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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:

Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome
Nicola Chiarelli, Giulia Carini, Nicoletta Zoppi, et al.
PLoS ONE (2018) Vol. 13, Iss. 1, pp. e0191220-e0191220
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases
Helena Kuivaniemi, Gerard Tromp
Gene (2019) Vol. 707, pp. 151-171
Open Access | Times Cited: 300
The Ehlers–Danlos syndromes
Fransiska Malfait, Marco Castori, Clair A. Francomano, et al.
Nature Reviews Disease Primers (2020) Vol. 6, Iss. 1
Closed Access | Times Cited: 218
Targetable cellular signaling events mediate vascular pathology in vascular Ehlers-Danlos syndrome
Caitlin J. Bowen, Juan F. Calderón, Zachary Burger, et al.
Journal of Clinical Investigation (2019) Vol. 130, Iss. 2, pp. 686-698
Open Access | Times Cited: 67
Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes
Nicola Chiarelli, Marco Ritelli, Nicoletta Zoppi, et al.
Genes (2019) Vol. 10, Iss. 8, pp. 609-609
Open Access | Times Cited: 64
Mechanisms of lower extremity vein dysfunction in chronic venous disease and implications in management of varicose veins
J.D. Raffetto, Raouf A. Khalil
Vessel Plus (2021)
Open Access | Times Cited: 45
Genome wide association and gene enrichment analysis reveal membrane anchoring and structural proteins associated with meat quality in beef
Joel D. Leal‐Gutiérrez, Mauricio A. Elzo, D. D. Johnson, et al.
BMC Genomics (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 50
Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
Vinh Toan Huynh, Marie‐Pierre Audrézet, John A. Sayer, et al.
Kidney International (2020) Vol. 98, Iss. 2, pp. 476-487
Open Access | Times Cited: 47
Collagen misfolding mutations: the contribution of the unfolded protein response to the molecular pathology
John F. Bateman, Matthew D. Shoulders, Shireen R. Lamandé
Connective Tissue Research (2022) Vol. 63, Iss. 3, pp. 210-227
Open Access | Times Cited: 16
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts
Nicoletta Zoppi, Nicola Chiarelli, Marco Ritelli, et al.
International Journal of Molecular Sciences (2018) Vol. 19, Iss. 4, pp. 982-982
Open Access | Times Cited: 31
Thrombospondin-4 mediates cardiovascular remodelling in angiotensin II-induced hypertension
Teresa Palao, Lejla Medzikovic, Catarina Rippe, et al.
Cardiovascular Pathology (2018) Vol. 35, pp. 12-19
Open Access | Times Cited: 29
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients’ skin fibroblasts
Nicola Chiarelli, Giulia Carini, Nicoletta Zoppi, et al.
PLoS ONE (2019) Vol. 14, Iss. 2, pp. e0211647-e0211647
Open Access | Times Cited: 28
Seeding decellularized nerve allografts with adipose-derived mesenchymal stromal cells: An in vitro analysis of the gene expression and growth factors produced
Nadia Rbia, Liselotte F. Bulstra, Eric A. Lewallen, et al.
Journal of Plastic Reconstructive & Aesthetic Surgery (2019) Vol. 72, Iss. 8, pp. 1316-1325
Closed Access | Times Cited: 27
Four decades in the making: Collagen III and mechanisms of vascular Ehlers Danlos Syndrome
Ramla Omar, Fransiska Malfait, Tom Van Agtmael
Matrix Biology Plus (2021) Vol. 12, pp. 100090-100090
Open Access | Times Cited: 21
Atypical COL3A1 variants (glutamic acid to lysine) cause vascular Ehlers–Danlos syndrome with a consistent phenotype of tissue fragility and skin hyperextensibility
Neeti Ghali, Duncan Baker, Angela F. Brady, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 9, pp. 2081-2091
Open Access | Times Cited: 24
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome
Anthony M. Vandersteen, Ruwan Weerakkody, David Parry, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 3, pp. 232-238
Open Access | Times Cited: 6
Transcriptome Profiling of Primary Skin Fibroblasts Reveal Distinct Molecular Features Between PLOD1- and FKBP14-Kyphoscoliotic Ehlers–Danlos Syndrome
Pei Jin Lim, Uschi Lindert, Lennart Opitz, et al.
Genes (2019) Vol. 10, Iss. 7, pp. 517-517
Open Access | Times Cited: 17
The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism
Tim Van Damme, Marlies Colman, Delfien Syx, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 265-265
Open Access | Times Cited: 9
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts
Nicola Chiarelli, Valeria Cinquina, Paolo Martini, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2023) Vol. 1870, Iss. 1, pp. 166915-166915
Open Access | Times Cited: 5
Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical review
Brent J. Doolan, Mark E. Lavallee, Ingrid Haußer, et al.
Journal of the American Academy of Dermatology (2023) Vol. 89, Iss. 3, pp. 551-559
Open Access | Times Cited: 4
Patient-derived extracellular matrix demonstrates role of COL3A1 in blood vessel mechanics
Elizabeth L. Doherty, Wen Yih Aw, Emily C. Warren, et al.
Acta Biomaterialia (2023) Vol. 166, pp. 346-359
Open Access | Times Cited: 4
Dysregulation of extracellular matrix and Lysyl Oxidase in Ehlers-Danlos syndrome type IV skin fibroblasts
Reece Foehr, Keith R. Anderson, Owen Dombrowski, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 1
Subpopulations of fibroblasts derived from human iPS cells
Takashi Kobayashi, Akihiro Yamashita, Noriyuki Tsumaki, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 1
The chemical chaperone 4-phenylbutyric acid rescues molecular cell defects of COL3A1 mutations that cause vascular Ehlers Danlos Syndrome
Ramla Omar, Michelle Lee, Laura Gonzalez-Trueba, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Pathogenic mechanisms in genetically defined Ehlers–Danlos syndromes
Delfien Syx, Fransiska Malfait
Trends in Molecular Medicine (2024) Vol. 30, Iss. 9, pp. 824-843
Closed Access | Times Cited: 1
Integrative Multi-Omics Approach in Vascular Ehlers–Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts
Nicola Chiarelli, Valeria Cinquina, Nicoletta Zoppi, et al.
Biomedicines (2024) Vol. 12, Iss. 12, pp. 2749-2749
Open Access | Times Cited: 1
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