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23 matching publication(s)

Publication	Journal	Year	Score	Verdict
A comparison across non-model animals suggests an optimal sequencing depth for de novo transcriptome assembly. PMID 23496952	BMC Genomics	2013	69	L1 69/100
The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases. PMID 28930663	Immunity	2017	67	L1 67/100
Endogenous retroviral elements LTR8B and MER65 rewire PSG9 regulation to control trophoblast syncytialization and pre-eclampsia risk. PMID 41796334	Genome Biol	2026	68	L1 68/100
Distinct senotypes in p16- and p21-positive cells across human and mouse aging tissues. PMID 41162753	EMBO J	2025	50	L1 50/100
A blood-based DNA damage signature in patients with Parkinson's disease is associated with disease progression. PMID 40913219	Nat Aging	2025	69	L1 69/100
MACanalyzeR scRNAseq analysis tool reveals PPARγHIGH/GDF15HIGH lipid-associated macrophages facilitate thermogenic ⚑ PMID 40450001	Nat Commun	2025	70	L1 70/100 ⚑
Chemical genomics informs antibiotic and essential gene function in Acinetobacter baumannii. PMID 40153700	PLoS Genet	2025	71	L1 71/100
Metabolic features that select for Bathyarchaeia in modern ferruginous lacustrine subsurface sediments. PMID 39660009	ISME Commun	2024	50	L1 50/100
Rfam 15: RNA families database in 2025. PMID 39526405	Nucleic Acids Res	2025	68	L1 68/100
Community assessment of methods to deconvolve cellular composition from bulk gene expression. PMID 39191725	Nat Commun	2024	63	L1 63/100
An atlas of the human liver diurnal transcriptome and its perturbation by hepatitis C virus infection. PMID 39209804	Nat Commun	2024	50	L1 50/100
Integrated drug resistance and leukemic stemness gene-expression scores predict outcomes in large cohort of over 3500 AML patients from 10 trials. PMID 39090192	NPJ Precis Oncol	2024	50	L1 50/100
The rates of adult neurogenesis and oligodendrogenesis are linked to cell cycle regulation through p27-dependent gene repression of SOX2. PMID 36627412	Cell Mol Life Sci	2023	59	L1 59/100
An individualized causal framework for learning intercellular communication networks that define microenvironments of individual tumors. PMID 36548438	PLoS Comput Biol	2022	67	L1 67/100
N6-methyladenosine (m6A) reader Pho92 is recruited co-transcriptionally and couples translation to mRNA decay to promote meiotic fitness in y ⚑ PMID 36422864	Elife	2022	55	L1 55/100 ⚑
The third international hackathon for applying insights into large-scale genomic composition to use cases in a wide range of organisms. PMID 36262335	F1000Res	2022	59	L1 59/100
Apoptotic brown adipocytes enhance energy expenditure via extracellular inosine PMID 35790189	—	2022	57	L1 57/100
Downstream high-speed plasma jet generation as a direct consequence of shock reformation. PMID 35105885	Nat Commun	2022	67	L1 67/100
Gene Set Enrichment Analysis Reveals Individual Variability in Host Responses in Tuberculosis Patients. PMID 34421903	Front Immunol	2021	71	71/100
Sustainable data analysis with Snakemake. PMID 34035898	F1000Res	2021	71	L1 71/100
A crowdsourced set of curated structural variants for the human genome. PMID 32559231	PLoS Comput Biol	2020	71	L1 71/100
miEAA 2.0: integrating multi-species microRNA enrichment analysis and workflow management systems. PMID 32374865	Nucleic Acids Res	2020	61	L1 61/100
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100