Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
Bobby Ng, Paulina Sosicka, François Fenaille, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 6, pp. 1040-1052
Open Access | Times Cited: 14

Showing 14 citing articles:

Clinical and biochemical footprints of congenital disorders of glycosylation: Proposed nosology
Bobby G. Ng, Hudson H. Freeze, Nastassja Himmelreich, et al.
Molecular Genetics and Metabolism (2024) Vol. 142, Iss. 1, pp. 108476-108476
Open Access | Times Cited: 24
The evolving genetic landscape of congenital disorders of glycosylation
Matthew P. Wilson, Gert Matthijs
Biochimica et Biophysica Acta (BBA) - General Subjects (2021) Vol. 1865, Iss. 11, pp. 129976-129976
Open Access | Times Cited: 29
CDG or not CDG
Hudson H. Freeze, Jaak Jaeken, Gert Matthijs
Journal of Inherited Metabolic Disease (2022) Vol. 45, Iss. 3, pp. 383-385
Open Access | Times Cited: 21
Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review
Federica Conte, Juda-El Sam, Dirk J. Lefeber, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 8632-8632
Open Access | Times Cited: 11
Hypoxia stress alters gene expression in the gills and spleen of greater amberjack (Seriola dumerili)
Duo Li, Weiwei Zhang, Tong Wang, et al.
Fish & Shellfish Immunology (2024) Vol. 150, pp. 109602-109602
Closed Access | Times Cited: 3
The landscape of CRISPR/Cas9 for inborn errors of metabolism
Andrés Felipe Leal, Nidhi Fnu, Eliana Benincore-Flórez, et al.
Molecular Genetics and Metabolism (2022) Vol. 138, Iss. 1, pp. 106968-106968
Open Access | Times Cited: 14
Hemostatic defects in congenital disorders of glycosylation
Tiffany Pascreau, Claire Auditeau, Delphine Borgel
Research and Practice in Thrombosis and Haemostasis (2023) Vol. 7, Iss. 3, pp. 100142-100142
Open Access | Times Cited: 7
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
Genetic aetiologies of acute liver failure
Robert Hegarty, Richard J. Thompson
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 4, pp. 582-597
Closed Access | Times Cited: 1
Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings
Matthew P. Wilson, Alejandro Garanto, Filippo Pinto e Vairo, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 11, pp. 2130-2144
Open Access | Times Cited: 8
SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy
Alexandre Raynor, Walid Haouari, Bobby Ng, et al.
Clinica Chimica Acta (2021) Vol. 521, pp. 104-106
Open Access | Times Cited: 5
The metabolic basis of inherited neutropenias
Usua Oyarbide, Genevieve M. Crane, Seth J. Corey
British Journal of Haematology (2023) Vol. 204, Iss. 1, pp. 45-55
Closed Access | Times Cited: 1
Coagulation dysfunction caused by a de novo mutation of gene SLC37A4
Mauro Guariento, Nicola Martinelli, Laura Pezzoli, et al.
Authorea (Authorea) (2024)
Open Access
Coagulation Dysfunction Caused by a De Novo Mutation of Gene SLC37A4
Mauro Guariento, Nicola Martinelli, Laura Pezzoli, et al.
Pediatric Blood & Cancer (2024)
Open Access
Page 1

Scroll to top