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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 26-50 of 58 citing articles:

Sources of gene expression variation in a globally diverse human cohort
Dylan J. Taylor, Surya B. Chhetri, Michael G. Tassia, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Sex-dependent placental methylation quantitative trait loci provide insight into the prenatal origins of childhood onset traits and conditions
William Casazza, Amy M. Inkster, Giulia Gobbo, et al.
iScience (2024) Vol. 27, Iss. 2, pp. 109047-109047
Open Access | Times Cited: 1
Development and Evaluation of a Comprehensive Prediction Model for Incident Coronary Heart Disease Using Genetic, Social, and Lifestyle–Psychological Factors: A Prospective Analysis of the UK Biobank
Mohammadreza Naderian, Kristján Norland, Daniel J. Schaid, et al.
Annals of Internal Medicine (2024)
Closed Access | Times Cited: 1
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1
Pilar Álvarez Jerez, Peter Wild Crea, Daniel M. Ramos, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Fine-mapping causal tissues and genes at disease-associated loci
Benjamin J. Strober, Martin Jinye Zhang, Tiffany Amariuta, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Comparative analysis of 136,401 Admixed Americans and 419,228 Europeans reveals ancestry-specific genetic determinants of clonal haematopoiesis
Sean Wen, Pablo Kuri‐Morales, Fengyuan Hu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Novel risk loci for COVID-19 hospitalization among admixed American populations
Silvia Diz‐de Almeida, Raquel Cruz, André Ducati Luchessi, et al.
(2024)
Open Access
Novel risk loci for COVID-19 hospitalization among admixed American populations
Silvia Diz‐de Almeida, Raquel Cruz, André Ducati Luchessi, et al.
eLife (2024) Vol. 13
Open Access
Multi-ancestry polygenic risk scores using phylogenetic regularization
Elliot Layne, Shadi Zabad, Yue Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Concordant B and T Cell Heterogeneity Inferred from the Multiomic Landscape of Peripheral Blood Mononuclear Cells in a Crohn’s Disease Cohort
Margaret Brown, Anne Dodd, Fang Shi, et al.
Journal of Crohn s and Colitis (2024)
Closed Access
Genetic epidemiology in the era of genomic medicine
Siana Nkya
Elsevier eBooks (2024), pp. 207-223
Closed Access
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
Min-Zhi Jiang, Sheila M. Gaynor, Xihao Li, et al.
PubMed (2024) Vol. 33, Iss. 16, pp. 1429-1441
Closed Access
Cell-type specific inference from bulk RNA-sequencing data by integrating single cell reference profiles via EPIC-unmix
Chenwei Tang, Quan Sun, Xinyue Zeng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
A unified framework for cell-type-specific eQTLs prioritization by integrating bulk and scRNA-seq data
Xinyi Yu, Xianghong Hu, Xiaomeng Wan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Variants in Vitamin D-related Genes and Prostate Cancer Risk in Black Men
Tracy M. Layne, Joseph H. Rothstein, Xiaoyu Song, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
A genome‐wide association study of alloimmunization in the TOPMed OMG‐SCD cohort identifies a locus on chromosome 12
Quan Sun, Matthew S. Karafin, Melanie E. Garrett, et al.
Transfusion (2024) Vol. 64, Iss. 9, pp. 1772-1783
Closed Access
Variants in Vitamin D-Related Genes and Prostate Cancer Risk in Black Men
Tracy M. Layne, Joseph H. Rothstein, Xiaoyu Song, et al.
(2024)
Open Access
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Yixuan He, Wenhan Lu, Yon Ho Jee, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Novel risk loci for COVID-19 hospitalization among admixed American populations
Silvia Diz‐de Almeida, Raquel Cruz, André Ducati Luchessi, et al.
(2024)
Open Access
Powerful mapping of cis-genetic effects on gene expression across diverse populations reveals novel disease-critical genes
Kai Akamatsu, Stephen Golzari, Tiffany Amariuta
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Cell-type specific inference from bulk RNA-sequencing data by integrating single cell reference profiles via EPIC-unmix
Chenwei Tang, Quan Sun, Xinyue Zeng, et al.
Research Square (Research Square) (2024)
Closed Access
Novel risk loci for COVID-19 hospitalization among admixed American populations
Silvia Diz‐de Almeida, Raquel Cruz, André Ducati Luchessi, et al.
eLife (2024) Vol. 13
Open Access
Public RNA-seq data are not representative of global human diversity
Irene Gallego Romero, Grace Rodenberg, Audrey M. Arner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Multiomics Resolves Regulatory Mechanisms in a Diverse Cohort of Crohn’s Disease
Randy Longman
Journal of Crohn s and Colitis (2024) Vol. 18, Iss. 12, pp. 1937-1938
Closed Access
CADET: Enhanced transcriptome-wide association analyses in admixed samples using eQTL summary data
S. Taylor Head, Qile Dai, Joellen Schildkraut, et al.
(2024)
Open Access

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