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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:

Prader-Willi syndrome: reflections on seminal studies and future therapies
Michael Chung, Maéva Langouët, Stormy J. Chamberlain, et al.
Open Biology (2020) Vol. 10, Iss. 9
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

A genome‐wide association meta‐analysis of all‐cause and vascular dementia
Bernard Fongang
Alzheimer s & Dementia (2024) Vol. 20, Iss. 9, pp. 5973-5995
Open Access | Times Cited: 9
Small nucleolar RNAs in plasma extracellular vesicles and their discriminatory power as diagnostic biomarkers of Alzheimer's disease
Nicholas F. Fitz, Jiebiao Wang, M. Ilyas Kamboh, et al.
Neurobiology of Disease (2021) Vol. 159, pp. 105481-105481
Open Access | Times Cited: 33
Diagnosis and management of sleep disorders in Prader-Willi syndrome
Jessica Duis, Lara C. Pullen, Maria Picone, et al.
Journal of Clinical Sleep Medicine (2022) Vol. 18, Iss. 6, pp. 1687-1696
Open Access | Times Cited: 26
Inpatient Hospitalizations for COVID‐19 Among Patients With Prader–Willi Syndrome: A National Inpatient Sample Analysis
James Luccarelli, Theresa V. Strong, Emily Rubin, et al.
American Journal of Medical Genetics Part A (2025)
Closed Access
Using Zebrafish Models to Study Epitranscriptomic Regulation of CNS Functions
Jianzhong Jiang, Yun‐Qian Zhang, Jiyi Wang, et al.
Journal of Neurochemistry (2025) Vol. 169, Iss. 1
Closed Access
Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing
Dahlia Rohm, Joshua B. Black, Sean R. McCutcheon, et al.
Cell Genomics (2025) Vol. 5, Iss. 2, pp. 100770-100770
Open Access
Epigenetics in Prader-Willi Syndrome
Aron Judd P. Mendiola, Janine M. LaSalle
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 26
Transcriptomic Analysis of Cardiomyocyte Extracellular Vesicles in Hypertrophic Cardiomyopathy Reveals Differential snoRNA Cargo
Victoria James, Zubair A. Nizamudeen, Daniel Lea, et al.
Stem Cells and Development (2021) Vol. 30, Iss. 24, pp. 1215-1227
Open Access | Times Cited: 24
Neuropeptide therapeutics to repress lateral septum neurons that disable sociability in an autism mouse model
Amélie M. Borie, Yann Dromard, Prabahan Chakraborty, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 11, pp. 101781-101781
Open Access | Times Cited: 3
The Role of Long Non-coding RNAs in Human Imprinting Disorders: Prospective Therapeutic Targets
Tingxuan Wang, Jian Jian Li, Liuyi Yang, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 22
Sex-Specific Transcriptomic Signatures in Brain Regions Critical for Neuropathic Pain-Induced Depression
Wei-Ping Dai, Shuying Huang, Yuan Luo, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 15
Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing
Dahlia Rohm, Joshua B. Black, Sean R. McCutcheon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Hormonal Imbalances in Prader–Willi and Schaaf–Yang Syndromes Imply the Evolution of Specific Regulation of Hypothalamic Neuroendocrine Function in Mammals
Maria Camila Hoyos Sanchez, Tara Bayat, Rebecca R. Florke Gee, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 17, pp. 13109-13109
Open Access | Times Cited: 5
Extracellular vesicles in Alzheimer's disease
Victor Hugo Berriel Pinho, João Paulo Lima Daher, Salim Kanaan, et al.
Arquivos de Neuro-Psiquiatria (2024) Vol. 82, Iss. 03, pp. 001-008
Open Access | Times Cited: 1
Acquiring Social Safety Engages Oxytocin Neurons in the Supraoptic Nucleus: Role of Magel2 Deficiency
Prabahan Chakraborty, Hugo Lamat, Emilie André, et al.
Neuroendocrinology (2024), pp. 1-16
Open Access | Times Cited: 1
Small Nucleolar RNAs and Their Comprehensive Biological Functions in Hepatocellular Carcinoma
Xiaoyu Liu, Wan Xie, Silu Meng, et al.
Cells (2022) Vol. 11, Iss. 17, pp. 2654-2654
Open Access | Times Cited: 6
A meta-analysis of genome-wide association studies identifies new genetic loci associated with all-cause and vascular dementia
Bernard Fongang, Muralidharan Sargurupremraj, Xueqiu Jian, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 6
Insulin secretion deficits in a Prader-Willi syndrome β-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperones
Erik Koppes, Marie A. Johnson, James J. Moresco, et al.
PLoS Genetics (2023) Vol. 19, Iss. 4, pp. e1010710-e1010710
Open Access | Times Cited: 3
The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome
Maria Rosaria Licenziati, Dario Bacchini, Antonino Crinò, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 5
Non-Syndromic Intellectual Disability and Its Pathways: A Long Noncoding RNA Perspective
Isabela Ichihara de Barros, Vitor Leão, Jessica Oliveira de Santis, et al.
Non-Coding RNA (2021) Vol. 7, Iss. 1, pp. 22-22
Open Access | Times Cited: 7
The Exon 3-Deleted Growth Hormone Receptor (d3GHR) Polymorphism—A Favorable Backdoor Mechanism for the GHR Function
Ghadeer Falah, Lital Sharvit, Gil Atzmon
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 13908-13908
Open Access | Times Cited: 2
Proteins and proteases of Prader–Willi syndrome: a comprehensive review and perspectives
Sanjukta Basak, Ajoy Basak
Bioscience Reports (2022) Vol. 42, Iss. 6
Open Access | Times Cited: 4
Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases
Zaletaev Dv, М. В. Немцова, V. V. Strelnikov
Molecular Biology (2022) Vol. 56, Iss. 1, pp. 1-28
Closed Access | Times Cited: 3
Genetic Disorders of Adipose Tissue
G. W. M. Millington
(2024), pp. 1-14
Closed Access
Differences in DNA methylation status explain phenotypic variability in patients with 5p− syndrome
Vanessa Tavares Almeida, Samar N. Chehimi, Gleyson Francisco Silva Carvalho, et al.
BMC Research Notes (2024) Vol. 17, Iss. 1
Open Access
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