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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:

Multifaceted Microcephaly-Related Gene MCPH1
Martina Kristofova, Alessandro Ori‬‬, Zhao‐Qi Wang
Cells (2022) Vol. 11, Iss. 2, pp. 275-275
Open Access | Times Cited: 20

Showing 20 citing articles:

TOP2A inhibition and its cellular effects related to cell cycle checkpoint adaptation pathway
M. López, María Ángeles Fernández-Mimbrera, E. Gollini, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 1
The analyses of human MCPH1 DNA repair machinery and genetic variations
O. Gabriel
Open Medicine (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Frontiers in Neurogenesis
Andreia Vaz, Inês Ribeiro, Luísa Pinto
Cells (2022) Vol. 11, Iss. 22, pp. 3567-3567
Open Access | Times Cited: 10
The emerging role of MCPH1/BRIT1 in carcinogenesis
Mona Alsolami, Doaa Aboalola, Dolal Malibari, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 5
The Role of Major Facilitator Superfamily Domain-Containing 2a in the Central Nervous System
Zhidong He, Yanan Zhao, Jing Sun
Cellular and Molecular Neurobiology (2022) Vol. 43, Iss. 2, pp. 639-647
Closed Access | Times Cited: 8
Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani family
Komal Aslam, Aysha Saeed, Iffat Jamil, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access | Times Cited: 1
Low-salt Diet Regulates the Metabolic and Signal Transduc-tion Genomic Fabrics, and Remodels the Cardiac Normal and Chronic Pathological Pathways
Dumitru A. Iacobaş, Haile Allen, Sanda Iacobaş
(2024)
Open Access | Times Cited: 1
Low-Salt Diet Regulates the Metabolic and Signal Transduction Genomic Fabrics, and Remodels the Cardiac Normal and Chronic Pathological Pathways
Dumitru A. Iacobaş, Haile Allen, Sanda Iacobaş
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 3, pp. 2355-2385
Open Access | Times Cited: 1
Functional analysis of a novel intronic variant of MCPH1 with autosomal recessive primary microcephaly
Shulin Luo, Lingyan Ren, Rongping Wang, et al.
Heliyon (2024) Vol. 10, Iss. 10, pp. e30285-e30285
Open Access | Times Cited: 1
Leveraging human–mouse studies to advance the genetics of hearing impairment in Africa
Kili James, O. Gabriel
The Journal of Gene Medicine (2024) Vol. 26, Iss. 7
Closed Access | Times Cited: 1
Advantages of CRISPR-Cas9 combined organoid model in the study of congenital nervous system malformations
Xiaoshuai Li, Qiushi Wang, Rui Wang
Frontiers in Bioengineering and Biotechnology (2022) Vol. 10
Open Access | Times Cited: 7
In vivo models to study neurogenesis and associated neurodevelopmental disorders—Microcephaly and autism spectrum disorder
Tuhina Prasad, Sharada Iyer, Sayoni Chatterjee, et al.
WIREs Mechanisms of Disease (2023) Vol. 15, Iss. 4
Closed Access | Times Cited: 3
The Central Domain of MCPH1 Controls Development of the Cerebral Cortex and Gonads in Mice
Yaru Wang, Wen Zong, Wenli Sun, et al.
Cells (2022) Vol. 11, Iss. 17, pp. 2715-2715
Open Access | Times Cited: 5
Epigenetic and transcriptional landscapes during cerebral cortex development in a microcephaly mouse model
Qing Yang, Qiang Cao, Yue Yu, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2023) Vol. 51, Iss. 4, pp. 419-432
Closed Access | Times Cited: 2
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis
Yoann Vial, Jeannette Nardelli, Adeline Bonnard, et al.
EMBO Reports (2024) Vol. 25, Iss. 5, pp. 2418-2440
Open Access
Generation and analysis of mouse embryonic stem cells with knockout of the Mcph1 (microcephalin) gene
A. M. Yunusova, A. V. Smirnov, Т. А. Шнайдер, et al.
Vavilov Journal of Genetics and Breeding (2024) Vol. 28, Iss. 5, pp. 487-494
Open Access
Can the male germline offer insight into mammalian brain size expansion?
Stephen J. Bush, Anne Goriely
Andrology (2024)
Closed Access
Chromosome engineering to restore euploidy in cells harboring a complex rearrangement of chromosome 8
Sophia N. Lee, Lu Qiao, Sarah Thompson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Evolutionary Analyses and Identification of Rare Pathogenic Variant in The MCPH1 BRCT3 Domain Broaden Its Role in Non-syndromic Hearing Impairment
O. Gabriel, Kili James, Ambroise Wonkam
Research Square (Research Square) (2022)
Open Access | Times Cited: 2
Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia
Tahereh Dianat, Dor Mohammad Kordi-Tamandani, Maryam Najafi, et al.
Disease and Diagnosis (2022) Vol. 11, Iss. 4, pp. 142-146
Open Access
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