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Vascular Anomalies and Treatments

TopicLeading institutions, researchers & key papers

Vascular Anomalies and Treatments is a topic indexed in ScholarIQ from OpenAlex.

What is known about Vascular Anomalies and Treatments?

ScholarIQrecord summary

This cluster of papers focuses on the diagnosis and management of hereditary hemorrhagic telangiectasia (HHT), a genetic disorder characterized by vascular malformations. It covers topics such as genetics, pulmonary arteriovenous malformations, embolization, epistaxis, liver involvement, SMAD4 mutations, and vascular anomalies.

How many works does Vascular Anomalies and Treatments have?

ScholarIQindexed works

Vascular Anomalies and Treatments has 94 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

What is the OpenAlex record for Vascular Anomalies and Treatments?

ScholarIQopenalex

The OpenAlex for Vascular Anomalies and Treatments is on the source record.

What are the most-cited papers on Vascular Anomalies and Treatments?

ScholarIQmost cited works
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
Kimberly A. McAllister, K.M. Grogg, David W. Johnson, Carol J. Gallione, Melanie A. Baldwin, Charles E. Jackson, E.A. Helmbold, Dorene S. Markel, Wendy McKinnon, J. Murrel, Mary Kay McCormick, M. A. Pericak‐Vance, Peter Heutink, Ben A. Oostra, T. Haitjema, C.J.J. Westerman, Mary Porteous, Alan E. Guttmacher, Michelle Letarte, Douglas A. Marchuk
Nature Genetics. 19941,503 CitationsOPEN ACCESS
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
David W. Johnson, Jonathan Berg, Melanie A. Baldwin, Carol J. Gallione, Ivonne Marondel, Sang-Heon Yoon, Timothy T. Stenzel, Marcy C. Speer, M. A. Pericak‐Vance, Austin G. Diamond, Alan E. Guttmacher, Charles E. Jackson, Liliana Attisano, Raju Kucherlapati, Mary Porteous, Douglas A. Marchuk
Nature Genetics. 19961,130 Citations
International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia
Marie E. Faughnan, Valerie A. Palda, Guadalupe García–Tsao, Urban W. Geisthoff, Jamie McDonald, Deborah D. Proctor, John C. Spears, Dale Brown, Elisabetta Buscarini, Mark S. Chesnutt, Vincent Cottin, Arupa Ganguly, James R. Gossage, Alan E. Guttmacher, Robert H. Hyland, Shelley Kennedy, Joshua R. Korzenik, Johannes J. Mager, Augustin Ozanne, Jay F. Piccirillo, Daniel Picus, Henri Plauchu, Mary Porteous, Reed E. Pyeritz, Douglas A. Ross, Carlo Sabbà, Karen L. Swanson, P. B. Terry, M. Christopher Wallace, C. J. J. Westermann, Robert I. White, Lawrence H. Young, Roberto Zarrabeitia
Journal of Medical Genetics. 20091,081 Citations
Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia
Vincent Cottin, Thierry Chinet, A. Lavolé, R. Corre, Éric Marchand, Martine Reynaud‐Gaubert, Henri Plauchu, Jean-François Cordier
Medicine. 2007215 CitationsOPEN ACCESS
Clinical Practice Guideline: Nosebleed (Epistaxis)
David E. Tunkel, Samantha Anne, Spencer C. Payne, Stacey L. Ishman, Richard M. Rosenfeld, Peter J. Abramson, Jacqueline D. Alikhaani, Margo McKenna Benoit, Rachel S. Bercovitz, Michael D. Brown, Boris Chernobilsky, David Feldstein, Jesse M. Hackell, Eric H. Holbrook, Sarah M. Holdsworth, Kenneth W. Lin, Meredith Merz Lind, David M. Poetker, Charles A. Riley, John S. Schneider, Michael D. Seidman, Venu Vadlamudi, Tulio A. Valdez, Lorraine C. Nnacheta, Taskin M. Monjur
Otolaryngology. 2020194 Citations

Where is Vascular Anomalies and Treatments research published, and who funds it?

ScholarIQvenues & funding sources

TOP FUNDERS

National Science Foundation—
NIH—
Wellcome Trust—
European Research Council—
Funder breakdown is a member featureSign up free to unlock

How much of the research on Vascular Anomalies and Treatments is open access?

ScholarIQopen access share
40%OPEN ACCESS
Gold
13%
Green
20%
Hybrid
0%
Bronze
7%
Closed
60%

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