Detalhe da pesquisa
1.
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels.
Blood
; 143(18): 1845-1855, 2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38320121
2.
CAVIN1-Mediated hERG Dynamics: A Novel Mechanism Underlying the Interindividual Variability in Drug-Induced Long QT.
Circulation
; 2024 Apr 29.
Artigo
Inglês
| MEDLINE | ID: mdl-38682330
3.
Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.
PLoS Genet
; 18(9): e1009923, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-36112662
4.
Novel Cardiokine GDF3 Predicts Adverse Fibrotic Remodeling After Myocardial Infarction.
Circulation
; 147(6): 498-511, 2023 02 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36484260
5.
Impaired balance between neutrophil extracellular trap formation and degradation by DNases in COVID-19 disease.
J Transl Med
; 22(1): 246, 2024 Mar 07.
Artigo
Inglês
| MEDLINE | ID: mdl-38454482
6.
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis.
Clin Genet
; 105(2): 185-189, 2024 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37904629
7.
Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays.
Blood
; 140(2): 140-151, 2022 07 14.
Artigo
Inglês
| MEDLINE | ID: mdl-35486842
8.
Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels.
Arterioscler Thromb Vasc Biol
; 43(7): e254-e269, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37128921
9.
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.
PLoS Genet
; 17(1): e1009284, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33465109
10.
Addressing unmeasured confounders in cohort studies: Instrumental variable method for a time-fixed exposure on an outcome trajectory.
Biom J
; 66(1): e2200358, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38098309
11.
A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling.
Am J Hum Genet
; 107(2): 211-221, 2020 08 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32649856
12.
Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation.
Blood
; 137(17): 2394-2402, 2021 04 29.
Artigo
Inglês
| MEDLINE | ID: mdl-33512453
13.
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.
Haematologica
; 108(3): 772-784, 2023 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35638551
14.
Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design.
BMC Med Res Methodol
; 23(1): 99, 2023 04 22.
Artigo
Inglês
| MEDLINE | ID: mdl-37087423
15.
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.
Brain
; 145(4): 1519-1534, 2022 05 24.
Artigo
Inglês
| MEDLINE | ID: mdl-34788392
16.
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease.
Blood
; 136(5): 533-541, 2020 07 30.
Artigo
Inglês
| MEDLINE | ID: mdl-32457982
17.
Single-Cell Study of Two Rat Models of Pulmonary Arterial Hypertension Reveals Connections to Human Pathobiology and Drug Repositioning.
Am J Respir Crit Care Med
; 203(8): 1006-1022, 2021 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33021809
18.
Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (HSD17B14) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes.
J Am Soc Nephrol
; 32(10): 2634-2651, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34261756
19.
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.
Eur Heart J
; 42(9): 919-933, 2021 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33532862
20.
OPTIMIR, a novel algorithm for integrating available genome-wide genotype data into miRNA sequence alignment analysis.
RNA
; 25(6): 657-668, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30819774