Frontiers in Genetics

Scope & Guideline

Connecting Researchers to the Future of Genetics

Introduction

Explore the comprehensive scope of Frontiers in Genetics through our detailed guidelines, including its aims and scope. Stay updated with trending and emerging topics, and delve into declining areas to understand shifts in academic interest. Our guidelines also showcase highly cited topics, featuring influential research making a significant impact. Additionally, discover the latest published papers and those with high citation counts, offering a snapshot of current scholarly conversations. Use these guidelines to explore Frontiers in Genetics in depth and align your research initiatives with current academic trends.
LanguageEnglish
ISSN-
PublisherFRONTIERS MEDIA SA
Support Open AccessNo
Country-
Type-
Converge-
AbbreviationFRONT GENET / Front. Genet.
Frequency1 issue/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressAVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE CH-1015, SWITZERLAND

Aims and Scopes

Frontiers in Genetics is a multidisciplinary journal that focuses on the vast field of genetics, encompassing a wide array of research areas that contribute to our understanding of genetic mechanisms, genomic technologies, and their applications in health, disease, and agriculture.
  1. Genetic Mechanisms and Pathways:
    Research exploring the fundamental genetic mechanisms that underlie various biological processes, including gene regulation, expression, and the role of non-coding RNAs in gene function.
  2. Disease Genetics and Genomics:
    Studies focusing on the genetic basis of diseases, including Mendelian disorders, complex diseases, and cancer genetics, utilizing approaches like genome-wide association studies (GWAS) and whole-exome sequencing.
  3. Bioinformatics and Computational Biology:
    Development of computational tools and bioinformatics approaches to analyze genomic data, predict gene functions, and understand the interactions within biological systems.
  4. Genetic Diversity and Population Genomics:
    Investigations into the genetic diversity of populations, including studies on evolutionary genetics, population structure, and the impact of genetic variation on traits and disease susceptibility.
  5. Applications of Genomics in Agriculture:
    Research aimed at improving crop and livestock genetics through genomic selection, marker-assisted breeding, and the exploration of genetic resources for enhancing agricultural productivity.
  6. Clinical Genetics and Precision Medicine:
    Exploration of genetic testing and personalized medicine implications, including pharmacogenomics, genetic counseling, and the integration of genomic data into clinical practice.
The journal Frontiers in Genetics is witnessing emerging trends that reflect the dynamic nature of the field, highlighting areas of growing interest and innovation in genetic research.
  1. Integration of Multi-Omics Data:
    There is a significant trend towards integrating various omics data (genomics, transcriptomics, proteomics) to provide a holistic view of biological systems and disease mechanisms.
  2. Mendelian Randomization Studies:
    Mendelian randomization is gaining traction as a powerful tool to infer causal relationships between genetic variants and diseases, particularly in understanding complex traits and conditions.
  3. Machine Learning and AI in Genomics:
    The application of machine learning and artificial intelligence in genomics is on the rise, enhancing predictive modeling, genomic data analysis, and biomarker discovery.
  4. Focus on Non-Coding RNAs:
    Research into non-coding RNAs, particularly their roles in cancer and other diseases, is increasingly prevalent, reflecting their importance in gene regulation and disease pathology.
  5. Genetic Contributions to Environmental Adaptation:
    Emerging studies are exploring how genetic factors contribute to adaptation to environmental changes, particularly in the context of climate change and agricultural sustainability.
  6. Personalized and Precision Medicine:
    There is a growing emphasis on research that supports personalized medicine approaches, utilizing genetic information to tailor treatments and improve patient outcomes.

Declining or Waning

While Frontiers in Genetics continues to thrive in numerous research domains, certain areas appear to be experiencing a decline in focus or publication frequency, reflecting shifts in research priorities or advancements in methodologies.
  1. Traditional Genetic Mapping Techniques:
    There is a noticeable decrease in publications focusing solely on classic genetic mapping techniques, as researchers increasingly adopt high-throughput sequencing and genomic approaches that provide more comprehensive insights.
  2. Single Trait Analysis:
    Research that focuses on single trait analysis is becoming less prevalent, with a growing emphasis on multi-trait analyses that better reflect the complex interactions between multiple genetic factors.
  3. Basic Genetic Mechanisms in Non-Model Organisms:
    While studies on model organisms remain strong, there seems to be a waning interest in basic genetic research in non-model organisms, as applied research and translational studies gain prominence.
  4. Historical Genetic Studies:
    Research focusing on historical genetic studies or retrospective analyses is declining, with a shift toward forward-looking, predictive models and real-time genomic assessments.
  5. Phenotypic Characterization Without Genomic Correlation:
    There is a reduction in studies that characterize phenotypes without linking them to genomic data, as the field moves toward integrative approaches that combine phenotypic and genomic analyses.

