Author

Leinøe Eva

Department of Haematology, Rigshospitalet, Copenhagen, Denmark - Cited by 438 - Platelets

Biography

Leinøe Eva, belonging to Department of Haematology, Herlev Hospital, Copenhagen University Hospital, Copenhagen, Denmark. Interested in the field of Megakaryocytic progenitors, Autograf.
Title
Cited by
Year
Prediction of haemorrhage in the early stage of acute myeloid leukaemia by flow cytometric analysis of platelet function
EB Leinoe, MH Hoffmann, E Kjaersgaard, JD Nielsen, OJ Bergmann, ...British journal of haematology 128 (4), 526-532, 2005200
72
2005
Application of whole‐exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia
E Leinøe, E Zetterberg, S Kinalis, O Østrup, P Kampmann, E Norström, ...British Journal of Haematology 179 (2), 308-322, 2017201
56
2017
A case of thrombocytopenia and multiple thromboses after vaccination with ChAdOx1 nCoV-19 against SARS-CoV-2
AL Tølbøll Sørensen, M Rolland, J Hartmann, ZB Harboe, C Roed, ...Blood advances 5 (12), 2569-2574, 2021202
39
2021
High syndecan-1 levels in acute myeloid leukemia are associated with bleeding, thrombocytopathy, endothelial cell damage, and leukocytosis
AM Larsen, EB Leinøe, PI Johansson, H Birgens, SR OstrowskiLeukemia research 37 (7), 777-783, 2013201
36
2013
Multiple platelet defects identified by flow cytometry at diagnosis in acute myeloid leukaemia
EB Leinoe, MH Hoffmann, E Kjaersgaard, HE JohnsenBritish journal of haematology 127 (1), 76-84, 2004200
33
2004
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
MC Sims, L Mayer, JH Collins, TK Bariana, K Megy, C Lavenu-Bombled, ...Blood, The Journal of the American Society of Hematology 136 (17), 1956-1967, 2020202
29
2020
Clinical management, ethics and informed consent related to multi‐gene panel‐based high throughput sequencing testing for platelet disorders: communication from the SSC of the ISTH
K Downes, P Borry, K Ericson, K Gomez, A Greinacher, M Lambert, ...Journal of Thrombosis and Haemostasis (10), 2751-2758, 2020202
18
2020
Haemostatic function and biomarkers of endothelial damage before and after RBC transfusion in patients with haematologic disease
AM Larsen, EB Leinøe, PI Johansson, H Birgens, SR OstrowskiVox Sanguinis 109 (1), 52-61, 2015201
18
2015
A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss-and a gain-of-function mutation of ITGB3: evidence of a dominant effect of gain-of-function mutations
L Bury, E Zetterberg, EB Leinøe, E Falcinelli, A Marturano, G Manni, ...Haematologica 103 (6), e259, 2018201
17
2018
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in …
K Megy, K Downes, MC Morel‐Kopp, JM Bastida, S Brooks, L Bury, ...Journal of Thrombosis and Haemostasis 19 (10), 2612-2617, 2021202
16
2021
Clinical impact of leukemic blast heterogeneity at diagnosis in cytogenetic intermediate‐risk acute myeloid leukemia
MH Hoffmann, TW Klausen, M Boegsted, SF Larsen, A Schmitz, ...Cytometry Part B: Clinical Cytometry 82 (3), 123-131, 2012201
14
2012
Outcome of an enhanced diagnostic pipeline for patients suspected of inherited thrombocytopenia
E Leinøe, M Gabrielaite, O Østrup, E Funding, A Greinacher, ...British Journal of Haematology 186 (2), 373-376, 2019201
13
2019
Haemostatic function and biomarkers of endothelial damage before and after platelet transfusion in patients with acute myeloid leukaemia
AM Larsen, EB Leinøe, PI Johansson, R Larsen, P Wantzin, H Birgens, ...Transfusion medicine 25 (3), 174-183, 2015201
12
2015
Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding
M Fager Ferrari, E Leinoe, M Rossing, E Norström, K Strandberg, ...Platelets 29 (1), 56-64, 2018201
11
2018
Whole-exome sequencing of a patient with severe and complex hemostatic abnormalities reveals a possible contributing frameshift mutation in C3AR1
E Leinøe, OJ Nielsen, L Jønson, M RossingMolecular Case Studies 2 (4), a000828, 2016201
9
2016
Measuring the impact of a restrictive transfusion guideline in patients with acute myeloid leukaemia
RT Hoeg, EB Leinoe, P Andersen, TW Klausen, HS BirgensVox Sanguinis 105 (1), 81-84, 2013201
7
2013
Subcommittee on Genomics in Thrombosis, Hemostasis. Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for …
K Downes, P Borry, K Ericson, K Gomez, A Greinacher, M Lambert, ...J Thromb Haemost 18 (10), 251-258, 2020202
7
2020
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
J Ghouse, V Tragante, G Ahlberg, SA Rand, JB Jespersen, EB Leinøe, ...Nature Genetics 55 (3), 399-409, 2023202
7
2023
The Copenhagen founder variant GP1BA c. 58T> G is the most frequent cause of inherited thrombocytopenia in Denmark
The Copenhagen founder variant GP1BA c. 8T> G is the most frequent cause of inherited thrombocytopenia in DenmarkE Leinøe, N Brøns, AØ Rasmussen, M Gabrielaite, C Zaninetti, ...Journal of Thrombosis and Haemostasis 19 (11), 2884-2892, 2021202
5
2021
Genetic screening of children with suspected inherited bleeding disorders
NG Andersson, M Rossing, M Fager Ferrari, M Gabrielaite, E Leinøe, ...Haemophilia 26 (2), 31-32, 2020202
4
2020

Referred From: https://scholar.google.dk/citations?user=spnjX_4AAAAJ&hl=da

Cited by
Citations 438
h-index 12
i10-index 14
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