Detalhe da pesquisa
1.
AI reveals insights into link between CD33 and cognitive impairment in Alzheimer's Disease.
PLoS Comput Biol
; 19(2): e1009894, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36780558
2.
GenRisk: a tool for comprehensive genetic risk modeling.
Bioinformatics
; 38(9): 2651-2653, 2022 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35266528
3.
SEEDS: data driven inference of structural model errors and unknown inputs for dynamic systems biology.
Bioinformatics
; 37(9): 1330-1331, 2021 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32931565
4.
Towards realizing the vision of precision medicine: AI based prediction of clinical drug response.
Brain
; 144(6): 1738-1750, 2021 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33734308
5.
Unraveling the heterogeneity in Alzheimer's disease progression across multiple cohorts and the implications for data-driven disease modeling.
Alzheimers Dement
; 18(2): 251-261, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34109729
6.
PathME: pathway based multi-modal sparse autoencoders for clustering of patient-level multi-omics data.
BMC Bioinformatics
; 21(1): 146, 2020 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32299344
7.
The EMT transcription factor Zeb2 controls adult murine hematopoietic differentiation by regulating cytokine signaling.
Blood
; 129(4): 460-472, 2017 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27683414
8.
From hype to reality: data science enabling personalized medicine.
BMC Med
; 16(1): 150, 2018 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30145981
9.
Towards clinically more relevant dissection of patient heterogeneity via survival-based Bayesian clustering.
Bioinformatics
; 33(22): 3558-3566, 2017 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28961917
10.
Linking metabolic network features to phenotypes using sparse group lasso.
Bioinformatics
; 33(21): 3445-3453, 2017 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29077809
11.
Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti.
Hum Genomics
; 11(1): 26, 2017 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29122006
12.
Inferring modulators of genetic interactions with epistatic nested effects models.
PLoS Comput Biol
; 13(4): e1005496, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28406896
13.
Ten quick tips for biomarker discovery and validation analyses using machine learning.
PLoS Comput Biol
; 18(8): e1010357, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35951526
14.
Key Players of Cisplatin Resistance: Towards a Systems Pharmacology Approach.
Int J Mol Sci
; 19(3)2018 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29518977
15.
Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson's disease revealed different epigenetic patterns in peripheral blood mononuclear cells.
Neurogenetics
; 18(1): 7-22, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27709425
16.
Changes in serum miRNAs following generalized convulsive seizures in human mesial temporal lobe epilepsy.
Biochem Biophys Res Commun
; 481(1-2): 13-18, 2016 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27833019
17.
biRte: Bayesian inference of context-specific regulator activities and transcriptional networks.
Bioinformatics
; 31(20): 3290-8, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26112290
18.
NEMix: single-cell nested effects models for probabilistic pathway stimulation.
PLoS Comput Biol
; 11(4): e1004078, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25879530
19.
Crowdsourced estimation of cognitive decline and resilience in Alzheimer's disease.
Alzheimers Dement
; 12(6): 645-53, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27079753
20.
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.
Int J Cancer
; 136(6): E578-89, 2015 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25219767