Detalhe da pesquisa
1.
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.
Genet Epidemiol
; 45(1): 4-15, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32964493
2.
Novel association of TM6SF2 rs58542926 genotype with increased serum tyrosine levels and decreased apoB-100 particles in Finns.
J Lipid Res
; 58(7): 1471-1481, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28539357
3.
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
; 174(4): 381-389, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28332277
4.
Autosomal dominant mannose-binding lectin deficiency is associated with worse neurodevelopmental outcomes after cardiac surgery in infants.
J Thorac Cardiovasc Surg
; 155(3): 1139-1147.e2, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29452463
5.
Concentration of Smaller High-Density Lipoprotein Particle (HDL-P) Is Inversely Correlated With Carotid Intima Media Thickening After Confounder Adjustment: The Multi Ethnic Study of Atherosclerosis (MESA).
J Am Heart Assoc
; 5(5)2016 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207961