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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:

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood
Ting Qi, Yang Wu, Jian Zeng, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 360

Showing 1-25 of 360 citing articles:

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Brian W. Kunkle, Benjamin Grenier‐Boley, Rebecca Sims, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 414-430
Open Access | Times Cited: 2487
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, et al.
The Lancet Neurology (2019) Vol. 18, Iss. 12, pp. 1091-1102
Open Access | Times Cited: 1973
Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry
Loïc Yengo, Julia Sidorenko, Kathryn E. Kemper, et al.
Human Molecular Genetics (2018) Vol. 27, Iss. 20, pp. 3641-3649
Open Access | Times Cited: 1970
Genome-wide association study identifies 30 loci associated with bipolar disorder
Eli A. Stahl, Gerome Breen, Andreas J. Forstner, et al.
Nature Genetics (2019) Vol. 51, Iss. 5, pp. 793-803
Open Access | Times Cited: 1449
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Urmo Võsa, Annique Claringbould, Harm-Jan Westra, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1300-1310
Open Access | Times Cited: 1177
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Angli Xue, Yang Wu, Zhihong Zhu, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 763
A saturated map of common genetic variants associated with human height
Loïc Yengo, Sailaja Vedantam, Eirini Marouli, et al.
Nature (2022) Vol. 610, Iss. 7933, pp. 704-712
Open Access | Times Cited: 501
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation
Josine L. Min, Gibran Hemani, Eilís Hannon, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1311-1321
Open Access | Times Cited: 351
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions
Solveig K. Sieberts, Thanneer M. Perumal, Minerva M. Carrasquillo, et al.
Scientific Data (2020) Vol. 7, Iss. 1
Open Access | Times Cited: 317
Abundant associations with gene expression complicate GWAS follow-up
Boxiang Liu, Michael J. Gloudemans, Abhiram Rao, et al.
Nature Genetics (2019) Vol. 51, Iss. 5, pp. 768-769
Open Access | Times Cited: 312
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Joana Revez, Tian Lin, Zhen Qiao, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 308
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
Naomi R. Wray, Cisca Wijmenga, Patrick F. Sullivan, et al.
Cell (2018) Vol. 173, Iss. 7, pp. 1573-1580
Open Access | Times Cited: 292
Multivariate genome-wide analyses of the well-being spectrum
Bart M. L. Baselmans, Rick Jansen, Hill F. Ip, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 445-451
Open Access | Times Cited: 285
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
Eleonora Porcu, Sina Rüeger, Kaido Lepik, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 269
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia
Pirro G. Hysi, Hélène Choquet, Anthony P. Khawaja, et al.
Nature Genetics (2020) Vol. 52, Iss. 4, pp. 401-407
Open Access | Times Cited: 243
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.
Brain (2019) Vol. 143, Iss. 1, pp. 234-248
Open Access | Times Cited: 200
Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders
Julien Bryois, Daniela Calini, Will Macnair, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 8, pp. 1104-1112
Open Access | Times Cited: 179
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: 169
GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression
Yeda Wu, Graham K. Murray, Enda M. Byrne, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 163
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, et al.
Movement Disorders (2019) Vol. 34, Iss. 12, pp. 1839-1850
Open Access | Times Cited: 158
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Nilüfer Rahmioğlu, Sally Mortlock, Marzieh Ghiasi, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 423-436
Open Access | Times Cited: 153
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
Julie Horowitz, Jack A. Kosmicki, Amy Damask, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 382-392
Open Access | Times Cited: 148
Prenatal Origins of ASD: The When, What, and How of ASD Development
Eric Courchesne, Vahid Gazestani, Nathan E. Lewis
Trends in Neurosciences (2020) Vol. 43, Iss. 5, pp. 326-342
Open Access | Times Cited: 145
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases
Niek de Klein, Ellen Tsai, Martijn Vochteloo, et al.
Nature Genetics (2023) Vol. 55, Iss. 3, pp. 377-388
Open Access | Times Cited: 145
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Zhe Wang, Andrew Emmerich, Nicolas J. Pillon, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1332-1344
Open Access | Times Cited: 133
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