Detalhe da pesquisa
1.
Dissecting the treatment-naive ecosystem of human melanoma brain metastasis.
Cell
; 185(14): 2591-2608.e30, 2022 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35803246
2.
Spatial multi-omic map of human myocardial infarction.
Nature
; 608(7924): 766-777, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35948637
3.
Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells.
PLoS Genet
; 19(3): e1010680, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36928188
4.
A 4-lineage Statistical Suite to Evaluate the Support of Large-Scale Retrotransposon Insertion Data to Reconstruct Evolutionary Trees.
Syst Biol
; 72(3): 649-661, 2023 06 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36688484
5.
Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories.
Mol Psychiatry
; 28(7): 2946-2963, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37131076
6.
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet
; 17(7): e1009679, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34324492
7.
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet
; 17(9): e1009809, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34547032
8.
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
PLoS Genet
; 12(10): e1006335, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27760138
9.
Triglyceride-derived fatty acids reduce autophagy in a model of retinal angiomatous proliferation.
JCI Insight
; 7(6)2022 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35167498
10.
Loss of ADAMTS19 causes progressive non-syndromic heart valve disease.
Nat Genet
; 52(1): 40-47, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31844321
11.
Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians.
Circ Genom Precis Med
; 12(6): e002481, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31184202
12.
Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene.
Eur J Hum Genet
; 27(7): 1033-1043, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30820038
13.
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
Nat Genet
; 51(1): 42-50, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30455415
14.
Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.
Front Physiol
; 8: 400, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28659821
15.
Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.
Front Physiol
; 8: 730, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28974934
16.
Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.
Can J Cardiol
; 32(1): 135.e1-7, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26148450
17.
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.
Nat Genet
; 46(11): 1245-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25282101