Claire L Shovlin (Claire Shovlin, C L Shovlin)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 27

Top Venues

Journal of clinical medicine

Blood

Emergency medicine journal : EMJ

Journal of medical genetics

Imperial College London (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Imperial College London

United Kingdom

PHD :: Molecular Medicine, including 3ys in Dept of Genetics, Harvard Medical School

Publications

Maria E Bernabéu-Herrero, Dilipkumar Patel, Adrianna Bielowka, JiaYi Zhu, Kinshuk Jain, Ian Stuart Mackay, Patricia Chaves Guerrero, Giulia Emanuelli, Luca Jovine, Michela Noseda, Stefan John Marciniak, Micheala A Aldred, Claire L Shovlin
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT. Blood 143 (22) (2024)
Maria E Bernabéu-Herrero, Dilipkumar Patel, Adrianna Bielowka, JiaYi Zhu, Kinshuk Jain, Ian Stuart Mackay, Patricia Chaves Guerrero, Giulia Emanuelli, Luca Jovine, Michela Noseda, Stefan John Marciniak, Micheala A Aldred, Claire L Shovlin
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT. Blood (2024)
Maria E Bernabéu-Herrero, Dilipkumar Patel, Adrianna Bielowka, JiaYi Zhu, Kinshuk Jain, Ian Stuart Mackay, Patricia Chaves Guerrero, Giulia Emanuelli, Luca Jovine, Michela Noseda, Stefan John Marciniak, Micheala A Aldred, Claire L Shovlin
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT. Blood (2024)
Maria E Bernabéu-Herrero, Dilipkumar Patel, Adrianna Bielowka, JiaYi Zhu, Kinshuk Jain, Ian Stuart Mackay, Patricia Chaves Guerrero, Giulia Emanuelli, Luca Jovine, Michela Noseda, Stefan John Marciniak, Micheala A Aldred, Claire L Shovlin
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT. Blood 143 (22) (2024)
Kinshuk Jain, Sarah C McCarley, Ghazel Mukhtar, Anna Ferlin, Andrew Fleming, Deborah J Morris-Rosendahl, Claire L Shovlin
Pathogenic Variant Frequencies in Hereditary Haemorrhagic Telangiectasia Support Clinical Evidence of Protection from Myocardial Infarction. Journal of clinical medicine 13 (1) (2023)
Kinshuk Jain, Sarah C McCarley, Ghazel Mukhtar, Anna Ferlin, Andrew Fleming, Deborah J Morris-Rosendahl, Claire L Shovlin
Pathogenic Variant Frequencies in Hereditary Haemorrhagic Telangiectasia Support Clinical Evidence of Protection from Myocardial Infarction. Journal of clinical medicine 13 (1) (2023)
Sarah C McCarley, Daniel A Murphy, Jack Thompson, Claire L Shovlin
Pharmacogenomic Considerations for Anticoagulant Prescription in Patients with Hereditary Haemorrhagic Telangiectasia. Journal of clinical medicine 12 (24) (2023)
Ghazel Mukhtar, Claire L Shovlin
Unsupervised machine learning algorithms identify expected haemorrhage relationships but define unexplained coagulation profiles mapping to thrombotic phenotypes in hereditary haemorrhagic telangiectasia. EJHaem 4 (3) (2023)
Omer F Eker, Sophie Dupuis-Girod, Claire L Shovlin, Edoardo Boccardi
Comment on Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12 , 2704. Journal of clinical medicine 12 (22) (2023)
Sarah C McCarley, Daniel A Murphy, Jack Thompson, Claire L Shovlin
Pharmacogenomic Considerations for Anticoagulant Prescription in Patients with Hereditary Haemorrhagic Telangiectasia. Journal of clinical medicine 12 (24) (2023)
Claire L Shovlin, Dilip Patel, Adrianna Bielowka, Jonathan A Ledermann, Atieh Modarresi, null null, Maria E Bernabeu-Herrero, Micheala A Aldred, Ali Alsafi
MEK 1 inhibition and bleeding in hereditary haemorrhagic telangiectasia. British journal of haematology (2023)
Sarah C McCarley, Daniel A Murphy, Jack Thompson, Claire L Shovlin
Pharmacogenomic Considerations for Anticoagulant Prescription in Patients with Hereditary Haemorrhagic Telangiectasia. Journal of clinical medicine 12 (24) (2023)
Claire L Shovlin, Fatma I Almaghlouth, Ali Alsafi, Nicola Coote, Catherine Rennie, Gillian Mf Wallace, Fatima S Govani, Genomics England Research Consortium
Updates on diagnostic criteria for hereditary haemorrhagic telangiectasia in the light of whole genome sequencing of 'gene-negative' individuals recruited to the 100 000 Genomes Project. Journal of medical genetics (2023)
Kinshuk Jain, Sarah C McCarley, Ghazel Mukhtar, Anna Ferlin, Andrew Fleming, Deborah J Morris-Rosendahl, Claire L Shovlin
Pathogenic Variant Frequencies in Hereditary Haemorrhagic Telangiectasia Support Clinical Evidence of Protection from Myocardial Infarction. Journal of clinical medicine 13 (1) (2023)
Emily Anderson, Lakshya Sharma, Ali Alsafi, Claire L Shovlin
Pulmonary arteriovenous malformations may be the only clinical criterion present in genetically confirmed hereditary haemorrhagic telangiectasia. Thorax 77 (6) (2022)
