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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:

Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits
Jacob C. Ulirsch, Satish K. Nandakumar, Li Wang, et al.
Cell (2016) Vol. 165, Iss. 6, pp. 1530-1545
Open Access | Times Cited: 333

Showing 1-25 of 333 citing articles:

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
William J. Astle, Heather Elding, Tao Jiang, et al.
Cell (2016) Vol. 167, Iss. 5, pp. 1415-1429.e19
Open Access | Times Cited: 1225
Activity-by-contact model of enhancer–promoter regulation from thousands of CRISPR perturbations
Charles P. Fulco, Joseph Nasser, Thouis R. Jones, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1664-1669
Open Access | Times Cited: 877
From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases
Eddie Cano-Gamez, Gosia Trynka
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 483
Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay
Ryan Tewhey, Dylan Kotliar, Daniel Park, et al.
Cell (2016) Vol. 165, Iss. 6, pp. 1519-1529
Open Access | Times Cited: 468
Linear models enable powerful differential activity analysis in massively parallel reporter assays
Leslie Myint, Dimitrios Avramopoulos, Loyal A. Goff, et al.
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 378
Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis
Rajiv K. Khajuria, Mathias Munschauer, Jacob C. Ulirsch, et al.
Cell (2018) Vol. 173, Iss. 1, pp. 90-103.e19
Open Access | Times Cited: 356
Variant Interpretation: Functional Assays to the Rescue
Lea M. Starita, Nadav Ahituv, Maitreya J. Dunham, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 3, pp. 315-325
Open Access | Times Cited: 340
Transcription factor–DNA binding: beyond binding site motifs
Sachi Inukai, Kian Hong Kock, Martha L. Bulyk
Current Opinion in Genetics & Development (2017) Vol. 43, pp. 110-119
Open Access | Times Cited: 323
Towards a comprehensive catalogue of validated and target-linked human enhancers
Molly Gasperini, Jacob M. Tome, Jay Shendure
Nature Reviews Genetics (2020) Vol. 21, Iss. 5, pp. 292-310
Open Access | Times Cited: 320
A Systematic p53 Mutation Library Links Differential Functional Impact to Cancer Mutation Pattern and Evolutionary Conservation
Eran Kotler, Odem Shani, Guy Goldfeld, et al.
Molecular Cell (2018) Vol. 71, Iss. 1, pp. 178-190.e8
Open Access | Times Cited: 248
Regulation of glucose and lipid metabolism in health and disease
Ligong Chen, Xiaowei Chen, Xun Huang, et al.
Science China Life Sciences (2019) Vol. 62, Iss. 11, pp. 1420-1458
Closed Access | Times Cited: 227
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect
Daniel Esposito, Jochen Weile, Jay Shendure, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 218
Saturation mutagenesis of twenty disease-associated regulatory elements at single base-pair resolution
Martin Kircher, Chenling Xiong, Beth Martin, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 210
Assessing sufficiency and necessity of enhancer activities for gene expression and the mechanisms of transcription activation
Rui R. Catarino, Alexander Stark
Genes & Development (2018) Vol. 32, Iss. 3-4, pp. 202-223
Open Access | Times Cited: 201
High-throughput identification of human SNPs affecting regulatory element activity
J.H.J. Janssen, Ludo Pagie, Vincent FitzPatrick, et al.
Nature Genetics (2019) Vol. 51, Iss. 7, pp. 1160-1169
Open Access | Times Cited: 189
The roles of RNA processing in translating genotype to phenotype
Kassie S. Manning, Thomas A. Cooper
Nature Reviews Molecular Cell Biology (2016) Vol. 18, Iss. 2, pp. 102-114
Open Access | Times Cited: 187
A systematic evaluation of the design and context dependencies of massively parallel reporter assays
Jason C. Klein, Vikram Agarwal, Fumitaka Inoue, et al.
Nature Methods (2020) Vol. 17, Iss. 11, pp. 1083-1091
Open Access | Times Cited: 177
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: 174
Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis
Leif S. Ludwig, Caleb A. Lareau, Erik L. Bao, et al.
Cell Reports (2019) Vol. 27, Iss. 11, pp. 3228-3240.e7
Open Access | Times Cited: 152
Multiple causal variants underlie genetic associations in humans
Nathan S. Abell, Marianne K. DeGorter, Michael J. Gloudemans, et al.
Science (2022) Vol. 375, Iss. 6586, pp. 1247-1254
Open Access | Times Cited: 138
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
Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 127
Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens
John Morris, Christina M. Caragine, Zharko Daniloski, et al.
Science (2023) Vol. 380, Iss. 6646
Open Access | Times Cited: 112
Functional regulatory variants implicate distinct transcriptional networks in dementia
Yonatan A. Cooper, Noam Teyssier, Nina M. Dräger, et al.
Science (2022) Vol. 377, Iss. 6608
Open Access | Times Cited: 88
Machine-guided design of cell-type-targeting cis-regulatory elements
Sager J. Gosai, Rodrigo Castro, Natalia Fuentes, et al.
Nature (2024) Vol. 634, Iss. 8036, pp. 1211-1220
Open Access | Times Cited: 26
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