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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:

A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing
Tao Chen, Bin Zhang, Thomas Ziegenhals, et al.
PLoS Genetics (2019) Vol. 15, Iss. 10, pp. e1008460-e1008460
Open Access | Times Cited: 20

Showing 20 citing articles:

Pan-cancer pervasive upregulation of 3′ UTR splicing drives tumourigenesis
Jia Jia Chan, Bin Zhang, Xiao Hong Chew, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 6, pp. 928-939
Open Access | Times Cited: 40
Dissecting the Genetic and Etiological Causes of Primary Microcephaly
Francesca Jean, Amanda L. Stuart, Maja Tarailo‐Graovac
Frontiers in Neurology (2020) Vol. 11
Open Access | Times Cited: 60
Biology of the mRNA Splicing Machinery and Its Dysregulation in Cancer Providing Therapeutic Opportunities
Maxime Blijlevens, Jing Li, Victor W. van Beusechem
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 10, pp. 5110-5110
Open Access | Times Cited: 30
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly
Maria Asif, Uzma Abdullah, Peter Nürnberg, et al.
Cells (2023) Vol. 12, Iss. 4, pp. 642-642
Open Access | Times Cited: 7
Update of recent findings in genetic hair disorders
Ryota Hayashi, Yutaka Shimomura
The Journal of Dermatology (2021) Vol. 49, Iss. 1, pp. 55-67
Closed Access | Times Cited: 17
The comprehensive expression and functional analysis of m6A modification “readers” in hepatocellular carcinoma
Sha Qin, Gaoming Liu, Haoer Jin, et al.
Aging (2022) Vol. 14, Iss. 15, pp. 6269-6298
Open Access | Times Cited: 11
The emerging significance of splicing in vertebrate development
Anouk Olthof, Alisa K. White, Rahul Kanadia
Development (2022) Vol. 149, Iss. 19
Open Access | Times Cited: 10
mRNA isoform balance in neuronal development and disease
Geneva LaForce, Polyxeni Philippidou, Ashleigh E. Schaffer
Wiley Interdisciplinary Reviews - RNA (2022) Vol. 14, Iss. 3
Open Access | Times Cited: 9
PSMC2, ORC5 and KRTDAP are specific biomarkers for HPV‑negative head and neck squamous cell carcinoma
Yushen Su, Zhirui Zeng, Dongyun Rong, et al.
Oncology Letters (2021) Vol. 21, Iss. 4
Open Access | Times Cited: 12
The Identification of RNA-Binding Proteins Functionally Associated with Tumor Progression in Gastrointestinal Cancer
Hiroaki Konishi, Shin Kashima, Takuma Goto, et al.
Cancers (2021) Vol. 13, Iss. 13, pp. 3165-3165
Open Access | Times Cited: 9
Genome-wide analysis of runs of homozygosity in Italian Mediterranean buffalo
Shen-he Liu, Xiaoya Ma, Faiz‐ul Hassan, et al.
Journal of Dairy Science (2022) Vol. 105, Iss. 5, pp. 4324-4334
Open Access | Times Cited: 6
Mutation of Arabidopsis SME1 and Sm core assembly improves oxidative stress resilience
Patrick J. Willems, Valerie Van Ruyskensvelde, Takanori Maruta, et al.
Free Radical Biology and Medicine (2023) Vol. 200, pp. 117-129
Open Access | Times Cited: 3
Do Fragile X Syndrome and Other Intellectual Disorders Converge at Aberrant Pre-mRNA Splicing?
Sneha Shah, Joel D. Richter
Frontiers in Psychiatry (2021) Vol. 12
Open Access | Times Cited: 7
Additional causal SNRPE mutations in hereditary hypotrichosis simplex
Pan Cheng, Aytaj Humbatova, Lan Zheng, et al.
British Journal of Dermatology (2021) Vol. 185, Iss. 2, pp. 439-441
Open Access | Times Cited: 4
Machine learning-based gene expression biomarkers to distinguish Zika and Dengue virus infections: implications for diagnosis
Ayesha Zeba, Aruna Rajalingam, K. Sekar, et al.
VirusDisease (2024) Vol. 35, Iss. 3, pp. 446-461
Closed Access
Hereditary hypotrichosis simplex with SNRPE gene mutation
Yumi Won, Byung Soo Kim, Moon-Bum Kim, et al.
Indian Journal of Dermatology Venereology and Leprology (2024), pp. 1-3
Open Access
Novel blended SNRPE‐related spliceosomopathy phenotype characterized by microcephaly and congenital atrichia
Shivarajan Amudhavalli, Victoria Paolillo, Caitlin E. Lawson, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 5, pp. 1425-1429
Closed Access | Times Cited: 1
Mammalian splicing divergence is shaped by drift, buffering in trans, and a scaling law
Xudong Zou, Bernhard Schaefke, Yisheng Li, et al.
Life Science Alliance (2021) Vol. 5, Iss. 4, pp. e202101333-e202101333
Open Access | Times Cited: 3
Mutation of Arabidopsis SME1 and Sm core assembly improves oxidative stress resilience
Patrick J. Willems, Valerie Van Ruyskensvelde, Takanori Maruta, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Two High-Quality Cygnus Genome Assemblies Reveal Genomic Variations Associated with Plumage Color
Yuqing Chong, Xiaolong Tu, Ying Lu, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 16953-16953
Open Access
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