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:

Genome-wide functional screen of 3′UTR variants uncovers causal variants for human disease and evolution
Dustin Griesemer, James R. Xue, Steven K. Reilly, et al.
Cell (2021) Vol. 184, Iss. 20, pp. 5247-5260.e19
Open Access | Times Cited: 128

Showing 1-25 of 128 citing articles:

MicroRNAs as therapeutic targets in cardiovascular disease
Bernhard Laggerbauer, Stefan Engelhardt
Journal of Clinical Investigation (2022) Vol. 132, Iss. 11
Open Access | Times Cited: 110
Human-specific genetics: new tools to explore the molecular and cellular basis of human evolution
Alex A. Pollen, Umut Kilik, Craig B. Lowe, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 10, pp. 687-711
Open Access | Times Cited: 97
The genetic and biochemical determinants of mRNA degradation rates in mammals
Vikram Agarwal, David R. Kelley
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 78
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
The functional and evolutionary impacts of human-specific deletions in conserved elements
James R. Xue, Ava Mackay-Smith, Kousuke Mouri, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 44
Machine Learning for Designing Next-Generation mRNA Therapeutics
Sebastian M. Castillo-Hair, Georg Seelig
Accounts of Chemical Research (2021) Vol. 55, Iss. 1, pp. 24-34
Open Access | Times Cited: 61
Prioritization of autoimmune disease-associated genetic variants that perturb regulatory element activity in T cells
Kousuke Mouri, Michael H. Guo, Carl G. de Boer, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 603-612
Open Access | Times Cited: 50
3’UTR Diversity: Expanding Repertoire of RNA Alterations in Human mRNAs
Dawon Hong, Sunjoo Jeong
Molecules and Cells (2023) Vol. 46, Iss. 1, pp. 48-56
Open Access | Times Cited: 37
Leveraging massively parallel reporter assays for evolutionary questions
Irene Gallego Romero, Amanda J. Lea
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 33
Decoding Non-coding Variants: Recent Approaches to Studying Their Role in Gene Regulation and Human Diseases
Edwin G. Peña-Martínez, José A. Rodríguez‐Martínez
Frontiers in Bioscience-Scholar (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 13
Massively parallel screen uncovers many rare 3′ UTR variants regulating mRNA abundance of cancer driver genes
Ting Fu, Kofi Amoah, Tracey W. Chan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 11
Functional dissection of complex and molecular trait variants at single nucleotide resolution
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
Regulatory features aid interpretation of 3′UTR variants
Lindsay Romo, Scott D. Findlay, Christopher B. Burge
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 350-363
Open Access | Times Cited: 10
Long-read sequencing for 29 immune cell subsets reveals disease-linked isoforms
Jun Inamo, Akari Suzuki, Mahoko Takahashi Ueda, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Linking genome variants to disease: scalable approaches to test the functional impact of human mutations
Gregory M. Findlay
Human Molecular Genetics (2021) Vol. 30, Iss. R2, pp. R187-R197
Open Access | Times Cited: 44
3′UTR heterogeneity and cancer progression
Jia Jia Chan, Hossein Tabatabaeian, Yvonne Tay
Trends in Cell Biology (2022) Vol. 33, Iss. 7, pp. 568-582
Closed Access | Times Cited: 38
Functional characterization of human genomic variation linked to polygenic diseases
Tania Fabo, Paul A. Khavari
Trends in Genetics (2023) Vol. 39, Iss. 6, pp. 462-490
Open Access | Times Cited: 19
Massively parallel functional dissection of schizophrenia-associated noncoding genetic variants
Christine K. Rummel, Miriam Gagliardi, Ruhel Ahmad, et al.
Cell (2023) Vol. 186, Iss. 23, pp. 5165-5182.e33
Open Access | Times Cited: 19
Focus on your locus with a massively parallel reporter assay
Jessica C. McAfee, Jessica Bell, Oleh Krupa, et al.
Journal of Neurodevelopmental Disorders (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 24
TOWARDS TRANSCRIPTOMICS AS A PRIMARY TOOL FOR RARE DISEASE INVESTIGATION
Stephen B. Montgomery, Jonathan A. Bernstein, Matthew T. Wheeler
Molecular Case Studies (2022), pp. mcs.a006198-mcs.a006198
Open Access | Times Cited: 23
Multi-level functional genomics reveals molecular and cellular oncogenicity of patient-based 3′ untranslated region mutations
Samantha L. Schuster, Sonali Arora, Cynthia L. Wladyka, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112840-112840
Open Access | Times Cited: 16
The Roles of microRNAs in the Cardiovascular System
Francesco Nappi, Sanjeet Singh, Vikram Jitendra, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 14277-14277
Open Access | Times Cited: 16
Quantifying negative selection in human 3ʹ UTRs uncovers constrained targets of RNA-binding proteins
Scott D. Findlay, Lindsay Romo, Christopher B. Burge
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Dissecting the biology of feeding and eating disorders
Laura M. Huckins, Kristen Brennand, Cynthia M. Bulik
Trends in Molecular Medicine (2024) Vol. 30, Iss. 4, pp. 380-391
Open Access | Times Cited: 5
Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance
Qingbo Wang, Takanori Hasegawa, Ho Namkoong, et al.
Nature Genetics (2024) Vol. 56, Iss. 10, pp. 2054-2067
Open Access | Times Cited: 5
Page 1 - Next Page

Scroll to top