Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome
Tom G. Richardson, Sean Harrison, Gibran Hemani, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 195

Showing 26-50 of 195 citing articles:

Brain Lipids and Lipid Droplet Dysregulation in Alzheimer’s Disease and Neuropsychiatric Disorders
Xiaojie Zhao, Siwei Zhang, Alan R. Sanders, et al.
Complex Psychiatry (2023) Vol. 9, Iss. 1-4, pp. 154-171
Open Access | Times Cited: 24
A cross-disorder PRS-pheWAS of 5 major psychiatric disorders in UK Biobank
Beate Leppert, Louise A C Millard, Lucy Riglin, et al.
PLoS Genetics (2020) Vol. 16, Iss. 5, pp. e1008185-e1008185
Open Access | Times Cited: 68
Association of Recent Stressful Life Events With Mental and Physical Health in the Context of Genomic and Exposomic Liability for Schizophrenia
Lotta-Katrin Pries, Jim van Os, Margreet ten Have, et al.
JAMA Psychiatry (2020) Vol. 77, Iss. 12, pp. 1296-1296
Open Access | Times Cited: 61
The patterns of family genetic risk scores for eleven major psychiatric and substance use disorders in a Swedish national sample
Kenneth S. Kendler, Henrik Ohlsson, Jan Sundquist, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 53
Mendelian randomization and pleiotropy analysis
Xiaofeng Zhu
Quantitative Biology (2020) Vol. 9, Iss. 2, pp. 122-132
Open Access | Times Cited: 50
Dietary and Lifestyle-Centered Approach in Gout Care and Prevention
Chio Yokose, Natalie McCormick, Hyon K. Choi
Current Rheumatology Reports (2021) Vol. 23, Iss. 7
Open Access | Times Cited: 49
Genetic insight into sick sinus syndrome
Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Hildur M. Aegisdottir, et al.
European Heart Journal (2021) Vol. 42, Iss. 20, pp. 1959-1971
Open Access | Times Cited: 45
Identifying behaviour-related and physiological risk factors for suicide attempts in the UK Biobank
Bei Zhang, Jia You, Edmund T. Rolls, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 9, pp. 1784-1797
Closed Access | Times Cited: 6
Subjective Cognitive Decline Plus and Longitudinal Assessment and Risk for Cognitive Impairment
Moon-Il Kang, Clara Li, Arnav Mahajan, et al.
JAMA Psychiatry (2024) Vol. 81, Iss. 10, pp. 993-993
Closed Access | Times Cited: 6
EpiGraphDB: a database and data mining platform for health data science
Yi Liu, Benjamin Elsworth, Pau Erola, et al.
Bioinformatics (2020) Vol. 37, Iss. 9, pp. 1304-1311
Open Access | Times Cited: 49
The role of cortisol in ischemic heart disease, ischemic stroke, type 2 diabetes, and cardiovascular disease risk factors: a bi-directional Mendelian randomization study
Man Ki Kwok, Ichiro Kawachi, David H. Rehkopf, et al.
BMC Medicine (2020) Vol. 18, Iss. 1
Open Access | Times Cited: 49
A role for vitamin D and omega-3 fatty acids in major depression? An exploration using genomics
Yuri Milaneschi, Wouter J. Peyrot, Michel G. Nivard, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 45
Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping
Kerry Geiler‐Samerotte, Shuang Li, Charalampos Lazaris, et al.
PLoS Biology (2020) Vol. 18, Iss. 8, pp. e3000836-e3000836
Open Access | Times Cited: 41
Non-genetic risk and protective factors and biomarkers for neurological disorders: a meta-umbrella systematic review of umbrella reviews
Alexios‐Fotios A. Mentis, Efthimios Dardiotis, Vasiliki Efthymiou, et al.
BMC Medicine (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 37
Research Review: A guide to computing and implementing polygenic scores in developmental research
Andrea G. Allegrini, Jessie R. Baldwin, Wikus Barkhuizen, et al.
Journal of Child Psychology and Psychiatry (2022) Vol. 63, Iss. 10, pp. 1111-1124
Open Access | Times Cited: 23
Harnessing tissue-specific genetic variation to dissect putative causal pathways between body mass index and cardiometabolic phenotypes
Genevieve M Leyden, Chin Yang Shapland, George Davey Smith, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 2, pp. 240-252
Open Access | Times Cited: 22
ExPRSweb: An online repository with polygenic risk scores for common health-related exposures
Ying Ma, Snehal Patil, Xiang Zhou, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 10, pp. 1742-1760
Open Access | Times Cited: 22
Genetic analyses implicate complex links between adult testosterone levels and health and disease
Jaakko T. Leinonen, Nina Mars, Leevi E. Lehtonen, et al.
Communications Medicine (2023) Vol. 3, Iss. 1
Open Access | Times Cited: 15
Genetic Variants That Impact Alternative Polyadenylation in Cancer Represent Candidate Causal Risk Loci
Bin Li, Yimin Cai, Can Chen, et al.
Cancer Research (2023) Vol. 83, Iss. 21, pp. 3650-3666
Closed Access | Times Cited: 15
Transforming polygenic risk prediction: functional annotation and digital twin modeling with whole-exome sequencing
Alejandro Correa Rojo, Toomas Kivisild, Dirk Valkenborg, et al.
Research Square (Research Square) (2025)
Closed Access
Identifying cross-disease components of genetic risk across hospital data in the UK Biobank
Adrián Cortés, Patrick K. Albers, Calliope A. Dendrou, et al.
Nature Genetics (2019) Vol. 52, Iss. 1, pp. 126-134
Open Access | Times Cited: 39
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 21
Constructing an atlas of associations between polygenic scores from across the human phenome and circulating metabolic biomarkers
Si Fang, Michael V. Holmes, Tom R. Gaunt, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 19
Sibling variation in polygenic traits and DNA recombination mapping with UK Biobank and IVF family data
Louis Lello, Maximus Hsu, Erik Widén, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 12
Genetic variants associated with syncope implicate neural and autonomic processes
Hildur M. Aegisdottir, Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, et al.
European Heart Journal (2023) Vol. 44, Iss. 12, pp. 1070-1080
Closed Access | Times Cited: 12

Scroll to top