Detalhe da pesquisa
1.
High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases.
Lab Invest
; 104(4): 100325, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38220043
2.
Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes.
J Hum Genet
; 66(6): 613-623, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33446885
3.
Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes.
Sci Rep
; 14(1): 13453, 2024 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38862513
4.
Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.
Genome Med
; 14(1): 132, 2022 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36419110
5.
Dissecting the contribution of single nucleotide polymorphisms in CCR9 and CCL25 genomic regions to the celiac disease phenotype.
J Transl Autoimmun
; 4: 100128, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34901814
6.
Phenome-wide association studies across large population cohorts support drug target validation.
Nat Commun
; 9(1): 4285, 2018 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30327483
7.
Accuracy of Programs for the Determination of Human Leukocyte Antigen Alleles from Next-Generation Sequencing Data.
Front Immunol
; 8: 1815, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29326702