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Plos Genetics
|
May 7, 2024
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
Nihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, et al.
Molecular Biology and Evolution
|
August 15, 2019
Sequenceserver: A Modern Graphical User Interface for Custom BLAST Databases
Anurag Priyam, Ben J Woodcroft, Vivek Rai, et al.
JAMA Ophthalmology
|
March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity
Siyin Liu, Amanda N Sadan, Nihar Bhattacharyya, et al.
Ophthalmology Science
|
July 31, 2025
Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases
Gunjan Naik, Saoud Al-Khuzaei, Ismail Moghul, et al.
Bioinformatics (Oxford, England)
|
March 24, 2017
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data
Nikolas Pontikos, Jing Yu, Ismail Moghul, et al.
BMJ Open
|
March 20, 2023
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene)
Quang Nguyen, William Woof, Nathaniel Kabiri, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 8, 2024
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom
William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Ophthalmology Science
|
February 3, 2025
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom
William A Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations
William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Nature Machine Intelligence
|
June 26, 2025
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene
Nikolas Pontikos, William A Woof, Siying Lin, et al.
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Search research articles
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Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Plos Genetics
|
May 7, 2024
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
Nihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, et al.
Molecular Biology and Evolution
|
August 15, 2019
Sequenceserver: A Modern Graphical User Interface for Custom BLAST Databases
Anurag Priyam, Ben J Woodcroft, Vivek Rai, et al.
JAMA Ophthalmology
|
March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity
Siyin Liu, Amanda N Sadan, Nihar Bhattacharyya, et al.
Ophthalmology Science
|
July 31, 2025
Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases
Gunjan Naik, Saoud Al-Khuzaei, Ismail Moghul, et al.
Bioinformatics (Oxford, England)
|
March 24, 2017
Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data
Nikolas Pontikos, Jing Yu, Ismail Moghul, et al.
BMJ Open
|
March 20, 2023
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene)
Quang Nguyen, William Woof, Nathaniel Kabiri, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 8, 2024
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom
William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Ophthalmology Science
|
February 3, 2025
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom
William A Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations
William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei, et al.
Nature Machine Intelligence
|
June 26, 2025
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene
Nikolas Pontikos, William A Woof, Siying Lin, et al.
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of 5