
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:
Opportunities and challenges for transcriptome-wide association studies
Michael Wainberg, Nasa Sinnott-Armstrong, Nicholas Mancuso, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 592-599
Open Access | Times Cited: 778
Michael Wainberg, Nasa Sinnott-Armstrong, Nicholas Mancuso, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 592-599
Open Access | Times Cited: 778
Showing 26-50 of 778 citing articles:
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: 102
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 102
The metabolomics of human aging: Advances, challenges, and opportunities
Daniel J. Panyard, Bing Yu, M Snyder
Science Advances (2022) Vol. 8, Iss. 42
Open Access | Times Cited: 93
Daniel J. Panyard, Bing Yu, M Snyder
Science Advances (2022) Vol. 8, Iss. 42
Open Access | Times Cited: 93
Statistical methods for cis‐Mendelian randomization with two‐sample summary‐level data
Apostolos Gkatzionis, Stephen Burgess, Paul J. Newcombe
Genetic Epidemiology (2022) Vol. 47, Iss. 1, pp. 3-25
Open Access | Times Cited: 84
Apostolos Gkatzionis, Stephen Burgess, Paul J. Newcombe
Genetic Epidemiology (2022) Vol. 47, Iss. 1, pp. 3-25
Open Access | Times Cited: 84
Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes
Jack Humphrey, Sanan Venkatesh, Rahat Hasan, et al.
Nature Neuroscience (2022) Vol. 26, Iss. 1, pp. 150-162
Open Access | Times Cited: 79
Jack Humphrey, Sanan Venkatesh, Rahat Hasan, et al.
Nature Neuroscience (2022) Vol. 26, Iss. 1, pp. 150-162
Open Access | Times Cited: 79
Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traits
Biao Zeng, Jaroslav Bendl, Roman Kosoy, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 161-169
Open Access | Times Cited: 74
Biao Zeng, Jaroslav Bendl, Roman Kosoy, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 161-169
Open Access | Times Cited: 74
Single-cell genomics meets human genetics
Anna Cuomo, Aparna Nathan, Soumya Raychaudhuri, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 535-549
Closed Access | Times Cited: 73
Anna Cuomo, Aparna Nathan, Soumya Raychaudhuri, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 535-549
Closed Access | Times Cited: 73
The schizophrenia syndrome, circa 2024: What we know and how that informs its nature
Rajiv Tandon, Henry A. Nasrallah, Schahram Akbarian, et al.
Schizophrenia Research (2023) Vol. 264, pp. 1-28
Open Access | Times Cited: 64
Rajiv Tandon, Henry A. Nasrallah, Schahram Akbarian, et al.
Schizophrenia Research (2023) Vol. 264, pp. 1-28
Open Access | Times Cited: 64
Transcriptome-wide association studies: recent advances in methods, applications and available databases
Jialin Mai, Mingming Lu, Qianwen Gao, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 59
Jialin Mai, Mingming Lu, Qianwen Gao, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 59
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: 52
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 52
Step by step: towards a better understanding of the genetic architecture of Alzheimer’s disease
Jean‐Charles Lambert, Alfredo Ramı́rez, Benjamin Grenier‐Boley, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 7, pp. 2716-2727
Open Access | Times Cited: 51
Jean‐Charles Lambert, Alfredo Ramı́rez, Benjamin Grenier‐Boley, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 7, pp. 2716-2727
Open Access | Times Cited: 51
Aberrant splicing prediction across human tissues
Nils Wagner, Muhammed Hasan Çelik, Florian R. Hölzlwimmer, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 861-870
Open Access | Times Cited: 50
Nils Wagner, Muhammed Hasan Çelik, Florian R. Hölzlwimmer, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 861-870
Open Access | Times Cited: 50
Shared genetic risk loci between Alzheimer’s disease and related dementias, Parkinson’s disease, and amyotrophic lateral sclerosis
Michael Wainberg, Shea J. Andrews, Shreejoy J. Tripathy
Alzheimer s Research & Therapy (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 49
Michael Wainberg, Shea J. Andrews, Shreejoy J. Tripathy
Alzheimer s Research & Therapy (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 49
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
Ashley Budu‐Aggrey, Anna Kilanowski, Maria Sobczyk, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 49
Ashley Budu‐Aggrey, Anna Kilanowski, Maria Sobczyk, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 49
Multi-omics data integration methods and their applications in psychiatric disorders
Anita Sathyanarayanan, Tamara T. Mueller, Mohammad Ali Moni, et al.
