
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:
The Parkinson's Disease Genome‐Wide Association Study Locus Browser
Francis P. Grenn, Jonggeol J. Kim, Mary B. Makarious, et al.
Movement Disorders (2020) Vol. 35, Iss. 11, pp. 2056-2067
Open Access | Times Cited: 87
Francis P. Grenn, Jonggeol J. Kim, Mary B. Makarious, et al.
Movement Disorders (2020) Vol. 35, Iss. 11, pp. 2056-2067
Open Access | Times Cited: 87
Showing 1-25 of 87 citing articles:
Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies
Kátia de Paiva Lopes, Gijsje J. L. Snijders, Jack Humphrey, et al.
Nature Genetics (2022) Vol. 54, Iss. 1, pp. 4-17
Open Access | Times Cited: 171
Kátia de Paiva Lopes, Gijsje J. L. Snijders, Jack Humphrey, et al.
Nature Genetics (2022) Vol. 54, Iss. 1, pp. 4-17
Open Access | Times Cited: 171
The Genetics of Parkinson’s Disease and Implications for Clinical Practice
Jacob Day, Stephen Mullin
Genes (2021) Vol. 12, Iss. 7, pp. 1006-1006
Open Access | Times Cited: 156
Jacob Day, Stephen Mullin
Genes (2021) Vol. 12, Iss. 7, pp. 1006-1006
Open Access | Times Cited: 156
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Nature Genetics (2023) Vol. 56, Iss. 1, pp. 27-36
Open Access | Times Cited: 80
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Nature Genetics (2023) Vol. 56, Iss. 1, pp. 27-36
Open Access | Times Cited: 80
Association of a common genetic variant with Parkinson’s disease is mediated by microglia
Rebekah G. Langston, Alexandra Beilina, Xylena Reed, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 655
Open Access | Times Cited: 70
Rebekah G. Langston, Alexandra Beilina, Xylena Reed, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 655
Open Access | Times Cited: 70
An astrocyte BMAL1-BAG3 axis protects against alpha-synuclein and tau pathology
Patrick W. Sheehan, Collin J. Nadarajah, Michael F. Kanan, et al.
Neuron (2023) Vol. 111, Iss. 15, pp. 2383-2398.e7
Open Access | Times Cited: 47
Patrick W. Sheehan, Collin J. Nadarajah, Michael F. Kanan, et al.
Neuron (2023) Vol. 111, Iss. 15, pp. 2383-2398.e7
Open Access | Times Cited: 47
Parkinson’s Disease is Predominantly a Genetic Disease
Shen‐Yang Lim, Christine Klein
Journal of Parkinson s Disease (2024) Vol. 14, Iss. 3, pp. 467-482
Open Access | Times Cited: 25
Shen‐Yang Lim, Christine Klein
Journal of Parkinson s Disease (2024) Vol. 14, Iss. 3, pp. 467-482
Open Access | Times Cited: 25
Pathogenesis of Parkinson’s Disease
Bin Xiao, Zhidong Zhou, Yinxia Chao, et al.
Neurologic Clinics (2025)
Closed Access | Times Cited: 2
Bin Xiao, Zhidong Zhou, Yinxia Chao, et al.
Neurologic Clinics (2025)
Closed Access | Times Cited: 2
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos
Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron, et al.
Annals of Neurology (2021) Vol. 90, Iss. 3, pp. 353-365
Open Access | Times Cited: 78
Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron, et al.
Annals of Neurology (2021) Vol. 90, Iss. 3, pp. 353-365
Open Access | Times Cited: 78
Molecular Mechanisms Underlying Synaptic and Axon Degeneration in Parkinson’s Disease
Nolwazi Z. Gcwensa, Drèson L. Russell, Rita M. Cowell, et al.
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 70
Nolwazi Z. Gcwensa, Drèson L. Russell, Rita M. Cowell, et al.
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 70
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism
Elisângela Bressan, Xylena Reed, V. Bansal, et al.
Cell Genomics (2023) Vol. 3, Iss. 3, pp. 100261-100261
Open Access | Times Cited: 34
Elisângela Bressan, Xylena Reed, V. Bansal, et al.
Cell Genomics (2023) Vol. 3, Iss. 3, pp. 100261-100261
Open Access | Times Cited: 34
Neurodegeneration cell per cell
Sriram Balusu, Roman Praschberger, Elsa Lauwers, et al.
Neuron (2023) Vol. 111, Iss. 6, pp. 767-786
Open Access | Times Cited: 31
Sriram Balusu, Roman Praschberger, Elsa Lauwers, et al.
Neuron (2023) Vol. 111, Iss. 6, pp. 767-786
Open Access | Times Cited: 31
A study of gene expression in the living human brain
Lora E. Liharska, You Jeong Park, Kimia Ziafat, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 25
Lora E. Liharska, You Jeong Park, Kimia Ziafat, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 25
Behavioral screening defines three molecular Parkinsonism subgroups in Drosophila
Natalie Kaempf, Jorge S. Valadas, Pieter Robberechts, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
Natalie Kaempf, Jorge S. Valadas, Pieter Robberechts, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
Heritability Enrichment Implicates Microglia in Parkinson's Disease Pathogenesis
Maren Stolp Andersen, Sara Bandrés‐Ciga, Regina H. Reynolds, et al.
