Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
Y. Henry Sun, Yueh-Lin Wu, Ben‐Yang Liao
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 10

Showing 10 citing articles:

LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation
Diana Rubalcava-Gracia, Kristina Bubb, Fredrik Levander, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 18, pp. 11266-11282
Open Access | Times Cited: 2
Effects on keratinocytes of the traditional combination of herb extract (Royal Oji Complex) implicated the improvement of young children's skin moisture and barrier
Thuy‐Tien Thi Trinh, Jae Hee Choi, Jee‐Eun Yang, et al.
Skin Research and Technology (2024) Vol. 30, Iss. 4
Open Access | Times Cited: 1
Advances in microbial decorations and its applications in drug delivery
Tongjiang He, Zhendong Zhao, Zhentao Luo, et al.
Acta Materia Medica (2023) Vol. 2, Iss. 4
Open Access | Times Cited: 3
Stochastic response of ultrasensitivity: Optimised switching of mitogen activated protein kinase (MAPK) cascade
Pallabi Roy, Sakuntala Chatterjee, Gautam Gangopadhyay
Chemical Physics (2024) Vol. 584, pp. 112327-112327
Closed Access
Low‐intensity noise exposure takes an essential part in the mechanism of late‐onset hereditary hearing loss caused by Abcc1 mutation
Mengzhu Jiang, Shuai Zhang, Jing Liu, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 462-475
Closed Access
Haploinsufficiency and Alzheimer’s Disease: The Possible Pathogenic and Protective Genetic Factors
Eva Bagyinszky, Seong Soo A. An
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 22, pp. 11959-11959
Open Access
MetaPhenotype: A Transferable Meta-Learning Model for Single-Cell Mass Spectrometry-Based Cell Phenotype Prediction Using Limited Number of Cells
Songyuan Yao, Tra D. Nguyen, Yunpeng Lan, et al.
Analytical Chemistry (2024) Vol. 96, Iss. 49, pp. 19238-19247
Closed Access
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter
Silvia Castiglioni, Laura Pezzoli, Lidia Pezzani, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Estimating the Genetic Risk of First-Degree Relatives for Chronic Diseases Using the Short Tandem Repeat Score as Model of Polygenic Inheritance
Qi Xia, Anwar Ullah, Weijian Yu, et al.
Biochemical Genetics (2024)
Closed Access
Brain heterogeneity in 1,792 individuals with schizophrenia: effects of illness stage, sites of origin and pathophysiology
Yuchao Jiang, Lena Palaniyappan, Xiao Chang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Page 1

Scroll to top