Detalhe da pesquisa
1.
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development.
PLoS Genet
; 17(8): e1009698, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34358225
2.
An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population.
Hum Mol Genet
; 30(9): 836-842, 2021 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33693786
3.
The functional role of sequentially neuromodulated synaptic plasticity in behavioural learning.
PLoS Comput Biol
; 17(6): e1009017, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34111110
4.
Mendelian Randomization Focused Analysis of Vitamin D on the Secondary Prevention of Ischemic Stroke.
Stroke
; 52(12): 3926-3937, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34565175
5.
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca.
Hum Mol Genet
; 27(2): 351-358, 2018 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29177441
6.
High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus.
Cardiovasc Diabetol
; 18(1): 171, 2019 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31847896
7.
Age-Biomarkers-Clinical Risk Factors for Prediction of Cardiovascular Events in Patients With Coronary Artery Disease.
Arterioscler Thromb Vasc Biol
; 38(10): 2519-2527, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30354221
8.
Seventy-five genetic loci influencing the human red blood cell.
Nature
; 492(7429): 369-75, 2012 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23222517
9.
Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals.
Diabetologia
; 60(1): 107-115, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27744525
10.
Genome-wide copy number variation study in anorectal malformations.
Hum Mol Genet
; 22(3): 621-31, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23108157
11.
Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism.
BMC Med Genet
; 16: 49, 2015 Jul 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26179878
12.
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.
J Allergy Clin Immunol
; 133(6): 1564-71, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24388013
13.
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
Hum Mol Genet
; 21(5): 1184-9, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22116939
14.
A gene-based test of association using canonical correlation analysis.
Bioinformatics
; 28(6): 845-50, 2012 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22296789
15.
GENOVA: gene overlap analysis of GWAS results.
Stat Appl Genet Mol Biol
; 11(3): Article 6, 2012 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22499700
16.
Differential vulnerability of hippocampal CA3-CA1 synapses to Aß.
Acta Neuropathol Commun
; 10(1): 45, 2022 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35379353
17.
Mendelian randomization analysis of vitamin D in the secondary prevention of hypertensive-diabetic subjects: role of facilitating blood pressure control.
Genes Nutr
; 17(1): 1, 2022 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35093020
18.
Impaired spatial learning and suppression of sharp wave ripples by cholinergic activation at the goal location.
Elife
; 102021 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33821790
19.
Cancer gene mutations in congenital pulmonary airway malformation patients.
ERJ Open Res
; 5(1)2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30740464
20.
Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects With Type 2 Diabetes.
Diabetes
; 68(1): 198-206, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30305369