Author details

Full Name

Myrto Kostadima

Affiliation

ORCID

Career Start Year

2011

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
32703790	Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas.	Haematologica	2021
33496751	Neutrophil specific granule and NETosis defects in gray platelet syndrome.	Blood Adv	2021
31691826	Ensembl 2020.	Nucleic Acids Res	2020
30407521	Ensembl 2019.	Nucleic Acids Res	2019
29785028	The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia.	Nat Med	2018
30184510	Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils.	Cell Rep	2018
30275110	A synthesis approach of mouse studies to identify genes and proteins in arterial thrombosis and bleeding.	Blood	2018
29155950	Ensembl 2018.	Nucleic Acids Res	2018
27899575	Ensembl 2017.	Nucleic Acids Res	2017
28385306	Detection of Atherosclerotic Inflammation by <sup>68</sup>Ga-DOTATATE PET Compared to [<sup>18</sup>F]FDG PET Imaging.	J Am Coll Cardiol	2017
28542600	SNP in human ARHGEF3 promoter is associated with DNase hypersensitivity, transcript level and platelet function, and Arhgef3 KO mice have increased mean platelet volume.	PLoS One	2017
28703137	Platelet function is modified by common sequence variation in megakaryocyte super enhancers.	Nat Commun	2017
27863249	Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters.	Cell	2016
26912466	A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.	Blood	2016
27084890	A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.	Blood	2016
27309738	Training in High-Throughput Sequencing: Common Guidelines to Enable Material Sharing, Dissemination, and Reusability.	PLoS Comput Biol	2016
26936507	A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.	Sci Transl Med	2016
27863252	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.	Cell	2016
25258084	Transcriptional diversity during lineage commitment of human blood progenitors.	Science	2014
23543352	Next-generation sequencing: a challenge to meet the increasing demand for training workshops in Australia.	Brief Bioinform	2013
23563608	SMIM1 underlies the Vel blood group and influences red blood cell traits.	Nat Genet	2013
22366785	Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.	Nat Genet	2012
22672625	Human gene correlation analysis (HGCA): a tool for the identification of transcriptionally co-expressed genes.	BMC Research Notes	2012
22819921	Towards the elucidation of the regulatory network guiding the insulin producing cells' differentiation.	Genomics	2012
21765411	Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.	Nat Genet	2011