Hereditas

Papers
(The TQCC of Hereditas is 5. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
Bioinformatic analysis identifies potential biomarkers and therapeutic targets of septic-shock-associated acute kidney injury31
The role of ceRNA-mediated diagnosis and therapy in hepatocellular carcinoma30
Mediators of SARS-CoV-2 entry are preferentially enriched in cardiomyocytes26
Population genomics of East Asian ethnic groups25
SLC3A2 inhibits ferroptosis in laryngeal carcinoma via mTOR pathway20
Performance comparison of four types of target enrichment baits for exome DNA sequencing20
Identification of a chromatin regulator signature and potential candidate drugs for bladder cancer19
Prognostic biomarkers and therapeutic targets in oral squamous cell carcinoma: a study based on cross-database analysis17
Identification of potential biomarkers for pathogenesis of Alzheimer’s disease15
Identification and validation of hub genes of synovial tissue for patients with osteoarthritis and rheumatoid arthritis14
Genomics in animal breeding from the perspectives of matrices and molecules13
Inhibition of USP14 suppresses ferroptosis and inflammation in LPS-induced goat mammary epithelial cells through ubiquitylating the IL-6 protein13
Identification of differentially expressed genes, signaling pathways and immune infiltration in rheumatoid arthritis by integrated bioinformatics analysis11
TGF-β1/SMOC2/AKT and ERK axis regulates proliferation, migration, and fibroblast to myofibroblast transformation in lung fibroblast, contributing with the asthma progression11
IFI27 may predict and evaluate the severity of respiratory syncytial virus infection in preterm infants11
RTP4 is a novel prognosis-related hub gene in cutaneous melanoma10
Monocytic THP-1 cells diverge significantly from their primary counterparts: a comparative examination of the chromosomal conformations and transcriptomes10
Susceptibility genes of hyperuricemia and gout10
Defining muscle-invasive bladder cancer immunotypes by introducing tumor mutation burden, CD8+ T cells, and molecular subtypes9
Identification of glioblastoma immune subtypes and immune landscape based on a large cohort9
Arecoline promotes proliferation and migration of human HepG2 cells through activation of the PI3K/AKT/mTOR pathway9
Identification and characterization of miRNAs associated with sterile flower buds in the tea plant based on small RNA sequencing9
RNA-Seq based transcriptome analysis in oral lichen planus9
Up-regulated RFC2 predicts unfavorable progression in hepatocellular carcinoma9
Dynamic co-expression modular network analysis in nonalcoholic fatty liver disease9
Bioinformatics analysis of differentially expressed genes and identification of an miRNA–mRNA network associated with entorhinal cortex and hippocampus in Alzheimer’s disease8
Exploring the mRNA expression level of RELN in peripheral blood of schizophrenia patients before and after antipsychotic treatment8
The homeodomain transcription factor Orthopedia is involved in development of the Drosophila hindgut8
ARG1 as a promising biomarker for sepsis diagnosis and prognosis: evidence from WGCNA and PPI network8
Screening of ulcerative colitis biomarkers and potential pathways based on weighted gene co-expression network, machine learning and ceRNA hypothesis8
miR-31-5p from placental and peripheral blood exosomes is a potential biomarker to diagnose preeclampsia8
Identification of biomarkers, immune infiltration landscape, and treatment targets of ischemia–reperfusion acute kidney injury at an early stage by bioinformatics methods8
SKA3 is a prognostic biomarker and associated with immune infiltration in bladder cancer7
Protein content and HvNAM alleles in Nordic barley (Hordeum vulgare) during a century of breeding7
Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathway7
Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese population6
SNP-based breeding for broiler resistance to ascites and evaluation of correlated production traits6
Identification of a novel four-gene diagnostic signature for patients with sepsis by integrating weighted gene co-expression network analysis and support vector machine algorithm6
SMPD1 expression profile and mutation landscape help decipher genotype–phenotype association and precision diagnosis for acid sphingomyelinase deficiency6
Discovering the key genes and important DNA methylation regions in breast cancer5
Identification of crucial genes involved in pathogenesis of regional weakening of the aortic wall5
Mechanisms of Cynarine for treatment of non-alcoholic fatty liver disease based on the integration of network pharmacology, molecular docking and cell experiment5
Two novel likely pathogenic variants of HARS2 identified in a Chinese family with sensorineural hearing loss5
Mutation update of SERPING1 related to hereditary angioedema in the Chinese population5
EZH2 regulates pancreatic cancer cells through E2F1, GLI1, CDK3, and Mcm45
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