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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 brief history of human disease genetics
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 603

Showing 1-25 of 603 citing articles:

A cross-population atlas of genetic associations for 220 human phenotypes
Saori Sakaue, Masahiro Kanai, Yosuke Tanigawa, et al.
Nature Genetics (2021) Vol. 53, Iss. 10, pp. 1415-1424
Open Access | Times Cited: 1411
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L. Bao, Parsa Akbari, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1214-1231.e11
Open Access | Times Cited: 556
Genome-wide enhancer maps link risk variants to disease genes
Joseph Nasser, Drew T. Bergman, Charles P. Fulco, et al.
Nature (2021) Vol. 593, Iss. 7858, pp. 238-243
Open Access | Times Cited: 526
The DisGeNET cytoscape app: Exploring and visualizing disease genomics data
Janet Piñero, Josep Saüch, Ferrán Sanz, et al.
Computational and Structural Biotechnology Journal (2021) Vol. 19, pp. 2960-2967
Open Access | Times Cited: 402
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Quanli Wang, Ryan S. Dhindsa, Keren Carss, et al.
Nature (2021) Vol. 597, Iss. 7877, pp. 527-532
Open Access | Times Cited: 368
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
Akl C. Fahed, Minxian Wang, Julian R. Homburger, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 360
Improving reporting standards for polygenic scores in risk prediction studies
Hannah Wand, Samuel A. Lambert, Cecelia P. Tamburro, et al.
Nature (2021) Vol. 591, Iss. 7849, pp. 211-219
Open Access | Times Cited: 358
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
Jing Hua Zhao, David Stacey, Niclas Eriksson, et al.
Nature Immunology (2023) Vol. 24, Iss. 9, pp. 1540-1551
Open Access | Times Cited: 356
A single-cell atlas of chromatin accessibility in the human genome
Kai Zhang, James D. Hocker, Michael Miller, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5985-6001.e19
Open Access | Times Cited: 327
A comparative genomics multitool for scientific discovery and conservation

Nature (2020) Vol. 587, Iss. 7833, pp. 240-245
Open Access | Times Cited: 307
Interpreting type 1 diabetes risk with genetics and single-cell epigenomics
Joshua Chiou, Ryan J. Geusz, Mei-Lin Okino, et al.
Nature (2021) Vol. 594, Iss. 7863, pp. 398-402
Open Access | Times Cited: 294
Strategic vision for improving human health at The Forefront of Genomics
Eric D. Green, Chris Gunter, Leslie G. Biesecker, et al.
Nature (2020) Vol. 586, Iss. 7831, pp. 683-692
Open Access | Times Cited: 267
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
EP Europace (2022) Vol. 24, Iss. 8, pp. 1307-1367
Open Access | Times Cited: 256
Genomic data in the All of Us Research Program
Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, et al.
Nature (2024) Vol. 627, Iss. 8003, pp. 340-346
Open Access | Times Cited: 244
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Nature Genetics (2020) Vol. 52, Iss. 9, pp. 969-983
Open Access | Times Cited: 215
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
Host genetics and infectious disease: new tools, insights and translational opportunities
Andrew Kwok, Alexander J. Mentzer, Julian C. Knight
Nature Reviews Genetics (2020) Vol. 22, Iss. 3, pp. 137-153
Open Access | Times Cited: 175
Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics
Craig J. Markin, Daniel A. Mokhtari, Fanny Sunden, et al.
Science (2021) Vol. 373, Iss. 6553
Open Access | Times Cited: 163
Variants of uncertain significance in the era of high-throughput genome sequencing: a lesson from breast and ovary cancers
G. Federici, Silvia Soddu
Journal of Experimental & Clinical Cancer Research (2020) Vol. 39, Iss. 1
Open Access | Times Cited: 162
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Heart Rhythm (2022) Vol. 19, Iss. 7, pp. e1-e60
Open Access | Times Cited: 158
Genomics of hypertension: the road to precision medicine
Sandosh Padmanabhan, Anna F. Dominiczak
Nature Reviews Cardiology (2020) Vol. 18, Iss. 4, pp. 235-250
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
An atlas of gene regulatory elements in adult mouse cerebrum
Yang Eric Li, Sebastian Preißl, Xiaomeng Hou, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 129-136
Open Access | Times Cited: 143
Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts
Rebecca Kingdom, Caroline F. Wright
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 141
LifeTime and improving European healthcare through cell-based interceptive medicine
Nikolaus Rajewsky, Geneviève Almouzni, Stanislaw A. Gorski, et al.
Nature (2020) Vol. 587, Iss. 7834, pp. 377-386
Open Access | Times Cited: 140
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