Similar Journals

Human Genome Variation

Unraveling the Secrets of Our DNA
Publisher: SPRINGERNATUREISSN: Frequency: 1 issue/year

Human Genome Variation, published by SpringerNature, is an esteemed open access journal dedicated to the field of genetic research and exploration. Since its inception in 2014, the journal has been at the forefront of advancing our understanding of human genome diversity and its implications in health and disease. With an E-ISSN of 2054-345X, it features a diverse array of studies that encompass biochemistry, genetics, and molecular biology, making it an invaluable resource for researchers and professionals alike. The journal holds a Q3 ranking in both biochemistry and genetics, and a Q4 ranking in molecular biology, highlighting its growing influence within these disciplines. As the landscape of genomics continues to evolve, Human Genome Variation serves as a platform for the dissemination of high-quality research, fostering collaboration and innovation within the scientific community. Researchers and academics are invited to contribute to this pivotal journal, which not only provides open access to its content since 2014 but also aims to bridge the gap between basic research and clinical applications in genetics.

npj Genomic Medicine

Empowering Global Collaboration in Genomics
Publisher: NATURE PORTFOLIOISSN: Frequency: 1 issue/year

npj Genomic Medicine is a leading open-access journal published by NATURE PORTFOLIO, specializing in the rapidly evolving areas of genomic medicine, including genetics, molecular biology, and clinical applications. Launched in 2016, the journal has quickly established itself within the academic community, boasting a prestigious Q1 ranking in multiple categories, including Genetics and Molecular Biology, with remarkable positions in both Scopus ranks and percentiles. With an emphasis on innovative genomic research that bridges the gap between laboratory findings and clinical implementation, npj Genomic Medicine aims to provide a platform for researchers, professionals, and students to share significant advancements and insights. Being an open-access journal enhances accessibility to cutting-edge research, ensuring that vital discoveries in genomics can benefit a global audience and facilitate interdisciplinary collaboration. The journal continues to contribute to the forefront of genomic research, impacting both academic scholarship and practical healthcare solutions.

INTERNATIONAL JOURNAL OF HUMAN GENETICS

Exploring the Depths of Genetic Knowledge
Publisher: KAMLA-RAJ ENTERPRISESISSN: 0972-3757Frequency: 4 issues/year

INTERNATIONAL JOURNAL OF HUMAN GENETICS is a distinguished publication dedicated to advancing knowledge in the fields of genetics and molecular biology. Published by KAMLA-RAJ ENTERPRISES, this journal explores critical developments and research findings from 2008 to 2016, though its coverage in Scopus has since been discontinued. With an ISSN of 0972-3757 and an E-ISSN of 2456-6330, the journal aimed to foster scholarly dialogue and serve as a resource for researchers, professionals, and students engaged in human genetics. While the journal holds a modest ranking in categories such as Biochemistry and Genetics, it remains a vital source for exploring niche topics within the realm of human genetics. Researchers interested in genetic screening, gene therapy, and clinical genetics will find valuable insights herein. Despite its pause in indexing, the journal continues to contribute to the academic discourse by disseminating critical research that bridges gaps in understanding human genetics.

MOLECULAR GENETICS AND GENOMICS

Innovating Insights in Genetics and Genomics
Publisher: SPRINGER HEIDELBERGISSN: 1617-4615Frequency: 6 issues/year

MOLECULAR GENETICS AND GENOMICS is a distinguished journal published by SPRINGER HEIDELBERG that serves as a pivotal platform for the communication of cutting-edge research and developments in the fields of genetics, molecular biology, and medicine. With an ISSN of 1617-4615 and an E-ISSN of 1617-4623, this journal has established itself since its inception in 1994 as a significant resource for researchers aiming to explore the complexities of genetic interactions and their implications in various biological systems. The journal is indexed in Scopus, with respectable rankings in the Genetics, Molecular Biology, and Biochemistry categories, showcasing its position within the academic community. It is categorized in the 2023 rankings as Q3 in Genetics, Q2 in Medicine (miscellaneous), and Q3 in Molecular Biology, indicating its relevance and quality in the scientific discourse. The journal also promotes open access, ensuring that researchers and professionals can easily share and advance knowledge in the rapidly evolving disciplines of molecular genetics and genomics. As the journal continues to bridge the gap between experimental and theoretical research, it presents a vital space for innovation, fostering collaborations and scholarly exchange among its readership.

BMC GENOMICS

Fostering collaboration through groundbreaking genomic insights.
Publisher: BMCISSN: 1471-2164Frequency: 1 issue/year

BMC Genomics is a premier open-access journal dedicated to advancing the field of genomics through the dissemination of high-quality research articles. Published by BMC, a renowned leader in open-access publishing, this journal has built a solid reputation since its inception in 2000, making significant contributions to the areas of biotechnology and genetics. Holding a prestigious Q1 ranking in Biotechnology and Q2 in Genetics as of 2023, it serves as an essential platform for researchers, professionals, and students alike, facilitating the exchange of innovative ideas and data. With an impactful presence in the Scopus rankings, BMC Genomics currently stands at Rank #90/347 in Genetics, reflecting its influence in the scientific community. Researchers are encouraged to explore the vast array of scholarly articles and engage with cutting-edge genomics research that is crucial for the evolution of various applications in medicine, agriculture, and environmental science. With its open access model, BMC Genomics ensures that groundbreaking research is freely available, fostering collaboration and accelerating scientific discovery on a global scale.

