Sadda, Andreas Wedrich, Michel Michaelides, Rupert W Strauss
Deep phenotyping of PROM1-associated retinal degeneration. The British journal of ophthalmology (2023)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Gernot Schließleder, Angelos Kalitzeos, Melissa Kasilian, Navjit Singh, Ziyuan Wang, Zhihong Jewel Hu, Manuel Großpötzl, SriniVas R Sadda, Andreas Wedrich, Michel Michaelides, Rupert W Strauss
Deep phenotyping of PROM1-associated retinal degeneration. The British journal of ophthalmology (2023)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Quang Nguyen, William Woof, Nathaniel Kabiri, Sagnik Sen, Malena Daich Varela, Thales Antonio Cabral de Guimaraes, Mital Shah, Dayyanah Sumodhee, Ismail Moghul, Saoud Al-Khuzaei, Yichen Liu, Catherine Hollyhead, Bhavna Tailor, Loy Lobo, Carl Veal, Stephen Archer, Jennifer Furman, Gavin Arno, Manuel Gomes, Kaoru Fujinami, Savita Madhusudhan, Omar A Mahroo, Andrew R Webster, Konstantinos Balaskas, Susan M Downes, Michel Michaelides, Nikolas Pontikos, null null
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene). BMJ open 13 (3) (2023)
Vanita Berry, Alexander Ionides, Michalis Georgiou, Roy A Quinlan, Michel Michaelides
Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British family. BMJ open ophthalmology 8 (1) (2023)
Gernot Schließleder, Angelos Kalitzeos, Melissa Kasilian, Navjit Singh, Ziyuan Wang, Zhihong Jewel Hu, Manuel Großpötzl, SriniVas R Sadda, Andreas Wedrich, Michel Michaelides, Rupert W Strauss
Deep phenotyping of PROM1-associated retinal degeneration. The British journal of ophthalmology (2023)
Gernot Schließleder, Angelos Kalitzeos, Melissa Kasilian, Navjit Singh, Ziyuan Wang, Zhihong Jewel Hu, Manuel Großpötzl, SriniVas R Sadda, Andreas Wedrich, Michel Michaelides, Rupert W Strauss
Deep phenotyping of PROM1-associated retinal degeneration. The British journal of ophthalmology (2023)
Anastasios Georgiadis, Alexander J Smith, Michel Michaelides, Stuart Naylor, Alexandria Forbes
Letter to the editor: 'Emerging gene therapy products for RPGR -associated X-linked retinitis pigmentosa'. Expert opinion on emerging drugs 27 (4) (2022)
Malena Daich Varela, Michel Michaelides
RDH12 retinopathy: clinical features, biology, genetics and future directions. Ophthalmic genetics (2022)
Vanita Berry, Kaoru Fujinami, Kiyofumi Mochizuki, Takeshi Iwata, Nikolas Pontikos, Roy A Quinlan, Michel Michaelides
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. Ophthalmic genetics 43 (5) (2022)
Declan C Murphy, Mohamed Katta, Catherine A Egan, Michel Michaelides, Louisa Wickham
Long-term vision outcomes for patients with albinism and diabetic retinopathy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 260 (7) (2022)
Anastasios Georgiadis, Alexander J Smith, Michel Michaelides, Stuart Naylor, Alexandria Forbes
Letter to the editor: 'Emerging gene therapy products for RPGR -associated X-linked retinitis pigmentosa'. Expert opinion on emerging drugs 27 (4) (2022)
Vanita Berry, Nikolas Pontikos, Alex Ionides, Angelos Kalitzeos, Roy A Quinlan, Michel Michaelides
Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataracts. Ophthalmic genetics (2021)
Serena Zaman, Thomas Kane, Mohamed Katta, Michalis Georgiou, Michel Michaelides
Photoaversion in inherited retinal diseases: clinical phenotypes, biological basis, and qualitative and quantitative assessment. Ophthalmic genetics 43 (2) (2021)
Austin D Igelman, Cristy Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena R Schiff, Byron L Lam, Eeva-Marja Sankila, Jeeyun Ahn, Lindsey Pyers, Ajoy Vincent, Juliana Maria Ferraz Sallum, Wadih M Zein, Jin Kyun Oh, Maldonado Ramiro S, Joseph Ryu, Stephen H Tsang, Michael B Gorin, Andrew R Webster, Michel Michaelides, Paul Yang, Mark E Pennesi
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic genetics 42 (6) (2021)
Vanita Berry, Alex Ionides, Nikolas Pontikos, Anthony T Moore, Roy A Quinlan, Michel Michaelides
Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts. Eye (London, England) (2021)
Bohdan Kousal, Filip Majer, Hana Vlaskova, Lenka Dvorakova, Lenka Piherová, Martin Meliska, Hana Langrová, Tomas Palecek, Milos Kubanek, Alice Krebsova, Jiri Gurka, Veronika Stara, Michel Michaelides, Tomáš Kalina, Jakub Sikora, Petra Liskova
Pigmentary retinopathy can indicate the presence of pathogenic LAMP2 variants even in somatic mosaic carriers with no additional signs of Danon disease. Acta ophthalmologica 99 (1) (2020)