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:
Whole Exome Sequencing of 20 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Cataracts
Patricia RodrÃguez-Solana, Natalia Arruti, M. Nieves-Moreno, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11429-11429
Open Access | Times Cited: 6
Patricia RodrÃguez-Solana, Natalia Arruti, M. Nieves-Moreno, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11429-11429
Open Access | Times Cited: 6
Showing 6 citing articles:
Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders
Francis Rossignol, Foudil Lamari, Grant A. Mitchell
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access | Times Cited: 1
Francis Rossignol, Foudil Lamari, Grant A. Mitchell
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access | Times Cited: 1
Through the Cat-Map Gateway: A Brief History of Cataract Genetics
Alan Shiels
Genes (2024) Vol. 15, Iss. 6, pp. 785-785
Open Access | Times Cited: 4
Alan Shiels
Genes (2024) Vol. 15, Iss. 6, pp. 785-785
Open Access | Times Cited: 4
Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract
Mauro Lecca, Lucia Mauri, Simone Gana, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 403-412
Closed Access | Times Cited: 2
Mauro Lecca, Lucia Mauri, Simone Gana, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 403-412
Closed Access | Times Cited: 2
Effect of clinical whole exome sequencing in aetiological investigation and reproductive risk prediction for a couple with monogenic inherited diseases
Yanan Wang, Yuqiong Chai, Jieqiong Wang, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Yanan Wang, Yuqiong Chai, Jieqiong Wang, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
PIKFYVE deficiency induces vacuole-like cataract via perturbing late endosome homeostasis
Xiaochen Ma, Sejie Yu, Min Zhang, et al.
Biochemical and Biophysical Research Communications (2024) Vol. 747, pp. 151123-151123
Closed Access
Xiaochen Ma, Sejie Yu, Min Zhang, et al.
Biochemical and Biophysical Research Communications (2024) Vol. 747, pp. 151123-151123
Closed Access
Genetic Variants in PIKFYVE: A Review of Ocular Phenotypes
Ehsan Misaghi, Pekka Kannus, Ian M. MacDonald, et al.
Experimental Eye Research (2024), pp. 110211-110211
Open Access
Ehsan Misaghi, Pekka Kannus, Ian M. MacDonald, et al.
Experimental Eye Research (2024), pp. 110211-110211
Open Access
