
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:
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: 344
Carles A. Boix, Benjamin T. James, Yongjin Park, et al.
Nature (2021) Vol. 590, Iss. 7845, pp. 300-307
Open Access | Times Cited: 344
Showing 1-25 of 344 citing articles:
GENCODE: reference annotation for the human and mouse genomes in 2023
Adam Frankish, Sílvia Carbonell Sala, Mark Diekhans, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D942-D949
Open Access | Times Cited: 367
Adam Frankish, Sílvia Carbonell Sala, Mark Diekhans, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D942-D949
Open Access | Times Cited: 367
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: 333
Kai Zhang, James D. Hocker, Michael Miller, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5985-6001.e19
Open Access | Times Cited: 333
Gene regulatory network inference in the era of single-cell multi-omics
Pau Badia-i-Mompel, Lorna Wessels, Sophia Müller‐Dott, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 11, pp. 739-754
Closed Access | Times Cited: 188
Pau Badia-i-Mompel, Lorna Wessels, Sophia Müller‐Dott, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 11, pp. 739-754
Closed Access | Times Cited: 188
Multi-Omics Profiling for Health
Mohan Babu, M Snyder
Molecular & Cellular Proteomics (2023) Vol. 22, Iss. 6, pp. 100561-100561
Open Access | Times Cited: 150
Mohan Babu, M Snyder
Molecular & Cellular Proteomics (2023) Vol. 22, Iss. 6, pp. 100561-100561
Open Access | Times Cited: 150
Characterizing cis-regulatory elements using single-cell epigenomics
Sebastian Preißl, Kyle J. Gaulton, Bing Ren
Nature Reviews Genetics (2022) Vol. 24, Iss. 1, pp. 21-43
Closed Access | Times Cited: 149
Sebastian Preißl, Kyle J. Gaulton, Bing Ren
Nature Reviews Genetics (2022) Vol. 24, Iss. 1, pp. 21-43
Closed Access | Times Cited: 149
Enhancers in disease: molecular basis and emerging treatment strategies
Annique Claringbould, Judith B. Zaugg
Trends in Molecular Medicine (2021) Vol. 27, Iss. 11, pp. 1060-1073
Open Access | Times Cited: 146
Annique Claringbould, Judith B. Zaugg
Trends in Molecular Medicine (2021) Vol. 27, Iss. 11, pp. 1060-1073
Open Access | Times Cited: 146
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
Hongbo Liu, Tomohito Doke, Dong Guo, et al.
Nature Genetics (2022) Vol. 54, Iss. 7, pp. 950-962
Closed Access | Times Cited: 144
Hongbo Liu, Tomohito Doke, Dong Guo, et al.
Nature Genetics (2022) Vol. 54, Iss. 7, pp. 950-962
Closed Access | Times Cited: 144
Pig genome functional annotation enhances the biological interpretation of complex traits and human disease
Zhangyuan Pan, Yuelin Yao, Hongwei Yin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 141
Zhangyuan Pan, Yuelin Yao, Hongwei Yin, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 141
Evolutionary constraint and innovation across hundreds of placental mammals
Matthew J. Christmas, Irene M. Kaplow, Diane P. Genereux, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 140
Matthew J. Christmas, Irene M. Kaplow, Diane P. Genereux, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 140
Sequence-based modeling of three-dimensional genome architecture from kilobase to chromosome scale
Jian Zhou
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 725-734
Open Access | Times Cited: 127
Jian Zhou
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 725-734
Open Access | Times Cited: 127
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: 125
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 125
Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
WhichTF is functionally important in your open chromatin data?
