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/vufind/Search/Results?lookfor=%22Downes%2C+Kate%22&type=Person&sort=year
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PubPharm (170)
1
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk
enthalten in:
bioRxiv.org
| 2024
von
Verdier, H.
|
Thomas, P.
|
Batista, J.
| +10
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2
Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework
enthalten in:
Journal of thrombosis and haemostasis : JTH
| 2024
von
Ross, J.
|
Mohan, S.
|
Zhang, J.
| +20
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3
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants
enthalten in:
Blood
| 2023
von
Stefanucci, L.
|
Collins, J.
|
Sims, M.
| +32
CommentIn: Blood. 2023 Dec 14;142(24):2037-2038. - PMID 38095926
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4
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk
enthalten in:
Blood
| 2023
von
Verdier, H.
|
Thomas, P.
|
Batista, J.
| +10
CommentIn: Blood. 2023 Nov 30;142(22):1851-1852. - PMID 38032670
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5
Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke
enthalten in:
TH open : companion journal to thrombosis and haemostasis
| 2023
von
Induruwa, I.
|
Kempster, C.
|
Thomas, P.
| +11
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6
Single cell transcriptional characterization of human megakaryocyte lineage commitment and maturation
enthalten in:
bioRxiv.org
| 2023
von
Choudry, F.
|
Bagger, F.
|
Macaulay, I.
| +15
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7
Genetic Analyses of Blood Cell Structure for Biological and Pharmacological Inference
enthalten in:
bioRxiv.org
| 2023
von
Akbari, P.
|
Vuckovic, D.
|
Jiang, T.
| +30
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8
Genome-wide Analysis of Differential Transcriptional and Epigenetic Variability Across Human Immune Cell Types
enthalten in:
bioRxiv.org
| 2023
von
Ecker, S.
|
Chen, L.
|
Pancaldi, V.
| +21
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9
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
enthalten in:
Nature communications
| 2023
von
Akbari, P.
|
Vuckovic, D.
|
Stefanucci, L.
| +29
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10
Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders : Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021 Oct;19(10):2612-2617
enthalten in:
Journal of thrombosis and haemostasis : JTH
| 2023
von
Megy, K.
|
Downes, K.
|
Morel-Kopp, M.
| +13
ErratumFor: J Thromb Haemost. 2021 Oct;19(10):2612-2617. - PMID 34355501
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