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:
NGLY1 Deficiency, a Congenital Disorder of Deglycosylation: From Disease Gene Function to Pathophysiology
Ashutosh Pandey, Joshua Adams, Seung Yeop Han, et al.
Cells (2022) Vol. 11, Iss. 7, pp. 1155-1155
Open Access | Times Cited: 28
Ashutosh Pandey, Joshua Adams, Seung Yeop Han, et al.
Cells (2022) Vol. 11, Iss. 7, pp. 1155-1155
Open Access | Times Cited: 28
Showing 1-25 of 28 citing articles:
HLA-DQB1*05 subtypes and not DRB1*10:01 mediates risk in anti-IgLON5 disease
Selina Yogeshwar, Sergio Muñiz‐Castrillo, Lídia Sabater, et al.
Brain (2024) Vol. 147, Iss. 7, pp. 2579-2592
Closed Access | Times Cited: 17
Selina Yogeshwar, Sergio Muñiz‐Castrillo, Lídia Sabater, et al.
Brain (2024) Vol. 147, Iss. 7, pp. 2579-2592
Closed Access | Times Cited: 17
Valosin containing protein (VCP): initiator, modifier, and potential drug target for neurodegenerative diseases
Siwei Chu, Xinyi Xie, Carla Payan, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 16
Siwei Chu, Xinyi Xie, Carla Payan, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 16
Interplay of Impaired Cellular Bioenergetics and Autophagy in PMM2-CDG
Anna N. Ligezka, Rohit Budhraja, Yurika Nishiyama, et al.
Genes (2023) Vol. 14, Iss. 8, pp. 1585-1585
Open Access | Times Cited: 13
Anna N. Ligezka, Rohit Budhraja, Yurika Nishiyama, et al.
Genes (2023) Vol. 14, Iss. 8, pp. 1585-1585
Open Access | Times Cited: 13
Gut barrier defects, intestinal immune hyperactivation and enhanced lipid catabolism drive lethality in NGLY1-deficient Drosophila
Ashutosh Pandey, Antonio Galeone, Seung Yeop Han, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Ashutosh Pandey, Antonio Galeone, Seung Yeop Han, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Increased Oxidative Stress and Autophagy in NGLY1 Patient iPSC-derived Neural Stem Cells
Zeenat A. Shyr, Soukaina Amniouel, Kofi Owusu-Ansah, et al.
Experimental Cell Research (2025), pp. 114540-114540
Open Access
Zeenat A. Shyr, Soukaina Amniouel, Kofi Owusu-Ansah, et al.
Experimental Cell Research (2025), pp. 114540-114540
Open Access
Applying the algorithm for Proven and young in GWAS Reveals high polygenicity for key traits in Nellore cattle
Adebisi R. Ogunbawo, Jorge Hidalgo, Henrique Alberto Mulim, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Adebisi R. Ogunbawo, Jorge Hidalgo, Henrique Alberto Mulim, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
NGLY1 deficiency: estimated incidence, clinical features, and genotypic spectrum from the NGLY1 Registry
Caroline R. Stanclift, Selina S. Dwight, Kevin Lee, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 12
Caroline R. Stanclift, Selina S. Dwight, Kevin Lee, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 12
NGLY1: A fascinating, multifunctional molecule
Tadashi Suzuki, Haruhiko Fujihira
Biochimica et Biophysica Acta (BBA) - General Subjects (2023) Vol. 1868, Iss. 2, pp. 130379-130379
Closed Access | Times Cited: 7
Tadashi Suzuki, Haruhiko Fujihira
Biochimica et Biophysica Acta (BBA) - General Subjects (2023) Vol. 1868, Iss. 2, pp. 130379-130379
Closed Access | Times Cited: 7
Quantifying Kinematic Tremor in an NGLY1-Deficient Individual: A Case Study
Brock Futrell, Christopher A. Malaya, Dacia Martinez Diaz, et al.
