Human Gene

Scope & Guideline

Transforming Genetic Knowledge into Health Solutions

Introduction

Explore the comprehensive scope of Human Gene 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 Human Gene in depth and align your research initiatives with current academic 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.

Similar Journals

HUMAN GENETICS

Transforming research into real-world health solutions.
Publisher: SPRINGERISSN: 0340-6717Frequency: 12 issues/year

HUMAN GENETICS, published by SPRINGER, stands as a cornerstone journal in the field of genetics, offering a wealth of research insights since its inception in 1964. Hailing from Germany, this esteemed journal boasts an impressive Q1 ranking in both Genetics and Clinical Genetics, marking it among the top quartile of journals in these categories for 2023. With a notable Scopus rank of #7 in Clinical Genetics and a percentile ranking of 93, HUMAN GENETICS attracts significant attention from researchers and professionals dedicated to advancing our understanding of genetic influences on human health and disease. Although it does not currently offer Open Access options, the journal provides a critical platform for scholarly communication, aimed at disseminating groundbreaking findings in genetics and biotechnology. As the field evolves, HUMAN GENETICS continues to play an instrumental role in bridging the gap between laboratory research and clinical application, making it an essential resource for students and seasoned researchers alike.

TRENDS IN GENETICS

Unraveling the Complexities of Genetic Science
Publisher: CELL PRESSISSN: 0168-9525Frequency: 12 issues/year

TRENDS IN GENETICS, published by CELL PRESS, is a leading journal in the field of genetics, recognized for its significant impact on research and advancements in the discipline. With an impressive Scopus ranking of #10 out of 347 in the category of Genetics and a 97th percentile ranking, this journal stands as a premier platform for publishing innovative, high-quality articles that shape the future of genetic research. Since its inception in 1985, TRENDS IN GENETICS has been at the forefront of the genetic sciences, continuously disseminating crucial findings while maintaining a strong commitment to scientific rigor and integrity. Although it does not currently offer open access options, its rigorous peer-review process ensures that only the most relevant and groundbreaking studies make it to publication. Scholars and practitioners in genetics will find this journal to be an invaluable resource for keeping abreast of the latest developments, trends, and methodologies that drive the field forward.

Genes

Fostering collaboration in the evolving landscape of genetics.
Publisher: MDPIISSN: Frequency: 12 issues/year

Genes is a leading open-access journal published by MDPI that focuses on advancing the field of genetics and genomics. Established in 2010 and based in Basel, Switzerland, this journal has made significant strides in promoting innovative research in both clinical genetics and molecular biology. With an impact factor reflecting its relevance and quality, Genes has been classified in the Q2 quartile for Genetics and the Q3 quartile for clinical Genetics as of 2023. The journal provides an accessible platform for researchers, professionals, and students to disseminate their findings and explore emerging trends across the genetics landscape. Accessible online since its inception, Genes allows for continuous engagement and collaboration within the scientific community, fostering a deeper understanding of genetic mechanisms and their implications in health and disease.

BIOCHEMICAL GENETICS

Advancing the Frontier of Biochemical Insights
Publisher: SPRINGER/PLENUM PUBLISHERSISSN: 0006-2928Frequency: 6 issues/year

BIOCHEMICAL GENETICS, published by Springer/Plenum Publishers, is a prominent journal in the fields of biochemistry, genetics, and molecular biology, with a substantial impact on the scientific community since its inception in 1967. The journal holds a significant position within various academic quartiles, ranking Q2 in Ecology, Evolution, Behavior and Systematics, and Q3 in Biochemistry, Genetics, and Medicine (miscellaneous), among others, demonstrating its diverse and interdisciplinary reach. With an ISSN of 0006-2928 and an E-ISSN of 1573-4927, it is recognized for contributing critical research insights and methodologies that drive the fields of biochemical genetics forward. Although it is not an Open Access journal, it provides vital access options and resources for researchers globally, facilitating the dissemination of knowledge across institutions. Positioned within the competitive landscape of Scopus rankings, it maintains respectable standings across its focused areas, making it an invaluable resource for researchers, professionals, and students seeking to deepen their understanding of genetic mechanisms and biochemical processes.

Journal of Genetics and Genomics

Bridging Theory and Practice in Genetics
Publisher: SCIENCE PRESSISSN: 1673-8527Frequency: 12 issues/year

The Journal of Genetics and Genomics, published by SCIENCE PRESS in China, stands as a significant contributor to the fields of Genetics and Molecular Biology. With an ISSN of 1673-8527 and E-ISSN 1873-5533, this esteemed journal has achieved a remarkable reputation, holding a prestigious Q1 ranking in both Genetics and Molecular Biology as of 2023. This journal not only showcases pioneering research but also fosters vital discussions on contemporary challenges and innovations within genomic sciences. As part of its commitment to facilitating scientific advancement, the journal encompasses a range of research articles, reviews, and short communications, all aiming to illuminate the complexities of genetic structures and functions from 2007 to 2024. Researchers, professionals, and students alike are encouraged to engage with its content, which ranks favorably in Scopus—placing it within the top tier of its categories. Join the community of academic excellence and explore the latest findings that shape our understanding of genomics.

