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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 26-50 of 360 citing articles:

Genetic control of RNA splicing and its distinct role in complex trait variation
Ting Qi, Yang Wu, Hailing Fang, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1355-1363
Open Access | Times Cited: 126
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
Melinda Mills, Felix C. Tropf, David M. Brazel, et al.
Nature Human Behaviour (2021) Vol. 5, Iss. 12, pp. 1717-1730
Open Access | Times Cited: 117
DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits
Meritxell Oliva, Kathryn Demanelis, Yihao Lu, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 112-122
Open Access | Times Cited: 117
Association of Antihypertensive Drug Target Genes With Psychiatric Disorders
Solal Chauquet, Zhihong Zhu, Michael O’Donovan, et al.
JAMA Psychiatry (2021) Vol. 78, Iss. 6, pp. 623-623
Open Access | Times Cited: 113
Integrative metabolomics‐genomics approach reveals key metabolic pathways and regulators of Alzheimer's disease
Emrin Horgusluoglu, Ryan Neff, Won‐Min Song, et al.
Alzheimer s & Dementia (2021) Vol. 18, Iss. 6, pp. 1260-1278
Open Access | Times Cited: 111
Identifying causal genes for depression via integration of the proteome and transcriptome from brain and blood
Yue‐Ting Deng, Ya‐Nan Ou, Bang‐Sheng Wu, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 6, pp. 2849-2857
Closed Access | Times Cited: 84
Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction
Rachel L. Kember, Rachel Vickers‐Smith, Heng Xu, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 10, pp. 1279-1287
Open Access | Times Cited: 72
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes
Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1483-1493
Open Access | Times Cited: 47
Systems biology dissection of PTSD and MDD across brain regions, cell types, and blood
Nikolaos P. Daskalakis, Artemis Iatrou, Chris Chatzinakos, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 24
Genomics yields biological and phenotypic insights into bipolar disorder
Kevin S. O’Connell, Maria Koromina, Tracey van der Veen, et al.
Nature (2025)
Closed Access | Times Cited: 12
Genome-wide association study identifies 48 common genetic variants associated with handedness
Gabriel Cuéllar-Partida, Joyce Y. Tung, Nicholas Eriksson, et al.
Nature Human Behaviour (2020) Vol. 5, Iss. 1, pp. 59-70
Open Access | Times Cited: 127
Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
Kimberley J. Billingsley, Inês A. Barbosa, Sara Bandrés‐Ciga, et al.
npj Parkinson s Disease (2019) Vol. 5, Iss. 1
Open Access | Times Cited: 125
Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 123
Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease
Costanza L. Vallerga, Futao Zhang, Javed Fowdar, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 118
Complex-Traits Genetics Virtual Lab: A community-driven web platform for post-GWAS analyses
Gabriel Cuéllar-Partida, Mischa Lundberg, Pik Fang Kho, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 115
Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours
Yordi J. van de Vegte, M. Abdullah Said, Michiel Rienstra, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 112
DNA methylation links prenatal smoking exposure to later life health outcomes in offspring
Petri Wiklund, Ville Karhunen, Rebecca C. Richmond, et al.
Clinical Epigenetics (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 109
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS
Wouter J. Peyrot, Alkes L. Price
Nature Genetics (2021) Vol. 53, Iss. 4, pp. 445-454
Open Access | Times Cited: 94
Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, et al.
(2018), pp. 388165
Open Access | Times Cited: 93
Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits
Eric R. Gamazon, Aeilko H. Zwinderman, Nancy J. Cox, et al.
Nature Genetics (2019) Vol. 51, Iss. 6, pp. 933-940
Open Access | Times Cited: 91
Shared genetic background between children and adults with attention deficit/hyperactivity disorder
Paula Rovira, Ditte Demontis, Cristina Sánchez‐Mora, et al.
Neuropsychopharmacology (2020) Vol. 45, Iss. 10, pp. 1617-1626
Open Access | Times Cited: 88
The Parkinson's Disease Genome‐Wide Association Study Locus Browser
Francis P. Grenn, Jonggeol J. Kim, Mary B. Makarious, et al.
Movement Disorders (2020) Vol. 35, Iss. 11, pp. 2056-2067
Open Access | Times Cited: 87
Dissecting polygenic signals from genome-wide association studies on human behaviour
Abdel Abdellaoui, Karin J. H. Verweij
Nature Human Behaviour (2021) Vol. 5, Iss. 6, pp. 686-694
Closed Access | Times Cited: 86
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders
Marta F. Nabais, Simon M. Laws, Tian Lin, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 81
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types
Sara Sáez-Atiénzar, Sara Bandrés‐Ciga, Rebekah G. Langston, et al.
Science Advances (2021) Vol. 7, Iss. 3
Open Access | Times Cited: 77

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