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Author Details
Full Name
Katrin Voss
Affiliation
ORCID
Career Start Year
2004
Papers
12
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
25258084
Transcriptional diversity during lineage commitment of human blood progenitors.
Science
2014
23570689
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.
Genome Res
2013
23222517
Seventy-five genetic loci influencing the human red blood cell.
Nature
2012
22972982
A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site.
Blood
2012
22139419
New gene functions in megakaryopoiesis and platelet formation.
Nature
2011
21765411
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.
Nat Genet
2011
19370760
Functional 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 Mutation
2009
18297070
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.
Nat Genet
2008
18300272
Novel 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 Mutation
2008
17657516
CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations.
Neurogenetics
2007
14691092
Acoustic communication in noise: regulation of call characteristics in a New World monkey.
Journal of Experimental Biology
2004
15114674
Inhibition of Notch signaling biases rat thymocyte development towards the NK cell lineage.
European Journal of Immunology
2004
1 - 12 of 12
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