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OpenAlex Citation Counts

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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:

Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases
Yoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Vida Baratang, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 2, pp. 384-394
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

Biosynthesis and biology of mammalian GPI-anchored proteins
Taroh Kinoshita
Open Biology (2020) Vol. 10, Iss. 3
Open Access | Times Cited: 238
Congenital disorders of glycosylation
Irene J. Chang, Miao He, Christina Lam
Annals of Translational Medicine (2018) Vol. 6, Iss. 24, pp. 477-477
Open Access | Times Cited: 192
Protein lipidation in health and disease: molecular basis, physiological function and pathological implication
Yuan Yuan, Peiyuan Li, Jianghui Li, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 24
Congenital disorders of glycosylation: Still “hot” in 2020
Nina Ondrušková, Anna Čechová, Hana Hansíková, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2020) Vol. 1865, Iss. 1, pp. 129751-129751
Closed Access | Times Cited: 114
Alkaline phosphatase in clinical practice in childhood: Focus on rickets
Giuseppe Cannalire, Simone Pilloni, Susanna Esposito, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 29
Recent advances in epilepsy genomics and genetic testing
Malavika Hebbar, Heather C. Mefford
F1000Research (2020) Vol. 9, pp. 185-185
Open Access | Times Cited: 69
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders
Jai Sidpra, Sniya Sudhakar, Asthik Biswas, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2775-2790
Open Access | Times Cited: 7
Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics
Yu‐Tzu Chang, Syuan‐Yu Hong, Wei‐De Lin, et al.
Children (2023) Vol. 10, Iss. 3, pp. 556-556
Open Access | Times Cited: 16
SMAD3 Hypomethylation as a Biomarker for Early Prediction of Colorectal Cancer
Muhamad Ansar, Chun-Jung Wang, Yu-Han Wang, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 19, pp. 7395-7395
Open Access | Times Cited: 37
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
Targeted lipidomics analysis of possible molecular mechanisms of lipid changes in temporal lobe epilepsy models
Huaiyu Sun, Xuewei Li, Zhiqing Chen, et al.
Frontiers in Pharmacology (2025) Vol. 15
Open Access
Gene Variant Analysis in Pediatrics with Early-Onset Epilepsy: Identification of Novel Gene Variants
Pooyan Alizadeh, Armin Jahangiri Babadi, Nemat Ghadiri, et al.
Practical Laboratory Medicine (2025), pp. e00462-e00462
Open Access
DOORS syndrome and a recurrent truncating ATP6V1B2 variant
Éliane Beauregard‐Lacroix, G. Pacheco-Cuellar, Norbert Fonya Ajeawung, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 149-154
Open Access | Times Cited: 25
Loss of the N-acetylgalactosamine side chain of the GPI-anchor impairs bone formation and brain functions and accelerates the prion disease pathology
Tetsuya Hirata, Atsushi Kobayashi, Tamio Furuse, et al.
Journal of Biological Chemistry (2022) Vol. 298, Iss. 3, pp. 101720-101720
Open Access | Times Cited: 14
Diverse Functions of Lipids and Lipid Metabolism in Development
Yan Yao, Long Ding, Xun Huang
Small Methods (2019) Vol. 4, Iss. 7
Closed Access | Times Cited: 23
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)
Miles D. Thompson, Xueying Li, Michele Spencer‐Manzon, et al.
Genes (2023) Vol. 14, Iss. 2, pp. 359-359
Open Access | Times Cited: 7
Expanding the phenotype of PIGS‐associated early onset epileptic developmental encephalopathy
Stéphanie Efthymiou, Marina Dutra‐Clarke, Reza Maroofian, et al.
Epilepsia (2021) Vol. 62, Iss. 2
Open Access | Times Cited: 16
Establishment of mouse model of inherited PIGO deficiency and therapeutic potential of AAV-based gene therapy
Ryoko Kuwayama, Keiichiro Suzuki, Jun Nakamura, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 11
Inherited glycosylphosphatidylinositol deficiency: a review from molecular and clinical perspectives
Shan Li, Qi Tang, Yuwu Jiang, et al.
Acta Biochimica et Biophysica Sinica (2024) Vol. 56, Iss. 8, pp. 1234-1243
Open Access | Times Cited: 2
Ethanolamine‐phosphate on the second mannose is a preferential bridge for some GPI‐anchored proteins
Mizuki Ishida, Yuta Maki, Akinori Ninomiya, et al.
EMBO Reports (2022) Vol. 23, Iss. 7
Open Access | Times Cited: 10
A CRISPR-Cas9–engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctions
Miguel Rodríguez de los Santos, Marion Rivalan, Friederike S. David, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 2
Open Access | Times Cited: 13
Spectrum of Neurological Symptoms in Glycosylphosphatidylinositol Biosynthesis Defects: Systematic Review
Justyna Paprocka, Michał Hutny, Jagoda Hofman, et al.
Frontiers in Neurology (2022) Vol. 12
Open Access | Times Cited: 9
Cerebral and portal vein thrombosis, macrocephaly and atypical absence seizures in Glycosylphosphatidyl inositol deficiency due to a PIGM promoter mutation
Ben Pode‐Shakked, Gali Heimer, Thierry Vilboux, et al.
Molecular Genetics and Metabolism (2019) Vol. 128, Iss. 1-2, pp. 151-161
Open Access | Times Cited: 13
A post glycosylphosphatidylinositol (GPI) attachment to proteins, type 2 (PGAP2) variant identified in Mabry syndrome index cases: Molecular genetics of the prototypical inherited GPI disorder
Miles D. Thompson, Alexej Knaus, Bruce A. Barshop, et al.
European Journal of Medical Genetics (2019) Vol. 63, Iss. 4, pp. 103822-103822
Closed Access | Times Cited: 13

Fahmil Haris, Johanri Taufan, Fauzan Aulia
Journal of Physical Education and Sport (2023) Vol. 23, Iss. 12
Open Access | Times Cited: 4
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