Case Reports in Clinical Medicine (2024) Vol. 13, Iss. 01, pp. 25-36
Open Access | Times Cited: 2
Brock Futrell, Christopher A. Malaya, Dacia Martinez Diaz, et al.
Case Reports in Clinical Medicine (2024) Vol. 13, Iss. 01, pp. 25-36
Open Access | Times Cited: 2
Doxorubicin induces deglycosylation of cancer cell‐intrinsic PD ‐1 by NGLY 1
Dexuan Wu, Zhen Wu, Han Yao, et al.
FEBS Letters (2024) Vol. 598, Iss. 12, pp. 1543-1553
Closed Access | Times Cited: 2
Dexuan Wu, Zhen Wu, Han Yao, et al.
FEBS Letters (2024) Vol. 598, Iss. 12, pp. 1543-1553
Closed Access | Times Cited: 2
Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature
Yuri Sonoda, Atsushi Fujita, Michiko Torio, et al.
European Journal of Medical Genetics (2023) Vol. 67, pp. 104895-104895
Open Access | Times Cited: 5
Yuri Sonoda, Atsushi Fujita, Michiko Torio, et al.
European Journal of Medical Genetics (2023) Vol. 67, pp. 104895-104895
Open Access | Times Cited: 5
NGLY1 deficiency: a prospective natural history study
Sandra Tong, Pamela Ventola, Christina H. Frater, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 18, pp. 2787-2796
Open Access | Times Cited: 4
Sandra Tong, Pamela Ventola, Christina H. Frater, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 18, pp. 2787-2796
Open Access | Times Cited: 4
Functional prediction of the potential NGLY1 mutations associated with rare disease CDG
Shuying Yuan, Yanwen Chen, Lin Zou, et al.
Heliyon (2024) Vol. 10, Iss. 8, pp. e28787-e28787
Open Access | Times Cited: 1
Shuying Yuan, Yanwen Chen, Lin Zou, et al.
Heliyon (2024) Vol. 10, Iss. 8, pp. e28787-e28787
Open Access | Times Cited: 1
Genetic disruption of mammalian endoplasmic reticulum‐associated protein degradation: Human phenotypes and animal and cellular disease models
Sally Badawi, Feda E. Mohamed, Divya Saro Varghese, et al.
Traffic (2023) Vol. 24, Iss. 8, pp. 312-333
Open Access | Times Cited: 3
Sally Badawi, Feda E. Mohamed, Divya Saro Varghese, et al.
Traffic (2023) Vol. 24, Iss. 8, pp. 312-333
Open Access | Times Cited: 3
3-Dimensional Kinematic Comparison of Arm Movements between an Individual with NGLY1 Deficiency and a Neurotypical Individual
Charles S. Layne, Christopher A. Malaya, Brock Futrell, et al.
Case Reports in Clinical Medicine (2024) Vol. 13, Iss. 04, pp. 122-146
Open Access
Charles S. Layne, Christopher A. Malaya, Brock Futrell, et al.
Case Reports in Clinical Medicine (2024) Vol. 13, Iss. 04, pp. 122-146
Open Access
Mouse Models Reveal the Physiological Functions of Cytosolic Peptide:<i>N</i>-Glycanase, NGLY1
Haruhiko Fujihira
Trends in Glycoscience and Glycotechnology (2024) Vol. 36, Iss. 211, pp. J52-J55
Closed Access
Haruhiko Fujihira
Trends in Glycoscience and Glycotechnology (2024) Vol. 36, Iss. 211, pp. J52-J55
Closed Access
Mouse Models Reveal the Physiological Functions of Cytosolic Peptide:<i>N</i>-Glycanase, NGLY1
Haruhiko Fujihira
Trends in Glycoscience and Glycotechnology (2024) Vol. 36, Iss. 211, pp. E51-E54
Closed Access
Haruhiko Fujihira
Trends in Glycoscience and Glycotechnology (2024) Vol. 36, Iss. 211, pp. E51-E54
Closed Access
Conformational disorder in the crystal structure of methyl 2-acetamido-2-deoxy-β-D -glucopyranosyl-(1→4)–2-acetamido-2-deoxy-β-D -glucopyranoside (methyl β-chitobioside) methanol monosolvate
Pradip Shit, Timothy Tetrault, Wenhui Zhang, et al.
