Detalhe da pesquisa
1.
Blocking HbS Polymerization in SCD.
Cell
; 180(5): 819, 2020 03 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32142671
2.
Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells.
PLoS Genet
; 19(3): e1010680, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36928188
3.
Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.
Hum Mol Genet
; 31(14): 2333-2347, 2022 07 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35138379
4.
Variation and impact of polygenic hematologic traits in monogenic sickle cell disease.
Haematologica
; 108(3): 870-881, 2023 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36226494
5.
Importance of genetic testing in unexplained cardiac arrest.
Eur Heart J
; 43(32): 3071-3081, 2022 08 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35352813
6.
Motif-Raptor: a cell type-specific and transcription factor centric approach for post-GWAS prioritization of causal regulators.
Bioinformatics
; 37(15): 2103-2111, 2021 Aug 09.
Artigo
Inglês
| MEDLINE | ID: mdl-33532840
7.
Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson's disease.
Proc Natl Acad Sci U S A
; 116(31): 15616-15624, 2019 07 30.
Artigo
Inglês
| MEDLINE | ID: mdl-31308240
8.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Genomics
; 22(1): 432, 2021 Jun 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34107879
9.
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans.
Hum Mol Genet
; 28(3): 515-523, 2019 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30307499
10.
Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.
Blood Cells Mol Dis
; 86: 102504, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32949984
11.
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
PLoS Genet
; 14(3): e1007293, 2018 03.
Artigo
Inglês
| MEDLINE | ID: mdl-29590102
12.
14q32 and let-7 microRNAs regulate transcriptional networks in fetal and adult human erythroblasts.
Hum Mol Genet
; 27(8): 1411-1420, 2018 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29432581
13.
Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated loci.
Proc Natl Acad Sci U S A
; 114(52): E11257-E11266, 2017 12 26.
Artigo
Inglês
| MEDLINE | ID: mdl-29229813
14.
Rare coding variants pinpoint genes that control human hematological traits.
PLoS Genet
; 13(8): e1006925, 2017 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-28787443
15.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
; 99(2): 481-8, 2016 08 04.
Artigo
Inglês
| MEDLINE | ID: mdl-27486782
16.
Testing the role of predicted gene knockouts in human anthropometric trait variation.
Hum Mol Genet
; 25(10): 2082-2092, 2016 05 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26908616
17.
PHACTR1 splicing isoforms and eQTLs in atherosclerosis-relevant human cells.
BMC Med Genet
; 19(1): 97, 2018 06 08.
Artigo
Inglês
| MEDLINE | ID: mdl-29884117
18.
Clonal hematopoiesis in sickle cell disease.
Blood
; 138(21): 2148-2152, 2021 11 25.
Artigo
Inglês
| MEDLINE | ID: mdl-34521115
19.
Re-assessing the effect of fetal hemoglobin on stroke in the Cooperative Study of Sickle Cell Disease.
Am J Hematol
; 98(11): E309-E311, 2023 11.
Artigo
Inglês
| MEDLINE | ID: mdl-37552626
20.
The genetics of platelet count and volume in humans.
Platelets
; 29(2): 125-130, 2018 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-28649937