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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:

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

Showing 26-50 of 53 citing articles:

PIGO‐CDG: A case study with a new genotype, expansion of the phenotype, literature review, and nosological considerations
Rodrigo Tzovenos Starosta, Nino Kerashvili, Cassandra Pruitt, et al.
JIMD Reports (2023) Vol. 64, Iss. 6, pp. 424-433
Open Access | Times Cited: 2
Prenatal ultrasound findings associated with PIGW variants: One more piece in the FRYNS syndrome puzzle? PIGW‐related prenatal findings
Luisa Ronzoni, Simona Boito, Camilla Meossi, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 12, pp. 1493-1502
Closed Access | Times Cited: 3
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)
Seda Süsgün, Afif Ben‐Mahmoud, Franz Rüschendorf, et al.
Human Mutation (2024) Vol. 2024, pp. 1-13
Open Access
Role of PIGM and PIGX in glycosylphosphatidylinositol biosynthesis and human health (Review)
Ángeles Torres‐Valdetano, Verónica Vallejo-Ruíz, Lorena Milflores‐Flores, et al.
Biomedical Reports (2024) Vol. 20, Iss. 4
Open Access
Genetic and Environmental Factors in Autoimmune Thyroid Disease: Exploring Associations with Selenium Levels and Novel Loci in a Latvian Cohort
Sabīne Upmale-Engela, Ieva Vaivode, Raitis Pečulis, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 3, pp. 2553-2565
Open Access
Prenatal Diagnosis of Fryns Syndrome through Identification of Two Novel Splice Variants in the PIGN Gene—A Case Series
Aruna Marchetto, Susanne Leidescher, Theresia van Hoi, et al.
Life (2024) Vol. 14, Iss. 5, pp. 628-628
Open Access
Spectrum of Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 (MCAHS3) Due to Phosphatidylinositol Glycan Biosynthesis Class T (PIGT) Gene Mutations: A Narrative Review
Ankit Ranjan, Md Shahbaz Alam, Vinod Kumar, et al.
Cureus (2024)
Open Access
Biallelic PIGM Coding Variant Causes Intractable Epilepsy and Intellectual Disability Without Thrombotic Events
Gali Heimer, Ben Pode‐Shakked, Dina Marek‐Yagel, et al.
Clinical Genetics (2024)
Open Access
A case report of PGAP2-related hyperphosphatasia with impaired intellectual development syndrome in a Chinese family and literature review
Yijun Pan, Bin Ren, Lijuan Chen, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access
Two Different Brain Injury Patterns Associated with Compound Heterozygosis of the PIGO Gene in a Term Newborn: A Case Report
Francesco Dellepiane, Giulia Moltoni, Sara Ronci, et al.
Biomedicines (2024) Vol. 12, Iss. 12, pp. 2779-2779
Open Access
CHIME Syndrome in a Child With Homozygous PIGL p.Leu167Pro Variant
Eszter Sára Arany, David Zocche, Jemima E. Mellerio, et al.
American Journal of Medical Genetics Part A (2024)
Closed Access
In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder
Agnese Feresin, Mathilde Lefebvre, Emilie Sjøstrøm, et al.
Biomolecules (2024) Vol. 14, Iss. 12, pp. 1626-1626
Open Access
Asfotase alfa improved skeletal mineralization and fracture healing in a child with MCAHS
Min Kang, Malinda Wu, Janet L. Crane
Bone (2023) Vol. 172, pp. 116778-116778
Open Access | Times Cited: 1
Characteristics of Neuroimaging and Behavioural Phenotype in Polish Patients with PIGV-CDG—An Observational Study and Literature Review
Michał Hutny, Patryk Lipiński, Aleksandra Jezela‐Stanek
Genes (2023) Vol. 14, Iss. 6, pp. 1208-1208
Open Access | Times Cited: 1
Perturbation of the insomniaWDR90GWAS 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.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Application of plasma metabolome for monitoring the effect of rivaroxaban in patients with nonvalvular atrial fibrillation
Mindi Zhao, Xiaoping Xiao, Xiaoxiao Bu, et al.
PeerJ (2022) Vol. 10, pp. e13853-e13853
Open Access | Times Cited: 1
Neurological Consequences of Congenital Disorders of Glycosylation
Justyna Paprocka
Advances in neurobiology (2022), pp. 219-253
Closed Access | Times Cited: 1
Congenital Disorders of Glycosylation, Peroxisomal Disorders, and Smith-Lemli-Opitz Syndrome
Janet A. Thomas, Christina Lam
Elsevier eBooks (2023), pp. 396-408.e4
Closed Access
Attenuated cerebellar phenotypes in Inpp4a truncation mutants with preserved phosphatase activity
Dang Minh Tran, Nozomu Yoshioka, Norihisa Bizen, et al.
Disease Models & Mechanisms (2023) Vol. 16, Iss. 7
Open Access
A Novel Homozygous GPAA1 Variant in a Patient with a Glycosylphosphatidylinositol Biosynthesis Defect
Paolo Fontana, Alberto Budillon, Domenico Simeone, et al.
Genes (2023) Vol. 14, Iss. 7, pp. 1444-1444
Open Access
Comparative putative metabolites profiling of Tachypleus gigas and Carcinoscorpius rotundicauda hemocytes stimulated with lipopolysaccharide
Nurhana Jasni, Chee Lee Wee, Noraznawati Ismail, et al.
Research Square (Research Square) (2023)
Open Access
PIGA mutations (can) cause juvenile hemochromatosis
Andrea U. Steinbicker
Blood (2022) Vol. 139, Iss. 9, pp. 1273-1275
Open Access
Peer Review #1 of "Application of plasma metabolome for monitoring the effect of rivaroxaban in patients with nonvalvular atrial fibrillation (v0.2)"
Mindi Zhao, Xiaoyan Liu, Xiaoxiao Bu, et al.
(2022)
Open Access
Peer Review #2 of "Application of plasma metabolome for monitoring the effect of rivaroxaban in patients with nonvalvular atrial fibrillation (v0.2)"
Mindi Zhao, Xiaoyan Liu, Xiaoxiao Bu, et al.
(2022)
Open Access
Peer Review #2 of "Application of plasma metabolome for monitoring the effect of rivaroxaban in patients with nonvalvular atrial fibrillation (v0.1)"
Mindi Zhao, Xiaoyan Liu, Xiaoxiao Bu, et al.
(2022)
Open Access

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