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:

The GTEx Consortium atlas of genetic regulatory effects across human tissues
François Aguet, Shankara Anand, Kristin Ardlie, et al.
Science (2020) Vol. 369, Iss. 6509, pp. 1318-1330
Open Access | Times Cited: 3765

Showing 51-75 of 3765 citing articles:

Plasma proteome analyses in individuals of European and African ancestry identify cis-pQTLs and models for proteome-wide association studies
Jingning Zhang, Diptavo Dutta, Anna Köttgen, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 593-602
Open Access | Times Cited: 228
Dynamic landscape of immune cell-specific gene regulation in immune-mediated diseases
Mineto Ota, Yasuo Nagafuchi, Hiroaki Hatano, et al.
Cell (2021) Vol. 184, Iss. 11, pp. 3006-3021.e17
Open Access | Times Cited: 227
Molecular and evolutionary processes generating variation in gene expression
Mark S. Hill, Pétra Vande Zande, Patricia J. Wittkopp
Nature Reviews Genetics (2020) Vol. 22, Iss. 4, pp. 203-215
Open Access | Times Cited: 224
A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis
Dan Zhou, Yi Jiang, Xue Zhong, et al.
Nature Genetics (2020) Vol. 52, Iss. 11, pp. 1239-1246
Open Access | Times Cited: 210
Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders
Chengran Yang, Fabiana Farias, Laura Ibáñez, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 9, pp. 1302-1312
Open Access | Times Cited: 203
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals
Kira J. Stanzick, Yong Li, Pascal Schlosser, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 198
Transcriptome variation in human tissues revealed by long-read sequencing
Dafni A. Glinos, Garrett Garborcauskas, Paul Hoffman, et al.
Nature (2022) Vol. 608, Iss. 7922, pp. 353-359
Open Access | Times Cited: 191
The single-cell eQTLGen consortium
Monique G.P. van der Wijst, DH de Vries, Hilde E. Groot, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 189
Exaggerated false positives by popular differential expression methods when analyzing human population samples
Yumei Li, Xinzhou Ge, Fanglue Peng, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 187
Towards a structurally resolved human protein interaction network
David F. Burke, Patrick Bryant, Inigo Barrio‐Hernandez, et al.
Nature Structural & Molecular Biology (2023) Vol. 30, Iss. 2, pp. 216-225
Open Access | Times Cited: 179
Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders
Julien Bryois, Daniela Calini, Will Macnair, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 8, pp. 1104-1112
Open Access | Times Cited: 178
Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia
Mercedes Prudencio, Jack Humphrey, Sarah Pickles, et al.
Journal of Clinical Investigation (2020) Vol. 130, Iss. 11, pp. 6080-6092
Open Access | Times Cited: 171
Single-cell multiomic profiling of human lungs reveals cell-type-specific and age-dynamic control of SARS-CoV2 host genes
Allen Wang, Joshua Chiou, Olivier Poirion, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 170
Common genetic variation influencing human white matter microstructure
Bingxin Zhao, Tengfei Li, Yue Yang, et al.
Science (2021) Vol. 372, Iss. 6548
Open Access | Times Cited: 168
Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies
Kátia de Paiva Lopes, Gijsje J. L. Snijders, Jack Humphrey, et al.
Nature Genetics (2022) Vol. 54, Iss. 1, pp. 4-17
Open Access | Times Cited: 168
A genome-wide association study of serum proteins reveals shared loci with common diseases
Alexander Guðjónsson, Valborg Guðmundsdóttir, G. Axelsson, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 168
Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases
E. Weeks, Jacob C. Ulirsch, Nathan Cheng, et al.
Nature Genetics (2023) Vol. 55, Iss. 8, pp. 1267-1276
Open Access | Times Cited: 168
A sequence-based global map of regulatory activity for deciphering human genetics
Kathleen Chen, Aaron K. Wong, Olga G. Troyanskaya, et al.
Nature Genetics (2022) Vol. 54, Iss. 7, pp. 940-949
Open Access | Times Cited: 157
Multimodal single-cell chromatin analysis with Signac
Tim Stuart, Avi Srivastava, Caleb A. Lareau, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 155
Systematic differences in discovery of genetic effects on gene expression and complex traits
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
Nature Genetics (2023) Vol. 55, Iss. 11, pp. 1866-1875
Closed Access | Times Cited: 155
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
Seyedeh M. Zekavat, Shu‐Hong Lin, Alexander G. Bick, et al.
Nature Medicine (2021) Vol. 27, Iss. 6, pp. 1012-1024
Open Access | Times Cited: 151
Synergistic insights into human health from aptamer- and antibody-based proteomic profiling
Maik Pietzner, Eleanor Wheeler, Julia Carrasco-Zanini, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 150
AnimalTFDB 4.0: a comprehensive animal transcription factor database updated with variation and expression annotations
Wen‐Kang Shen, Si‐Yi Chen, Zi-Quan Gan, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D39-D45
Open Access | Times Cited: 150
Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus
Damien J. Downes, Amy Cross, Hua Peng, et al.
Nature Genetics (2021) Vol. 53, Iss. 11, pp. 1606-1615
Open Access | Times Cited: 149
Nrf2 for protection against oxidant generation and mitochondrial damage in cardiac injury
Qin M. Chen
Free Radical Biology and Medicine (2021) Vol. 179, pp. 133-143
Closed Access | Times Cited: 149

Scroll to top