Yosuke Tanigawa, Ethan S. Dyer, Gill Bejerano
PLoS Computational Biology (2022) Vol. 18, Iss. 8, pp. e1010378-e1010378
Open Access | Times Cited: 90
Yosuke Tanigawa, Ethan S. Dyer, Gill Bejerano
PLoS Computational Biology (2022) Vol. 18, Iss. 8, pp. e1010378-e1010378
Open Access | Times Cited: 90
Annotating and prioritizing human non-coding variants with RegulomeDB v.2
Shengcheng Dong, Nanxiang Zhao, Emma Spragins, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 724-726
Open Access | Times Cited: 88
Shengcheng Dong, Nanxiang Zhao, Emma Spragins, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 724-726
Open Access | Times Cited: 88
Complementary Alu sequences mediate enhancer–promoter selectivity
Liang Liang, Changchang Cao, Lei Ji, et al.
Nature (2023) Vol. 619, Iss. 7971, pp. 868-875
Closed Access | Times Cited: 87
Liang Liang, Changchang Cao, Lei Ji, et al.
Nature (2023) Vol. 619, Iss. 7971, pp. 868-875
Closed Access | Times Cited: 87
Cell fate decisions, transcription factors and signaling during early retinal development
Raven Diacou, Prithviraj Nandigrami, András Fiser, et al.
Progress in Retinal and Eye Research (2022) Vol. 91, pp. 101093-101093
Open Access | Times Cited: 80
Raven Diacou, Prithviraj Nandigrami, András Fiser, et al.
Progress in Retinal and Eye Research (2022) Vol. 91, pp. 101093-101093
Open Access | Times Cited: 80
Single-nucleus multiregion transcriptomic analysis of brain vasculature in Alzheimer’s disease
Na Sun, Leyla Anne Akay, Mitchell H. Murdock, et al.
Nature Neuroscience (2023) Vol. 26, Iss. 6, pp. 970-982
Open Access | Times Cited: 79
Na Sun, Leyla Anne Akay, Mitchell H. Murdock, et al.
Nature Neuroscience (2023) Vol. 26, Iss. 6, pp. 970-982
Open Access | Times Cited: 79
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
Genetic variation in the immunoglobulin heavy chain locus shapes the human antibody repertoire
Oscar L. Rodriguez, Yana Safonova, Catherine A. Silver, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 53
Oscar L. Rodriguez, Yana Safonova, Catherine A. Silver, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 53
An encyclopedia of enhancer-gene regulatory interactions in the human genome
Andreas R. Gschwind, Kristy S. Mualim, Alireza Karbalayghareh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 45
Andreas R. Gschwind, Kristy S. Mualim, Alireza Karbalayghareh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 45
Conserved and divergent gene regulatory programs of the mammalian neocortex
Nathan R. Zemke, Ethan J. Armand, Wenliang Wang, et al.
Nature (2023) Vol. 624, Iss. 7991, pp. 390-402
Open Access | Times Cited: 44
Nathan R. Zemke, Ethan J. Armand, Wenliang Wang, et al.
Nature (2023) Vol. 624, Iss. 7991, pp. 390-402
Open Access | Times Cited: 44
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 33
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 33
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma
Shefali S. Verma, Harini V. Gudiseva, Venkata Ramana Murthy Chavali, et al.
Cell (2024) Vol. 187, Iss. 2, pp. 464-480.e10
Open Access | Times Cited: 25
Shefali S. Verma, Harini V. Gudiseva, Venkata Ramana Murthy Chavali, et al.
Cell (2024) Vol. 187, Iss. 2, pp. 464-480.e10
Open Access | Times Cited: 25
Tissue-specific enhancer–gene maps from multimodal single-cell data identify causal disease alleles
Saori Sakaue, Kathryn Weinand, Shakson Isaac, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 615-626
Open Access | Times Cited: 23
Saori Sakaue, Kathryn Weinand, Shakson Isaac, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 615-626
Open Access | Times Cited: 23
A review of cancer data fusion methods based on deep learning
Yuxin Zhao, Xiaobo Li, Changjun Zhou, et al.
Information Fusion (2024) Vol. 108, pp. 102361-102361
Closed Access | Times Cited: 19
Yuxin Zhao, Xiaobo Li, Changjun Zhou, et al.
Information Fusion (2024) Vol. 108, pp. 102361-102361
Closed Access | Times Cited: 19