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:
Metabolic adaptation of human skin fibroblasts to ER stress caused by glycosylation defect in PMM2-CDG
Lucie Zdražilová, Tereza Rákosníková, Nastassja Himmelreich, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 4, pp. 107629-107629
Open Access | Times Cited: 6
Lucie Zdražilová, Tereza Rákosníková, Nastassja Himmelreich, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 4, pp. 107629-107629
Open Access | Times Cited: 6
Showing 6 citing articles:
Biochemical diagnosis of congenital disorders of glycosylation
Alexandre Raynor, Walid Haouari, Elodie Lebredonchel, et al.
Advances in clinical chemistry (2024), pp. 1-43
Closed Access | Times Cited: 5
Alexandre Raynor, Walid Haouari, Elodie Lebredonchel, et al.
Advances in clinical chemistry (2024), pp. 1-43
Closed Access | Times Cited: 5
Increased Oxidative Stress and Autophagy in NGLY1 Patient iPSC-derived Neural Stem Cells
Zeenat A. Shyr, Soukaina Amniouel, Kofi Owusu-Ansah, et al.
Experimental Cell Research (2025), pp. 114540-114540
Open Access
Zeenat A. Shyr, Soukaina Amniouel, Kofi Owusu-Ansah, et al.
Experimental Cell Research (2025), pp. 114540-114540
Open Access
Targeted metabolomic evaluation of peripheral blood mononucleated cells from patients with PMM2-CDG
Renata Mangione, Lara Cirnigliaro, Miriam Wissam Saab, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Renata Mangione, Lara Cirnigliaro, Miriam Wissam Saab, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Complex metabolic disharmony in PMM2-CDG paves the way to new therapeutic approaches
Nastassja Himmelreich, Frauke Kikul, Lucie Zdražilová, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 3, pp. 107610-107610
Closed Access | Times Cited: 6
Nastassja Himmelreich, Frauke Kikul, Lucie Zdražilová, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 3, pp. 107610-107610
Closed Access | Times Cited: 6
Deficient glycan extension and endoplasmic reticulum stresses in ALG3‐CDG
Earnest James Paul Daniel, Andrew C. Edmondson, Yair Argon, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 4, pp. 766-777
Closed Access | Times Cited: 1
Earnest James Paul Daniel, Andrew C. Edmondson, Yair Argon, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 4, pp. 766-777
Closed Access | Times Cited: 1
HepG2 PMM2-CDG knockout model: A versatile platform for variant and therapeutic evaluation
Alicia Vilas, Alvaro Briso‐Montiano, Cristina Segovia‐Falquina, et al.
Molecular Genetics and Metabolism (2024) Vol. 143, Iss. 1-2, pp. 108538-108538
Open Access | Times Cited: 1
Alicia Vilas, Alvaro Briso‐Montiano, Cristina Segovia‐Falquina, et al.
Molecular Genetics and Metabolism (2024) Vol. 143, Iss. 1-2, pp. 108538-108538
Open Access | Times Cited: 1
Large TRAPPC11 gene deletions as a cause of muscular dystrophy and their estimated genesis
Johana Kopčilová, Hana Ptáčková, Tereza Kramářová, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 9, pp. 908-913
Closed Access
Johana Kopčilová, Hana Ptáčková, Tereza Kramářová, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 9, pp. 908-913
Closed Access
