
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:
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
Showing 1-25 of 91 citing articles:
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, et al.
Nature Genetics (2023) Vol. 55, Iss. 2, pp. 198-208
Open Access | Times Cited: 374
Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, et al.
Nature Genetics (2023) Vol. 55, Iss. 2, pp. 198-208
Open Access | Times Cited: 374
Polygenic architecture of rare coding variation across 394,783 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 111
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 111
The missing link between genetic association and regulatory function
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 100
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 100
Epigenomic dissection of Alzheimer’s disease pinpoints causal variants and reveals epigenome erosion
Xushen Xiong, Benjamin T. James, Carles A. Boix, et al.
Cell (2023) Vol. 186, Iss. 20, pp. 4422-4437.e21
Open Access | Times Cited: 90
Xushen Xiong, Benjamin T. James, Carles A. Boix, et al.
Cell (2023) Vol. 186, Iss. 20, pp. 4422-4437.e21
Open Access | Times Cited: 90
Precise modulation of transcription factor levels identifies features underlying dosage sensitivity
Sahin Naqvi, Seungsoo Kim, Hanne Hoskens, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 841-851
Open Access | Times Cited: 67
Sahin Naqvi, Seungsoo Kim, Hanne Hoskens, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 841-851
Open Access | Times Cited: 67
Molecular quantitative trait loci
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 50
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 50
Common genetic factors among autoimmune diseases
Adil Harroud, David A. Hafler
Science (2023) Vol. 380, Iss. 6644, pp. 485-490
Closed Access | Times Cited: 47
Adil Harroud, David A. Hafler
Science (2023) Vol. 380, Iss. 6644, pp. 485-490
Closed Access | Times Cited: 47
Genetic and molecular architecture of complex traits
Tuuli Lappalainen, Yang Li, Sohini Ramachandran, et al.
Cell (2024) Vol. 187, Iss. 5, pp. 1059-1075
Open Access | Times Cited: 21
Tuuli Lappalainen, Yang Li, Sohini Ramachandran, et al.
Cell (2024) Vol. 187, Iss. 5, pp. 1059-1075
Open Access | Times Cited: 21
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain
Cindy Wen, Michael Margolis, Rujia Dai, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 18
Cindy Wen, Michael Margolis, Rujia Dai, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 18
Single-cell multiome of the human retina and deep learning nominate causal variants in complex eye diseases
Sean K. Wang, Surag Nair, Rui Li, et al.
Cell Genomics (2022) Vol. 2, Iss. 8, pp. 100164-100164
Open Access | Times Cited: 43
Sean K. Wang, Surag Nair, Rui Li, et al.
Cell Genomics (2022) Vol. 2, Iss. 8, pp. 100164-100164
Open Access | Times Cited: 43
Relating pathogenic loss-of-function mutations in humans to their evolutionary fitness costs
Ipsita Agarwal, Zachary L. Fuller, Simon Myers, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 35
Ipsita Agarwal, Zachary L. Fuller, Simon Myers, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 35
From ‘Omics to Multi-omics Technologies: the Discovery of Novel Causal Mediators
Pedrum Mohammadi‐Shemirani, Tushar Sood, Guillaume Paré
Current Atherosclerosis Reports (2023) Vol. 25, Iss. 2, pp. 55-65
Open Access | Times Cited: 30
Pedrum Mohammadi‐Shemirani, Tushar Sood, Guillaume Paré
Current Atherosclerosis Reports (2023) Vol. 25, Iss. 2, pp. 55-65
Open Access | Times Cited: 30
Proteogenomic links to human metabolic diseases
Mine Koprulu, Julia Carrasco-Zanini, Eleanor Wheeler, et al.
Nature Metabolism (2023) Vol. 5, Iss. 3, pp. 516-528
Open Access | Times Cited: 26
Mine Koprulu, Julia Carrasco-Zanini, Eleanor Wheeler, et al.
