Myrto Kostadima - Concepedia

Author

Myrto Kostadima

Also Known As

Andrew R. Harper, Christopher Kressler, Kostadima, Myrto, M. Kostadima, Myrto A Kostadima, Myrto A. Kostadima, Myrto Kostadima, Myrto-Areti Kostadima, Nathalie Kingston, Praveen Jeevaratnam

Publications

12.1K

Citations

H-Index

Concepts

All Affiliations

University of Cambridge European Bioinformatics Institute Wellcome Sanger Institute National Health Service NHS Blood and Transplant

About

Myrto Kostadima is an author at University of Cambridge specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	6.4K
2	Biology	4	4	5.5K
3	Engineering	3	3	4.5K
4	Cell Biology	2	2	139
5	Immunology	1	1	120

Myrto Kostadima

Publications

10.7K

Citations

H-Index

Page 1

	Year	Citations
Ensembl 2018 Daniel R. Zerbino, Premanand Achuthan, Wasiu Akanni, Nucleic Acids Research EngineeringGeneticsGenomicsBioinformatics DatabaseHigh Throughput Sequencing	2017	2.8K
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease William J. Astle, Heather Elding, Tao Jiang, Cell	2016	1.4K
Ensembl 2020 Andrew Yates, Premanand Achuthan, Wasiu Akanni, Nucleic Acids Research EngineeringGeneticsGenome AnnotationGenomicsBioinformatics Database	2019	1.2K
Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters Biola M. Javierre, Oliver S. Burren, Steven P. Wilder, Cell	2016	1.1K
Ensembl 2019 Fiona Cunningham, Premanand Achuthan, Wasiu Akanni, Nucleic Acids Research BiologyFunctional GenomicsBioinformatics DatabaseBiological DatabaseGene Sequence Annotation	2018	1K
Ensembl 2017 Bronwen Aken, Premanand Achuthan, Wasiu Akanni, Nucleic Acids Research EngineeringGeneticsGenomicsGenome VariationBioinformatics Database	2016	546
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome Cornelis A. Albers, Dirk S. Paul, Harald Schulze, Nature Genetics Compound InheritanceMendelian DisorderGenetic DisorderGeneticsGenomic Mechanism	2012	419
Detection of Atherosclerotic Inflammation by 68 Ga-DOTATATE PET Compared to [ 18 F]FDG PET Imaging Jason M. Tarkin, Francis R. Joshi, Nicholas R. Evans, Journal of the American College of Cardiology	2017	413
Transcriptional diversity during lineage commitment of human blood progenitors Lu Chen, Myrto Kostadima, Joost H.A. Martens, Science	2014	296
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome Cornelis A. Albers, Ana Cvejic, Rémi Favier, Nature Genetics ThrombopoiesisThrombosisBlood PlateletGenetic DisorderGenetics	2011	274

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