
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 Glycosylphosphatidylinositol biosynthesis pathway in human diseases
Tenghui Wu, Fei Yin, Shiqi Guang, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 53
Tenghui Wu, Fei Yin, Shiqi Guang, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 53
Showing 1-25 of 53 citing articles:
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
Giuseppe Cannalire, Simone Pilloni, Susanna Esposito, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 29
Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders
Francis Rossignol, Foudil Lamari, Grant A. Mitchell
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access | Times Cited: 1
Francis Rossignol, Foudil Lamari, Grant A. Mitchell
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access | Times Cited: 1
Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
Christina Lam, Fernando Scaglia, Susan A. Berry, et al.
Molecular Genetics and Metabolism (2024) Vol. 142, Iss. 4, pp. 108509-108509
Closed Access | Times Cited: 8
Christina Lam, Fernando Scaglia, Susan A. Berry, et al.
Molecular Genetics and Metabolism (2024) Vol. 142, Iss. 4, pp. 108509-108509
Closed Access | Times Cited: 8
Ketogenic diet therapy for pediatric epilepsy is associated with alterations in the human gut microbiome that confer seizure resistance in mice
Gregory R. Lum, Sung Min Ha, C. Anders Olson, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113521-113521
Open Access | Times Cited: 14
Gregory R. Lum, Sung Min Ha, C. Anders Olson, et al.
Cell Reports (2023) Vol. 42, Iss. 12, pp. 113521-113521
Open Access | Times Cited: 14
The GPI-anchor biosynthesis pathway is critical for syncytiotrophoblast differentiation and placental development
Andrea Álvarez-Sánchez, Johanna Grinat, Paula Doria-Borrell, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 5
Andrea Álvarez-Sánchez, Johanna Grinat, Paula Doria-Borrell, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 5
Neuronal Wiring Receptors Dprs and DIPs Are GPI Anchored and This Modification Contributes to Their Cell Surface Organization
Meike Lobb-Rabe, Wioletta I. Nawrocka, Ruiling Zhang, et al.
eNeuro (2024) Vol. 11, Iss. 2, pp. ENEURO.0184-23.2023
Open Access | Times Cited: 4
Meike Lobb-Rabe, Wioletta I. Nawrocka, Ruiling Zhang, et al.
eNeuro (2024) Vol. 11, Iss. 2, pp. ENEURO.0184-23.2023
Open Access | Times Cited: 4
Recurrent status epilepticus and severe bifrontal hypometabolism in PGAP1 ‐related neurodevelopmental disorder
Samia Benabess, Kenneth A. Myers
Epileptic Disorders (2025)
Open Access
Samia Benabess, Kenneth A. Myers
Epileptic Disorders (2025)
Open Access
Genetic Study and Prenatal Diagnosis of Inherited Glycosylphosphatidylinositol Disorders due to Novel Variants in Phosphatidylinositol Glycan Genes
Zhenhua Zhao, Jinglin Zhou, Qi Wang, et al.
Clinical Genetics (2025)
Closed Access
Zhenhua Zhao, Jinglin Zhou, Qi Wang, et al.
Clinical Genetics (2025)
Closed Access
Biochemical testing for congenital disorders of glycosylation: A technical standard of the American College of Medical Genetics and Genomics (ACMG)
Patricia Hall, Christina Lam, Lynne A. Wolfe, et al.
Genetics in Medicine (2025), pp. 101328-101328
Closed Access
Patricia Hall, Christina Lam, Lynne A. Wolfe, et al.
Genetics in Medicine (2025), pp. 101328-101328
Closed Access
Integrated Proteomics and Lipidomics Analysis of Hippocampus to Reveal the Metabolic Landscape of Epilepsy
Yinyu Chen, Qianyun Nie, Tao Song, et al.
ACS Omega (2025) Vol. 10, Iss. 9, pp. 9351-9367
Open Access
Yinyu Chen, Qianyun Nie, Tao Song, et al.
ACS Omega (2025) Vol. 10, Iss. 9, pp. 9351-9367
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
Pooyan Alizadeh, Armin Jahangiri Babadi, Nemat Ghadiri, et al.
Practical Laboratory Medicine (2025), pp. e00462-e00462
Open Access
Glycosylphosphatidylinositol biosynthesis defect due to novel biallelic pathogenic variants in PIGW
Nazim Rabouhi, Smrithi Salian, Hind Benkerroum, et al.
Pediatric Neurology (2025)
Open Access
Nazim Rabouhi, Smrithi Salian, Hind Benkerroum, et al.
Pediatric Neurology (2025)
Open Access
Hypometabolism in Autism Spectrum Disorder: Insights from Brain and Blood Transcriptomics
Rami Balasubramanian, Debajit Saha, A. Arun, et al.
Molecular Neurobiology (2025)
Closed Access
Rami Balasubramanian, Debajit Saha, A. Arun, et al.
