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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:

Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture
Linda Kachuri, Angel C. Y. Mak, Donglei Hu, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 952-963
Open Access | Times Cited: 58

Showing 1-25 of 58 citing articles:

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study
Mie Rizig, Sara Bandrés‐Ciga, Mary B. Makarious, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 11, pp. 1015-1025
Open Access | Times Cited: 86
Gene–environment interactions in human health
Esther Herrera-Luis, Kelly S. Benke, Heather E. Volk, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 11, pp. 768-784
Closed Access | Times Cited: 20
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: 19
Quantitative proteomics of cerebrospinal fluid from African Americans and Caucasians reveals shared and divergent changes in Alzheimer’s disease
Erica Modeste, Lingyan Ping, Caroline M. Watson, et al.
Molecular Neurodegeneration (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 39
Epigenomic insights into common human disease pathology
Christopher G. Bell
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 11
Gene expression and splicing QTL analysis of blood cells in African American participants from the Jackson Heart Study
Jia Wen, Quan Sun, Le Huang, et al.
Genetics (2024) Vol. 228, Iss. 1
Open Access | Times Cited: 6
A noncoding regulatory variant in IKZF1 increases acute lymphoblastic leukemia risk in Hispanic/Latino children
Adam J. de Smith, Lara Wahlster, Soyoung Jeon, et al.
Cell Genomics (2024) Vol. 4, Iss. 4, pp. 100526-100526
Open Access | Times Cited: 6
The role of patient-specific variables in protein corona formation and therapeutic efficacy in nanomedicine
Ethan Cisneros, Brinkley Morse, Ani Savk, et al.
Journal of Nanobiotechnology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 5
Improved multi-ancestry fine-mapping identifiescis-regulatory variants underlying molecular traits and disease risk
Zeyun Lu, Xinran Wang, Matthew Carr, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson’s Disease in African and African Admixed Populations
Mie Rizig, Sara Bandrés‐Ciga, Mary B. Makarious, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 10
A unified framework for cell-type-specific eQTL prioritization by integrating bulk and scRNA-seq data
Xinyi Yu, Xianghong Hu, Xiaomeng Wan, et al.
The American Journal of Human Genetics (2025)
Closed Access
Vitamin D-related genetic variants and prostate cancer risk in Black men
Tracy M. Layne, Joseph H. Rothstein, Xiaoyu Song, et al.
Cancer Epidemiology (2025) Vol. 95, pp. 102742-102742
Closed Access
Prediction and Characterization of Genetically Regulated Expression of Target Tissues in Asthma
Sarah D. Slack, Erika Esquinca, Christopher H. Arehart, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis
Sean Wen, Pablo Kuri‐Morales, Fengyuan Hu, et al.
Nature Genetics (2025)
Open Access
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed
Peter Orchard, Thomas W. Blackwell, Linda Kachuri, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Chromosome 1 variants associated with decreased HIV set-point viral load correlate with PRKAB2 expression changes
Riley H. Tough, Paul J. McLaren
Frontiers in Genetics (2025) Vol. 16
Open Access
Admixed gene expression models expand molecular and neurological insights into 6 major psychiatric disorders
Eric R. Gamazon
Research Square (Research Square) (2025)
Closed Access
Multi-omics characterization of type 2 diabetes associated genetic variation.
Ravi Mandla, Kimberly Lorenz, Xianyong Yin, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Single-nucleus chromatin accessibility and transcriptomic map of breast tissues of women of diverse genetic ancestry
Poornima Bhat‐Nakshatri, Hongyu Gao, Aditi S. Khatpe, et al.
Nature Medicine (2024)
Open Access | Times Cited: 3
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Odessica N. Hughes, Amy R. Bentley, Charles E. Breeze, et al.
Cell Genomics (2023) Vol. 4, Iss. 1, pp. 100468-100468
Open Access | Times Cited: 7
Brain eQTLs of European, African American, and Asian ancestry improve interpretation of schizophrenia GWAS
Yu Chen, Sihan Liu, Zongyao Ren, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Precision medicine for asthma treatment: Unlocking the potential of the epigenome and microbiome
Javier Pérez-García, Andres Cardenas, Fabian Lorenzo-Diaz, et al.
Journal of Allergy and Clinical Immunology (2024)
Open Access | Times Cited: 2
The Role of the Neural Exposome as a Novel Strategy to Identify and Mitigate Health Inequities in Alzheimer’s Disease and Related Dementias
Ravid Granov, Skyler Vedad, Shu-Han Wang, et al.
Molecular Neurobiology (2024)
Open Access | Times Cited: 2
Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies
Yu Chen, Sihan Liu, Zongyao Ren, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 11, pp. 2444-2457
Open Access | Times Cited: 2
Multivariate adaptive shrinkage improves cross-population transcriptome prediction and association studies in underrepresented populations
Daniel S. Araújo, Chris Nguyen, Xiaowei Hu, et al.
Human Genetics and Genomics Advances (2023) Vol. 4, Iss. 4, pp. 100216-100216
Open Access | Times Cited: 6
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