OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Bardet-Biedl syndrome-7 (BBS7) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate model
Tomas S. Alemán, Erin O'Neil, Keli O’Connor, et al.
Ophthalmic Genetics (2021) Vol. 42, Iss. 3, pp. 252-265
Open Access | Times Cited: 15
Tomas S. Alemán, Erin O'Neil, Keli O’Connor, et al.
Ophthalmic Genetics (2021) Vol. 42, Iss. 3, pp. 252-265
Open Access | Times Cited: 15
Showing 15 citing articles:
Nonhuman primate genetic models for the study of rare diseases
Eric J. Vallender, Charlotte E. Hotchkiss, Anne D. Lewis, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 19
Eric J. Vallender, Charlotte E. Hotchkiss, Anne D. Lewis, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 19
New-Onset Type 1 Diabetes in a Child with Joubert Syndrome: A Rare Endocrine Complication
Yutaka Furuta, Erica T. Nelson, Rory J. Tinker, et al.
Reports — Medical Cases Images and Videos (2025) Vol. 8, Iss. 2, pp. 57-57
Open Access
Yutaka Furuta, Erica T. Nelson, Rory J. Tinker, et al.
Reports — Medical Cases Images and Videos (2025) Vol. 8, Iss. 2, pp. 57-57
Open Access
Comparative Natural History of Visual Function From Patients With Biallelic Variants inBBS1andBBS10
Monika K. Grudzinska Pechhacker, Samuel G. Jacobson, Arlene V. Drack, et al.
Investigative Ophthalmology & Visual Science (2021) Vol. 62, Iss. 15, pp. 26-26
Open Access | Times Cited: 20
Monika K. Grudzinska Pechhacker, Samuel G. Jacobson, Arlene V. Drack, et al.
Investigative Ophthalmology & Visual Science (2021) Vol. 62, Iss. 15, pp. 26-26
Open Access | Times Cited: 20
Adaptive optics imaging in inherited retinal diseases: A scoping review of the clinical literature
Alexis Ceecee Britten‐Jones, Lawrence Thai, Jeremy P.M. Flanagan, et al.
Survey of Ophthalmology (2023) Vol. 69, Iss. 1, pp. 51-66
Open Access | Times Cited: 8
Alexis Ceecee Britten‐Jones, Lawrence Thai, Jeremy P.M. Flanagan, et al.
Survey of Ophthalmology (2023) Vol. 69, Iss. 1, pp. 51-66
Open Access | Times Cited: 8
Ophthalmic and Genetic Features of Bardet Biedl Syndrome in a German Cohort
Fadi Nasser, Susanne Kohl, Anne Kurtenbach, et al.
Genes (2022) Vol. 13, Iss. 7, pp. 1218-1218
Open Access | Times Cited: 11
Fadi Nasser, Susanne Kohl, Anne Kurtenbach, et al.
Genes (2022) Vol. 13, Iss. 7, pp. 1218-1218
Open Access | Times Cited: 11
Near-Infrared Autofluorescence: Early Detection of Retinal Pigment Epithelial Alterations in Inherited Retinal Dystrophies
Simone Kellner, Silke Weinitz, Ghazaleh Farmand, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 22, pp. 6886-6886
Open Access | Times Cited: 2
Simone Kellner, Silke Weinitz, Ghazaleh Farmand, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 22, pp. 6886-6886
Open Access | Times Cited: 2
Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model
Sara Mayer, Jacintha Thomas, Megan Helms, et al.
Disease Models & Mechanisms (2022) Vol. 15, Iss. 9
Open Access | Times Cited: 10
Sara Mayer, Jacintha Thomas, Megan Helms, et al.
Disease Models & Mechanisms (2022) Vol. 15, Iss. 9
Open Access | Times Cited: 10
Molecular mechanisms of the obesity associated with Bardet‐Biedl syndrome: An update
Banghua Zhong, Ning Nie, Ming Dong
Obesity Reviews (2024)
Open Access | Times Cited: 1
Banghua Zhong, Ning Nie, Ming Dong
Obesity Reviews (2024)
Open Access | Times Cited: 1
Syndromic Retinitis Pigmentosa
Jessica S. Karuntu, Hind Almushattat, Xuan‐Thanh‐An Nguyen, et al.
Progress in Retinal and Eye Research (2024), pp. 101324-101324
Open Access | Times Cited: 1
Jessica S. Karuntu, Hind Almushattat, Xuan‐Thanh‐An Nguyen, et al.
Progress in Retinal and Eye Research (2024), pp. 101324-101324
Open Access | Times Cited: 1
A Genotype–Phenotype Analysis of the Bardet–Biedl Syndrome in Puerto Rico
Gabriel Guardiola, Fabiola Ramos, Natalio Izquierdo, et al.
Clinical ophthalmology (2021) Vol. Volume 15, pp. 3757-3764
Open Access | Times Cited: 9
Gabriel Guardiola, Fabiola Ramos, Natalio Izquierdo, et al.
Clinical ophthalmology (2021) Vol. Volume 15, pp. 3757-3764
Open Access | Times Cited: 9
Detailed phenotype and long-term follow-up of RAB28- associated cone-rod dystrophy
Nitya T. Rao, Alexander Sumaroka, Arlene J. Santos, et al.
Ophthalmic Genetics (2024) Vol. 45, Iss. 5, pp. 506-515
Closed Access | Times Cited: 1
Nitya T. Rao, Alexander Sumaroka, Arlene J. Santos, et al.
Ophthalmic Genetics (2024) Vol. 45, Iss. 5, pp. 506-515
Closed Access | Times Cited: 1
A CASE OF ALSTRÖM SYNDROME WITH A NOVEL VARIANT IN ALMS1 GENE PRESENTING WITH CONE ROD DYSTROPHY AS FIRST FINDING
B. Lin Ju Yen, Mukaddes Damla Çiftçi, Filiz Afrashı, et al.
Retinal Cases & Brief Reports (2024) Vol. 19, Iss. 3, pp. 413-417
Closed Access
B. Lin Ju Yen, Mukaddes Damla Çiftçi, Filiz Afrashı, et al.
Retinal Cases & Brief Reports (2024) Vol. 19, Iss. 3, pp. 413-417
Closed Access
Generation and characterization of Ccdc28b mutant mice links the Bardet-Biedl associated gene with mild social behavioral phenotypes
Matias Fábregat, Sofía Niño-Rivero, Sabrina Pose, et al.
PLoS Genetics (2022) Vol. 18, Iss. 6, pp. e1009896-e1009896
Open Access | Times Cited: 2
Matias Fábregat, Sofía Niño-Rivero, Sabrina Pose, et al.
PLoS Genetics (2022) Vol. 18, Iss. 6, pp. e1009896-e1009896
Open Access | Times Cited: 2
NPHP1 FULL DELETION CAUSES NEPHRONOPHTHISIS AND A CONE–ROD DYSTROPHY
Zujaja Tauqeer, Erin O'Neil, Alexander J. Brucker, et al.
Retinal Cases & Brief Reports (2021)
Closed Access | Times Cited: 2
Zujaja Tauqeer, Erin O'Neil, Alexander J. Brucker, et al.
Retinal Cases & Brief Reports (2021)
Closed Access | Times Cited: 2
Generation and characterization ofCcdc28bmutant mice links the Bardet-Biedl associated gene with social behavioral phenotypes
Matias Fábregat, Sofía Niño, Sabrina Pose, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
Matias Fábregat, Sofía Niño, Sabrina Pose, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
