Detalhe da pesquisa
1.
Fast and accurate recurrent event analysis for genome-wide association studies.
Genet Epidemiol
; 47(5): 365-378, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37060326
2.
Genomics Research of Lifetime Depression in the Netherlands: The BIObanks Netherlands Internet Collaboration (BIONIC) Project.
Twin Res Hum Genet
; : 1-11, 2024 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38497097
3.
Genome-wide association study identifies 74 loci associated with educational attainment.
Nature
; 533(7604): 539-42, 2016 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27225129
4.
Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6-Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia.
Int J Mol Sci
; 23(3)2022 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35163840
5.
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Mol Psychiatry
; 25(9): 2047-2057, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30116028
6.
Sex-Specific Regulation of Inflammation and Metabolic Syndrome in Obesity.
Arterioscler Thromb Vasc Biol
; 40(7): 1787-1800, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32460579
7.
Integrating Metabolomics, Genomics, and Disease Pathways in Age-Related Macular Degeneration: The EYE-RISK Consortium.
Ophthalmology
; 127(12): 1693-1709, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32553749
8.
Measurement and genetic architecture of lifetime depression in the Netherlands as assessed by LIDAS (Lifetime Depression Assessment Self-report).
Psychol Med
; : 1-10, 2020 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32102724
9.
Standardized serum hepcidin values in Dutch children: Set point relative to body iron changes during childhood.
Pediatr Blood Cancer
; 67(3): e28038, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31724793
10.
Cigarette Smoking and the Risk of Cutaneous Melanoma: A Case-Control Study.
Dermatology
; 236(3): 228-236, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31505496
11.
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
12.
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
13.
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
PLoS Genet
; 10(2): e1004123, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24586183
14.
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.
Hum Mol Genet
; 23(20): 5545-57, 2014 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24861552
15.
Known susceptibility SNPs for sporadic prostate cancer show a similar association with "hereditary" prostate cancer.
Prostate
; 75(5): 474-83, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25560306
16.
Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?
BMC Genet
; 16: 79, 2015 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26159428
17.
Serum hepcidin is associated with presence of plaque in postmenopausal women of a general population.
Arterioscler Thromb Vasc Biol
; 34(2): 446-56, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24334869
18.
Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study.
J Med Genet
; 50(9): 593-8, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23794717
19.
Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomization analysis.
Int J Epidemiol
; 53(1)2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38124529
20.
Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis.
EBioMedicine
; 100: 104991, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38301482