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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:

Structural elucidation of the cis -prenyltransferase NgBR/DHDDS complex reveals insights in regulation of protein glycosylation
Ban H. Edani, Kariona A. Grabińska, Rong Zhang, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 34, pp. 20794-20802
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes
Carolina Courage, Karen Oliver, Eon Joo Park, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 722-738
Open Access | Times Cited: 65
The cis‐prenyltransferase protein family in Taraxacum koksaghyz
Boje Müller, Eva Niephaus, Wolfgang Eisenreich, et al.
The Plant Journal (2025) Vol. 121, Iss. 3
Open Access | Times Cited: 1
Lysosomal cholesterol accumulation contributes to the movement phenotypes associated with NUS1 haploinsufficiency
Seok‐Ho Yu, Tong Wang, Kali Wiggins, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 7, pp. 1305-1314
Open Access | Times Cited: 30
Modeling Retinitis Pigmentosa 59: Dhdds T206A and Dhdds K42E knock-in mutant mice are phenotypically similar.
Mai Nguyen, Dibyendu Chakraborty, Jeffrey D. Messinger, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Niemann-Pick C-like Endolysosomal Dysfunction in DHDDS Patient Cells, a Congenital Disorder of Glycosylation, Can Be Treated with Miglustat
Hannah L. Best, Sophie R. Cook, Helen Waller‐Evans, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1471-1471
Open Access
Lipid-metabolism-focused CRISPR screens identify enzymes of the mevalonate pathway as essential for prostate cancer growth
Gio Fidelito, Izabela Todorovski, Leonie A. Cluse, et al.
Cell Reports (2025) Vol. 44, Iss. 4, pp. 115470-115470
Open Access
Insights from natural rubber biosynthesis evolution for pathway engineering
Yin-Hong Cao, Qingwen Chen, Xia Xu, et al.
Trends in Plant Science (2025)
Closed Access
Genetic study of the NUS1 gene variants in Han Chinese patients with Parkinson’s disease
Cui Gao, Lamei Yuan, Wen Zheng, et al.
Ageing and Neurodegenerative Diseases (2025)
Open Access
Structural basis of heterotetrameric assembly and disease mutations in the human cis-prenyltransferase complex
Michal Lisnyansky, Pavla Vaňková, Adva Yeheskel, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 29
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus
Serena Galosi, Ban H. Edani, Simone Martinelli, et al.
Brain (2021) Vol. 145, Iss. 1, pp. 208-223
Open Access | Times Cited: 24
Plant molecular engine out of the chassis: Natural rubber synthesis in cell-free systems
Abdul Wakeel, Jong‐Chan Park, Tengfang Ling, et al.
Industrial Crops and Products (2023) Vol. 195, pp. 116166-116166
Closed Access | Times Cited: 8
DHDDS and NUS1: A Converging Pathway and Common Phenotype
Laura Williams, Sophie Waller, Jessica Qiu, et al.
Movement Disorders Clinical Practice (2023) Vol. 11, Iss. 1, pp. 76-85
Open Access | Times Cited: 8
Reconstitution of prenyltransferase activity on nanodiscs by components of the rubber synthesis machinery of the Para rubber tree and guayule
Fu Kuroiwa, Akira Nishino, Yasuko Mandal, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 13
Case Report: Clinical Features of a Chinese Boy With Epileptic Seizures and Intellectual Disabilities Who Carries a Truncated NUS1 Variant
Pingli Zhang, Di Cui, Peiyuan Liao, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 13
Adult‐onset rapidly worsening progressive myoclonic epilepsy caused by a novel variant in DHDDS
Seondeuk Kim, Man Jin Kim, Hyoshin Son, et al.
Annals of Clinical and Translational Neurology (2021) Vol. 8, Iss. 12, pp. 2319-2326
Open Access | Times Cited: 12
Novel NUS1 variant in a Chinese patient with progressive myoclonus epilepsy: a case report and systematic review
Caihong Ji, Jiajia Zhao, Jianfang Zhang, et al.
Neurological Sciences (2023) Vol. 44, Iss. 10, pp. 3495-3498
Closed Access | Times Cited: 4
Discovery, Structure, and Engineering of a cis‐Geranylfarnesyl Diphosphate Synthase
Fang‐Ru Li, Qingling Wang, Xingming Pan, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 27
Closed Access | Times Cited: 1
Acetazolamide treatment in late onset CDG type 1 due to biallelic pathogenic DHDDS variants
Jehan Mousa, Larissa Veres, Anab Mohamed, et al.
Molecular Genetics and Metabolism Reports (2022) Vol. 32, pp. 100901-100901
Open Access | Times Cited: 7
The promoter sequences of lettuce cis-prenyltransferase and its binding protein specify gene expression in laticifers
Elysabeth K. Barnes, Moonhyuk Kwon, Connor L. Hodgins, et al.
Planta (2021) Vol. 253, Iss. 2
Closed Access | Times Cited: 9
Structural basis for long-chain isoprenoid synthesis by cis -prenyltransferases
Moshe Giladi, Michal Lisnyansky, Pavla Vaňková, et al.
Science Advances (2022) Vol. 8, Iss. 20
Open Access | Times Cited: 6
Phenotype of heterozygous variants of dehydrodolichol diphosphate synthase
Xianru Jiao, Yi-Nan Xue, Sai Yang, et al.
Developmental Medicine & Child Neurology (2021) Vol. 64, Iss. 1, pp. 125-134
Open Access | Times Cited: 8
Knockdown of Dehydrodolichyl Diphosphate Synthase in the Drosophila Retina Leads to a Unique Pattern of Retinal Degeneration
Tal Brandwine, Reut Ifrah, Tzofia Bialistoky, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 6
Complexation and evolution of cis‐prenyltransferase homologues in Cinnamomum kanehirae deduced from kinetic and functional characterizations
Jia‐Jin Liu, Po‐Huang Liang
Protein Science (2023) Vol. 32, Iss. 12
Closed Access | Times Cited: 2
DHDDS -related disease; biallelic missense novel variant causing major severity with an early-onset epilepsy and hyperkinetic movement disorder
Hande Gazeteci Tekin, Pınar Edem
International Journal of Neuroscience (2024), pp. 1-5
Closed Access
NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation
Nan-Xiang Shen, Xiao-Chong Qu, Jing Yu, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 11, pp. 8518-8530
Closed Access
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