Detalhe da pesquisa
1.
Exploring miRNA-target gene pair detection in disease with coRmiT.
Brief Bioinform
; 25(2)2024 Jan 22.
Artigo
Inglês
| MEDLINE | ID: mdl-38436559
2.
Deepening the knowledge of rare diseases dependent on angiogenesis through semantic similarity clustering and network analysis.
Brief Bioinform
; 23(4)2022 07 18.
Artigo
Inglês
| MEDLINE | ID: mdl-35731990
3.
Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2.
J Med Genet
; 60(4): 406-415, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36243518
4.
Integrating differential expression, co-expression and gene network analysis for the identification of common genes associated with tumor angiogenesis deregulation.
J Biomed Inform
; 144: 104421, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37315831
5.
Phenotype-genotype comorbidity analysis of patients with rare disorders provides insight into their pathological and molecular bases.
PLoS Genet
; 16(10): e1009054, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-33001999
6.
Assigning protein function from domain-function associations using DomFun.
BMC Bioinformatics
; 23(1): 43, 2022 Jan 15.
Artigo
Inglês
| MEDLINE | ID: mdl-35033002
7.
Protein residues determining interaction specificity in paralogous families.
Bioinformatics
; 37(8): 1076-1082, 2021 05 23.
Artigo
Inglês
| MEDLINE | ID: mdl-33135068
8.
Systematic identification of genetic systems associated with phenotypes in patients with rare genomic copy number variations.
Hum Genet
; 140(3): 457-475, 2021 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-32778951
9.
Regulatory variants: from detection to predicting impact.
Brief Bioinform
; 20(5): 1639-1654, 2019 09 27.
Artigo
Inglês
| MEDLINE | ID: mdl-29893792
10.
How can functional annotations be derived from profiles of phenotypic annotations?
BMC Bioinformatics
; 18(1): 96, 2017 Feb 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28183267
11.
Systematic identification of phenotypically enriched loci using a patient network of genomic disorders.
BMC Genomics
; 17: 232, 2016 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26980139
12.
Insights into polypharmacology from drug-domain associations.
Bioinformatics
; 29(16): 1934-7, 2013 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23740740
13.
CoMentG: comprehensive retrieval of generic relationships between biomedical concepts from the scientific literature.
Database (Oxford)
; 20242024 Apr 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38564426
14.
Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease.
Biomolecules
; 14(2)2024 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-38397401
15.
Transcriptomic analysis identifies dysregulated pathways and therapeutic targets in PMM2-CDG.
Biochim Biophys Acta Mol Basis Dis
; 1870(5): 167163, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38599261
16.
Bone metabolism and inflammatory biomarkers in radiographic and non-radiographic axial spondyloarthritis patients: a comprehensive evaluation.
Front Endocrinol (Lausanne)
; 15: 1227196, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38449853
17.
Evolutionary expansion of the Ras switch regulatory module in eukaryotes.
Nucleic Acids Res
; 39(13): 5526-37, 2011 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-21447561
18.
Genetic signature detected in T cell receptors from patients with severe COVID-19.
iScience
; 26(10): 107735, 2023 Oct 20.
Artigo
Inglês
| MEDLINE | ID: mdl-37720084
19.
Erratum to: How can functional annotations be derived from profiles of phenotypic annotations?
BMC Bioinformatics
; 18(1): 194, 2017 03 27.
Artigo
Inglês
| MEDLINE | ID: mdl-28347274
20.
CoMent: Relationships Between Biomedical Concepts Inferred From the Scientific Literature.
J Mol Biol
; 434(11): 167568, 2022 06 15.
Artigo
Inglês
| MEDLINE | ID: mdl-35662459