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:

17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes
Kathryn R. Bowles, Derian A. Pugh, Yiyuan Liu, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Functional regulatory variants implicate distinct transcriptional networks in dementia
Yonatan A. Cooper, Noam Teyssier, Nina M. Dräger, et al.
Science (2022) Vol. 377, Iss. 6608
Open Access | Times Cited: 87

Disentangling tau: One protein, many therapeutic approaches
Courtney Lane‐Donovan, Adam L. Boxer
Neurotherapeutics (2024) Vol. 21, Iss. 2, pp. e00321-e00321
Open Access | Times Cited: 18

Cell state-dependent allelic effects and contextual Mendelian randomization analysis for human brain phenotypes
Alexander Haglund, Verena Zuber, Maya Abouzeid, et al.
Nature Genetics (2025)
Open Access | Times Cited: 3

Interindividual variation in human cortical cell type abundance and expression
Nelson Johansen, Saroja Somasundaram, Kyle J. Travaglini, et al.
Science (2023) Vol. 382, Iss. 6667
Open Access | Times Cited: 36

Neuronal MAPT expression is mediated by long-range interactions with cis-regulatory elements
Brianne B. Rogers, Ashlyn G. Anderson, Shelby N. Lauzon, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 259-279
Open Access | Times Cited: 7

Deciphering the role of a SINE-VNTR-Alu retrotransposon polymorphism as a biomarker of Parkinson’s disease progression
Alexander Fröhlich, Abigail L. Pfaff, Ben Middlehurst, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 7

Chromosomal inversion polymorphisms shape human brain morphology
Hao Wang, Carolina Makowski, Yanxiao Zhang, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112896-112896
Open Access | Times Cited: 16

Shared Genetics and Comorbid Genes of Amyotrophic Lateral Sclerosis and Parkinson's Disease
Ye Tian, Guochen Ma, Haoqi Li, et al.
Movement Disorders (2023) Vol. 38, Iss. 10, pp. 1813-1821
Closed Access | Times Cited: 13

Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
Chiara Pedicone, Sarah A. Weitzman, Alan E. Renton, et al.
Molecular Neurodegeneration (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 5

Transcriptomic analysis of the human habenula in schizophrenia
Ege A Yalcinbas, Bukola Ajanaku, Erik D. Nelson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4

MAPT haplotype-associated transcriptomic changes in progressive supranuclear palsy
Hadley W. Ressler, Jack Humphrey, Ricardo A. Vialle, et al.
Acta Neuropathologica Communications (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 4

Exome sequencing identifies genes for socioeconomic status in 350,770 individuals
Xinrui Wu, Yang Liu, Bang‐Sheng Wu, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 2
Open Access

Structural variation, selection, and diversification of theNPIPgene family from the human pangenome
Philip C. Dishuck, Katherine M. Munson, Alexandra P. Lewis, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Genetic architectures of the human hippocampus and those involved in neuropsychiatric traits
Caibo Ning, Jin Meng, Yimin Cai, et al.
BMC Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2

CRISPR deletion of a SINE-VNTR-Alu (SVA_67) retrotransposon demonstrates its ability to differentially modulate gene expression at the MAPT locus
Alexander Fröhlich, Lauren S. Hughes, Ben Middlehurst, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 6

A single-cell eQTL atlas of the human cerebellum reveals vulnerability of oligodendrocytes in essential tremor
Guy A. Rouleau, Charles-Etienne Castonguay, Farah Aboasali, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 1

Bioinformatics analysis of an immunotherapy responsiveness- related gene signature in predicting lung adenocarcinoma prognosis
Yupeng Jiang, Bacha Hammad, Hong Huang, et al.
Translational Lung Cancer Research (2024) Vol. 13, Iss. 6, pp. 1277-1295
Open Access | Times Cited: 1

Integration of estimated regional gene expression with neuroimaging and clinical phenotypes at biobank scale
Nhung Hoang, Neda Sardaripour, Grace Ramey, et al.
PLoS Biology (2024) Vol. 22, Iss. 9, pp. e3002782-e3002782
Open Access | Times Cited: 1

MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset
Olaitan Okunoye, Oluwadamilola O. Ojo, Oladunni Abiodun, et al.
Parkinsonism & Related Disorders (2023) Vol. 113, pp. 105517-105517
Open Access | Times Cited: 3

The influence of 17q21.31 and APOE genetic ancestry on neurodegenerative disease risk
Nadia V. Harerimana, Alison Goate, Kathryn R. Bowles
Frontiers in Aging Neuroscience (2022) Vol. 14
Open Access | Times Cited: 4

Validation of Enhancer Regions in Primary Human Neural Progenitor Cells using Capture STARR-seq
Sophia C. Gaynor-Gillett, Lijun Cheng, Manman Shi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Induction of acrosome reaction by 4-Br-A23187 alters the glycoproteomic profile of boar spermatozoa
David Martín‐Hidalgo, M. Izquierdo, Nicolás Garrido, et al.
Theriogenology (2024) Vol. 223, pp. 108-114
Open Access

Critical reasoning on the co-expression module QTL in the dorsolateral prefrontal cortex
Alanna C. Cote, Hannah E. Young, Laura M. Huckins
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100311-100311
Open Access

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