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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:

Integrated analysis of direct and proxy genome wide association studies highlights polygenicity of Alzheimer’s disease outside of the APOE region
Javier de la Fuente, Andrew D. Grotzinger, Riccardo E. Marioni, et al.
PLoS Genetics (2022) Vol. 18, Iss. 6, pp. e1010208-e1010208
Open Access | Times Cited: 16

Showing 16 citing articles:

The complex genetic architecture of Alzheimer's disease: novel insights and future directions
Shea J. Andrews, Alan E. Renton, Brian Fulton‐Howard, et al.
EBioMedicine (2023) Vol. 90, pp. 104511-104511
Open Access | Times Cited: 191
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: 49
Artificial intelligence for dementia genetics and omics
Conceição Bettencourt, Nathan Skene, Sara Bandrés‐Ciga, et al.
Alzheimer s & Dementia (2023) Vol. 19, Iss. 12, pp. 5905-5921
Open Access | Times Cited: 17
Pervasive biases in proxy genome-wide association studies based on parental history of Alzheimer’s disease
Yuchang Wu, Zhongxuan Sun, Qinwen Zheng, et al.
Nature Genetics (2024)
Closed Access | Times Cited: 6
Exploring the Genetic Link Between Thyroid Dysfunction and Common Psychiatric Disorders: A Specific Hormonal or a General Autoimmune Comorbidity
Sourena Soheili‐Nezhad, Emma Sprooten, Indira Tendolkar, et al.
Thyroid (2022) Vol. 33, Iss. 2, pp. 159-168
Open Access | Times Cited: 25
Transcriptome-wide and stratified genomic structural equation modeling identify neurobiological pathways shared across diverse cognitive traits
Andrew D. Grotzinger, Javier de la Fuente, Gail Davies, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 21
Patient stratification by genetic risk in Alzheimer’s disease is only effective in the presence of phenotypic heterogeneity
Jack Euesden, Muhammad Ali, Chloe Robins, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0310977-e0310977
Open Access
Development of a k-Nearest Neighbors Model for the Prediction of Late-Onset Alzheimer’s Risk by Combining Polygenic Risk Scores and Phenotypic Variables
Santiago Fernando Suárez López, Rosana Ferrero, Jorge Blom-Dahl, et al.
Genes (2025) Vol. 16, Iss. 4, pp. 377-377
Open Access
Interpretation of 10 years of Alzheimer’s disease genetic findings in the perspective of statistical heterogeneity
Shan Gao, Tao Wang, Zhifa Han, et al.
Briefings in Bioinformatics (2024) Vol. 25, Iss. 3
Open Access | Times Cited: 3
Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic review
Shiying Liu, William S. Bush, Rufus Akinyemi, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Modeling Alzheimer’s Disease: A Review of Gene-Modified and Induced Animal Models, Complex Cell Culture Models, and Computational Modeling
Anna M. Timofeeva, Kseniya S. Aulova, Georgy A. Nevinsky
Brain Sciences (2025) Vol. 15, Iss. 5, pp. 486-486
Open Access
Pervasive biases in proxy GWAS based on parental history of Alzheimer’s disease
Yuchang Wu, Zhongxuan Sun, Qinwen Zheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 8
Mendelian Randomization of Blood Metabolites Suggests Circulating Glutamine Protects Against Late-Onset Alzheimer’s Disease
Ferris A. Ramadan, Gayatri Arani, Ayan Jafri, et al.
Journal of Alzheimer s Disease (2024) Vol. 98, Iss. 3, pp. 1069-1078
Closed Access | Times Cited: 2
Exploring the Genetic Predisposition to Epigenetic Changes in Alzheimer’s Disease
L. O. Bryzgalov, Elena E. Korbolina, Т. И. Меркулова
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 7955-7955
Open Access | Times Cited: 5
Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study
Gunn-Helen Moen, Michel G. Nivard, Laxmi Bhatta, et al.
Behavior Genetics (2022) Vol. 53, Iss. 1, pp. 40-52
Open Access | Times Cited: 6
DINGO: increasing the power of locus discovery in maternal and fetal genome-wide association studies of perinatal traits
Liang‐Dar Hwang, Gabriel Cuéllar-Partida, Loïc Yengo, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Direct and INdirect effects analysis of Genetic lOci (DINGO): A software package to increase the power of locus discovery in GWAS meta-analyses of perinatal phenotypes and traits influenced by indirect genetic effects
Liang‐Dar Hwang, Gabriel Cuéllar-Partida, Loïc Yengo, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Genetic Architecture of Neurological Disorders and Their Endophenotypes: Insights from Genetic Association Studies
Muralidharan Sargurupremraj
Current topics in behavioral neurosciences (2024), pp. 109-128
Closed Access
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