
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:
Making sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genome
Yu Gyoung Tak, Peggy Farnham
Epigenetics & Chromatin (2015) Vol. 8, Iss. 1
Open Access | Times Cited: 338
Yu Gyoung Tak, Peggy Farnham
Epigenetics & Chromatin (2015) Vol. 8, Iss. 1
Open Access | Times Cited: 338
Showing 26-50 of 338 citing articles:
Disease-Associated SNPs in Inflammation-Related lncRNAs
Ainara Castellanos‐Rubio, Sankar Ghosh
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 85
Ainara Castellanos‐Rubio, Sankar Ghosh
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 85
DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning
Janine Arloth, Gökçen Eraslan, Till F. M. Andlauer, et al.
PLoS Computational Biology (2020) Vol. 16, Iss. 2, pp. e1007616-e1007616
Open Access | Times Cited: 82
Janine Arloth, Gökçen Eraslan, Till F. M. Andlauer, et al.
PLoS Computational Biology (2020) Vol. 16, Iss. 2, pp. e1007616-e1007616
Open Access | Times Cited: 82
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism
Nana Matoba, Dan Liang, Huaigu Sun, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 82
Nana Matoba, Dan Liang, Huaigu Sun, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 82
The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseases
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 55
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 55
FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases
Charles E. Breeze, Eric Haugen, María Gutiérrez‐Arcelus, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 16
Charles E. Breeze, Eric Haugen, María Gutiérrez‐Arcelus, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 16
Decoding Non-coding Variants: Recent Approaches to Studying Their Role in Gene Regulation and Human Diseases
Edwin G. Peña-Martínez, José A. Rodríguez‐Martínez
Frontiers in Bioscience-Scholar (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 13
Edwin G. Peña-Martínez, José A. Rodríguez‐Martínez
Frontiers in Bioscience-Scholar (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 13
Enhancer RNA Transcriptome‐Wide Association Study Reveals a Distinctive Class of Pan‐Cancer Susceptibility eRNAs
Wenyan Chen, Zeyang Wang, Yinuo Wang, et al.
Advanced Science (2025)
Open Access | Times Cited: 1
Wenyan Chen, Zeyang Wang, Yinuo Wang, et al.
Advanced Science (2025)
Open Access | Times Cited: 1
Improved regulatory element prediction based on tissue-specific local epigenomic signatures
Yupeng He, David U. Gorkin, Diane E. Dickel, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 9
Open Access | Times Cited: 83
Yupeng He, David U. Gorkin, Diane E. Dickel, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 9
Open Access | Times Cited: 83
High-throughput screening of prostate cancer risk loci by single nucleotide polymorphisms sequencing
Peng Zhang, Ji‐Han Xia, Jing Zhu, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 82
Peng Zhang, Ji‐Han Xia, Jing Zhu, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 82
Using single‐cell multiple omics approaches to resolve tumor heterogeneity
Michael A. Ortega, Olivier Poirion, Xun Zhu, et al.
Clinical and Translational Medicine (2017) Vol. 6, Iss. 1
Open Access | Times Cited: 81
Michael A. Ortega, Olivier Poirion, Xun Zhu, et al.
Clinical and Translational Medicine (2017) Vol. 6, Iss. 1
Open Access | Times Cited: 81
Osteoarthritis year in review 2016: genetics, genomics and epigenetics
Joyce B. J. van Meurs
Osteoarthritis and Cartilage (2017) Vol. 25, Iss. 2, pp. 181-189
Open Access | Times Cited: 77
Joyce B. J. van Meurs
Osteoarthritis and Cartilage (2017) Vol. 25, Iss. 2, pp. 181-189
Open Access | Times Cited: 77
DIVAN: accurate identification of non-coding disease-specific risk variants using multi-omics profiles
Li Chen, Peng Jin, Zhaohui Qin
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 76
Li Chen, Peng Jin, Zhaohui Qin
Genome biology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 76
microRNA single polynucleotide polymorphism influences on microRNA biogenesis and mRNA target specificity
Jarosław Króliczewski, Aleksandra Sobolewska, Dawid Lejnowski, et al.
Gene (2017) Vol. 640, pp. 66-72
Closed Access | Times Cited: 76
Jarosław Króliczewski, Aleksandra Sobolewska, Dawid Lejnowski, et al.
Gene (2017) Vol. 640, pp. 66-72
Closed Access | Times Cited: 76
A genome-wide long noncoding RNA CRISPRi screen identifies PRANCR as a novel regulator of epidermal homeostasis
Pengfei Cai, Auke B.C. Otten, Binbin Cheng, et al.
