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38 matching publication(s)

Publication	Journal	Year	Score	Verdict
COVID-19 lung disease shares driver AT2 cytopathic features with Idiopathic pulmonary fibrosis. PMID 35870428	EBioMedicine	2022	85	L1 85/100
Perturbation of placental protein glycosylation by endoplasmic reticulum stress promotes maladaptation of maternal hepatic glucose metabolism. PMID 36660474	iScience	2022	71	L1 71/100
Disentangling the causal relationship between rabbit growth and cecal microbiota through structural equation models. PMID 36536288	Genet Sel Evol	2022	93	L1 93/100
Integrating transcriptomic datasets across neurological disease identifies unique myeloid subpopulations driving disease-specific signatures. ⚑ PMID 36527260	Glia	2022	26	L1 26/100 ⚑
Extensive androgen receptor enhancer heterogeneity in primary prostate cancers underlies transcriptional diversity and metastatic potential. PMID 36450752	Nat Commun	2022	70	L1 70/100
Spatial transcriptomics demonstrates the role of CD4 T cells in effector CD8 T cell differentiation during chronic viral infection. PMID 36450262	Cell Rep	2022	50	L1 50/100
Specific signature biomarkers highlight the potential mechanisms of circulating neutrophils in aneurysmal subarachnoid hemorrhage. PMID 36438795	Front Pharmacol	2022	80	L1 80/100
Dissecting lncRNA-mRNA competitive regulatory network in human islet tissue exosomes of a type 1 diabetes model reveals exosome miRNA markers. PMID 36440209	Front Endocrinol (Lausanne)	2022	50	L1 50/100
Optimisation of the core subset for the APY approximation of genomic relationships. PMID 36418945	Genet Sel Evol	2022	85	L1 85/100
RNA Editing Alterations Define Disease Manifestations in the Progression of Experimental Autoimmune Encephalomyelitis (EAE). ⚑ PMID 36429012	Cells	2022	37	L1 37/100 ⚑
Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing. PMID 36401180	Genet Sel Evol	2022	50	L1 50/100
CHD7 regulates otic lineage specification and hair cell differentiation in human inner ear organoids. PMID 36396635	Nat Commun	2022	50	L1 50/100
An integrated in silico-in vitro approach for identifying therapeutic targets against osteoarthritis. PMID 36352408	BMC Biol	2022	84	L1 84/100
Stromal androgen signaling acts as tumor niches to drive prostatic basal epithelial progenitor-initiated oncogenesis. ⚑ PMID 36323713	Nat Commun	2022	63	L1 63/100 ⚑
CASK loss of function differentially regulates neuronal maturation and synaptic function in human induced cortical excitatory neurons. PMID 36262316	iScience	2022	62	L1 62/100
Artificial Intelligence Meets Whole Slide Images: Deep Learning Model Shapes an Immune-Hot Tumor and Guides Precision Therapy in Bladder Cancer. PMID 36245985	J Oncol	2022	—	not yet assessed
miR-4478 Accelerates Nucleus Pulposus Cells Apoptosis Induced by Oxidative Stress by Targeting MTH1. PMID 36130054	Spine (Phila Pa 1976)	2022	100	L1 100/100
AI-assisted discovery of an ethnicity-influenced driver of cell transformation in esophageal and gastroesophageal junction adenocarcinomas. PMID 36134663	JCI Insight	2022	84	L1 84/100
CCL8 as a promising prognostic factor in diffuse large B-cell lymphoma via M2 macrophage interactions: A bioinformatic analysis of the tumor microenviron PMID 36072582	Front Immunol	2022	81	L1 81/100
Assessment of genotyping array performance for genome-wide association studies and imputation in African cattle. PMID 36057548	Genet Sel Evol	2022	90	L1 90/100
Systematic analysis of CNGCs in cotton and the positive role of GhCNGC32 and GhCNGC35 in salt tolerance. PMID 35931984	BMC Genomics	2022	—	not yet assessed
Analyzing biomarker discovery: Estimating the reproducibility of biomarker sets. PMID 35901020	PLoS One	2022	83	L1 83/100
Identification of the stress granule transcriptome via RNA-editing in single cells and in vivo. PMID 35784648	Cell Rep Methods	2022	66	L1 66/100
GeMI: interactive interface for transformer-based Genomic Metadata Integration. PMID 35657113	Database (Oxford)	2022	64	L1 64/100
Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets. PMID 35672799	Genome Biol	2022	—	L1 No data access
TFAP2 paralogs facilitate chromatin access for MITF at pigmentation and cell proliferation genes. PMID 35580127	PLoS Genet	2022	95	L2 95/100
Deconvolution of the hematopoietic stem cell microenvironment reveals a high degree of specialization and conservation. PMID 35494238	iScience	2022	60	L1 60/100
Comprehensive enhancer-target gene assignments improve gene set level interpretation of genome-wide regulatory data. PMID 35473573	Genome Biol	2022	—	not yet assessed
Transcriptomic Data Meta-Analysis Sheds Light on High Light Response in Arabidopsis thaliana L. PMID 35457273	Int J Mol Sci	2022	88	L1 88/100
NUSAP1 Could be a Potential Target for Preventing NAFLD Progression to Liver Cancer. ⚑ PMID 35431924	Front Pharmacol	2022	45	L1 45/100 ⚑
Identification of phenotype-specific networks from paired gene expression-cell shape imaging data. PMID 35197309	Genome Res	2022	100	L1 100/100
Integrated Analysis of Multiple Microarrays Based on Raw Data Identified Novel Gene Signatures in Recurrent Implantation Failure. PMID 35197930	Front Endocrinol (Lausanne)	2022	85	L1 85/100
Comparative analysis of molecular signatures reveals a hybrid approach in breast cancer: Combining the Nottingham Prognostic Index with gene expressions into a ⚑ PMID 35143511	PLoS One	2022	48	L1 48/100 ⚑
Effect of PAIP1 on the metastatic potential and prognostic significance in oral squamous cell carcinoma. ⚑ PMID 35153296	Int J Oral Sci	2022	10	L1 10/100 ⚑
Downstream high-speed plasma jet generation as a direct consequence of shock reformation. PMID 35105885	Nat Commun	2022	67	L1 67/100
ddRAD-seq reveals the genetic structure and detects signals of selection in Italian brown trout. PMID 35100964	Genet Sel Evol	2022	87	L1 87/100
A comprehensive framework for analysis of microRNA sequencing data in metastatic colorectal cancer. PMID 35047825	NAR Cancer	2022	100	L1 100/100
Systematic identification of ACE2 expression modulators reveals cardiomyopathy as a risk factor for mortality in COVID-19 patients. PMID 35012625	Genome Biol	2022	68	L1 68/100