Acta Crystallographica Section C Structural Chemistry (2024) Vol. 80, Iss. 7, pp. 331-336
Closed Access
Pradip Shit, Timothy Tetrault, Wenhui Zhang, et al.
Acta Crystallographica Section C Structural Chemistry (2024) Vol. 80, Iss. 7, pp. 331-336
Closed Access
Mutations in nucleotide metabolism genes bypass proteasome defects in png-1/NGLY1-deficient Caenorhabditis elegans
Katherine S. Yanagi, Briar E. Jochim, Sheikh Omar Kunjo, et al.
PLoS Biology (2024) Vol. 22, Iss. 7, pp. e3002720-e3002720
Open Access
Katherine S. Yanagi, Briar E. Jochim, Sheikh Omar Kunjo, et al.
PLoS Biology (2024) Vol. 22, Iss. 7, pp. e3002720-e3002720
Open Access
AP3B1 facilitates PDIA3/ERP57 function to regulate rabies virus glycoprotein selective degradation and viral entry
Yuelan Zhang, Xinyi Zhang, Xueli Yang, et al.
Autophagy (2024) Vol. 20, Iss. 12, pp. 2785-2803
Closed Access
Yuelan Zhang, Xinyi Zhang, Xueli Yang, et al.
Autophagy (2024) Vol. 20, Iss. 12, pp. 2785-2803
Closed Access
Ubiquitin gets sweet: Sugar-mediated ubiquitination regulates Nrf1 function
Alison Mody, Christina M. Woo
Molecular Cell (2024) Vol. 84, Iss. 16, pp. 3003-3005
Closed Access
Alison Mody, Christina M. Woo
Molecular Cell (2024) Vol. 84, Iss. 16, pp. 3003-3005
Closed Access
Development of new NGLY1 assay systems – toward developing an early screening method for NGLY1 deficiency
Hiroto Hirayama, Haruhiko Fujihira, Tadashi Suzuki
Glycobiology (2024) Vol. 34, Iss. 11
Open Access
Hiroto Hirayama, Haruhiko Fujihira, Tadashi Suzuki
Glycobiology (2024) Vol. 34, Iss. 11
Open Access
Anything you can do, glycans do better: deglycosylation and noncanonical ubiquitination vie to rule the proteasome
Nicolas J. Lehrbach
Trends in Biochemical Sciences (2024)
Closed Access
Nicolas J. Lehrbach
Trends in Biochemical Sciences (2024)
Closed Access
An Assay System for Plate-based Detection of Endogenous Peptide:<em>N</em>-glycanase/NGLY1 Activity Using A Fluorescence-based Probe
Hiroto Hirayama, Tadashi Suzuki
BIO-PROTOCOL (2024) Vol. 15, Iss. 1362
Closed Access
Hiroto Hirayama, Tadashi Suzuki
BIO-PROTOCOL (2024) Vol. 15, Iss. 1362
Closed Access
NGLY1 Deficiency: A Rare Genetic Disorder Unlocks Therapeutic Potential for Common Diseases
Simon Walber, Georgia Partalidou, Ulla I. M. Gerling‐Driessen
Israel Journal of Chemistry (2022) Vol. 63, Iss. 1-2
Open Access | Times Cited: 1
Simon Walber, Georgia Partalidou, Ulla I. M. Gerling‐Driessen
Israel Journal of Chemistry (2022) Vol. 63, Iss. 1-2
Open Access | Times Cited: 1
