Author details

Full Name

Tieliu Shi

Affiliation

ORCID

Career Start Year

2001

Papers

174

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37427124	Mapping knowledge landscapes and emerging trends of the biomarkers in melanoma: a bibliometric analysis from 2004 to 2022.		2023
37649370	HiFun: homology independent protein function prediction by a novel protein-language self-attention model.	Brief Bioinform	2023
37089192	Was Wuhan the early epicenter of the COVID-19 pandemic?-A critique.		2023
36907956	SMPD1 expression profile and mutation landscape help decipher genotype-phenotype association and precision diagnosis for acid sphingomyelinase deficiency.	Hereditas	2023
36873188	The role of CYP1A1/2 in cholesterol ester accumulation provides a new perspective for the treatment of hypercholesterolemia.	Acta Pharm Sin B	2023
36858955	Gene expression variability across cells and species shapes the relationship between renal resident macrophages and infiltrated macrophages.		2023
34637759	Annotating unknown species of urban microorganisms on a global scale unveils novel functional diversity and local environment association.	Environ Res	2022
36299999	A history of the MetaSUB consortium: Tracking urban microbes around the globe.	iScience	2022
36271146	IL-17D-induced inhibition of DDX5 expression in keratinocytes amplifies IL-36R-mediated skin inflammation.	Nature Immunology	2022
36132143	Transcriptome sequencing of hepatocellular carcinoma uncovers multiple types of dysregulated ncRNAs.	Frontiers in Oncology	2022
35479398	ToPP: Tumor online prognostic analysis platform for prognostic feature selection and clinical patient subgroup selection.	iScience	2022
35479329	Editorial: Emerging Technologies Powering Rare and Neglected Disease Diagnosis and Theraphy Development.	Front Pharmacol	2022
36468018	Prognostic value of <i>PNN</i> in prostate cancer and its correlation with therapeutic significance.	Front Genet	2022
36467581	MagMD: Database summarizing the metabolic action of gut microbiota to drugs.	Computational and Structural Biotechnology Journal	2022
33811136	Whole genome and exome sequencing identify mutations as a new cause of progressive cavitating leukoencephalopathy.	Journal of Medical Genetics	2022
34159505	Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia.	Science China Life Sciences	2022
34980216	Assessing reproducibility of inherited variants detected with short-read whole genome sequencing.	Genome Biol	2022
35264626	Computational identification of new potential transcriptional partners of ERRÎ± in breast cancer cells: specific partners for specific targets.	Scientific Reports	2022
34367235	A Novel Germline Compound Heterozygous Mutation of Gene Associated With Familial Peripheral Neuroblastic Tumors in Two Siblings.	Frontiers in Genetics	2021
33482149	Biochemical features and mutations of key proteins in SARS-CoV-2 and their impacts on RNA therapeutics.	Biochem Pharmacol	2021
33846644	Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology.	Nat Biotechnol	2021
33892143	Towards population-specific pharmacogenomics in the era of next-generation sequencing.	Drug Discov Today	2021
34258712	Proteomics provides individualized options of precision medicine for patients with gastric cancer.	Science China Life Sciences	2021
33655229	COVID-19 drug practices risk antimicrobial resistance evolution.	Lancet Microbe	2021
33863366	A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency.	Genome Biol	2021
33863344	Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.	Genome Biol	2021
32654205	Perturbation of Specific Signaling Pathways Is Involved in Initiation of Mouse Liver Fibrosis.	Hepatology	2021
32572807	Single-cell transcriptomic analysis reveals dynamic alternative splicing and gene regulatory networks among pancreatic islets.	Science China Life Sciences	2021
33219693	AtMAD: Arabidopsis thaliana multi-omics association database.	Nucleic Acids Research	2021
34868213	A Novel Risk-Score Model With Eight MiRNA Signatures for Overall Survival of Patients With Lung Adenocarcinoma.	Frontiers in Genetics	2021
34407882	X-CNV: genome-wide prediction of the pathogenicity of copy number variations.	Genome Med	2021
33000697	Comprehensive Characterization of Circular RNAs in Neuroblastoma Cell Lines.	Technology in Cancer Research and Treatment	2020
31598709	DNMIVD: DNA methylation interactive visualization database.	Nucleic Acids Research	2020
32372448	UHRF2 promotes intestinal tumorigenesis through stabilization of TCF4 mediated Wnt/Î²-catenin signaling.	Int J Cancer	2020
32128068	Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.	Computational and Structural Biotechnology Journal	2020
32064261	Co-occurrence and Mutual Exclusivity Analysis of DNA Methylation Reveals Distinct Subtypes in Multiple Cancers.	Frontiers in Cell and Developmental Biology	2020
32349771	Genotype-phenotype correlations of Berardinelli-Seip congenital lipodystrophy and novel candidate genes prediction.	Orphanet Journal of Rare Diseases	2020
32337245	Discovery of Urinary Proteomic Signature for Differential Diagnosis of Acute Appendicitis.	Biomed Res Int	2020
33101045	Editorial: Advancing Genomics for Rare Disease Diagnosis and Therapy Development.	Front Pharmacol	2020
32749457	A comprehensive rat transcriptome built from large scale RNA-seq-based annotation.	Nucleic Acids Res	2020
31338106	Five-Feature Model for Developing the Classifier for Synergistic vs. Antagonistic Drug Combinations Built by XGBoost.	Front Genet	2019
31591431	Static magnetic field regulates Arabidopsis root growth via auxin signaling.	Scientific Reports	2019
31680973	Genotype-Phenotype Association Analysis Reveals New Pathogenic Factors for Osteogenesis Imperfecta Disease.	Frontiers in Pharmacology	2019
32116662	Corrigendum: Genotype-Phenotype Association Analysis Reveals New Pathogenic Factors for Osteogenesis Imperfecta Disease.	Frontiers in Pharmacology	2019
31572191	Systematically Analyzing the Pathogenic Variations for Acute Intermittent Porphyria.	Frontiers in Pharmacology	2019
31824949	Comprehensive Identification and Characterization of Human Secretome Based on Integrative Proteomic and Transcriptomic Data.	Frontiers in Cell and Developmental Biology	2019
31807992	Innovation for better health of children.	Science China Life Sciences	2019
31751824	Phosphoproteomics Enables Molecular Subtyping and Nomination of Kinase Candidates for Individual Patients of Diffuse-Type Gastric Cancer.	iScience	2019
30604760	A region-resolved mucosa proteome of the human stomach.	Nature Communications	2019
30696380	Integrative analysis identifies potential DNA methylation biomarkers for pan-cancer diagnosis and prognosis.	Epigenetics	2019