Gillian Lowe - Concepedia

Author

Gillian Lowe

University of Birmingham ORCID

Also Known As

G LOWE, G Lowe, G. C. Lowe, G. Lowe, G.C. Lowe, GC Lowe, Gerry Gilleran, Gill Lowe, Gillian C Lowe, Gillian C. Lowe

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

University of Birmingham University Hospitals Birmingham NHS Foundation Trust University of Sheffield Queen Elizabeth Hospital Birmingham University of Bristol

About

Gillian Lowe is an author at University of Birmingham specializing in medicine, hematology, and thrombosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	520
2	Public Health	3	3	103
3	Health Sciences	1	1	22
4	Allergy	1	1	15
5	Biomedical Engineering	1	1	22

Gillian Lowe

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Real-world experience with caplacizumab in the management of acute TTP Tina Dutt, Rebecca Shaw, Matthew Stubbs, Blood	2020	150
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
Rituximab prophylaxis to prevent thrombotic thrombocytopenic purpura relapse: outcome and evaluation of dosing regimens John‐Paul Westwood, Mari Thomas, Ferras Alwan, Blood Advances	2017	118
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
A novel mutation in the P2Y12 receptor and a function‐reducing polymorphism in protease‐activated receptor 1 in a patient with chronic bleeding Yesha Patel, Marie Lordkipanidzé, Gillian Lowe, Journal of Thrombosis and Haemostasis Function‐reducing PolymorphismMedicineP2y12 ReceptorHematologyPathology	2014	54

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