Detalhe da pesquisa
1.
Large-scale plasma proteomics comparisons through genetics and disease associations.
Nature;
622(7982): 348-358, 2023 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37794188
2.
The sequences of 150,119 genomes in the UK Biobank.
Nature;
607(7920): 732-740, 2022 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35859178
3.
Actionable Genotypes and Their Association with Life Span in Iceland.
N Engl J Med;
389(19): 1741-1752, 2023 Nov 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37937776
4.
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease.
Nature;
584(7822): 619-623, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32581359
5.
Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations.
Nature;
630(8015): E3, 2024 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38778117
6.
Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis.
Br J Cancer;
129(7): 1142-1151, 2023 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37596405
7.
Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.
Ann Rheum Dis;
82(6): 873-880, 2023 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36931692
8.
Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Nature;
549(7673): 519-522, 2017 09 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28959963
9.
Sequence variants associating with urinary biomarkers.
Hum Mol Genet;
28(7): 1199-1211, 2019 04 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30476138
10.
A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury.
Gastroenterology;
156(6): 1707-1716.e2, 2019 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30664875
11.
Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome.
J Med Genet;
56(7): 462-470, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30877237
12.
Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.
N Engl J Med;
374(22): 2131-41, 2016 Jun 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27192541
13.
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.
Blood;
130(6): 742-752, 2017 08 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28483762
14.
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.
Nature;
497(7450): 517-20, 2013 May 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23644456
15.
Profile of common prostate cancer risk variants in an unscreened Romanian population.
J Cell Mol Med;
22(3): 1574-1582, 2018 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29266682
16.
Identification of Lynch syndrome risk variants in the Romanian population.
J Cell Mol Med;
22(12): 6068-6076, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30324682
17.
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry.
Hum Mol Genet;
25(6): 1203-14, 2016 Mar 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26732427
18.
Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer.
Hum Mol Genet;
25(5): 1008-18, 2016 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26740556
19.
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.
PLoS Genet;
11(9): e1005379, 2015 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26327206
20.
Detection of sharing by descent, long-range phasing and haplotype imputation.
Nat Genet;
40(9): 1068-75, 2008 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19165921