Genome Research (2019) Vol. 30, Iss. 1, pp. 22-34
Open Access | Times Cited: 76
Pengfei Cai, Auke B.C. Otten, Binbin Cheng, et al.
Genome Research (2019) Vol. 30, Iss. 1, pp. 22-34
Open Access | Times Cited: 76
Exploring the epigenetic drug discovery landscape
Veda Prachayasittikul, Philip Prathipati, Reny Pratiwi, et al.
Expert Opinion on Drug Discovery (2017) Vol. 12, Iss. 4, pp. 345-362
Closed Access | Times Cited: 73
Veda Prachayasittikul, Philip Prathipati, Reny Pratiwi, et al.
Expert Opinion on Drug Discovery (2017) Vol. 12, Iss. 4, pp. 345-362
Closed Access | Times Cited: 73
CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops
Yu Guo, Andrew Perez, Dennis J. Hazelett, et al.
Genome biology (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 70
Yu Guo, Andrew Perez, Dennis J. Hazelett, et al.
Genome biology (2018) Vol. 19, Iss. 1
Open Access | Times Cited: 70
Genome-wide enhancer annotations differ significantly in genomic distribution, evolution, and function
Mary Lauren Benton, Sai Charan Talipineni, Dennis Kostka, et al.
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 58
Mary Lauren Benton, Sai Charan Talipineni, Dennis Kostka, et al.
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 58
Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits
Chelsea K. Raulerson, Arthur Ko, John Kidd, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 4, pp. 773-787
Open Access | Times Cited: 58
Chelsea K. Raulerson, Arthur Ko, John Kidd, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 4, pp. 773-787
Open Access | Times Cited: 58
Signature-based approaches for informed drug repurposing: targeting CNS disorders
Rammohan Shukla, Nicholas Henkel, Khaled Alganem, et al.
Neuropsychopharmacology (2020) Vol. 46, Iss. 1, pp. 116-130
Open Access | Times Cited: 55
Rammohan Shukla, Nicholas Henkel, Khaled Alganem, et al.
Neuropsychopharmacology (2020) Vol. 46, Iss. 1, pp. 116-130
Open Access | Times Cited: 55
Advanced Breeding Strategies and Future Perspectives of Salinity Tolerance in Rice
M. A. Haque, Mohd Y. Rafii, Martini Mohammad Yusoff, et al.
Agronomy (2021) Vol. 11, Iss. 8, pp. 1631-1631
Open Access | Times Cited: 51
M. A. Haque, Mohd Y. Rafii, Martini Mohammad Yusoff, et al.
Agronomy (2021) Vol. 11, Iss. 8, pp. 1631-1631
Open Access | Times Cited: 51
From Junk to Function: LncRNAs in CNS Health and Disease
Rafaela Policarpo, Annerieke Sierksma, Bart De Strooper, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 48
Rafaela Policarpo, Annerieke Sierksma, Bart De Strooper, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 48
Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations
Charles E. Breeze, Eric Haugen, Alex Reynolds, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 30
Charles E. Breeze, Eric Haugen, Alex Reynolds, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 30
Single-nucleotide variants within heart enhancers increase binding affinity and disrupt heart development
Granton A. Jindal, Alexis Bantle, Joe J. Solvason, et al.
Developmental Cell (2023) Vol. 58, Iss. 21, pp. 2206-2216.e5
Open Access | Times Cited: 23
Granton A. Jindal, Alexis Bantle, Joe J. Solvason, et al.
Developmental Cell (2023) Vol. 58, Iss. 21, pp. 2206-2216.e5
Open Access | Times Cited: 23
Integrative mapping of the dog epigenome: Reference annotation for comparative intertissue and cross-species studies
Keun Hong Son, Mark Borris D. Aldonza, A-Reum Nam, et al.
Science Advances (2023) Vol. 9, Iss. 27
Open Access | Times Cited: 18
Keun Hong Son, Mark Borris D. Aldonza, A-Reum Nam, et al.
Science Advances (2023) Vol. 9, Iss. 27
Open Access | Times Cited: 18
RNA‐binding proteins implicated in neurodegenerative diseases
Mark Cookson
Wiley Interdisciplinary Reviews - RNA (2016) Vol. 8, Iss. 1
Open Access | Times Cited: 58
Mark Cookson
Wiley Interdisciplinary Reviews - RNA (2016) Vol. 8, Iss. 1
Open Access | Times Cited: 58