Marie Lordkipanidzé

Author

Marie Lordkipanidzé

Also Known As

Lordkipanidzé, Marie, M Lordkipanidzé, M. LORDKIPANIDZÉ, M. Lordkipanidze, M. Lordkipanidzé, MARIE LORDKIPANIDZÉ, Marie Lordkipanidze, Marie Lordkipanidzé, Ying Sia

164

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

Université de Montréal Montreal Heart Institute University of Birmingham University of Bristol Hôpital du Sacré-Cœur de Montréal

About

Marie Lordkipanidzé is an author at Université de Montréal specializing in medicine, hematology, and thrombosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	21	973
2	Public Health	4	4	259
3	Health Sciences	2	2	64
4	Engineering	1	1	17
5	Allergy	1	1	39

Marie Lordkipanidzé

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
A comparison of six major platelet function tests to determine the prevalence of aspirin resistance in patients with stable coronary artery disease Marie Lordkipanidzé, C. Pharand, Érick Schampaert, European Heart Journal	2007	521
Comparison of four tests to assess inhibition of platelet function by clopidogrel in stable coronary artery disease patients Marie Lordkipanidzé, C. Pharand, Theresa Nguyen, European Heart Journal	2008	142
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects Benjamin C. Johnson, Gillian Lowe, Jane Wong Fütterer, Haematologica	2016	138
Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders Gillian Lowe, Marie Lordkipanidzé, Steve P. Watson Journal of Thrombosis and Haemostasis Platelet BiologyThrombosisThrombopoiesisCardiovascular DiseaseBlood Platelet	2013	123
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects Jacqueline Stockley, Neil V. Morgan, Danai Bem, Blood	2013	122
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC Paolo Gresele, Sara Orsini, Patrizia Noris, Journal of Thrombosis and Haemostasis ThrombopoiesisThrombosisPlatelet Physiology SscCardiovascular DiseaseInherited Platelet Disorders	2019	116
Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel Ban B. Dawood, Gillian Lowe, Marie Lordkipanidzé, Blood	2012	113
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects Sarah J. Fletcher, Ben Johnson, Gillian Lowe, Journal of Clinical Investigation Slfn14 MutationsFamily MembersGeneticsImmunologyPathology	2015	93
Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders Vincenzo Leo, Neil V. Morgan, Danai Bem, Journal of Thrombosis and Haemostasis Platelet BiologyThrombosisEpidemiologyNext‐generation SequencingUnderlying Defects	2014	69
Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay Marie Lordkipanidzé, Gillian Lowe, Nicholas S. Kirkby, Blood	2014	69

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