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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:

Genetic association of molecular traits: A help to identify causative variants in complex diseases
Claire Vandiedonck
Clinical Genetics (2017) Vol. 93, Iss. 3, pp. 520-532
Open Access | Times Cited: 53

Showing 1-25 of 53 citing articles:

Genetic impacts on DNA methylation: research findings and future perspectives
Sergio Villicaña, Jordana T. Bell
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 166
High-Diversity Mouse Populations for Complex Traits
Michael C. Saul, Vivek M. Philip, Laura G. Reinholdt, et al.
Trends in Genetics (2019) Vol. 35, Iss. 7, pp. 501-514
Open Access | Times Cited: 150
QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes
Zhanye Zheng, Dandan Huang, Jianhua Wang, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. D1, pp. D983-D991
Open Access | Times Cited: 115
Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations
Chiara Auwerx, Marie C. Sadler, Tristan Woh, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 25
Genetic variation and microRNA targeting of A-to-I RNA editing fine tune human tissue transcriptomes
Eddie Park, Yan Jiang, Lili Hao, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 50
Genetic approaches for increasing fitness in endangered species
Tiffany A. Kosch, Anthony W. Waddle, Caitlin Cooper, et al.
Trends in Ecology & Evolution (2022) Vol. 37, Iss. 4, pp. 332-345
Closed Access | Times Cited: 37
How dysregulation of the immune system promotes diabetes mellitus and cardiovascular risk complications
Diane Girard, Claire Vandiedonck
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 30
Genetics and Functional Genomics of Spondyloarthritis
Félicie Costantino, Maxime Bréban, Henri‐Jean Garchon
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 54
Strengthening Causal Inference for Complex Disease Using Molecular Quantitative Trait Loci
Sonja Neumeyer, Gibran Hemani, Eleftheria Zeggini
Trends in Molecular Medicine (2019) Vol. 26, Iss. 2, pp. 232-241
Open Access | Times Cited: 46
Primo: integration of multiple GWAS and omics QTL summary statistics for elucidation of molecular mechanisms of trait-associated SNPs and detection of pleiotropy in complex traits
Kevin J. Gleason, Fan Yang, Brandon L. Pierce, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 40
Genome-wide analysis of expression QTL (eQTL) and allele-specific expression (ASE) in pig muscle identifies candidate genes for meat quality traits
Yan Liu, Xiaolei Liu, Zhiwei Zheng, et al.
Genetics Selection Evolution (2020) Vol. 52, Iss. 1
Open Access | Times Cited: 39
Regulation of inflammation in diabetes: From genetics to epigenomics evidence
Marc Diedisheim, Elena Carcarino, Claire Vandiedonck, et al.
Molecular Metabolism (2020) Vol. 41, pp. 101041-101041
Open Access | Times Cited: 34
CancerImmunityQTL: a database to systematically evaluate the impact of genetic variants on immune infiltration in human cancer
Jianbo Tian, Yimin Cai, Yue Li, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1065-D1073
Open Access | Times Cited: 31
QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes
Dandan Huang, Xiangling Feng, Hongxi Yang, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1122-D1128
Open Access | Times Cited: 18
Genetic variation in histone modifications and gene expression identifies regulatory variants in the mammary gland of cattle
Claire Prowse-Wilkins, Thomas Lopdell, Ruidong Xiang, et al.
BMC Genomics (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 17
From the Genetics of Ankylosing Spondylitis to New Biology and Drug Target Discovery
Nancy Zaarour, Yan Li, Hui Shi, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 21
Genetic risk variants for multiple sclerosis are linked to differences in alternative pre-mRNA splicing
Elena Putscher, Michael Hecker, Brit Fitzner, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 13
Multi-omic and multi-species meta-analyses of nicotine consumption
Rohan H. C. Palmer, Chelsie E. Benca‐Bachman, Spencer B. Huggett, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 16
Interpretation of the role of germline and somatic non-coding mutations in cancer: expression and chromatin conformation informed analysis
Michael Pudjihartono, Jo K. Perry, Cristin G. Print, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 11
Increasing diversity of functional genetics studies to advance biological discovery and human health
Sophia George, Alejandra Medina-Rivera, Youssef Idaghdour, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 12, pp. 1996-2002
Open Access | Times Cited: 5
Implication of genetic variants in primary microRNA processing sites in the risk of multiple sclerosis
Michael Hecker, Brit Fitzner, Elena Putscher, et al.
EBioMedicine (2022) Vol. 80, pp. 104052-104052
Open Access | Times Cited: 8
Using Gene Expression to Annotate Cardiovascular GWAS Loci
Matthias Heinig
Frontiers in Cardiovascular Medicine (2018) Vol. 5
Open Access | Times Cited: 14
Soluble biochemical markers of osteoarthritis: Are we close to using them in clinical practice?
Ali Mobasheri, Anne‐Christine Bay‐Jensen, Oreste Gualillo, et al.
Best Practice & Research Clinical Rheumatology (2017) Vol. 31, Iss. 5, pp. 705-720
Closed Access | Times Cited: 13
Mouse Models and Online Resources for Functional Analysis of Osteoporosis Genome-Wide Association Studies
Robert Maynard, Cheryl L. Ackert‐Bicknell
Frontiers in Endocrinology (2019) Vol. 10
Open Access | Times Cited: 13
ReQTL: identifying correlations between expressed SNVs and gene expression using RNA-sequencing data
Liam F. Spurr, Nawaf Alomran, Pavlos Bousounis, et al.
Bioinformatics (2019) Vol. 36, Iss. 5, pp. 1351-1359
Open Access | Times Cited: 12
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