OOIR: Observatory of International Research

Papers

(The H4-Index of Frontiers in Genetics is 52. 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 2022-08-01 to 2026-08-01.)

Article	Citations
Subject clustering by IF-PCA and several recent methods	188
RET splice site variants in medullary thyroid carcinoma	171
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in PARD6G-AS1 promotor in a case with arthrogryposis	129
Editorial: Epigenetic mechanisms and epigenetic-based therapies in cardiometabolic and vascular disease	125
Geographical distribution of ALDH2 rs671 polymorphism in Chinese angina pectoris patients	120
Panoramic analysis of the biological function and clinical value of SLC38A2 in human cancers: a study based on pan-cancer and single-cell analysis	119
Moral judgment of genetic technologies: validation of the genetic technologies questionnaire in the German-speaking population	117
The potential impact of GLS and PDHA1 on tumor immunity and immunotherapy response in LUSC	104
Editorial: Forensic investigative genetic genealogy and fine-scale structure of human populations	101
Editorial: New insights in cellular and molecular biology of cancer stem cells	99
Editorial: High-throughput sequencing-based investigation of chronic disease markers and mechanisms, volume II	98
Association between arthropathies and postpartum hemorrhage: a bidirectional Mendelian randomization study	97
Regulatory role of N6-Methyladenosine on skeletal muscle development in Hu sheep	95
Metabolic reprogramming and prognostic modeling in pancreatic cancer: insights from WGCNA	93
Editorial: Genetic and epigenetic aspects of non-coding RNAs in physiology and disease	93
Editorial: Genetics of reproduction for livestock species	91
Editorial: Computational methods to analyze RNA data for human diseases	89
Editorial: Prediction and explanation in biomedicine using network-based approaches	86
A comprehensive splicing characterization of COL4A5 mutations and prognostic significance in a single cohort with X-linked alport syndrome	83
Early-Life Exposure of Pigs to Topsoil Alters miRNA and mRNA Expression in Peripheral Blood Mononuclear Cells	82
FGF/FGFR-related lncRNAs based classification predicts prognosis and guides therapy in gastric cancer	80
Skin-specific transgenic overexpression of ovine β-catenin in mice	79
Development and validation of a chromatin regulator prognostic signature in colon adenocarcinoma	78
Identification of discriminant features from stationary pattern of nucleotide bases and their application to essential gene classification	78
Mutational signatures representative transcriptomic perturbations in hepatocellular carcinoma	78

Two machine learning-derived nomogram for predicting the occurrence and severity of acute graft-versus-host disease: a retrospective study based on serum biomarkers	78
Construction of a prognostic model related to copper dependence in breast cancer by single-cell sequencing analysis	76
Neoepitope load, T cell signatures and PD-L2 as combined biomarker strategy for response to checkpoint inhibition immunotherapy	76
Editorial: The ethics and challenges of studying the genetics of marginalized populations	75
Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases	74
An immune infiltration-related long non-coding RNAs signature predicts prognosis for hepatocellular carcinoma	74
Construction of ceRNA network based on RNA-seq for identifying prognostic lncRNA biomarkers in Perthes disease	72
Systemic inflammatory regulators and preeclampsia: a two-sample bidirectional Mendelian randomization study	66
From genetic data to kinship clarity: employing machine learning for detecting incestuous relations	65
KLF4 loss in hepatocellular carcinoma: Improving prognostic prediction and correlating immune infiltrates	64
Bioinformatics revealed biomarkers for diagnosis in kidney stones	63
Bioinformatics analysis reveals the landscape of immune cell infiltration and novel immune-related biomarkers in moyamoya disease	62
Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis	61
Comprehensive analysis of molecular features, prognostic values, and immune landscape association of m6A-regulated immune-related lncRNAs in smoking-associated lung squamous cell carcinoma	60
Epigenome-wide DNA methylation profiling in comparison between pathological and physiological hypertrophy of human cardiomyocytes	60
Genome-wide identification and expression analysis of WRKY family genes under soft rot in Chinese cabbage	59
Development and validation of a TRP-related gene signature for overall survival prediction in lung adenocarcinoma	59
Identification of resistance gene analogs of the NBS-LRR family through transcriptome probing and in silico prediction of the expressome of Dalbergia sissoo under dieback disease stress	59
Potential immunomodulatory effects of the extract from Artemisia frigida Willd on loaches infested with Aeromonas hydrophila revealed by microRNA analysis	59
Prioritizing potential circRNA biomarkers for bladder cancer and bladder urothelial cancer based on an ensemble model	57
Genetic and clinical landscape of Duchenne muscular dystrophy in Guatemala: insights from a national study	57
Editorial: Multi-omics studies and applications in precision medicine	56
ARGem: a new metagenomics pipeline for antibiotic resistance genes: metadata, analysis, and visualization	55
Identifying mitochondrial genes and potential biological functions in pre-eclampsia: bioinformatics and experimental insights	54
Genetic analysis of a bronze age individual from Ulug-depe (Turkmenistan)	54
BANSMDA: a computational model for predicting potential microbe-disease associations based on bilinear attention networks and sparse autoencoders	52
LRRC56 deficiency cause motile ciliopathies in humans and mice	52