Human Gene

Scope & Guideline

Unlocking the Secrets of Our DNA

Introduction

Immerse yourself in the scholarly insights of Human Gene with our comprehensive guidelines detailing its aims and scope. This page is your resource for understanding the journal's thematic priorities. Stay abreast of trending topics currently drawing significant attention and explore declining topics for a full picture of evolving interests. Our selection of highly cited topics and recent high-impact papers is curated within these guidelines to enhance your research impact.
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

Molecular Genetics & Genomic Medicine

Bridging research and real-world medical solutions.
Publisher: WILEYISSN: 2324-9269Frequency: 12 issues/year

Molecular Genetics & Genomic Medicine, published by WILEY, is an esteemed and open-access journal that has been a prominent source of knowledge in the fields of genetics and molecular biology since its establishment in 2013. With an ISSN of 2324-9269, it aims to provide a platform for the dissemination of novel findings and innovative research that pushes the boundaries of genomics and its clinical applications. The journal holds a Q3 categorization in Genetics, Clinical Genetics, and Molecular Biology, reflecting its growing influence in these disciplines, as evidenced by its Scopus rankings. Researchers, professionals, and students alike will find valuable insights and advancements in genomic medicine, making this journal an essential resource for those dedicated to the understanding and application of genetic and molecular research in healthcare. Located at 111 River St, Hoboken, NJ, Molecular Genetics & Genomic Medicine continues to foster a global dialogue within the scientific community, ensuring accessible knowledge for all.

Human Genomics

Elevating Genomic Research to New Heights
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 GENETICS

Shaping the Future of Genetic Understanding
Publisher: NATURE PORTFOLIOISSN: 1061-4036Frequency: 12 issues/year

Nature Genetics is a premier journal in the field of genetics published by NATURE PORTFOLIO, renowned for its impactful research and significant contributions to the understanding of genetic mechanisms and their implications for human health. Since its establishment in 1992, the journal has continually maintained a strong reputation, evidenced by its impressive Q1 ranking in the Genetics category and a commendable Scopus ranking of #4 out of 347 in Genetics, placing it in the 98th percentile. Although it does not currently offer Open Access options, Nature Genetics remains a critical resource for researchers and practitioners, providing cutting-edge studies and papers that drive advancements in both fundamental and applied genetic research. With a global readership and contributions from leading scientists around the world, this journal is a vital platform for disseminating innovative findings and fostering discussions at the frontier of genetics.

JOURNAL OF GENE MEDICINE

Connecting Researchers to Transformative Genetic Insights
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.

BIOCHEMICAL GENETICS

Innovating the Understanding of Genetic Mechanisms
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.

MOLECULAR PSYCHIATRY

Transforming Understanding of Psychiatric Disorders through Molecular Research
Publisher: SPRINGERNATUREISSN: 1359-4184Frequency: 12 issues/year

MOLECULAR PSYCHIATRY, published by SpringerNature, is a premier peer-reviewed journal that has established itself as a leading platform for the dissemination of cutting-edge research in the fields of neuroscience, molecular biology, and psychiatry. With an impressive impact factor and a reputation for excellence, the journal is ranked Q1 in key categories, signifying its high academic quality and relevance. The journal’s scope spans groundbreaking studies and innovative therapeutic approaches that intersect at the molecular and cellular levels, providing invaluable insights into the biological underpinnings of psychiatric disorders. Since its inception in 1996, MOLECULAR PSYCHIATRY has evolved to support both established and emerging researchers, fostering a collaborative environment that enhances the understanding of mental health. It is committed to improving access to scientific knowledge, although it currently does not offer open access options. With its headquarters in London, the journal continues to play a pivotal role in enhancing the global dialogue on psychiatric and neurological advancements, making it an essential resource for academics and professionals dedicated to advancing mental health sciences.

TRENDS IN GENETICS

Pioneering Insights in the World of Genetics
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 & GENETIC SYSTEMS

Shaping the Future of Genetic Science and Medicine
Publisher: GENETICS SOC JAPANISSN: 1341-7568Frequency: 6 issues/year

GENES & GENETIC SYSTEMS, an esteemed journal published by the Genetics Society of Japan, serves as a vital platform for the dissemination of innovative research within the fields of genetics, molecular biology, and medicine. Established in 1996 and based in Mishima, Shizuoka, Japan, this journal has actively contributed to the academic community, fostering collaboration and knowledge sharing among researchers and professionals. The journal’s impact can be seen through its category quartiles, which reflect its position in Genetics, Molecular Biology, and Medicine, and while it currently ranks in Q4 in Genetics and Q3 in Medicine (miscellaneous), it is poised for growth as it continues to publish pivotal studies. With a commitment to open access, GENES & GENETIC SYSTEMS ensures that research findings are freely accessible to the global scientific community, promoting a more inclusive approach to knowledge distribution. This journal is essential for students, researchers, and professionals seeking to stay informed of advancements in genetic research and its implications for the broader field of medicine.

Genes and Nutrition

Advancing Health Through Genetic Insights and Nutritional Science
Publisher: BMCISSN: 1555-8932Frequency: 1 issue/year

Genes and Nutrition is a prominent open access journal published by BMC in the United Kingdom, dedicated to advancing knowledge at the intersection of nutrition, genetics, and human health. With the aim of making cutting-edge research available to a global audience, the journal has been a vital platform for sharing discoveries since its inception in 2007, and it continues to thrive with a convergence period extending to 2024. Recognized for its high-quality contributions, Genes and Nutrition is rated in the Q2 category within both Endocrinology, Diabetes, and Metabolism and Genetics as of 2023, reflecting its esteemed position in these fields (Scopus Ranks leaderboard places it at #72/244 and #109/347, respectively). This journal is an invaluable resource for researchers, professionals, and students alike, fostering collaboration and innovation in the understanding of how genetic factors influence nutrition and health outcomes. Accessible to all since 2016, it encourages dialogue and discovery, positioning itself as a leader in genetic and nutritional science.

Frontiers in Genetics

Unlocking the Secrets of Genetics for All
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.