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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:

Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions
Ryan O. Snodgrass, Tim Chico, Helen M. Arthur
Genes (2021) Vol. 12, Iss. 2, pp. 174-174
Open Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

The role of endothelial cell–pericyte interactions in vascularization and diseases
Li Gan, Junjie Gao, Peng Ding, et al.
Journal of Advanced Research (2024)
Open Access | Times Cited: 18
Hereditary hemorrhagic telangiectasia: from signaling insights to therapeutic advances
Tala Al Tabosh, Mohammad Al Tarrass, Laura Tourvieilhe, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 4
Open Access | Times Cited: 16
Endovascular treatment in the multimodality management of brain arteriovenous malformations: report of the Society of NeuroInterventional Surgery Standards and Guidelines Committee
Reade De Leacy, Sameer A. Ansari, Clemens M. Schirmer, et al.
Journal of NeuroInterventional Surgery (2022) Vol. 14, Iss. 11, pp. 1118-1124
Open Access | Times Cited: 52
Myostatin/Activin Receptor Ligands in Muscle and the Development Status of Attenuating Drugs
Buel D. Rodgers, Christopher W. Ward
Endocrine Reviews (2021) Vol. 43, Iss. 2, pp. 329-365
Open Access | Times Cited: 53
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT
María E Bernabeu-Herrero, Dilipkumar Patel, Adrianna Bielowka, et al.
Blood (2024) Vol. 143, Iss. 22, pp. 2314-2331
Open Access | Times Cited: 7
An update on preclinical models of hereditary haemorrhagic telangiectasia: Insights into disease mechanisms
Helen M. Arthur, Beth L. Roman
Frontiers in Medicine (2022) Vol. 9
Open Access | Times Cited: 24
Vascular defects associated with hereditary hemorrhagic telangiectasia revealed in patient-derived isogenic iPSCs in 3D vessels on chip
Valeria V. Orlova, Dennis M. Nahon, Amy Cochrane, et al.
Stem Cell Reports (2022) Vol. 17, Iss. 7, pp. 1536-1545
Open Access | Times Cited: 23
Hereditary haemorrhagic telangiectasia
Ruben Hermann, Claire L. Shovlin, Raj S. Kasthuri, et al.
Nature Reviews Disease Primers (2025) Vol. 11, Iss. 1
Closed Access
Molecular basis for pericyte-induced capillary tube network assembly and maturation
Scott S. Kemp, Prisca K. Lin, Zheying Sun, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 18
BMP10 functions independently from BMP9 for the development of a proper arteriovenous network
Hyunwoo Choi, Bo-Gyeong Kim, Yong Hwan Kim, et al.
Angiogenesis (2022) Vol. 26, Iss. 1, pp. 167-186
Open Access | Times Cited: 18
Brain arteriovenous malformation in hereditary hemorrhagic telangiectasia: Recent advances in cellular and molecular mechanisms
Elise Drapé, Typhaine Anquetil, Bruno Larrivée, et al.
Frontiers in Human Neuroscience (2022) Vol. 16
Open Access | Times Cited: 14
Pathological Background and Clinical Procedures in Oral Surgery Haemostasis Disorders: A Narrative Review
Federica Pulicari, Matteo Pellegrini, Andrea Scribante, et al.
Applied Sciences (2023) Vol. 13, Iss. 4, pp. 2076-2076
Open Access | Times Cited: 8
Therapeutic targeting of vascular malformation in a zebrafish model of hereditary haemorrhagic telangiectasia
Ryan O. Snodgrass, Karan Govindpani, Karen Plant, et al.
Disease Models & Mechanisms (2023) Vol. 16, Iss. 4
Open Access | Times Cited: 8
Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1
Desiree DeMille, Jamie McDonald, Carmelo Bernabéu, et al.
Human Mutation (2024) Vol. 2024, pp. 1-13
Open Access | Times Cited: 2
Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variation
Katie E. Joyce, Ebun Onabanjo, S Brownlow, et al.
Blood Advances (2022) Vol. 6, Iss. 13, pp. 3956-3969
Open Access | Times Cited: 12
Genetics of brain arteriovenous malformations and cerebral cavernous malformations
Hiroki Hongo, Satoru Miyawaki, Yu Teranishi, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 157-167
Closed Access | Times Cited: 10
Myostatin/Activin-A Signaling in the Vessel Wall and Vascular Calcification
Pasquale Esposito, Daniela Verzola, Daniela Picciotto, et al.
Cells (2021) Vol. 10, Iss. 8, pp. 2070-2070
Open Access | Times Cited: 13
Oxidative stress-induced MMP- and γ-secretase-dependent VE-cadherin processing is modulated by the proteasome and BMP9/10
Caterina Ivaldo, Mario Passalacqua, Anna Lisa Furfaro, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 5
Pericytes and vascular smooth muscle cells in central nervous system arteriovenous malformations
Sera Nakisli, Alfonso Lagares, Corinne M. Nielsen, et al.
Frontiers in Physiology (2023) Vol. 14
Open Access | Times Cited: 5
CDK6-mediated endothelial cell cycle acceleration drives arteriovenous malformations in hereditary hemorrhagic telangiectasia
Sajeth Dinakaran, Haitian Zhao, Yuefeng Tang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
Seven cases of hereditary haemorrhagic telangiectasia-like hepatic vascular abnormalities associated withEPHB4pathogenic variants
A Guilhem, Sophie Dupuis‐Girod, Olivier Espitia, et al.
Journal of Medical Genetics (2023) Vol. 60, Iss. 9, pp. 905-909
Closed Access | Times Cited: 4
Glycosylation: A new signaling paradigm for the neurovascular diseases
Dapinder Kaur, Heena Khan, Amarjot Kaur Grewal, et al.
Life Sciences (2023) Vol. 336, pp. 122303-122303
Closed Access | Times Cited: 4
A Microphysiological HHT-on-a-Chip Platform Recapitulates Patient Vascular Lesions
Jennifer S. Fang, Christopher J. Hatch, Jillian W. Andrejecsk, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
"Recent Advances in Hereditary Hemorrhagic Telangiectasia Pathogenesis and Therapies"
Y Alka, Zahra Shabani, Jasneet Kaur Dhaliwal, et al.
(2024)
Open Access | Times Cited: 1
A Microphysiological HHT-on-a-Chip Platform Recapitulates Patient Vascular Lesions
Christopher C.W. Hughes, Jennifer S. Fang, Christopher J. Hatch, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 1
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