Pinar Bayrak-Toydemir

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 4

Top Topics

Intellectual Disability

Papillary Thyroid

Top Venues

International journal of molecular sciences

Molecular genetics & genomic medicine

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)
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)