Annals of Neurology (2021) Vol. 89, Iss. 5, pp. 942-951
Open Access | Times Cited: 56
Maren Stolp Andersen, Sara Bandrés‐Ciga, Regina H. Reynolds, et al.
Annals of Neurology (2021) Vol. 89, Iss. 5, pp. 942-951
Open Access | Times Cited: 56
Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
Cornelis Blauwendraat, Hirotaka Iwaki, Mary B. Makarious, et al.
Annals of Neurology (2021) Vol. 90, Iss. 1, pp. 35-42
Open Access | Times Cited: 46
Cornelis Blauwendraat, Hirotaka Iwaki, Mary B. Makarious, et al.
Annals of Neurology (2021) Vol. 90, Iss. 1, pp. 35-42
Open Access | Times Cited: 46
Brain atrophy progression in Parkinson’s disease is shaped by connectivity and local vulnerability
Christina Tremblay, Shady Rahayel, Andrew Vo, et al.
Brain Communications (2021) Vol. 3, Iss. 4
Open Access | Times Cited: 45
Christina Tremblay, Shady Rahayel, Andrew Vo, et al.
Brain Communications (2021) Vol. 3, Iss. 4
Open Access | Times Cited: 45
Expanding causal genes for Parkinson’s disease via multi-omics analysis
Xiaojing Gu, Wei‐Ming Su, Meng Dou, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 21
Xiaojing Gu, Wei‐Ming Su, Meng Dou, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 21
Identification of Parkinson’s disease PACE subtypes and repurposing treatments through integrative analyses of multimodal data
Chang Su, Yu Hou, Jielin Xu, et al.
npj Digital Medicine (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 8
Chang Su, Yu Hou, Jielin Xu, et al.
npj Digital Medicine (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 8
Pathological Relevance of Post-Translationally Modified Alpha-Synuclein (pSer87, pSer129, nTyr39) in Idiopathic Parkinson’s Disease and Multiple System Atrophy
Berkiye Sonustun, Melek Firat Altay, Catherine Strand, et al.
Cells (2022) Vol. 11, Iss. 5, pp. 906-906
Open Access | Times Cited: 26
Berkiye Sonustun, Melek Firat Altay, Catherine Strand, et al.
Cells (2022) Vol. 11, Iss. 5, pp. 906-906
Open Access | Times Cited: 26
A hidden layer of structural variation in transposable elements reveals potential genetic modifiers in human disease-risk loci
Elisabeth J. van Bree, Rita L. F. P. Guimarães, Mischa Lundberg, et al.
Genome Research (2022) Vol. 32, Iss. 4, pp. 656-670
Open Access | Times Cited: 23
Elisabeth J. van Bree, Rita L. F. P. Guimarães, Mischa Lundberg, et al.
Genome Research (2022) Vol. 32, Iss. 4, pp. 656-670
Open Access | Times Cited: 23
Common genetic risk for Parkinson's disease and dysfunction of the endo-lysosomal system
Noopur Bhore, Erin C. Bogacki, Benjamin O’Callaghan, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2024) Vol. 379, Iss. 1899
Open Access | Times Cited: 5
Noopur Bhore, Erin C. Bogacki, Benjamin O’Callaghan, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2024) Vol. 379, Iss. 1899
Open Access | Times Cited: 5
Fine-mapping of Parkinson’s disease susceptibility loci identifies putative causal variants
Brian M. Schilder, Towfique Raj
Human Molecular Genetics (2021) Vol. 31, Iss. 6, pp. 888-900
Open Access | Times Cited: 32
Brian M. Schilder, Towfique Raj
Human Molecular Genetics (2021) Vol. 31, Iss. 6, pp. 888-900
Open Access | Times Cited: 32
Parkinson's disease risk genes act in glia to control neuronal α-synuclein toxicity
Abby L. Olsen, Mel Β. Feany
Neurobiology of Disease (2021) Vol. 159, pp. 105482-105482
Open Access | Times Cited: 30
Abby L. Olsen, Mel Β. Feany
Neurobiology of Disease (2021) Vol. 159, pp. 105482-105482
Open Access | Times Cited: 30
Multi-omic insights into Parkinson's Disease: From genetic associations to functional mechanisms
Brian M. Schilder, Elisa Navarro, Towfique Raj
Neurobiology of Disease (2021) Vol. 163, pp. 105580-105580
Open Access | Times Cited: 30
Brian M. Schilder, Elisa Navarro, Towfique Raj
Neurobiology of Disease (2021) Vol. 163, pp. 105580-105580
Open Access | Times Cited: 30
Neuroticism and Risk of Parkinson's Disease: A Meta‐Analysis
Antonio Terracciano, Damaris Aschwanden, Yannick Stéphan, et al.
Movement Disorders (2021) Vol. 36, Iss. 8, pp. 1863-1870
Open Access | Times Cited: 29
Antonio Terracciano, Damaris Aschwanden, Yannick Stéphan, et al.
Movement Disorders (2021) Vol. 36, Iss. 8, pp. 1863-1870
Open Access | Times Cited: 29