Nature Metabolism (2023) Vol. 5, Iss. 3, pp. 516-528
Open Access | Times Cited: 26
Methods and Insights from Single-Cell Expression Quantitative Trait Loci
Joyce B. Kang, Alessandro Raveane, Aparna Nathan, et al.
Annual Review of Genomics and Human Genetics (2023) Vol. 24, Iss. 1, pp. 277-303
Open Access | Times Cited: 26
Joyce B. Kang, Alessandro Raveane, Aparna Nathan, et al.
Annual Review of Genomics and Human Genetics (2023) Vol. 24, Iss. 1, pp. 277-303
Open Access | Times Cited: 26
Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 24
Jessica C. McAfee, Sool Lee, Jiseok Lee, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100404-100404
Open Access | Times Cited: 24
From genetic associations to genes: methods, applications, and challenges
Ting Qi, Liyang Song, Yazhou Guo, et al.
Trends in Genetics (2024) Vol. 40, Iss. 8, pp. 642-667
Open Access | Times Cited: 15
Ting Qi, Liyang Song, Yazhou Guo, et al.
Trends in Genetics (2024) Vol. 40, Iss. 8, pp. 642-667
Open Access | Times Cited: 15
Regulatory features aid interpretation of 3′UTR variants
Lindsay Romo, Scott D. Findlay, Christopher B. Burge
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 350-363
Open Access | Times Cited: 10
Lindsay Romo, Scott D. Findlay, Christopher B. Burge
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 350-363
Open Access | Times Cited: 10
The genetic regulation of protein expression in cerebrospinal fluid
Oskar Hansson, Atul Kumar, Shorena Janelidze, et al.
EMBO Molecular Medicine (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 35
Oskar Hansson, Atul Kumar, Shorena Janelidze, et al.
EMBO Molecular Medicine (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 35
Multi-layered genetic approaches to identify approved drug targets
Marie C. Sadler, Chiara Auwerx, Patrick Deelen, et al.
Cell Genomics (2023) Vol. 3, Iss. 7, pp. 100341-100341
Open Access | Times Cited: 20
Marie C. Sadler, Chiara Auwerx, Patrick Deelen, et al.
Cell Genomics (2023) Vol. 3, Iss. 7, pp. 100341-100341
Open Access | Times Cited: 20
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs
Seong Kyu Han, Michelle Mcnulty, Christopher J. Benway, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 19
Seong Kyu Han, Michelle Mcnulty, Christopher J. Benway, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 19
Cell type-specific and disease-associated eQTL in the human lung
Heini M. Natri, Christina B. Azodi, Lance Peter, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 17
Heini M. Natri, Christina B. Azodi, Lance Peter, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 17
SURGE: uncovering context-specific genetic-regulation of gene expression from single-cell RNA sequencing using latent-factor models
Benjamin J. Strober, Karl Tayeb, Joshua M Popp, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Benjamin J. Strober, Karl Tayeb, Joshua M Popp, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Mapping the functional impact of non-coding regulatory elements in primary T cells through single-cell CRISPR screens
Celia Alda-Catalinas, Ximena Ibarra-Soria, Christina Flouri, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Celia Alda-Catalinas, Ximena Ibarra-Soria, Christina Flouri, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Genetic regulatory effects in response to a high-cholesterol, high-fat diet in baboons
Wenhe Lin, Jeffrey D. Wall, Ge Li, et al.
Cell Genomics (2024) Vol. 4, Iss. 3, pp. 100509-100509
Open Access | Times Cited: 6
Wenhe Lin, Jeffrey D. Wall, Ge Li, et al.
Cell Genomics (2024) Vol. 4, Iss. 3, pp. 100509-100509
Open Access | Times Cited: 6
Massively parallel characterization of psychiatric disorder-associated and cell-type-specific regulatory elements in the developing human cortex
Chengyu Deng, Sean Whalen, Marilyn Steyert, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16
Chengyu Deng, Sean Whalen, Marilyn Steyert, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16