Detalhe da pesquisa
1.
Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters.
Cell
; 167(5): 1369-1384.e19, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27863249
2.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
Cell
; 167(5): 1415-1429.e19, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27863252
3.
Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas.
Haematologica
; 106(10): 2613-2623, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32703790
4.
A synthesis approach of mouse studies to identify genes and proteins in arterial thrombosis and bleeding.
Blood
; 132(24): e35-e46, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30275110
5.
Ensembl 2018.
Nucleic Acids Res
; 46(D1): D754-D761, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29155950
6.
Ensembl 2017.
Nucleic Acids Res
; 45(D1): D635-D642, 2017 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27899575
7.
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.
Blood
; 127(23): 2903-14, 2016 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26912466
8.
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
Blood
; 127(23): 2791-803, 2016 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27084890
9.
Training in High-Throughput Sequencing: Common Guidelines to Enable Material Sharing, Dissemination, and Reusability.
PLoS Comput Biol
; 12(6): e1004937, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27309738
10.
Next-generation sequencing: a challenge to meet the increasing demand for training workshops in Australia.
Brief Bioinform
; 14(5): 563-74, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23543352
11.
Towards the elucidation of the regulatory network guiding the insulin producing cells' differentiation.
Genomics
; 100(4): 212-21, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22819921
12.
Neutrophil specific granule and NETosis defects in gray platelet syndrome.
Blood Adv
; 5(2): 549-564, 2021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33496751
13.
Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils.
Cell Rep
; 24(10): 2784-2794, 2018 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30184510
14.
The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia.
Nat Med
; 24(6): 868-880, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29785028
15.
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
; 12(5): e0178095, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28542600
16.
Detection of Atherosclerotic Inflammation by 68Ga-DOTATATE PET Compared to [18F]FDG PET Imaging.
J Am Coll Cardiol
; 69(14): 1774-1791, 2017 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385306
17.
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.
Sci Transl Med
; 8(328): 328ra30, 2016 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26936507
18.
Transcriptional diversity during lineage commitment of human blood progenitors.
Science
; 345(6204): 1251033, 2014 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25258084
19.
SMIM1 underlies the Vel blood group and influences red blood cell traits.
Nat Genet
; 45(5): 542-545, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23563608
20.
Human gene correlation analysis (HGCA): a tool for the identification of transcriptionally co-expressed genes.
BMC Res Notes
; 5: 265, 2012 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22672625