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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:

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

Showing 26-50 of 189 citing articles:

Uncovering the whole genome silencers of human cells via Ss-STARR-seq
Xiusheng Zhu, Lei Huang, Chao Wang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation
Antoinette F. van Ouwerkerk, Amelia Weber Hall, Zachary A. Kadow, et al.
Circulation Research (2020) Vol. 127, Iss. 1, pp. 34-50
Open Access | Times Cited: 65
Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variation
Shuquan Rao, Yao Yao, Daniel E. Bauer
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 56
Local adaptation and archaic introgression shape global diversity at human structural variant loci
Stephanie M. Yan, Rachel M. Sherman, Dylan J. Taylor, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 44
Challenges and opportunities associated with rare-variant pharmacogenomics
Yitian Zhou, Roman Tremmel, Elke Schaeffeler, et al.
Trends in Pharmacological Sciences (2022) Vol. 43, Iss. 10, pp. 852-865
Open Access | Times Cited: 33
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements
Peter Dixon, Adam P. Levine, Inês Cebola, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 31
Enhancer–silencer transitions in the human genome
Di Huang, Ivan Ovcharenko
Genome Research (2022) Vol. 32, Iss. 3, pp. 437-448
Open Access | Times Cited: 29
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
Neuronal MAPT expression is mediated by long-range interactions with cis-regulatory elements
Brianne B. Rogers, Ashlyn G. Anderson, Shelby N. Lauzon, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 259-279
Open Access | Times Cited: 7
Massively parallel techniques for cataloguing the regulome of the human brain
Kayla G. Townsley, Kristen Brennand, Laura M. Huckins
Nature Neuroscience (2020) Vol. 23, Iss. 12, pp. 1509-1521
Open Access | Times Cited: 49
Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract
Rik Westland, Kirsten Y. Renkema, Nine V.A.M. Knoers
Clinical Journal of the American Society of Nephrology (2020) Vol. 16, Iss. 1, pp. 128-137
Open Access | Times Cited: 47
Massively Parallel Reporter Assays: Defining Functional Psychiatric Genetic Variants Across Biological Contexts
Bernard Mulvey, Tomás Lagunas, Joseph D. Dougherty
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 76-89
Open Access | Times Cited: 44
Deregulated Regulators: Disease-Causing cis Variants in Transcription Factor Genes
Robin van der Lee, Solenne Correard, Wyeth W. Wasserman
Trends in Genetics (2020) Vol. 36, Iss. 7, pp. 523-539
Open Access | Times Cited: 42
Neanderthal introgression reintroduced functional ancestral alleles lost in Eurasian populations
David C. Rinker, Corinne Simonti, Evonne McArthur, et al.
Nature Ecology & Evolution (2020) Vol. 4, Iss. 10, pp. 1332-1341
Open Access | Times Cited: 42
Identification of Functional Variant Enhancers Associated With Atrial Fibrillation
Antoinette F. van Ouwerkerk, Fernanda M. Bosada, Jia Liu, et al.
Circulation Research (2020) Vol. 127, Iss. 2, pp. 229-243
Open Access | Times Cited: 40
Enhancer RNAs step forward: new insights into enhancer function
Laura J. Harrison, Daniel Bose
Development (2022) Vol. 149, Iss. 16
Open Access | Times Cited: 26
Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity
Erping Long, Jinhu Yin, Karen Funderburk, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 12, pp. 2210-2229
Open Access | Times Cited: 25
The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force
Qingbo Wang, Ryuya Edahiro, Ho Namkoong, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 24
Functional noncoding SNPs in human endothelial cells fine-map vascular trait associations
Anu Toropainen, Lindsey K. Stolze, Tiit Örd, et al.
Genome Research (2022) Vol. 32, Iss. 3, pp. 409-424
Open Access | Times Cited: 23
In it for the long run: perspectives on exploiting long-read sequencing in livestock for population scale studies of structural variants
Tuan V. Nguyen, Christy J. Vander Jagt, Jianhui Wang, et al.
Genetics Selection Evolution (2023) Vol. 55, Iss. 1
Open Access | Times Cited: 16
DNA variants affecting the expression of numerous genes in trans have diverse mechanisms of action and evolutionary histories
Sheila Lutz, Christian Brion, Margaret Kliebhan, et al.
PLoS Genetics (2019) Vol. 15, Iss. 11, pp. e1008375-e1008375
Open Access | Times Cited: 36
Missing heritability in Parkinson’s disease: the emerging role of non-coding genetic variation
Jochen Ohnmacht, Patrick May, Lasse Sinkkonen, et al.
Journal of Neural Transmission (2020) Vol. 127, Iss. 5, pp. 729-748
Open Access | Times Cited: 35
Fine-mapping of Parkinson’s disease susceptibility loci identifies putative causal variants
Brian M. Schilder, Towfique Raj
Human Molecular Genetics (2021) Vol. 31, Iss. 6, pp. 888-900
Open Access | Times Cited: 32
Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex
Evgeniia Golovina, Tayaza Fadason, Thierry Lints, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 29
Computational and experimental methods for classifying variants of unknown clinical significance.
Malte Spielmann, Martin Kircher
PubMed (2022) Vol. 8, Iss. 3
Closed Access | Times Cited: 21

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