Detalhe da pesquisa
1.
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project.
J Med Genet
; 60(3): 247-253, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35595280
2.
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project.
Hum Genet
; 142(12): 1737-1745, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37938362
3.
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.
Hum Mutat
; 42(4): 434-444, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33502061
4.
Clinical Predictors of Multiple Organ Dysfunction Syndromes in Pediatric patients with Scrub Typhus.
J Trop Pediatr
; 63(3): 167-173, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27697827
5.
Increased GABA signaling in liver macrophage promotes HBV replication in HBV-carrier mice.
Virus Res
; 344: 199366, 2024 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38548137
6.
Cyanidin-3-O-glucoside alleviates ethanol-induced liver injury by promoting mitophagy in a Gao-binge mouse model of alcohol-associated liver disease.
Biochim Biophys Acta Mol Basis Dis
; 1870(6): 167259, 2024 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38796918
7.
Correlation of DNA load, genotyping, and clinical phenotype of Mycoplasma pneumoniae infection in children.
Front Pediatr
; 12: 1369431, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38655275
8.
Delivery room resuscitation intensity and associated neonatal outcomes of 24+0-31+6 weeks' preterm infants in China: a retrospective cross-sectional study.
World J Pediatr
; 20(1): 64-72, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37389785
9.
Neurosonography: Shaping the future of neuroprotection strategies in extremely preterm infants.
Heliyon
; 10(11): e31742, 2024 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38845994
10.
Brain development in newborns and infants after ECMO.
World J Pediatr
; 2024 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38238638
11.
Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder.
Gene
; 887: 147723, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37598788
12.
Incidence of Neonatal Seizures in China Based on Electroencephalogram Monitoring in Neonatal Neurocritical Care Units.
JAMA Netw Open
; 6(7): e2326301, 2023 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37505497
13.
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project.
Kidney Int Rep
; 8(11): 2376-2384, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-38025242
14.
Integration of Urine Proteomic and Metabolomic Profiling Reveals Novel Insights Into Neuroinflammation in Autism Spectrum Disorder.
Front Psychiatry
; 13: 780747, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35615451
15.
A frameshift mutation of TMPRSS3 in a Chinese family with non-syndromic hearing loss.
Front Pediatr
; 10: 1032659, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36568422
16.
Machine learning approach identifies meconium metabolites as potential biomarkers of neonatal hyperbilirubinemia.
Comput Struct Biotechnol J
; 20: 1778-1784, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35495115
17.
Identifying Rare Genetic Variants of Immune Mediators as Risk Factors for Autism Spectrum Disorder.
Genes (Basel)
; 13(6)2022 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35741860
18.
Estimation of hereditary fructose intolerance prevalence in the Chinese population.
Orphanet J Rare Dis
; 17(1): 326, 2022 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36028839
19.
Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of CTTNBP2 in a Quad Family Affected by Autism Spectrum Disorder.
Children (Basel)
; 10(1)2022 Dec 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36670631
20.
Inductively coupled plasma mass spectrometry based urine metallome to construct clinical decision models for autism spectrum disorder.
Metallomics
; 14(12)2022 12 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36442146