Detalhe da pesquisa
1.
Leveraging cross-species transcription factor binding site patterns: from diabetes risk loci to disease mechanisms.
Cell
; 156(1-2): 343-58, 2014 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-24439387
2.
Plasma proteomic associations with genetics and health in the UK Biobank.
Nature
; 622(7982): 329-338, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794186
3.
wnt16 regulates spine and muscle morphogenesis through parallel signals from notochord and dermomyotome.
PLoS Genet
; 18(11): e1010496, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36346812
4.
Microbiome signatures associated with clinical stages of gastric Cancer: whole metagenome shotgun sequencing study.
BMC Microbiol
; 24(1): 139, 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658841
5.
Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder.
Mol Psychiatry
; 2023 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37433967
6.
Blood transcriptomic signature in type-2 biomarker-low severe asthma and asthma control.
J Allergy Clin Immunol
; 152(4): 876-886, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37315813
7.
Molecular and Genetics-Based Systems for Tracing the Evolution and Exploring the Mechanisms of Human Norovirus Infections.
Int J Mol Sci
; 24(10)2023 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37240438
8.
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach.
Br J Psychiatry
; : 1-10, 2022 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35225756
9.
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder.
Mol Psychiatry
; 26(6): 2457-2470, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32203155
10.
Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.
Mol Psychiatry
; 25(7): 1420-1429, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30626913
11.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature
; 526(7571): 112-7, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26367794
12.
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis.
Am J Hum Genet
; 101(2): 227-238, 2017 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28757204
13.
IConMHC: a deep learning convolutional neural network model to predict peptide and MHC-I binding affinity.
Immunogenetics
; 72(5): 295-304, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32577798
14.
Meta-analysis of epigenome-wide association studies of cognitive abilities.
Mol Psychiatry
; 23(11): 2133-2144, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29311653
15.
The association of obesity and coronary artery disease genes with response to SSRIs treatment in major depression.
J Neural Transm (Vienna)
; 126(1): 35-45, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30610379
16.
Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study.
Hum Mol Genet
; 25(23): 5234-5243, 2016 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27616567
17.
FTO Obesity Variant Circuitry and Adipocyte Browning in Humans.
N Engl J Med
; 373(10): 895-907, 2015 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26287746
18.
Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
Ann Rheum Dis
; 77(3): 378-385, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29170203
19.
Bivariate Genome-Wide Association Study of Depressive Symptoms With Type 2 Diabetes and Quantitative Glycemic Traits.
Psychosom Med
; 80(3): 242-251, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29280852
20.
Associations of methylenetetrahydrofolate reductase C677T genotype with blood pressure levels in Chinese population with essential hypertension.
Clin Exp Hypertens
; 40(3): 207-212, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29436860