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Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease
(JAMA neurology, 2022-05-31)Article de revue -
PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases
(International Journal of Cancer. vol. 144, n° 3, pp. 533-544, 2019-02-01)Article de revue -
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome
(Journal of the American Society of Nephrology. vol. 29, n° 7, pp. 2000-2013, 2018-07)Article de revue -
Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse
(Circulation-Genomic and Precision Medicine. vol. 14, n° 5, pp. CIRCGEN120003148, 2021-08-31)Article de revue -
Association of ABO haplotypes with the risk of venous thrombosis: impact on disease risks estimation
(Blood, 2020-12-22)Article de revue -
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
(Nature Genetics. vol. 52, n° 12, pp. 1303-1313, 2020-12)Article de revue -
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
(Acta Neuropathologica. vol. 144, n° 5, pp. 821-842, 2022-11)Article de revueLibre acceso -
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
(Nature Genetics. vol. 51, n° 1, pp. 51-62, 2019-01)Article de revueLibre acceso -
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke
(PLoS ONE. vol. 13, n° 11, pp. e0206554, 2018-11-02)Article de revue -
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
(European Heart Journal, 2022-03-04)Article de revue