Detalhe da pesquisa
1.
Cell-free DNA in maternal blood and artificial intelligence: accurate prenatal detection of fetal congenital heart defects.
Am J Obstet Gynecol
; 228(1): 76.e1-76.e10, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35948071
2.
Alzheimer's Precision Neurology: Epigenetics of Cytochrome P450 Genes in Circulating Cell-Free DNA for Disease Prediction and Mechanism.
Int J Mol Sci
; 24(3)2023 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36769199
3.
Maternal opioid use disorder: Placental transcriptome analysis for neonatal opioid withdrawal syndrome.
Genomics
; 113(6): 3610-3617, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34352367
4.
Placental DNA methylation profiles in opioid-exposed pregnancies and associations with the neonatal opioid withdrawal syndrome.
Genomics
; 113(3): 1127-1135, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33711455
5.
Haplotype analysis of ADAM33 polymorphisms in asthma: A pilot study.
Indian J Med Res
; 150(3): 272-281, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31719298
6.
Deep Learning/Artificial Intelligence and Blood-Based DNA Epigenomic Prediction of Cerebral Palsy.
Int J Mol Sci
; 20(9)2019 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31035542
7.
A candidate gene identification strategy utilizing mouse to human big-data mining: "3R-tenet" in COPD genetic research.
Respir Res
; 19(1): 92, 2018 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29871630
8.
Transcriptomic analysis comparing mouse strains with extreme total lung capacities identifies novel candidate genes for pulmonary function.
Respir Res
; 18(1): 152, 2017 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28793908
9.
Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
Genet Res (Camb)
; 97: e18, 2015 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26390810
10.
IL-10 and IL-17F Promoter Single Nucleotide Polymorphism and Asthma: A Case-Control Study in South India.
Lung
; 193(5): 739-47, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26108303
11.
Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays.
Genet Res (Camb)
; 96: e17, 2014 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-25578402
12.
Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma.
Ann Allergy Asthma Immunol
; 113(4): 418-24.e1, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25155083
13.
Serum levels of IL-10, IL-17F and IL-33 in patients with asthma: a case-control study.
J Asthma
; 51(10): 1004-13, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24960440
14.
Insertion-deletions burden in copy number polymorphisms of the Tibetan population.
Indian J Hum Genet
; 20(2): 166-74, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25400346
15.
Precision oncology: Artificial intelligence, circulating cell-free DNA, and the minimally invasive detection of pancreatic cancer-A pilot study.
Cancer Med
; 12(19): 19644-19655, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37787018
16.
Association between ADAM33 Single-Nucleotide Polymorphisms and Treatment Response to Inhaled Corticosteroids and a Long-Acting Beta-Agonist in Asthma.
Diagnostics (Basel)
; 13(3)2023 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36766510
17.
Placental microRNA methylome signatures may serve as biomarkers and therapeutic targets for prenatally opioid-exposed infants with neonatal opioid withdrawal syndrome.
Front Genet
; 14: 1215472, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37434949
18.
Integrative Analysis Unveils the Correlation of Aminoacyl-tRNA Biosynthesis Metabolites with the Methylation of the SEPSECS Gene in Huntington's Disease Brain Tissue.
Genes (Basel)
; 14(9)2023 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37761892
19.
Placental cytochrome P450 methylomes in infants exposed to prenatal opioids: exploring the effects of neonatal opioid withdrawal syndrome on health horizons.
Front Genet
; 14: 1292148, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38264209
20.
Artificial intelligence and placental DNA methylation: newborn prediction and molecular mechanisms of autism in preterm children.
J Matern Fetal Neonatal Med
; 35(25): 8150-8159, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34404318