Dr David Rabbolini

BSc MBBCh (Witw.) PhD (SyD) FRACP FRCPA
Clinical lecturer, Northern Clinical School / Northern Clinical School


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Awards and honours

2016AHCDO ASTH Conference Grant Recipient,Awarded to the author of the best abstract in the bleeding disorders field submitted to either HAA or the ASTH scientific workshop.

2016ASTH Scientific Medal – Runner up.

2015ASTH Scientific Medal - Winner, Awarded for the best presentation at the annual scientific meeting, Adelaide, SA, 2015.

- The award is intended forindividuals working in clinical and laboratory research in the field of thrombosis and haemostasis.

- The award is judged on the basis of abstracts submitted to the annual combined meeting of the ASTH and the Haematology Society of Australia and New Zealand (HSANZ) and Australian and New Zealand Society of Blood Transfusion (ANZSBT).

2015 Abstract selected as one of theOutstanding young scientist abstracts from the Asia - Pacific region.

-Presented as an oral presentation at theAsia-Pacific society of Thrombosis and Haemostasis (APSTH)/ Japanese Society of Thrombosis and Haemostasis (JSTH) joint symposium in May 2015

Keywords

Stem cells; Genetic diseases; Haematology

Clinical Specialty

Haematology

Selected publications

Download citations: PDF RTF Endnote

Book Chapters

  • Rabbolini, D., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2015). DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-generation Sequencing Technology with a Candidate Gene Array. In Jerzy K Kulski (Eds.), Next Generation Sequencing: Advances, Applications and Challenges, (pp. 387-408). Rijeka, Croatia: InTech Publishers. [More Information]

Journals

  • Fixter, K., Rabbolini, D., Valecha, B., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2018). Mean platelet diameter measurements to classify inherited thrombocytopenias. International Journal of Laboratory Hematology, 40(2), 187-195. [More Information]
  • Mundell, S., Rabbolini, D., Gabrielli, S., Chen, Q., Aungraheeta, R., Hutchinson, J., Kilo, T., Mackay, J., Ward, C., Stevenson, W., Morel-Kopp, M. (2018). Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding. Journal of Thrombosis and Haemostasis, 16(1), 44-53. [More Information]
  • Rabbolini, D., Gardiner, E., Morel-Kopp, M., Dunkley, S., Jahangiri, A., Lee, C., Stevenson, W., Ward, C. (2017). Anti-glycoprotein VI mediated immune thrombocytopenia: An under-recognized and significant entity? Research and Practice in Thrombosis and Haemostasis, 1, 291-295.
  • Rabbolini, D., Morel-Kopp, M., Ward, C., Stevenson, W. (2017). GFI1B variants associated with thrombocytopenia. Platelets, 28(5), 525-527. [More Information]
  • Rabbolini, D., Morel-Kopp, M., Chen, Q., Gabrielli, S., Dunlop, L., Chew, L., Blair, N., Brighton, T., Singh, N., Ng, A., Ward, C., Stevenson, W. (2017). Thrombocytopenia and CD34 expression is decoupled from (alpha)-granule deficiency with mutation of the first growth factor-independent 1B zinc finger. Journal of Thrombosis and Haemostasis, 15(11), 2245-2258. [More Information]
  • Rabbolini, D., Morel-Kopp, M., Stevenson, W., Ward, C. (2014). Inherited Macrothrombocytopenias. Seminars in Thrombosis and Hemostasis, 40(7), 774-784. [More Information]

2018

  • Fixter, K., Rabbolini, D., Valecha, B., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2018). Mean platelet diameter measurements to classify inherited thrombocytopenias. International Journal of Laboratory Hematology, 40(2), 187-195. [More Information]
  • Mundell, S., Rabbolini, D., Gabrielli, S., Chen, Q., Aungraheeta, R., Hutchinson, J., Kilo, T., Mackay, J., Ward, C., Stevenson, W., Morel-Kopp, M. (2018). Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding. Journal of Thrombosis and Haemostasis, 16(1), 44-53. [More Information]

2017

  • Rabbolini, D., Gardiner, E., Morel-Kopp, M., Dunkley, S., Jahangiri, A., Lee, C., Stevenson, W., Ward, C. (2017). Anti-glycoprotein VI mediated immune thrombocytopenia: An under-recognized and significant entity? Research and Practice in Thrombosis and Haemostasis, 1, 291-295.
  • Rabbolini, D., Morel-Kopp, M., Ward, C., Stevenson, W. (2017). GFI1B variants associated with thrombocytopenia. Platelets, 28(5), 525-527. [More Information]
  • Rabbolini, D., Morel-Kopp, M., Chen, Q., Gabrielli, S., Dunlop, L., Chew, L., Blair, N., Brighton, T., Singh, N., Ng, A., Ward, C., Stevenson, W. (2017). Thrombocytopenia and CD34 expression is decoupled from (alpha)-granule deficiency with mutation of the first growth factor-independent 1B zinc finger. Journal of Thrombosis and Haemostasis, 15(11), 2245-2258. [More Information]

2015

  • Rabbolini, D., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2015). DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-generation Sequencing Technology with a Candidate Gene Array. In Jerzy K Kulski (Eds.), Next Generation Sequencing: Advances, Applications and Challenges, (pp. 387-408). Rijeka, Croatia: InTech Publishers. [More Information]

2014

  • Rabbolini, D., Morel-Kopp, M., Stevenson, W., Ward, C. (2014). Inherited Macrothrombocytopenias. Seminars in Thrombosis and Hemostasis, 40(7), 774-784. [More Information]

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