Detalhe da pesquisa
1.
Toll-like Receptor Signaling Rewires Macrophage Metabolism and Promotes Histone Acetylation via ATP-Citrate Lyase.
Immunity
; 51(6): 997-1011.e7, 2019 12 17.
Artigo
Inglês
| MEDLINE | ID: mdl-31851905
2.
The genetic regulation of the gastric transcriptome is associated with metabolic and obesity-related traits and diseases.
Physiol Genomics
; 56(5): 384-396, 2024 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38406838
3.
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level.
Gut
; 72(4): 612-623, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35882562
4.
Pathogen-specific innate immune response patterns are distinctly affected by genetic diversity.
Nat Commun
; 14(1): 3239, 2023 06 05.
Artigo
Inglês
| MEDLINE | ID: mdl-37277347
5.
Elucidation of the genetic causes of bicuspid aortic valve disease.
Cardiovasc Res
; 119(3): 857-866, 2023 05 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35727948
6.
Dissecting the genetic heterogeneity of gastric cancer.
EBioMedicine
; 92: 104616, 2023 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-37209533
7.
Allele-specific transcription factor binding in a cellular model of orofacial clefting.
Sci Rep
; 12(1): 1807, 2022 02 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35110662
8.
Genome-wide association study in patients with posterior urethral valves.
Front Pediatr
; 10: 988374, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36238604
9.
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Commun Biol
; 5(1): 1203, 2022 11 09.
Artigo
Inglês
| MEDLINE | ID: mdl-36352089
10.
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.
HGG Adv
; 3(2): 100093, 2022 Apr 14.
Artigo
Inglês
| MEDLINE | ID: mdl-35199045
11.
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.
PLoS One
; 15(6): e0234246, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32502225
12.
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene.
Birth Defects Res
; 110(7): 587-597, 2018 04 17.
Artigo
Inglês
| MEDLINE | ID: mdl-29388391
13.
Evidence for PTGER4, PSCA, and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level.
Cancer Med
; 7(10): 5057-5065, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30191681
14.
Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer".
EBioMedicine
; 94: 104709, 2023 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37480624