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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:

Interpreting noncoding genetic variation in complex traits and human disease
Lucas D. Ward, Manolis Kellis
Nature Biotechnology (2012) Vol. 30, Iss. 11, pp. 1095-1106
Open Access | Times Cited: 497

Showing 1-25 of 497 citing articles:

The Ensembl Variant Effect Predictor
William McLaren, Laurent Gil, Sarah Hunt, et al.
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 6463
A general framework for estimating the relative pathogenicity of human genetic variants
Martin Kircher, Daniela Witten, Preti Jain, et al.
Nature Genetics (2014) Vol. 46, Iss. 3, pp. 310-315
Open Access | Times Cited: 5832
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
Kristin G. Ardlie, David S. DeLuca, Ayellet V. Segrè, et al.
Science (2015) Vol. 348, Iss. 6235, pp. 648-660
Open Access | Times Cited: 5018
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Michael J. Gandal, Pan Zhang, Evi Hadjimichael, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 1069
HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease
Lucas D. Ward, Manolis Kellis
Nucleic Acids Research (2015) Vol. 44, Iss. D1, pp. D877-D881
Open Access | Times Cited: 862
IL-12 and IL-23 cytokines: from discovery to targeted therapies for immune-mediated inflammatory diseases
Michele W.L. Teng, Edward P. Bowman, Joshua McElwee, et al.
Nature Medicine (2015) Vol. 21, Iss. 7, pp. 719-729
Closed Access | Times Cited: 779
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants
Stephen C. J. Parker, Michael L. Stitzel, D. Leland Taylor, et al.
Proceedings of the National Academy of Sciences (2013) Vol. 110, Iss. 44, pp. 17921-17926
Open Access | Times Cited: 669
Genetics of autism spectrum disorders
Daniel H. Geschwind
Trends in Cognitive Sciences (2011) Vol. 15, Iss. 9, pp. 409-416
Open Access | Times Cited: 667
Pharmacogenomics of GPCR Drug Targets
Alexander S. Hauser, Sreenivas Chavali, Ikuo Masuho, et al.
Cell (2017) Vol. 172, Iss. 1-2, pp. 41-54.e19
Open Access | Times Cited: 564
Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression
Frank Soldner, Yonatan Stelzer, Chikdu Shivalila, et al.
Nature (2016) Vol. 533, Iss. 7601, pp. 95-99
Open Access | Times Cited: 487
Molecular control of activation and priming in macrophages
Christopher K. Glass, Gioacchino Natoli
Nature Immunology (2015) Vol. 17, Iss. 1, pp. 26-33
Open Access | Times Cited: 460
The PsychENCODE project
Schahram Akbarian, Chunyu Liu, James A. Knowles, et al.
Nature Neuroscience (2015) Vol. 18, Iss. 12, pp. 1707-1712
Open Access | Times Cited: 416
The Ensembl Variant Effect Predictor
William McLaren, Laurent Gil, Sarah Hunt, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2016)
Open Access | Times Cited: 378
Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics
Ekta Khurana, Yao Fu, Vincenza Colonna, et al.
Science (2013) Vol. 342, Iss. 6154
Open Access | Times Cited: 375
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood
Ting Qi, Yang Wu, Jian Zeng, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 355
Abundant contribution of short tandem repeats to gene expression variation in humans
Melissa Gymrek, Thomas Willems, Audrey Guilmatre, et al.
Nature Genetics (2015) Vol. 48, Iss. 1, pp. 22-29
Open Access | Times Cited: 354
FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer
Yao Fu, Zhu Liu, Shaoke Lou, et al.
Genome biology (2014) Vol. 15, Iss. 10
Open Access | Times Cited: 351
The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis
Luis de la Torre-Ubieta, Jason L. Stein, Hyejung Won, et al.
Cell (2018) Vol. 172, Iss. 1-2, pp. 289-304.e18
Open Access | Times Cited: 345
Regulatory genomic circuitry of human disease loci by integrative epigenomics
Carles A. Boix, Benjamin T. James, Yongjin Park, et al.
Nature (2021) Vol. 590, Iss. 7845, pp. 300-307
Open Access | Times Cited: 340
Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases
Daniel Marbach, David Lamparter, Gerald Quon, et al.
Nature Methods (2016) Vol. 13, Iss. 4, pp. 366-370
Open Access | Times Cited: 338
HDL-targeted therapies: progress, failures and future
Bronwyn A. Kingwell, M. John Chapman, Anatol Kontush, et al.
Nature Reviews Drug Discovery (2014) Vol. 13, Iss. 6, pp. 445-464
Closed Access | Times Cited: 328
Driver and Passenger Mutations in Cancer
Julia R. Pon, Marco A. Marra
Annual Review of Pathology Mechanisms of Disease (2014) Vol. 10, Iss. 1, pp. 25-50
Open Access | Times Cited: 327
Transgenerational epigenetic inheritance: how important is it?
Ueli Grossniklaus, William G. Kelly, Anne C. Ferguson‐Smith, et al.
Nature Reviews Genetics (2013) Vol. 14, Iss. 3, pp. 228-235
Open Access | Times Cited: 287
Collective judgment predicts disease-associated single nucleotide variants
Emidio Capriotti, Russ B. Altman, Yana Bromberg
BMC Genomics (2013) Vol. 14, Iss. Suppl 3, pp. S2-S2
Open Access | Times Cited: 278
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
Damian Smedley, Max Schubach, Julius O.B. Jacobsen, et al.
The American Journal of Human Genetics (2016) Vol. 99, Iss. 3, pp. 595-606
Open Access | Times Cited: 261
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