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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:

PTPRD: neurobiology, genetics, and initial pharmacology of a pleiotropic contributor to brain phenotypes
George R. Uhl, María Jimena Martínez
Annals of the New York Academy of Sciences (2019) Vol. 1451, Iss. 1, pp. 112-129
Open Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

Restless legs syndrome
Mauro Manconi, Diego García‐Borreguero, Barbara Schormair, et al.
Nature Reviews Disease Primers (2021) Vol. 7, Iss. 1
Closed Access | Times Cited: 157
Connectomics of predicted Sst transcriptomic types in mouse visual cortex
Clare Gamlin, Casey M Schneider-Mizell, Matthew Mallory, et al.
Nature (2025) Vol. 640, Iss. 8058, pp. 497-505
Open Access | Times Cited: 5
Synaptic promiscuity in brain development
Neele Wolterhoff, P. Robin Hiesinger
Current Biology (2024) Vol. 34, Iss. 3, pp. R102-R116
Open Access | Times Cited: 8
Behavioral Abnormalities, Cognitive Impairments, Synaptic Deficits, and Gene Replacement Therapy in a CRISPR Engineered Rat Model of 5p15.2 Deletion Associated With Cri du Chat Syndrome
Jingjing Shen, Yan Wang, Yang Liu, et al.
Advanced Science (2025)
Open Access | Times Cited: 1
The Protein Tyrosine Phosphatase Receptor Delta Regulates Developmental Neurogenesis
Hideaki Tomita, Francisca Cornejo, Begoña Aranda-Pino, et al.
Cell Reports (2020) Vol. 30, Iss. 1, pp. 215-228.e5
Open Access | Times Cited: 63
Genetic contributions to alcohol use disorder treatment outcomes: a genome-wide pharmacogenomics study
Joanna M. Biernacka, Brandon J. Coombes, Anthony Batzler, et al.
Neuropsychopharmacology (2021) Vol. 46, Iss. 12, pp. 2132-2139
Open Access | Times Cited: 36
Protein tyrosine phosphatase receptor δ serves as the orexigenic asprosin receptor
Ila Mishra, Wei Rose Xie, Juan C. Bournat, et al.
Cell Metabolism (2022) Vol. 34, Iss. 4, pp. 549-563.e8
Open Access | Times Cited: 26
Genome-wide meta-analysis, functional genomics and integrative analyses implicate new risk genes and therapeutic targets for anxiety disorders
Wenqiang Li, Rui Chen, Laipeng Feng, et al.
Nature Human Behaviour (2023) Vol. 8, Iss. 2, pp. 361-379
Closed Access | Times Cited: 15
Systems genetics analysis reveals the common genetic basis for pain sensitivity and cognitive function
Fuyi Xu, Anran Chen, Shuijing Pan, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 2
Open Access | Times Cited: 5
Genome-wide association study implicates lipid pathway dysfunction in antipsychotic-induced weight gain: multi-ancestry validation
Yundan Liao, Hao Yu, Yuyanan Zhang, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 6, pp. 1857-1868
Closed Access | Times Cited: 5
Splice‐dependent trans‐synaptic PTP δ– IL 1 RAPL 1 interaction regulates synapse formation and non‐ REM sleep
Haram Park, Yeonsoo Choi, Hwajin Jung, et al.
The EMBO Journal (2020) Vol. 39, Iss. 11
Open Access | Times Cited: 39
Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders
Cynthia Okhuijsen‐Pfeifer, Marte Z. van der Horst, Chad A. Bousman, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 21
Widespread dysregulation of mRNA splicing implicates RNA processing in the development and progression of Huntington's disease
Vincent Tano, Kagistia Hana Utami, Nur Amirah Binte Mohammad Yusof, et al.
EBioMedicine (2023) Vol. 94, pp. 104720-104720
Open Access | Times Cited: 11
Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies
Antonino Zito, Jeannie T. Lee
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 9
Open Access | Times Cited: 4
The cerebellum modulates thirst
Ila Mishra, Bing Feng, B. BASU, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 9, pp. 1745-1757
Closed Access | Times Cited: 4
Disrupted synaptic gene expression in Fabry disease: Findings from RNA sequencing
Laura López-Valverde, M.E. Vázquez-Mosquera, Cristóbal Colón, et al.
Neurobiology of Disease (2025) Vol. 209, pp. 106908-106908
Open Access
Dairy Cattle Reproduction, Production, and Disease Resistance in the Omics Era: Genome-Wide Selection Signatures Identify Candidate Genes in Sahiwal Cattle
Pradeep Chaudhary, Ankit Magotra, Rani Alex, et al.
OMICS A Journal of Integrative Biology (2025)
Closed Access
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy
Delnaz Roshandel, Eric J. Sanders, Amy Shakeshaft, et al.
npj Genomic Medicine (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 9
Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores
Javad Jamshidi, Leanne M. Williams, Peter R. Schofield, et al.
Genes Brain & Behavior (2020) Vol. 19, Iss. 8
Open Access | Times Cited: 27
Feature Fusion and Detection in Alzheimer’s Disease Using a Novel Genetic Multi-Kernel SVM Based on MRI Imaging and Gene Data
Xianglian Meng, Qingpeng Wei, Meng Li, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 837-837
Open Access | Times Cited: 15
Genetic testing in the evaluation of individuals with clinical diagnosis of atypicalSturge–Webersyndrome
SangEun Yeom, Bernard A. Cohen, Clifford R. Weiss, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 4, pp. 983-994
Open Access | Times Cited: 9
Genetic architecture of plasma Alzheimer disease biomarkers
Joseph Bradley, Priyanka Gorijala, Suzanne E. Schindler, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 15, pp. 2532-2543
Open Access | Times Cited: 8
Protein tyrosine phosphatase receptor type D (PTPRD)—mediated signaling pathways for the potential treatment of hepatocellular carcinoma: a narrative review
Xuejing Huang, Feizhang Qin, Qiuhua Meng, et al.
Annals of Translational Medicine (2020) Vol. 8, Iss. 18, pp. 1192-1192
Open Access | Times Cited: 23
Comparing RNA‐sequencing datasets from astrocytes, oligodendrocytes, and microglia in multiple sclerosis identifies novel dysregulated genes relevant to inflammation and myelination
Sienna Drake, Aliyah Zaman, Tristan Simas, et al.
WIREs Mechanisms of Disease (2023) Vol. 15, Iss. 2
Closed Access | Times Cited: 7
Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs
Martina Servetti, Livia Pisciotta, Elisa Tassano, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 17
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