Molecular Neurobiology (2025)
Closed Access
PIGT promotes cell growth, glycolysis, and metastasis in bladder cancer by modulating GLUT1 glycosylation and membrane trafficking
Mingyue Tan, Qi Pan, Chao Yu, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 3
Mingyue Tan, Qi Pan, Chao Yu, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 3
Early-Onset Dystonia and Visual Impairment Preceding Epileptic Encephalopathy Associated with PIGA Gene Mutation
Catarina Franquelim, Andreia Romana, Augusto Rachão, et al.
Neuropediatrics (2024) Vol. 55, Iss. 04, pp. 265-268
Closed Access | Times Cited: 3
Catarina Franquelim, Andreia Romana, Augusto Rachão, et al.
Neuropediatrics (2024) Vol. 55, Iss. 04, pp. 265-268
Closed Access | Times Cited: 3
Deciphering the premature mortality in PIGA-CDG – An untold story
Allan Bayat, Marius Kløvgaard, Katrine M. Johannesen, et al.
Epilepsy Research (2020) Vol. 170, pp. 106530-106530
Open Access | Times Cited: 23
Allan Bayat, Marius Kløvgaard, Katrine M. Johannesen, et al.
Epilepsy Research (2020) Vol. 170, pp. 106530-106530
Open Access | Times Cited: 23
Investigating Developmental and Epileptic Encephalopathy Using Drosophila melanogaster
Akari Takai, Masamitsu Yamaguchi, Hideki Yoshida, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 17, pp. 6442-6442
Open Access | Times Cited: 19
Akari Takai, Masamitsu Yamaguchi, Hideki Yoshida, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 17, pp. 6442-6442
Open Access | Times Cited: 19
Perturbation of the insomnia WDR90 genome-wide association studies locus pinpoints rs3752495 as a causal variant influencing distal expression of neighboring gene, PIG-Q
Shilpa Sonti, Sheridan H. Littleton, Matthew C. Pahl, et al.
SLEEP (2024) Vol. 47, Iss. 7
Closed Access | Times Cited: 2
Shilpa Sonti, Sheridan H. Littleton, Matthew C. Pahl, et al.
SLEEP (2024) Vol. 47, Iss. 7
Closed Access | Times Cited: 2
Rare Genetic Developmental Disabilities: Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) Disorders
Miles D. Thompson, Alexej Knaus
Genes (2024) Vol. 15, Iss. 5, pp. 619-619
Open Access | Times Cited: 2
Miles D. Thompson, Alexej Knaus
Genes (2024) Vol. 15, Iss. 5, pp. 619-619
Open Access | Times Cited: 2
Hyperphosphatasia with mental retardation syndrome 3: Cerebrospinal fluid abnormalities and correction with pyridoxine and Folinic acid
Martina Messina, Emanuela Manea, Thomas Cullup, et al.
JIMD Reports (2022) Vol. 64, Iss. 1, pp. 42-52
Open Access | Times Cited: 10
Martina Messina, Emanuela Manea, Thomas Cullup, et al.
JIMD Reports (2022) Vol. 64, Iss. 1, pp. 42-52
Open Access | Times Cited: 10
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
Justyna Paprocka, Michał Hutny, Jagoda Hofman, et al.
Frontiers in Neurology (2022) Vol. 12
Open Access | Times Cited: 9
Neuronal wiring receptors Dprs and DIPs are GPI anchored and this modification contributes to their cell surface organization
Meike Lobb-Rabe, Wioletta I. Nawrocka, Robert A. Carrillo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
Meike Lobb-Rabe, Wioletta I. Nawrocka, Robert A. Carrillo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
An Exploratory Study of the Metabolite Profiling from Pesticides Exposed Workers
Daniela Magalhães Nolasco, Michele P. R. Mendes, Luiz Paulo de Aguiar Marciano, et al.
Metabolites (2023) Vol. 13, Iss. 5, pp. 596-596
Open Access | Times Cited: 4
Daniela Magalhães Nolasco, Michele P. R. Mendes, Luiz Paulo de Aguiar Marciano, et al.
Metabolites (2023) Vol. 13, Iss. 5, pp. 596-596
Open Access | Times Cited: 4
Comparative putative metabolites profiling of Tachypleus gigas and Carcinoscorpius rotundicauda hemocytes stimulated with lipopolysaccharide
Nurhana Jasni, Chee Lee Wee, Noraznawati Ismail, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Nurhana Jasni, Chee Lee Wee, Noraznawati Ismail, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype–phenotype correlation
Ameni Aguech, L. Sfaihi, Olfa Alila‐Fersi, et al.
Metabolic Brain Disease (2023) Vol. 38, Iss. 8, pp. 2665-2678
Closed Access | Times Cited: 2
Ameni Aguech, L. Sfaihi, Olfa Alila‐Fersi, et al.
Metabolic Brain Disease (2023) Vol. 38, Iss. 8, pp. 2665-2678
Closed Access | Times Cited: 2