1. Tissue‐specific mosaicism in hereditary hemorrhagic telangiectasia: Implications for genetic testing in families. Issue 7 (7th May 2018) Authors: McDonald, Jamie; Wooderchak‐Donahue, Whitney L.; Henderson, Katharine; Paul, Eleri; Morris, Ashley; Bayrak‐Toydemir, Pinar Journal: American journal of medical genetics Issue: Volume 176:Issue 7(2018) Page Start: 1618 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. No Access New York City : The City’s Hidden Treasures, Haunts, and Forgotten Places /: The City’s Hidden Treasures, Haunts, and Forgotten Places. (2018) Authors: McDonald, Jamie Record Type: Book Extent: 1 online resource (288 pages), (250 illustrations) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An evaluation of the severity and progression of epistaxis in hereditary hemorrhagic telangiectasia 1 versus hereditary hemorrhagic telangiectasia 2. (15th September 2015) Authors: Hunter, Benjamin N.; Timmins, Benjamin H.; McDonald, Jamie; Whitehead, Kevin J.; Ward, P. Daniel; Wilson, Kevin F. Journal: Laryngoscope Issue: Volume 126:Number 4(2016:Apr.) Page Start: 786 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mosaic ACVRL1 and ENG mutations in hereditary haemorrhagic telangiectasia patients. Issue 5 (4th March 2011) Authors: Best, D Hunter; Vaughn, Cecily; McDonald, Jamie; Damjanovich, Kristy; Runo, James R; Chibuk, Jason M; Bayrak-Toydemir, Pinar Journal: Journal of medical genetics Issue: Volume 48:Issue 5(2011) Page Start: 358 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 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. Issue 12 (9th April 2021) Authors: Hodgson, Joshua; Ruiz‐Llorente, Lidia; McDonald, Jamie; Quarrell, Oliver; Ugonna, Kelechi; Bentham, James; Mason, Rebecca; Martin, Jennifer; Moore, David; Bergstrom, Katie; Bayrak‐Toydemir, Pinar; Wooderchak‐Donahue, Whitney; Morrell, Nicholas W.; Condliffe, Robin; Bernabeu, Carmelo; Upton, Paul D. Journal: Molecular genetics & genomic medicine Issue: Volume 9:Issue 12(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Vitamin D levels are associated with epistaxis severity and bleeding duration in hereditary hemorrhagic telangiectasia. (April 2018) Authors: Weber, Lauren Marissa; McDonald, Jamie; Whitehead, Kevin Journal: Biomarkers in medicine Issue: Volume 12:Number 4(2018) Page Start: 365 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Decolonizing Organizational Communication. (August 2022) Authors: Pal, Mahuya; Kim, Heewon; Harris, Kate L.; Long, Ziyu; Linabary, Jasmine; Wilhoit Larson, Elizabeth; Jensen, Peter R.; Gist-Mackey, Angela N.; McDonald, Jamie; Nieto-Fernandez, Beatriz; Jiang, Jing; Misra, Smita; Dempsey, Sarah E. Journal: Management communication quarterly Issue: Volume 36:Number 3(2022) Page Start: 547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A rare neuromyelitis optica mimic: Primary CNS histiocytic sarcoma. (September 2022) Authors: Rogawski, David S; Nirschl, Jeffrey J; McDonald, Jamie; Nie, Esther; Schwartz, Nicholas U; Vogel, Hannes; Scott, Brian J; Gold, Carl A; Kipp, Lucas B Journal: Multiple sclerosis Issue: Volume 28:Number 10(2022) Page Start: 1651 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Movements in organizational communication research : current issues and future directions /: current issues and future directions. (2019) Editors: McDonald, Jamie; Mitra, Rahul Record Type: Book Extent: 1 online resource, illustrations (black and white) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia. Issue 12 (22nd September 2018) Authors: Wooderchak-Donahue, Whitney L.; McDonald, Jamie; Farrell, Andrew; Akay, Gulsen; Velinder, Matt; Johnson, Peter; VanSant-Webb, Chad; Margraf, Rebecca; Briggs, Eric; Whitehead, Kevin J; Thomson, Jennifer; Lin, Angela E; Pyeritz, Reed E; Marth, Gabor; Bayrak-Toydemir, Pinar Journal: Journal of medical genetics Issue: Volume 55:Issue 12(2018) Page Start: 824 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