CURRENT GENOMICS

Illuminating the path of genetic discovery.
Publisher: BENTHAM SCIENCE PUBL LTDISSN: 1389-2029Frequency: 8 issues/year

CURRENT GENOMICS is a premier journal published by Bentham Science Publishers that focuses on the expansive field of genomics, including both clinical and molecular genetics. With the ISSN 1389-2029 and E-ISSN 1875-5488, this esteemed journal has been disseminating significant scientific insights since its inception in 2000 and continues to contribute to the field through 2024. Based in the United Arab Emirates, CURRENT GENOMICS boasts a Q3 ranking in both the genetics and clinical genetics categories for 2023, reflecting its growing impact in the scientific community. Although not an open-access journal, it provides valuable content that supports researchers and professionals in navigating the complexities of genetic research and its applications. By publishing original research articles, reviews, and case studies, CURRENT GENOMICS aims to foster a deeper understanding of genomic science and its implications for medicine, thus playing a critical role in the advancement of genetics and biomedical research.

Genetics Research

Driving Progress in Genetic and Medical Sciences
Publisher: HINDAWI LTDISSN: 0016-6723Frequency: 1 issue/year

Genetics Research, published by HINDAWI LTD, is a distinguished open access journal that has been at the forefront of genetic studies since its inception in 1960. With the transition to open access in 2019, this journal has expanded its accessibility, fostering knowledge dissemination across the global scientific community. Operating out of the United Kingdom, it provides a platform for innovative research in the fields of genetics and molecular biology, encompassing a broad range of topics that are highly relevant to medical sciences. As of 2023, it holds a Q4 classification in Genetics and a Q3 classification in miscellaneous Medicine, reflecting its ongoing commitment to scholarly excellence amidst shifting academic landscapes. While the journal's H-index remains unlisted, its indexed ranking within Scopus, with a rank of #325/328 in the Genetics category highlights the challenges ligated to its niche audience. Nevertheless, it serves as a crucial resource for researchers, professionals, and students eager to contribute to and stay informed on the latest genetic research trends and breakthroughs.

Human Genomics

Bridging Knowledge and Accessibility in Genomics
Publisher: BMCISSN: 1473-9542Frequency: 1 issue/year

Human Genomics, published by BMC, is a leading open-access journal dedicated to advancing the field of genomics and its applications in health and disease. Since its inception in 2003, the journal has provided a vital platform for researchers to disseminate groundbreaking findings related to genetic research, contributing significantly to areas such as Drug Discovery, Genetics, Molecular Biology, and Molecular Medicine, as reflected in its Q1 and Q2 quartile rankings throughout 2023. With an ISSN of 1473-9542 and an E-ISSN of 1479-7364, Human Genomics not only delivers high-quality, peer-reviewed research but also ensures accessibility to a broader audience, empowering professionals, students, and academics to stay at the forefront of genomic science. Through its rigorous editorial standards and impactful publications, the journal fosters a collaborative environment for innovative research across the globe from its base in the United Kingdom. By promoting open access since its launch, Human Genomics continues to enhance the visibility and impact of genetic studies, making it an essential resource for anyone involved in the rapidly evolving field of human genomics.

NATURE REVIEWS GENETICS

Exploring the Depths of Genetic Innovation.
Publisher: NATURE PORTFOLIOISSN: 1471-0056Frequency: 12 issues/year

NATURE REVIEWS GENETICS, published by NATURE PORTFOLIO, stands as a leading journal in the field of genetics, boasting a remarkable reputation reflected in its Q1 ranking across multiple categories including Genetics, Clinical Genetics, and Molecular Biology. With an impressive percentile of 99th in both Genetics and Clinical Genetics, as well as a solid rank in Molecular Biology, this journal is pivotal for researchers, professionals, and students alike who seek to stay informed on the latest advancements and comprehensive reviews in genetic research. The journal's scope encompasses a wide array of topics, providing in-depth insights from fundamental genetic principles to clinical applications, underscoring its importance in bridging basic science and medical practice. Though not an open-access publication, it remains accessible through various academic institutions, enhancing its reach and influence within the scientific community. With publication years spanning from 2000 to 2024, NATURE REVIEWS GENETICS continues to shape the future of genetics research and education.

Genes & Genomics

Unlocking the Secrets of Genomic Science
Publisher: SPRINGERISSN: 1976-9571Frequency: 6 issues/year

Genes & Genomics is a prominent academic journal dedicated to the fields of biochemistry, genetics, and molecular biology, published by Springer from South Korea. With an evolving focus on innovative genetic research and its implications, this journal serves as a crucial platform for disseminating knowledge within the scientific community. The journal has been indexed in Scopus and boasts a Q3 quartile ranking in 2023 for its contributions to these disciplines, highlighting its relevance and growing impact. In addition to traditional subscription options, Genes & Genomics supports Open Access, offering broader accessibility for researchers and enthusiasts eager to explore the latest advancements in genetic studies. Since its inception in 2008, the journal has committed to publishing high-quality research that drives forward our understanding of genetics and its applications, making it an essential resource for researchers, professionals, and students alike who are passionate about the complexities and breakthroughs in genomic sciences.