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:
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases
Li Shu, Tatiana Maroilley, Maja Tarailo‐Graovac
Genes (2023) Vol. 14, Iss. 1, pp. 196-196
Open Access | Times Cited: 6
Li Shu, Tatiana Maroilley, Maja Tarailo‐Graovac
Genes (2023) Vol. 14, Iss. 1, pp. 196-196
Open Access | Times Cited: 6
Showing 6 citing articles:
How to customize common data models for rare diseases: an OMOP-based implementation and lessons learned
Najia Ahmadi, Michéle Zoch, Oya Guengoeze, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 3
Najia Ahmadi, Michéle Zoch, Oya Guengoeze, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 3
Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders
Ana Zamora-Cánovas, Belén de la Morena‐Barrio, Ana Marín‐Quílez, et al.
Journal of Thrombosis and Haemostasis (2023) Vol. 22, Iss. 3, pp. 851-859
Closed Access | Times Cited: 3
Ana Zamora-Cánovas, Belén de la Morena‐Barrio, Ana Marín‐Quílez, et al.
Journal of Thrombosis and Haemostasis (2023) Vol. 22, Iss. 3, pp. 851-859
Closed Access | Times Cited: 3
How to customize Common Data Models for rare diseases: an OMOP-based implementation and lessons learned
Najia Ahmadi, Michéle Zoch, Oya Guengoeze, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
Najia Ahmadi, Michéle Zoch, Oya Guengoeze, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
Single variant, yet “double trouble”: TSC and KBG syndrome because of a large de novo inversion
Victoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, et al.
Life Science Alliance (2024) Vol. 7, Iss. 4, pp. e202302115-e202302115
Open Access
Victoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, et al.
Life Science Alliance (2024) Vol. 7, Iss. 4, pp. e202302115-e202302115
Open Access
Novel Biallelic Synonymous Exonic Variant in VPS13A Affecting mRNA Splicing
Rebecca Hui Min Hoe, Yi Zhao, Helen L. Ong, et al.
Neurology Genetics (2024) Vol. 10, Iss. 6
Closed Access
Rebecca Hui Min Hoe, Yi Zhao, Helen L. Ong, et al.
Neurology Genetics (2024) Vol. 10, Iss. 6
Closed Access
Un protocolo para el análisis de los problemas de lenguaje en las enfermedades raras
Antonio Benítez‐Burraco, Ma Salud Jiménez-Romero, Maite Fernández-Urquiza
(2023)
Open Access
Antonio Benítez‐Burraco, Ma Salud Jiménez-Romero, Maite Fernández-Urquiza
(2023)
Open Access
