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Author Details

Katrin Voss
2004
12
12
PMIDPaper TitleJournal TitlePublished Year
25258084Transcriptional diversity during lineage commitment of human blood progenitors.Science2014
23570689Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.Genome Res2013
23222517Seventy-five genetic loci influencing the human red blood cell.Nature2012
22972982A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site.Blood2012
22139419New gene functions in megakaryopoiesis and platelet formation.Nature2011
21765411Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.Nat Genet2011
19370760Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 protein.Human Mutation2009
18297070G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.Nat Genet2008
18300272Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.Human Mutation2008
17657516CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations.Neurogenetics2007
14691092Acoustic communication in noise: regulation of call characteristics in a New World monkey.Journal of Experimental Biology2004
15114674Inhibition of Notch signaling biases rat thymocyte development towards the NK cell lineage.European Journal of Immunology2004
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Genomics England Ltd
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Lee Kong Chian School of Medicine, Nanyang Technological University
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William Harvey Research Institute, Queen Mary University of London
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London NorthWest Healthcare NHS Trust
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University Hospital Augsburg
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Medical Research Council Integrative Epidemiology Unit at the University of Bristol
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King's College London
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