European Neuropsychopharmacology (2023) Vol. 69, pp. 26-46
Open Access | Times Cited: 48
Anita Sathyanarayanan, Tamara T. Mueller, Mohammad Ali Moni, et al.
European Neuropsychopharmacology (2023) Vol. 69, pp. 26-46
Open Access | Times Cited: 48
Decoding the genetic and epigenetic basis of asthma
Bernard Stikker, Rudi W. Hendriks, Ralph Stadhouders
Allergy (2023) Vol. 78, Iss. 4, pp. 940-956
Open Access | Times Cited: 47
Bernard Stikker, Rudi W. Hendriks, Ralph Stadhouders
Allergy (2023) Vol. 78, Iss. 4, pp. 940-956
Open Access | Times Cited: 47
Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits
Siming Zhao, Wesley L. Crouse, Sheng Qian, et al.
Nature Genetics (2024)
Open Access | Times Cited: 36
Siming Zhao, Wesley L. Crouse, Sheng Qian, et al.
Nature Genetics (2024)
Open Access | Times Cited: 36
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
Integrative bioinformatics approach identifies novel drug targets for hyperaldosteronism, with a focus on SHMT1 as a promising therapeutic candidate
Minyue Jia, Liya Lin, Hanxiao Yu, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Minyue Jia, Liya Lin, Hanxiao Yu, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Multi-omics approaches for understanding gene-environment interactions in noncommunicable diseases: techniques, translation, and equity issues
Robel Alemu, Nigussie Tadesse Sharew, Yodit Y. Arsano, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Robel Alemu, Nigussie Tadesse Sharew, Yodit Y. Arsano, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access | Times Cited: 2
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
Nick Dand, Philip E. Stuart, John Bowes, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Nick Dand, Philip E. Stuart, John Bowes, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2
A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants
Alexander Gusev, Kate Lawrenson, Xianzhi Lin, et al.
Nature Genetics (2019) Vol. 51, Iss. 5, pp. 815-823
Open Access | Times Cited: 111
Alexander Gusev, Kate Lawrenson, Xianzhi Lin, et al.
Nature Genetics (2019) Vol. 51, Iss. 5, pp. 815-823
Open Access | Times Cited: 111
Probabilistic colocalization of genetic variants from complex and molecular traits: promise and limitations
Abhay Hukku, Milton Pividori, Francesca Luca, et al.
The American Journal of Human Genetics (2020) Vol. 108, Iss. 1, pp. 25-35
Open Access | Times Cited: 106
Abhay Hukku, Milton Pividori, Francesca Luca, et al.
The American Journal of Human Genetics (2020) Vol. 108, Iss. 1, pp. 25-35
Open Access | Times Cited: 106
Enhancer Domains Predict Gene Pathogenicity and Inform Gene Discovery in Complex Disease
Xinchen Wang, David B. Goldstein
The American Journal of Human Genetics (2020) Vol. 106, Iss. 2, pp. 215-233
Open Access | Times Cited: 98
Xinchen Wang, David B. Goldstein
The American Journal of Human Genetics (2020) Vol. 106, Iss. 2, pp. 215-233
Open Access | Times Cited: 98
Genetic drivers of m6A methylation in human brain, lung, heart and muscle
Xushen Xiong, Lei Hou, Yongjin Park, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1156-1165
Open Access | Times Cited: 95
Xushen Xiong, Lei Hou, Yongjin Park, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1156-1165
Open Access | Times Cited: 95
The Human Immunopeptidome Project: A Roadmap to Predict and Treat Immune Diseases
Juan Antonio Vizcaíno, Peter Kubiniok, Kevin A. Kovalchik, et al.
Molecular & Cellular Proteomics (2019) Vol. 19, Iss. 1, pp. 31-49
Open Access | Times Cited: 93
Juan Antonio Vizcaíno, Peter Kubiniok, Kevin A. Kovalchik, et al.
Molecular & Cellular Proteomics (2019) Vol. 19, Iss. 1, pp. 31-49
Open Access | Times Cited: 93