Found: 17
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Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
- Published in:
- BioData Mining, 2017, v. 10, p. 1, doi. 10.1186/s13040-017-0145-5
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- Publication type:
- Article
Vaccine‐induced immune thrombocytopenia and thrombosis: The decline in anti‐platelet factor 4 antibodies is assay‐dependent.
- Published in:
- British Journal of Haematology, 2022, v. 197, n. 4, p. 428, doi. 10.1111/bjh.18022
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- Publication type:
- Article
A novel variant causing α2 antiplasmin deficiency: case report and experience in a UK centre.
- Published in:
- British Journal of Haematology, 2019, v. 187, n. 2, p. e42, doi. 10.1111/bjh.16165
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- Publication type:
- Article
Treatment of post‐transfusion hyperhaemolysis syndrome in Sickle Cell Disease with the anti‐IL6R humanised monoclonal antibody Tocilizumab.
- Published in:
- British Journal of Haematology, 2019, v. 186, n. 6, p. e212, doi. 10.1111/bjh.16103
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- Publication type:
- Article
Artificial intelligence and machine learning in haematology.
- Published in:
- British Journal of Haematology, 2019, v. 185, n. 2, p. 207, doi. 10.1111/bjh.15774
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- Publication type:
- Article
Diagnosis of inherited bleeding disorders in the genomic era.
- Published in:
- British Journal of Haematology, 2017, v. 179, n. 3, p. 363, doi. 10.1111/bjh.14796
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- Publication type:
- Article
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.
- Published in:
- Nature Genetics, 2011, v. 43, n. 8, p. 735, doi. 10.1038/ng.885
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- Publication type:
- Article
Mutation in KERA Identified by Linkage Analysis and Targeted Resequencing in a Pedigree with Premature Atherosclerosis.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098289
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- Article
Monocyte Gene Expression Signature of Patients with Early Onset Coronary Artery Disease.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0032166
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- Publication type:
- Article
Platelets in Patients with Premature Coronary Artery Disease Exhibit Upregulation of miRNA340* and miRNA624*.
- Published in:
- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0025946
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- Publication type:
- Article
Common genetic variants do not associate with CAD in familial hypercholesterolemia.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 6, p. 809, doi. 10.1038/ejhg.2013.242
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- Publication type:
- Article
Low-density lipoprotein receptor mutations generate synthetic genome-wide associations.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 563, doi. 10.1038/ejhg.2012.207
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- Article
More outreach for young scientists.
- Published in:
- Nature, 2010, v. 467, n. 7314, p. 401, doi. 10.1038/467401a
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- Publication type:
- Article
Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002139
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- Publication type:
- Article
Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.
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- 2016
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- Publication type:
- journal article
Mendelian randomization of blood lipids for coronary heart disease.
- Published in:
- European Heart Journal, 2015, v. 36, n. 9, p. 539
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- Publication type:
- Article
Hemostatic abnormalities in critically ill patients.
- Published in:
- Internal & Emergency Medicine, 2015, v. 10, n. 3, p. 287, doi. 10.1007/s11739-014-1176-2
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- Publication type:
- Article