ATHN CV: Peer-Reviewed Publications

Radionuclide synovectomy/synoviorthesis (RS) in patients with bleeding disorders: A review of patient and procedure demographics and functional outcomes in the ATHNdataset.
Authors: McGuinn C, Cheng D, Aschman D, Carpenter SL, Sidonio R, Soni A, Tarantino MD, Wheeler AP, Dunn AL, ATHN3 Working Group. Haemophilia. 2017 Aug 24. doi: 10.1111/hae.13318. [Epub ahead of print]

Radionuclide Synovectomy/Synoviorthesis (RS) in Persons with Bleeding Disorders: A Review of Impact of National Guidance on Frequency of RS using the ATHNdataset
Authors: Sharma, R, Dunn, A, Aschman, D, Cheng, D, Wheeler, A, Soni, A, McGuinn, C, Knoll, C, Stein, DT, Young, G, French, J, Sanders, J, Davis, JA, Tarantino, M, Lim, M,Gruppo, R, Sidonio, R, Ahuja, S, Carpenter, S, Pipe, S, Shapiro, A Haemophilia. 2017 Jul; 23(4):e385-e388. Epub 2017 May 24.

Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative
Authors: Johnsen JM, Fletcher SN, Huston H, Roberge S, Martin BK, Kircher M, Josephson NC, Shendure J, Ruuska S, Koerper MA, Morales J, Pierce G, Aschman DJ, Konkle B Blood Advances 2017 May;1(13):824-834.

Genetic Analysis of Bleeding Disorders
Edison E, Konkle BA, Goodeve AC Haemophilia (2016), 22 (Supp.5), pg. 79.

National Needs Assessment of Patients Treated at the United States Federally Funded Hemophilia Treatment Centers
Authors: Butler RB, Cheadle A, Aschman DJ, Riske B, Senter S, McLaughlin K, Young G, Ahuja S and Forsberg A Haemophilia (2015) 1-7 DOI:10:111/hae.12810.

Hemophilia and Von Willebrand Disease Patients’ Perceptions of Care at US Hemophilia Treatment Centers
Authors: Aschman DJ on behalf of the NHPCC Needs Assessment Working Group, Shapiro AD, Butler RD, Sharathkumar A, Skinner M and Forsberg A Haemophilia (2014), 2 (Suppl.2), pg. 13. Based upon presentation at the 7th Annual Congress of the European Association of Haemophilia and Allied Disorders, Brussels, Belgium, February 26-28, 2014.

The ATHNdataset: A Community Resource for Outcomes Analysis, Public Health Surveillance and Research
Authors: Konkle B, Abshire T and Aschman D on behalf of the American Thrombosis and Hemostasis Network Affiliates American Journal of Hematology (2012), 87 (Suppl.1), pg. S159-60. Based upon presentation poster at Thrombosis and Hemostasis Summit of North America Scientific Meeting, Chicago IL, April 29, 2012.

The ATHNdataset: A U.S.-Based Dataset for Outcomes Analysis, Public Health Surveillance and Research
Authors: Konkle B, Abshire T and Aschman D on behalf of the American Thrombosis and Hemostasis Network Affiliates Haemophilia (2012), 18 (Suppl.1), pg. 27. Based upon presentation poster at the 5th Annual Congress of the European Association of Haemophilia and Allied Disorders, Rome, Italy, February 22-24, 2012.

Knowledge and Therapeutic Gaps: A Major Public Health Problem Highlighted in the Rare Coagulation Disorders
Authors: Shapiro A, Soucie JM, Peyvandi, F, Aschman DJ, DiMichele DM on behalf of the UDC Rare Bleeding and Clotting Disorders Working Group and the European Network of Rare Bleeding Disorders Database American Journal of Preventive Medicine (2011, December) (Suppl.4), pg. S324-331.

Establishing Community-Based Partnerships to Create a Standards-Based Information Infrastructure
Authors: Aschman DJ, Abshire TC, Shapiro AD, Lusher JM, Forsberg AD and Kulkarni R American Journal of Preventive Medicine (2011, December), (Suppl.4), pg. 332-337.