Detalhe da pesquisa
1.
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature
; 586(7831): 763-768, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057201
2.
DLRAPom: a hybrid pipeline of Optimized XGBoost-guided integrative multiomics analysis for identifying targetable disease-related lncRNA-miRNA-mRNA regulatory axes.
Brief Bioinform
; 23(2)2022 03 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35224615
3.
Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses.
Mol Psychiatry
; 28(7): 2913-2921, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37340172
4.
The interactions between host genome and gut microbiome increase the risk of psychiatric disorders: Mendelian randomization and biological annotation.
Brain Behav Immun
; 113: 389-400, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37557965
5.
Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction.
Mol Psychiatry
; 27(1): 113-126, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34193973
6.
Survival Association of Angiotensin Inhibitors in Heart Failure With Reduced Ejection Fraction: Comparisons Using Self-Identified Race and Genomic Ancestry.
J Card Fail
; 28(2): 215-225, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34425222
7.
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature
; 591(7851): E27, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33707633
8.
Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans.
Am J Respir Crit Care Med
; 203(4): 424-436, 2021 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32966749
9.
Genetics of heart rate in heart failure patients (GenHRate).
Hum Genomics
; 13(1): 22, 2019 05 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31113495
10.
Integrative approach identifies corticosteroid response variant in diverse populations with asthma.
J Allergy Clin Immunol
; 143(5): 1791-1802, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30367910
11.
Corrigendum to "The interactions between host genome and gut microbiome increase the risk of psychiatric disorders: Mendelian randomization and biological annotation" [Brain, behav. Immun., 113 october (2023) 389-400].
Brain Behav Immun
; 116: 422, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38065811
12.
Correction: Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses.
Mol Psychiatry
; 2023 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38086974
13.
Association of Regulatory Genetic Variants for Protein Kinase Cα with Mortality and Drug Efficacy in Patients with Heart Failure.
Cardiovasc Drugs Ther
; 33(6): 693-700, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31728800
14.
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Hum Mol Genet
; 25(23): 5265-5275, 2016 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27702942
15.
Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function.
Gastroenterology
; 153(1): 139-153.e8, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28342760
16.
Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population.
Am J Med Genet B Neuropsychiatr Genet
; 177(1): 86-92, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29150900
17.
Identification of GLI Mutations in Patients With Hirschsprung Disease That Disrupt Enteric Nervous System Development in Mice.
Gastroenterology
; 149(7): 1837-1848.e5, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26261006
18.
Targeted next-generation sequencing on Hirschsprung disease: a pilot study exploits DNA pooling.
Ann Hum Genet
; 78(5): 381-7, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24947032
19.
GATES: a rapid and powerful gene-based association test using extended Simes procedure.
Am J Hum Genet
; 88(3): 283-93, 2011 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21397060
20.
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases.
Nucleic Acids Res
; 40(7): e53, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22241780