Human Gene

Scope & Guideline

Connecting Discoveries in Genetics and Clinical Applications

Introduction

Delve into the academic richness of Human Gene with our guidelines, detailing its aims and scope. Our resource identifies emerging and trending topics paving the way for new academic progress. We also provide insights into declining or waning topics, helping you stay informed about changing research landscapes. Evaluate highly cited topics and recent publications within these guidelines to align your work with influential scholarly trends.
LanguageEnglish
ISSN2773-0441
PublisherELSEVIER
Support Open AccessNo
CountryNetherlands
TypeJournal
Convergefrom 2022 to 2024
AbbreviationHUM GENE / Hum. Gene
Frequency4 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressRADARWEG 29, 1043 NX AMSTERDAM, NETHERLANDS

Aims and Scopes

The journal 'Human Gene' focuses on the intricate relationships between human genetics and various health outcomes, emphasizing molecular mechanisms, genetic variations, and their implications in disease pathology and therapy. This journal serves as a platform for innovative research that combines both basic and applied genetic studies.
  1. Genetic Epidemiology and Disease Associations:
    The journal publishes studies that explore the associations between genetic variations, such as single nucleotide polymorphisms (SNPs), and the susceptibility to various diseases, including cancer, diabetes, and cardiovascular conditions.
  2. Molecular Pathogenesis and Mechanisms:
    Research highlighting the molecular pathways involved in disease progression, including the role of gene expression, mutations, and epigenetic factors, is a core focus of the journal.
  3. Innovative Diagnostic and Therapeutic Approaches:
    The journal encourages submissions that propose novel biomarkers or therapeutic targets based on genetic findings, integrating bioinformatics and computational biology to enhance understanding and treatment of diseases.
  4. Translational Research:
    A significant aim is to bridge the gap between laboratory findings and clinical applications, showcasing research that has the potential to impact patient care through genetic insights.
  5. Bioinformatics and Computational Genetics:
    With the advancements in technology, the journal promotes studies that utilize bioinformatics tools to analyze genetic data for better understanding of human health and disease.
Recent publications in 'Human Gene' reveal several emerging themes that reflect the evolving landscape of genetic research. These trends highlight the journal's responsiveness to contemporary scientific challenges and interests.
  1. Integrative Omics Approaches:
    There is a growing trend towards using integrative omics approaches, combining genomics, transcriptomics, and proteomics to provide a more comprehensive understanding of diseases, particularly cancers.
  2. Impact of MicroRNAs in Disease:
    Research focusing on the role of microRNAs in cancer and other diseases is on the rise, reflecting their importance as regulatory molecules and potential therapeutic targets.
  3. Long Non-Coding RNAs (lncRNAs):
    The exploration of lncRNAs and their role in gene regulation and disease mechanisms is gaining traction, with studies increasingly linking them to various health conditions.
  4. AI and Machine Learning in Genetics:
    The application of artificial intelligence and machine learning techniques for genetic data analysis and disease prediction is emerging as a significant trend, showcasing innovative methodologies in genetics.
  5. Environmental and Lifestyle Factors in Genomics:
    There is an increasing emphasis on understanding how environmental factors and lifestyle choices interact with genetic predispositions to influence disease outcomes.

Declining or Waning

While 'Human Gene' remains a vibrant platform for genetic research, certain themes have shown a decline in publication frequency or emphasis over recent years. These waning scopes may reflect shifts in research focus or a saturation of certain topics.
  1. Traditional Genetic Testing Techniques:
    There has been a noticeable decline in studies focusing solely on traditional genetic testing methods, as the field shifts towards more advanced genomic technologies and personalized medicine.
  2. Basic Genetic Mapping Studies:
    Research that solely concentrates on basic genetic mapping without integrating functional studies or clinical implications appears to be decreasing, as the emphasis now favors more comprehensive analyses.
  3. Single Disease Focus:
    Papers that examine genetic factors related to single diseases without considering comorbidities or broader health implications are less frequent, indicating a trend towards multi-faceted research approaches.
  4. Population-Specific Studies:
    While still relevant, the number of studies focusing exclusively on specific populations without broader applicability or comparative analyses has been waning, possibly due to a shift towards global health perspectives.

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