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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 the phosphatidylinositol glycan C (PIGC) gene are associated with epilepsy and intellectual disability
Simon Edvardson, Yoshiko Murakami, Thi Tuyet Mai Nguyen, et al.
Journal of Medical Genetics (2016) Vol. 54, Iss. 3, pp. 196-201
Closed Access | Times Cited: 46

Showing 1-25 of 46 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 (CDG): Quo vadis?
Romain Péanne, Pascale de Lonlay, François Foulquier, et al.
European Journal of Medical Genetics (2017) Vol. 61, Iss. 11, pp. 643-663
Open Access | Times Cited: 235
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
Locus for severity implicates CNS resilience in progression of multiple sclerosis
Adil Harroud, Pernilla Stridh, Jacob L. McCauley, et al.
Nature (2023) Vol. 619, Iss. 7969, pp. 323-331
Open Access | Times Cited: 123
What is new in CDG?
Jaak Jaeken, Romain Péanne
Journal of Inherited Metabolic Disease (2017) Vol. 40, Iss. 4, pp. 569-586
Closed Access | Times Cited: 148
Clinical variability in inherited glycosylphosphatidylinositol deficiency disorders
Kara Bellai‐Dussault, Thi Tuyet Mai Nguyen, Nissan Vida Baratang, et al.
Clinical Genetics (2018) Vol. 95, Iss. 1, pp. 112-121
Closed Access | Times Cited: 98
Adaptive introgression reveals the genetic basis of a sexually selected syndrome in wall lizards
Nathalie Feiner, Weizhao Yang, Ignas Bunikis, et al.
Science Advances (2024) Vol. 10, Iss. 14
Open Access | Times Cited: 8
Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis
Alexej Knaus, Jean Tori Pantel, Manuela Pendziwiat, et al.
Genome Medicine (2018) Vol. 10, Iss. 1
Open Access | Times Cited: 80
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
Mutations in GPAA1 , Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
Thi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 5, pp. 856-865
Open Access | Times Cited: 60
Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy
Thi Tuyet Mai Nguyen, Yoshiko Murakami, Kristen Wigby, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 4, pp. 602-611
Open Access | Times Cited: 57
Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy
Devon L. Johnstone, Thi-Tuyet-Mai Nguyen, Yoshiko Murakami, et al.
Human Molecular Genetics (2017) Vol. 26, Iss. 9, pp. 1706-1715
Open Access | Times Cited: 43
Organization of GPI-anchored proteins at the cell surface and its physiopathological relevance
Stéphanie Lebreton, Chiara Zurzolo, Simona Paladino
Critical Reviews in Biochemistry and Molecular Biology (2018) Vol. 53, Iss. 4, pp. 403-419
Closed Access | Times Cited: 39
Epidemiology of congenital disorders of glycosylation (CDG)—overview and perspectives
Ana Piedade, Rita Francisco, Jaak Jaeken, et al.
Journal of Rare Diseases (2022) Vol. 1, Iss. 1
Open Access | Times Cited: 19
Identifying behavior regulatory leverage over mental disorders transcriptomic network hubs toward lifestyle-dependent psychiatric drugs repurposing
Mennatullah Abdelzaher Turky, Ibrahim Youssef, Azza El Amir
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
Early infantile epileptic-dyskinetic encephalopathy due to biallelic PIGP mutations
Annalisa Vetro, Tiziana Pisano, Silvia Chiaro, et al.
Neurology Genetics (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 28
Significantly different clinical phenotypes associated with mutations in synthesis and transamidase+remodeling glycosylphosphatidylinositol (GPI)-anchor biosynthesis genes
Leigh Carmody, Hannah Blau, Daniel Daniš, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 28
Phenotype-genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties
Junpei Tanigawa, Haruka Mimatsu, Seiji Mizuno, et al.
Human Mutation (2017) Vol. 38, Iss. 7, pp. 805-815
Open Access | Times Cited: 32
CNTNAP4 Impacts Epilepsy Through GABAA Receptors Regulation: Evidence From Temporal Lobe Epilepsy Patients and Mouse Models
Yafei Shangguan, Xin Xu, Baigalimaa Ganbat, et al.
Cerebral Cortex (2017) Vol. 28, Iss. 10, pp. 3491-3504
Open Access | Times Cited: 29
PIGT-CDG, a disorder of the glycosylphosphatidylinositol anchor: description of 13 novel patients and expansion of the clinical characteristics
Allan Bayat, Alexej Knaus, Annika Wollenberg Juul, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 10, pp. 2216-2223
Open Access | Times Cited: 27
Deep Feature Selection and Causal Analysis of Alzheimer’s Disease
Yuanyuan Liu, Zhouxuan Li, Qiyang Ge, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 25
Abnormal ER quality control of neural GPI-anchored proteins via dysfunction in ER export processing in the frontal cortex of elderly subjects with schizophrenia
Pitna Kim, Madeline R. Scott, James H. Meador‐Woodruff
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 20
Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency
Mariska Davids, Minal Menezes, Yiran Guo, et al.
Molecular Genetics and Metabolism (2020) Vol. 130, Iss. 1, pp. 49-57
Open Access | Times Cited: 19
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
A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephaly
Alistair T. Pagnamenta, Yoshiko Murakami, Consuelo Anzilotti, et al.
Human Mutation (2018) Vol. 39, Iss. 6, pp. 822-826
Open Access | Times Cited: 19
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