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:

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
Alicia R. Martin, Christopher R. Gignoux, Raymond K. Walters, et al.
The American Journal of Human Genetics (2020) Vol. 107, Iss. 4, pp. 788-789
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

Efficient ancestry and mutation simulation with msprime 1.0
Franz Baumdicker, Gertjan Bisschop, Daniel Goldstein, et al.
Genetics (2021) Vol. 220, Iss. 3
Open Access | Times Cited: 283
Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
Nature Genetics (2024) Vol. 56, Iss. 7, pp. 1386-1396
Open Access | Times Cited: 21
Sources of gene expression variation in a globally diverse human cohort
Dylan J. Taylor, Surya B. Chhetri, Michael G. Tassia, et al.
Nature (2024) Vol. 632, Iss. 8023, pp. 122-130
Open Access | Times Cited: 20
Genetics of multiple sclerosis: lessons from polygenicity
An Goris, Marijne Vandebergh, Jacob L. McCauley, et al.
The Lancet Neurology (2022) Vol. 21, Iss. 9, pp. 830-842
Closed Access | Times Cited: 62
Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits
Ananyo Choudhury, Jean‐Tristan Brandenburg, Tinashe Chikowore, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 40
Characterizing features affecting local ancestry inference performance in admixed populations
Jessica Honorato‐Mauer, Nirav N. Shah, Adam X. Maihofer, et al.
The American Journal of Human Genetics (2025)
Open Access | Times Cited: 1
The evolution of group differences in changing environments
Arbel Harpak, Molly Przeworski
PLoS Biology (2021) Vol. 19, Iss. 1, pp. e3001072-e3001072
Open Access | Times Cited: 48
Beyond the Human Genome Project: The Age of Complete Human Genome Sequences and Pangenome References
Dylan J. Taylor, Jordan M. Eizenga, Qiuhui Li, et al.
Annual Review of Genomics and Human Genetics (2024) Vol. 25, Iss. 1, pp. 77-104
Open Access | Times Cited: 7
Evaluating the power and limitations of genome-wide association studies in Caenorhabditis elegans
Samuel J. Widmayer, Kathryn S. Evans, Stefan Zdraljevic, et al.
G3 Genes Genomes Genetics (2022) Vol. 12, Iss. 7
Open Access | Times Cited: 28
Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 10
Characterizing substructure via mixture modeling in large-scale genetic summary statistics
Hayley R Stoneman, Adelle Price, Nikole Scribner Trout, et al.
The American Journal of Human Genetics (2025)
Open Access
Clinical use of polygenic scores in type 2 diabetes: challenges and possibilities
Rashmi B. Prasad, Liisa Hakaste, Jaakko Tuomilehto
Diabetologia (2025)
Open Access
Advancing drug discovery using the power of the human genome
Karl Heilbron, Sahar V. Mozaffari, Vladimir Vacic, et al.
The Journal of Pathology (2021) Vol. 254, Iss. 4, pp. 418-429
Open Access | Times Cited: 19
Polygenic risk scores and risk stratification in deep vein thrombosis
Valeria Lo Faro, Therese Johansson, Julia Höglund, et al.
Thrombosis Research (2023) Vol. 228, pp. 151-162
Open Access | Times Cited: 7
The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits
Inês Barroso
Diabetologia (2021) Vol. 64, Iss. 12, pp. 2653-2664
Open Access | Times Cited: 15
PGS-Depot: a comprehensive resource for polygenic scores constructed by summary statistics based methods
Chen Cao, Shuting Zhang, Jianhua Wang, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D963-D971
Open Access | Times Cited: 6
Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes
Andrés Jimenez-Kaufmann, Amanda Y. Chong, Adrián Cortés, et al.
Frontiers in Genetics (2022) Vol. 12
Open Access | Times Cited: 9
Associations of externalizing polygenic scores with externalizing disorders among Mexican youth
Gabriela Ariadna Martínez-Levy, Mateo Maya-Martínez, Luis M. García‐Marín, et al.
Journal of Psychiatric Research (2024) Vol. 171, pp. 346-353
Closed Access | Times Cited: 1
Characterizing substructure via mixture modeling of genetic similarity in large-scale summary statistics
Hayley R Stoneman, Adelle Price, Nikole Scribner Trout, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
A Polygenic Risk Analysis for Identifying Ulcerative Colitis Patients with European Ancestry
Ling Liu, Yiming Wu, Yizhou Li, et al.
Genes (2024) Vol. 15, Iss. 6, pp. 684-684
Open Access | Times Cited: 1
Polygenic scores and their applications in kidney disease
Atlas Khan, Krzysztof Kiryluk
Nature Reviews Nephrology (2024)
Closed Access | Times Cited: 1
A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16
Elin Barnekow, Wen Liu, Hafdís T. Helgadóttir, et al.
Cancers (2022) Vol. 14, Iss. 5, pp. 1206-1206
Open Access | Times Cited: 6
Genotype imputation and polygenic score estimation in northwestern Russian population
Nikita Kolosov, Valeriia Rezapova, О. P. Rotar, et al.
PLoS ONE (2022) Vol. 17, Iss. 6, pp. e0269434-e0269434
Open Access | Times Cited: 6
Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol
James J. Crowley, Carolina Cappi, Marcos E Ochoa-Panaifo, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2023) Vol. 195, Iss. 4
Open Access | Times Cited: 3
Page 1 - Next Page

Scroll to top