2021 Publications
Antithrombin deficiency: A pediatric disorder
Smith N, Warren BB, Smith J, Jacobson L, Armstrong J, Kim J, Di Paola J, Manco-Johnson M. Antithrombin deficiency: A pediatric disorder. Thromb Res. 2021 Jun;202:45-51.
ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease
James PD, Connell NT, Ameer B, Di Paola J, Eikenboom J, Giraud N, Haberichter S, Jacobs-Pratt V, Konkle B, McLintock C, McRae S, R Montgomery R, O'Donnell JS, Scappe N, Sidonio R, Flood VH, Husainat N, Kalot MA, Mustafa RA. ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease. Blood Adv. 2021 Jan 12;5(1):280-300.
ETV6-related Thrombocytopenia and Platelet Dysfunction
Di Paola J, Fisher MH. ETV6-related thrombocytopenia and platelet dysfunction. January 2021. Platelets. 2020;1‐3.
Negatively charged nanoparticles of multiple materials inhibit shear-induced platelet accumulation
Griffin MT, Ashworth K, Hill N, von Behren J, Di Paola J, Ku DN. Negatively charged nanoparticles of multiple materials inhibit shear-induced platelet accumulation. Nanomedicine. 2021 Jul;35:102405.
Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel
Ross JE, Zhang BM, Lee K, Mohan S, Branchford BR, Bray P, Dugan SN, Freson K, Heller PG, Kahr WHA, Lambert MP, Luchtman-Jones L, Luo M, Perez Botero J, Rondina MT, Ryan G, Westbury S, Bergmeier W, Di Paola J. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel. Blood Adv. January 2021; 5(2):414-431.
von Willebrand disease: proposing definitions for future research
Connell NT, James PD, Brignardello-Petersen R, Abdul-Kadir R, Ameer B, Arapshian A, Couper S, Di Paola J, Eikenboom J, Giraud N, Grow JM, Haberichter S, Jacobs-Pratt V, Konkle BA, Kouides P, Laffan M, Lavin M, Leebeek FWG, McLintock C, McRae S, Montgomery R, O'Brien SH, O'Donnell JS, Ozelo MC, Scappe N, Sidonio R, Tosetto A, Weyand AC, Kalot MA, Husainat N, Mustafa RA, Flood VH. von Willebrand disease: proposing definitions for future research. Blood Adv. January 2021; 5(2):565-569.
von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene
Sadler B, Christopherson PA, Haller G, Montgomery RR, Di Paola J. von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene. Blood. 2021 Jun 10;137(23):3277-3283.