Hereditas

Papers
(The median citation count of Hereditas is 2. 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
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
RTP4 is a novel prognosis-related hub gene in cutaneous melanoma10
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
Defining muscle-invasive bladder cancer immunotypes by introducing tumor mutation burden, CD8+ T cells, and molecular subtypes9
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
Nucleo-cytoplasmic shuttling of murine RBPJ by Hairless protein matches that of Su(H) protein in the model system Drosophila melanogaster4
A cuproptosis-related lncRNA signature for predicting prognosis and immunotherapy response of lung adenocarcinoma4
Stable populations and Hardy-Weinberg equilibrium4
Identification of four novel hub genes as monitoring biomarkers for colorectal cancer4
Regulatory modules mediating the complex neural expression patterns of the homeobrain gene during Drosophila brain development4
Identification of tubulointerstitial genes and ceRNA networks involved in diabetic nephropathy via integrated bioinformatics approaches4
CCR5 as a prognostic biomarker correlated with immune infiltrates in head and neck squamous cell carcinoma by bioinformatic study4
Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database4
HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity4
Identification of metabolism genes related to hepatocarcinogenesis and progression in type 2 diabetes mellitus via co-expression networks analysis4
Immunological analysis and differential genes screening of venous thromboembolism4
N6-methyladenosine-related lncRNAs is a potential marker for predicting prognosis and immunotherapy in ovarian cancer4
Enhancer analysis of the Drosophila zinc finger transcription factor Earmuff by gene targeting4
A novel mutation of CTC1 leads to telomere shortening in a chinese family with interstitial lung disease3
Leopard syndrome: the potential cardiac defect underlying skin phenotypes3
Network analysis of potential risk genes for psoriasis3
Identification of a five-miRNA signature as a novel potential prognostic biomarker in patients with nasopharyngeal carcinoma3
NPM3 as a novel oncogenic factor and poor prognostic marker contributes to cell proliferation and migration in lung adenocarcinoma3
A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome3
Development and validation of an RBP gene signature for prognosis prediction in colorectal cancer based on WGCNA3
Identification of the prognostic value of Th1/Th2 ratio and a novel prognostic signature in basal-like breast cancer3
A guide to barley mutants3
Favorable function of Ectonucleoside triphosphate diphosphohydrolase 1 high expression in thyroid carcinoma3
LncRNA WAC-AS1 expression in human tumors correlates with immune infiltration and affects prognosis3
Complex vascular anomalies and tissue overgrowth of limbs associated with increased skin temperature and peripheral venous dilatation: parks weber syndrome or PROS?3
The reversal of human phylogeny: Homo left Africa as erectus, came back as sapiens sapiens3
Development and analysis of long non-coding RNA-associated competing endogenous RNA network for osteosarcoma metastasis3
RNA sequencing analyses in infants patients with coarctation of the aorta3
PeakMatcher facilitates updated Aedes aegypti embryonic cis-regulatory element map3
Göte Turesson’s research legacy to Hereditas: from the ecotype concept in plants to the analysis of landraces’ diversity in crops2
Exploration of the underlying comorbidity mechanism in psoriasis and periodontitis: a bioinformatics analysis2
Race biology2
Bioinformatics analysis of diagnostic biomarkers for Alzheimer's disease in peripheral blood based on sex differences and support vector machine algorithm2
Transcriptome sequencing reveals core regulation modules and gene signatures of Zusanli acupoints in response to different moxibustion warm stimulation in adjuvant arthritis rat2
Trimeric complexes of Antp-TBP with TFIIEβ or Exd modulate transcriptional activity2
Mutations in the acetolactate synthase (ALS) enzyme affect shattercane (Sorghum bicolor) response to ALS-inhibiting herbicides2
Functional analysis of enhancer elements regulating the expression of the Drosophila homeodomain transcription factor DRx by gene targeting2
Regulation of DNA methylation on key parasitism genes of Cysticercus cellulosae revealed by integrative epigenomic-transcriptomic analyses2
Insulin-like growth factor binding protein 2: a core biomarker of left ventricular dysfunction in dilated cardiomyopathy2
Variations in the TAS2R38 gene among college students in Hubei2
Genetic polymorphism of IDOL gene was associated with the susceptibility of coronary artery disease in Han population in Xinjiang, China2
Single-nucleotide polymorphisms and activities of indoleamine 2,3-dioxygenase isoforms, IDO1 and IDO2, in tuberculosis patients2
Multiomics landscape of the autosomal dominant osteopetrosis type II disease-specific induced pluripotent stem cells2
Insights into AIM-InDel diversities in Yunnan Miao and Hani ethnic groups of China for forensic and population genetic purposes2
Identification and development of the novel 7-genes diagnostic signature by integrating multi cohorts based on osteoarthritis2
A century of Hereditas: from local publication to international journal2
Comprehensive analysis to identify pseudogenes/lncRNAs-hsa-miR-200b-3p-COL5A2 network as a prognostic biomarker in gastric cancer2
LPAR2 correlated with different prognosis and immune cell infiltration in head and neck squamous cell carcinoma and kidney renal clear cell carcinoma2
Forkhead box P3 gene polymorphisms predispose to type 2 diabetes and diabetic nephropathy in the Han Chinese populations: a genetic-association and gender-based evaluation study2
FBXW7 gene polymorphism is associated with type 2 diabetes in the Uygur population in Xinjiang, China2
Genetic analysis of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family2
Circular RNA circHMCU promotes breast tumorigenesis through miR-4458/PGK1 regulatory cascade2
Understanding the contemporary high obesity rate from an evolutionary genetic perspective2
Elevated HMGB1 promotes the malignant progression and contributes to cisplatin resistance of non-small cell lung cancer2
Cell-free DNA from plasma as a promising alternative for detection of gene mutations in patients with Maffucci syndrome2
Identification of key apoptosis-related genes and immune infiltration in the pathogenesis of psoriasis2
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