PLoS Genetics

Unlocking the mysteries of genetics, one breakthrough at a time.
Publisher: PUBLIC LIBRARY SCIENCEISSN: 1553-7404Frequency: 12 issues/year

PLoS Genetics, published by the PUBLIC LIBRARY SCIENCE, is a leading open-access journal dedicated to advancing the field of genetics, molecular biology, and related disciplines. With its ISSN of 1553-7404, this esteemed journal has been offering unrestricted access to its content since 2005, fostering a global community of researchers, professionals, and students. Situated in the United States, its contributions can be found at 1160 Battery Street, Ste 100, San Francisco, CA 94111. As of 2023, PLoS Genetics proudly holds a Q1 ranking in multiple categories including Cancer Research, Ecology, Evolution, Behavior and Systematics, Genetics, and Molecular Biology, underscoring its impact in these vital scientific areas. The journal's commitment to disseminating high-quality research is reflected in its impressive Scopus rankings, with notable positions in various fields of study, ensuring that it remains a crucial resource for cutting-edge research and innovation. By providing an open-access platform, PLoS Genetics not only enhances the visibility of genetic research but also encourages collaborations and the sharing of knowledge that can lead to significant breakthroughs in science.

RUSSIAN JOURNAL OF GENETICS

Shaping the Future of Genetic Understanding
Publisher: PLEIADES PUBLISHING INCISSN: 1022-7954Frequency: 12 issues/year

RUSSIAN JOURNAL OF GENETICS is a significant platform in the field of genetics, published by PLEIADES PUBLISHING INC since its inception in 1996. With an ISSN of 1022-7954 and an E-ISSN of 1608-3369, the journal focuses on a wide array of topics within genetics, providing researchers, professionals, and students with insights into advancements and discoveries in this ever-evolving discipline. While it currently holds a Q4 ranking in the 2023 Genetics category according to Scopus, representing invaluable opportunities for knowledge dissemination, the journal is actively working to enhance its impact in future rankings. Readers will find the journal a repository of diverse genetic research findings, methodologies, and theoretical advancements. Although it is not an open-access journal, it is committed to serving the academic community through rigorous peer-reviewed articles. With a consistent publication trajectory spanning to 2024, the RUSSIAN JOURNAL OF GENETICS remains a crucial resource for those aspiring to stay at the forefront of genetic research and applications.

MOLECULAR GENETICS AND GENOMICS

Unraveling the Complexities of Life at the Molecular Level
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.

Frontiers in Genetics

Pioneering Interdisciplinary Insights in Genetics
Publisher: FRONTIERS MEDIA SAISSN: Frequency: 1 issue/year

Frontiers in Genetics is a premier academic journal dedicated to advancing the field of genetics through high-quality, peer-reviewed research. Published by FRONTIERS MEDIA SA in Switzerland since 2010, this Open Access journal provides a platform for researchers and practitioners to disseminate innovative findings across various subfields, including clinical genetics and molecular medicine. With a notable emphasis on interdisciplinary approaches, the journal holds a strong position in the academic landscape, achieving Q2 rankings in key categories such as Genetics and Molecular Medicine in 2023. Not only does Frontiers in Genetics contribute to the scholarly dialogue by publishing impactful studies, but it also promotes accessibility to vital research, ensuring that knowledge is available to a global audience. This journal is a vital resource for researchers, professionals, and students looking to stay at the forefront of genetic discoveries and their applications, reflective of its engagement with contemporary challenges in genetics and healthcare.

JOURNAL OF GENE MEDICINE

Elevating Standards in Gene Medicine Research
Publisher: WILEYISSN: 1099-498XFrequency: 12 issues/year

The Journal of Gene Medicine, published by Wiley, stands as a pivotal resource in the field of gene therapy and molecular medicine, with a rich history of dissemination of impactful research since its inception in 1998. With an ISSN of 1099-498X and an E-ISSN of 1521-2254, this esteemed journal plays a crucial role in advancing our understanding of genetics and drug discovery, reflected in its impressive 2023 Scopus rankings where it holds a Q2 classification in Drug Discovery and Q3 in several genetics-related categories. The journal aims to facilitate the exchange of high-quality research findings that bridge the gap between laboratory and clinical applications, making it an essential platform for researchers, academics, and healthcare professionals committed to the forefront of genetic innovation. Although it does not currently offer open access options, its reputation for rigorous peer review ensures that all published work meets the highest academic standards, providing a reliable reference for scientific inquiry in the United States and beyond. As the field rapidly evolves, the Journal of Gene Medicine remains at the helm, guiding future discoveries with its influential publications and comprehensive insights.