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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:

Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy
Thi Tuyet Mai Nguyen, Yoshiko Murakami, Sabrina Mobilio, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 4, pp. 484-495
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

Computed structures of core eukaryotic protein complexes
Ian R. Humphreys, Jimin Pei, Minkyung Baek, et al.
Science (2021) Vol. 374, Iss. 6573
Open Access | Times Cited: 454
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
Proteomic screens of SEL1L-HRD1 ER-associated degradation substrates reveal its role in glycosylphosphatidylinositol-anchored protein biogenesis
Xiaoqiong Wei, You Lu, Liangguang Leo Lin, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8
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
Novel insights into the roles of migrasome in cancer
Sijun Deng, Yiwen Wu, Sheng Huang, et al.
Discover Oncology (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Structure of human glycosylphosphatidylinositol transamidase
Hongwei Zhang, Jiawei Su, Li Bin, et al.
Nature Structural & Molecular Biology (2022) Vol. 29, Iss. 3, pp. 203-209
Closed Access | Times Cited: 23
Deep brain stimulation of thalamic nucleus reuniens promotes neuronal and cognitive resilience in an Alzheimer’s disease mouse model
Shiri Shoob, Nadav Buchbinder, Ortal Shinikamin, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 14
Unveiling the Potential of Migrasomes: A Machine-Learning-Driven Signature for Diagnosing Acute Myocardial Infarction
Yihao Zhu, Yuxi Chen, Jiajin Xu, et al.
Biomedicines (2024) Vol. 12, Iss. 7, pp. 1626-1626
Open Access | Times Cited: 5
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
Molecular insights into biogenesis of glycosylphosphatidylinositol anchor proteins
Yidan Xu, Guowen Jia, Tingting Li, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 19
Selection Signatures in Italian Goat Populations Sharing the “facciuto” Phenotype
Simona Tarricone, Nikola Schlosserová, Silvia Bruno, et al.
Genes (2025) Vol. 16, Iss. 4, pp. 390-390
Open Access
The Regulatory Roles of Cerebellar Glycosphingolipid Microdomains/Lipid Rafts
Keisuke Komatsuya, Norihito Kikuchi, Tetsuya Hirabayashi, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 6, pp. 5566-5566
Open Access | Times Cited: 8
Structures of core eukaryotic protein complexes
Ian R. Humphreys, Jimin Pei, Minkyung Baek, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 16
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
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
Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis
Xin Chen, Wu Yin, Siyi Chen, et al.
Human Genetics (2021) Vol. 140, Iss. 5, pp. 791-803
Closed Access | Times Cited: 11
A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizures
Kenichiro Sadamitsu, Kumiko Yanagi, Yuiko Hasegawa, et al.
Journal of Human Genetics (2024) Vol. 69, Iss. 11, pp. 553-563
Closed Access | Times Cited: 1
PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiation
Siyi Chen, Jiali You, Xiaowei Zhou, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 11
Open Access | Times Cited: 1
PIGG variant pathogenicity assessment reveals characteristic features within 19 families
Camille Tremblay‐Laganière, Reza Maroofian, Thi Tuyet Mai Nguyen, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 10, pp. 1873-1881
Open Access | Times Cited: 10
Functional Analysis of the GPI Transamidase Complex by Screening for Amino Acid Mutations in Each Subunit
Sisi Liu, Fei Jin, Yi‐Shi Liu, et al.
Molecules (2021) Vol. 26, Iss. 18, pp. 5462-5462
Open Access | Times Cited: 8
Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1
Alison M. R. Castle, Smrithi Salian, Haim Bassan, et al.
Neurology Genetics (2021) Vol. 7, Iss. 6
Open Access | Times Cited: 6
Lipid Dyshomeostasis and Inherited Cerebellar Ataxia
Jin Zhao, Huan Zhang, Xueyu Fan, et al.
Molecular Neurobiology (2022) Vol. 59, Iss. 6, pp. 3800-3828
Open Access | Times Cited: 3
Structure and Function of the Glycosylphosphatidylinositol Transamidase, a Transmembrane Complex Catalyzing GPI Anchoring of Proteins
Dianfan Li
Sub-cellular biochemistry/Subcellular biochemistry (2024), pp. 425-458
Closed 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
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