Katie E Joyce, Ebun Onabanjo, Sheila Brownlow, Fadumo Nur, Kike Olupona, Kehinde Fakayode, Manveer Sroya, Geraldine A Thomas, Teena Ferguson, Julian Redhead, Carolyn M Millar, Nichola Cooper, D Mark Layton, Freya Boardman-Pretty, Mark J Caulfield, null null, Claire L Shovlin
Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variation. Blood advances 6 (13) (2022)
Srimmitha Balachandar, Tamara J Graves, Anika Shimonty, Katie Kerr, Jill Kilner, Sihao Xiao, Richard Slade, Manveer Sroya, Mary Alikian, Emanuel Curetean, Ellen Thomas, Vivienne P M McConnell, Shane McKee, Freya Boardman-Pretty, Andrew Devereau, Tom A Fowler, Mark J Caulfield, Eric W Alton, Teena Ferguson, Julian Redhead, Amy J McKnight, Geraldine A Thomas, null null, Micheala A Aldred, Claire L Shovlin
Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations. American journal of medical genetics. Part A 188 (3) (2021)
Karan K Topiwala, Smit D Patel, Jeffrey L Saver, Christopher D Streib, Claire L Shovlin
Ischemic Stroke and Pulmonary Arteriovenous Malformations: A Review. Neurology (2021)
Marie E Faughnan, Johannes J Mager, Steven W Hetts, Valerie A Palda, Kelly Lang-Robertson, Elisabetta Buscarini, Erik Deslandres, Raj S Kasthuri, Andrea Lausman, David Poetker, Felix A Ratjen, Mark S Chesnutt, Marianne S Clancy, Kevin J Whitehead, David J Kuter, Murali M Chakinala, Miles B Conrad, Daniel Cortes, Claudia Crocione, Jama Darling, Els de Gussem, Carol Derksen, Sophie Dupuis-Girod, Patrick Foy, Urban W Geisthoff, James R Gossage, Adrienne M Hammilll, Ketil Heimdal, Katharine Henderson, Vivek N Iyer, Anette Drøhse Kjeldsen, Masaki Komiyama, Kevin Korenblatt, Jamie McDonald, Jack McMahon, Justin P McWilliams, Mary E Meek, Meir Mei Zahav, Scott Olitsky, Sara Palmer, Rose Pantalone, Jay F Piccirillo, Beth Plahn, Mary E M Porteous, Marco C Post, Ivan Radovanovic, Paul J Rochon, Josanna Rodriguez-Lopez, Carlo Sabba, Marcelo Martín Serra, Claire L Shovlin, Dennis Sprecher, Andrew J White, Ingrid Winship, Roberto Zarrabeitia
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia. Annals of internal medicine 173 (12) (2020)
Claire L Shovlin, Marcela P Vizcaychipi
Implications for COVID-19 triage from the ICNARC report of 2204 COVID-19 cases managed in UK adult intensive care units. Emergency medicine journal : EMJ 37 (6) (2020)
Marcela P Vizcaychipi, Claire L Shovlin, Alex McCarthy, Alice Howard, Alexander Brown, Michelle Hayes, Suveer Singh, Linsey Christie, Alice Sisson, Roger Davies, Christopher Lockie, Monica Popescu, Amandeep Gupta, James Armstrong, Hisham Said, Timothy Peters, Richard T Keays, null null
Development and implementation of a COVID-19 near real-time traffic light system in an acute hospital setting. Emergency medicine journal : EMJ 37 (10) (2020)
Jessica M Clarke, Mary Alikian, Sihao Xiao, Dalia Kasperaviciute, Ellen Thomas, Isobel Turbin, Kike Olupona, Elna Cifra, Emanuel Curetean, Teena Ferguson, Julian Redhead, null null, Claire L Shovlin
Low grade mosaicism in hereditary haemorrhagic telangiectasia identified by bidirectional whole genome sequencing reads through the 100,000 Genomes Project clinical diagnostic pipeline. Journal of medical genetics 57 (12) (2020)
Filip Gawecki, Jonathan Myers, Claire L Shovlin
Veterans Specific Activity Questionnaire (VSAQ): a new and efficient method of assessing exercise capacity in patients with pulmonary arteriovenous malformations. BMJ open respiratory research 6 (1) (2019)
Jillian W Andrejecsk, Anna E Hosman, Luisa Maria Botella, Claire L Shovlin, Helen M Arthur, Sophie Dupuis-Girod, Elisabetta Buscarini, Christopher C W Hughes, Franck Lebrin, Christine L Mummery, Marco C Post, Johannes J Mager
Executive summary of the 12th HHT international scientific conference. Angiogenesis 21 (1) (2019)
Abeer Rizvi, Patricia Macedo, Lydia Babawale, Hannah C Tighe, J Michael B Hughes, James E Jackson, Claire L Shovlin
Hemoglobin Is a Vital Determinant of Arterial Oxygen Content in Hypoxemic Patients with Pulmonary Arteriovenous Malformations. Annals of the American Thoracic Society 14 (6) (2018)
Claire L Shovlin, Elisabetta Buscarini, Anette D Kjeldsen, Hans Jurgen Mager, Carlo Sabba, Freya Droege, Urban Geisthoff, Sara Ugolini, Sophie Dupuis-Girod
European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT). Orphanet journal of rare diseases 13 (1) (2018)
A E Hosman, Claire L Shovlin
Cancer and hereditary haemorrhagic telangiectasia. Journal of cancer research and clinical oncology 143 (2) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Claire L Shovlin (Claire Shovlin, C L Shovlin)