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:
Normal transferrin patterns in congenital disorders of glycosylation with Golgi homeostasis disruption: apolipoprotein C-III at the rescue!
Alexandre Raynor, Catherine Vincent‐Delorme, Anne-Sophie Alaix, et al.
Clinica Chimica Acta (2021) Vol. 519, pp. 285-290
Open Access | Times Cited: 9
Alexandre Raynor, Catherine Vincent‐Delorme, Anne-Sophie Alaix, et al.
Clinica Chimica Acta (2021) Vol. 519, pp. 285-290
Open Access | Times Cited: 9
Showing 9 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
SLC10A7 regulates O-GalNAc glycosylation and Ca2+ homeostasis in the secretory pathway: insights into SLC10A7-CDG
Zoé Durin, Aurore Layotte, Willy Morelle, et al.
Cellular and Molecular Life Sciences (2025) Vol. 82, Iss. 1
Open Access
Zoé Durin, Aurore Layotte, Willy Morelle, et al.
Cellular and Molecular Life Sciences (2025) Vol. 82, Iss. 1
Open Access
Diagnostic and Therapeutic Approaches in Congenital Disorders of Glycosylation
Alexandre Raynor, Élodie Lebredonchel, François Foulquier, et al.
Handbook of experimental pharmacology (2025)
Closed Access
Alexandre Raynor, Élodie Lebredonchel, François Foulquier, et al.
Handbook of experimental pharmacology (2025)
Closed Access
Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2021–2022
David J. Harvey
Mass Spectrometry Reviews (2024)
Open Access | Times Cited: 2
David J. Harvey
Mass Spectrometry Reviews (2024)
Open Access | Times Cited: 2
Normal transferrin glycosylation does not rule out severe ALG1 deficiency
Inez Bosnyák, Mustafa Sadek, Wasantha Ranatunga, et al.
JIMD Reports (2024) Vol. 65, Iss. 3, pp. 135-143
Open Access | Times Cited: 1
Inez Bosnyák, Mustafa Sadek, Wasantha Ranatunga, et al.
JIMD Reports (2024) Vol. 65, Iss. 3, pp. 135-143
Open Access | Times Cited: 1
Electrospray Ionization Mass Spectrometry of Apolipoprotein CIII to Evaluate <i>O</i>-glycan Site Occupancy and Sialylation in Congenital Disorders of Glycosylation
Yoshinao Wada, Nobuhiko Okamoto
Mass Spectrometry (2022) Vol. 11, Iss. 1, pp. A0104-A0104
Open Access | Times Cited: 3
Yoshinao Wada, Nobuhiko Okamoto
Mass Spectrometry (2022) Vol. 11, Iss. 1, pp. A0104-A0104
Open Access | Times Cited: 3
Identification of a novel intronic variant of ATP6V0A2 in a Han-Chinese family with cutis laxa
Ying Zhang, Mei Sun, Na Li, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access
Ying Zhang, Mei Sun, Na Li, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access
SLC10A7 regulates O-GalNAc glycosylation and Ca2+ homeostasis in the secretory pathway: insights into SLC10A7-CDG
Zoé Durin, Aurore Layotte, Willy Morelle, et al.
Research Square (Research Square) (2024)
Open Access
Zoé Durin, Aurore Layotte, Willy Morelle, et al.
Research Square (Research Square) (2024)
Open Access
Higher frequency of TMEM199-CDG in the southern mediterranean area is associated with c.92G>C (p.Arg31Pro) mutation
Agata Fiumara, Annamaria Sapuppo, Lorenzo Ferri, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 3, pp. 104709-104709
Closed Access | Times Cited: 1
Agata Fiumara, Annamaria Sapuppo, Lorenzo Ferri, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 3, pp. 104709-104709
Closed Access | Times Cited: 1
