Jamie McDonald

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 10

Top Topics

Epithelial Mesenchymal Transition

Polycyclic Aromatic Hydrocarbons

Chronic Rhinosinusitis

Top Venues

International journal of molecular sciences

Journal of clinical medicine

Molecular genetics & genomic medicine

Science signaling

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

Publications

Kevin J Whitehead, Doruk Toydemir, Whitney Wooderchak-Donahue, Gretchen M Oakley, Bryan McRae, Angelica Putnam, Jamie McDonald, Pinar Bayrak-Toydemir
Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT). International journal of molecular sciences 25 (14) (2024)
Kevin J Whitehead, Doruk Toydemir, Whitney Wooderchak-Donahue, Gretchen M Oakley, Bryan McRae, Angelica Putnam, Jamie McDonald, Pinar Bayrak-Toydemir
Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT). International journal of molecular sciences 25 (14) (2024)
Kevin J Whitehead, Doruk Toydemir, Whitney Wooderchak-Donahue, Gretchen M Oakley, Bryan McRae, Angelica Putnam, Jamie McDonald, Pinar Bayrak-Toydemir
Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT). International journal of molecular sciences 25 (14) (2024)
Alexandra Kilian, Giuseppe A Latino, Andrew J White, Felix A Ratjen, Jamie McDonald, Kevin J Whitehead, James R Gossage, Timo Krings, Michael T Lawton, Helen Kim, Marie E Faughnan, null The Brain Vascular Malformation Consortium Hht Investigator Group
Reply to Eker et al. 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 (23) (2023)
Alexandra Kilian, Giuseppe A Latino, Andrew J White, Felix Ratjen, Jamie McDonald, Kevin J Whitehead, James R Gossage, Timo Krings, Michael T Lawton, Helen Kim, Marie E Faughnan, null The Brain Vascular Malformation Consortium Hht Investigator Group
Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. Journal of clinical medicine 12 (7) (2023)
Joshua Mark Hodgson, Lidia Ruiz-Llorente, Jamie McDonald, Oliver W J Quarrell, Kelechi Ugonna, James Bentham, Rebecca Mason, Jennifer M Martin, Alejandro Sifrim, Katie Bergstrom, Pinar Bayrak-Toydemir, Whitney L Wooderchak-Donahue, Nicholas W Morrell, Robin Condliffe, Carmelo Bernabéu, Paul D Upton
Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT-like" syndrome in children. Molecular genetics & genomic medicine (2021)
Jamie McDonald, Pinar Bayrak-Toydemir, Desiree DeMille, Whitney Wooderchak-Donahue, Kevin Whitehead
Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2). Genetics in medicine : official journal of the American College of Medical Genetics 22 (7) (2020)
Xuan Jiang, Whitney L Wooderchak-Donahue, Jamie McDonald, Prajakta Ghatpande, Mai Baalbaki, Melissa Sandoval, Daniel Hart, Hilary Clay, Shaun R Coughlin, Giorgio Lagna, Pinar Bayrak-Toydemir, Akiko Hata
Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia. Science signaling 11 (513) (2018)
Rhett S Thomson, Nicole L Molin, Kevin J Whitehead, Shaelene Ashby, Leland Johnson, P Daniel Ward, Bryan R McRae, Kevin F Wilson, Jamie McDonald
The effects of nasal closure on quality of life in patients with hereditary hemorrhagic telangiectasia. Laryngoscope investigative otolaryngology 3 (3) (2018)
Jamie McDonald, Whitney L Wooderchak-Donahue, Katharine Henderson, Eleri Paul, Ashley Morris, Pinar Bayrak-Toydemir
Tissue-specific mosaicism in hereditary hemorrhagic telangiectasia: Implications for genetic testing in families. American journal of medical genetics. Part A 176 (7) (2018)