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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 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

Showing 1-25 of 29 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
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
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
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
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
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
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
Enhanced Immune Response Against Echinococcus Granulosus Through a CTLA-4/B7 Affinity-Based Vaccine
Yuejie Zhu, Y He, Zhen‐Yu Yin, et al.
Vaccines (2024) Vol. 12, Iss. 12, pp. 1440-1440
Open Access
Case analysis of epilepsy, neurodevelopmental disorder, and motor disorders associated with mutations in the dehydrodolichyl diphosphate synthase gene
Ting Lv, Junxian Fu, Xiaoyang Liu, et al.
Seizure (2023) Vol. 110, pp. 126-135
Open Access | Times Cited: 1
Perspectives on Retinal Dolichol Metabolism, and Visual Deficits in Dolichol Metabolism-Associated Inherited Disorders
Sriganesh Ramachandra Rao, Steven J. Pittler, Steven J. Fliesler
Advances in experimental medicine and biology (2023), pp. 449-456
Closed Access | Times Cited: 1
A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmission
Mai Nguyen, Dibyendu Chakraborty, Sriganesh Ramachandra Rao, et al.
Cell Death and Disease (2023) Vol. 14, Iss. 7
Open Access | Times Cited: 1
Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonus
Yi Dong, Yi Zhang, Yue Sheng, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 1
Evidence that nuclear receptors are related to terpene synthases
Douglas R. Houston, Jane G. Hanna, J Constance Lathe, et al.
Journal of Molecular Endocrinology (2022) Vol. 68, Iss. 3, pp. 153-166
Open Access | Times Cited: 2
Vertebrate Animal Models of RP59: Current Status and Future Prospects
Steven J. Fliesler, Sriganesh Ramachandra Rao, Mai Nhu Nguyen, et al.
(2022)
Open Access | Times Cited: 2
Role of Neurite Outgrowth Inhibitor B Receptor in hepatic steatosis
Fangzhi Chen, Zhongcheng Mo, Qiaoqing Zhong, et al.
Acta Histochemica (2022) Vol. 124, Iss. 8, pp. 151977-151977
Closed Access | Times Cited: 2
Identification and biochemical characterization of a heteromeric cis-prenyltransferase from the thermophilic archaeon Archaeoglobus fulgidus
Kitty Sompiyachoke, Arisa Nagasaka, Tomokazu Ito, et al.
The Journal of Biochemistry (2022) Vol. 171, Iss. 6, pp. 641-651
Closed Access | Times Cited: 1
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.
Vide Leaf, Hyderabad eBooks (2022)
Open Access | Times Cited: 1
From the Desk of the Editor‑in‑Chief: Excerpts from the Society for Neurochemistry (ESN) Future Perspectives for European Neurochemistry Highlighting the Symposium Asking “Autism, Epilepsy, Intellectual Disability Where Do These All Meet?”
Illana Gozes
Journal of Molecular Neuroscience (2022) Vol. 72, Iss. 7, pp. 1527-1529
Open Access
A Dhdds K42E knock-in RP59 mouse model shows inner retina pathology and defective synaptic transmission
Mai Nguyen, Dibyendu Chakraborty, Sriganesh Ramachandra Rao, et al.
Research Square (Research Square) (2022)
Open Access
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