Genes and Environment

Scope & Guideline

Transforming Research into Policy for Healthier Futures

Introduction

Welcome to your portal for understanding Genes and Environment, featuring guidelines for its aims and scope. Our guidelines cover trending and emerging topics, identifying the forefront of research. Additionally, we track declining topics, offering insights into areas experiencing reduced scholarly attention. Key highlights include highly cited topics and recently published papers, curated within these guidelines to assist you in navigating influential academic dialogues.
LanguageEnglish
ISSN1880-7046
PublisherBMC
Support Open AccessYes
CountryUnited Kingdom
TypeJournal
Convergefrom 2006 to 2007, from 2009 to 2024
AbbreviationGENES ENVIRON / Gene Environ.
Frequency1 issue/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressCAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND

Aims and Scopes

The journal 'Genes and Environment' focuses on the intersection of genetic and environmental factors influencing health, disease, and cancer. It emphasizes innovative methodologies for studying these complex interactions and aims to advance understanding in molecular biology, toxicology, and epidemiology.
  1. Genetic and Environmental Interactions:
    The journal investigates how genetic predispositions interact with environmental exposures to influence health outcomes, particularly in relation to cancer.
  2. Molecular Mechanisms of Disease:
    Research published in this journal frequently explores the molecular pathways involved in disease processes, including the role of genes, non-coding RNAs, and epigenetic modifications.
  3. Toxicology and Genotoxicity Assessment:
    A core focus is on the assessment of environmental toxins and their genotoxic effects, employing in vivo and in vitro methodologies to evaluate the impacts on human health.
  4. Cancer Research and Biomarkers:
    The journal contributes to the field of cancer research by identifying genetic mutations, biomarkers, and therapeutic targets, particularly in relation to environmental carcinogens.
  5. Epidemiological Studies:
    It encompasses epidemiological studies that examine the correlation between environmental factors and disease incidence, highlighting the relevance of population health.
The journal has identified and embraced several emerging themes that reflect current scientific interests and societal concerns. These trends indicate a proactive approach to addressing contemporary challenges in health and disease.
  1. Integrative Exposomics:
    There is a growing emphasis on exposomics, which involves the comprehensive study of environmental exposures and their cumulative effects on health, particularly in relation to cancer risk.
  2. Long Non-Coding RNAs:
    Research on long non-coding RNAs (lncRNAs) has surged, highlighting their roles in gene regulation and disease processes, particularly in cancer biology.
  3. Precision Medicine and Genomic Profiling:
    The journal is increasingly publishing studies focused on precision medicine, utilizing genomic profiling to tailor treatments based on individual genetic and environmental factors.
  4. Artificial Intelligence in Toxicology:
    Emerging methodologies utilizing artificial intelligence and machine learning for predicting toxicological outcomes and assessing environmental risks are gaining traction.
  5. Epigenetics in Disease Mechanisms:
    There is an expanding interest in the role of epigenetic modifications in disease mechanisms, particularly in how these changes are influenced by environmental factors.

Declining or Waning

While 'Genes and Environment' continues to evolve, certain themes have seen a decline in prominence over recent years. These waning scopes may reflect shifts in research focus or a saturation of findings in specific areas.
  1. Traditional Mutagenicity Testing:
    There has been a noticeable reduction in studies focusing on conventional mutagenicity testing methods, as newer, more sophisticated techniques are being developed and adopted.
  2. Single Environmental Factors:
    Research concentrating exclusively on single environmental factors, without consideration of genetic interactions, has become less frequent, indicating a shift towards more integrative approaches.
  3. Basic Toxicology Studies:
    There is a decreasing trend in basic toxicology studies that do not link findings to broader genetic or epidemiological implications, as the field moves toward more applied, translational research.

Similar Journals

Genes and Nutrition

Bridging Genetics and Nutrition for Better Health
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.

MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS

Fostering innovation in genetic research for public health advancements.
Publisher: ELSEVIERISSN: 1383-5718Frequency: 12 issues/year

MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, published by Elsevier, is a renowned journal that explores critical advancements in the field of genetic toxicology and environmental mutagenesis. With an ISSN of 1383-5718 and an E-ISSN of 1879-3592, it ranks in Q3 for Genetics and Q2 for Health, Toxicology, and Mutagenesis as of 2023. This journal not only emphasizes the importance of environmental factors in genetic material alterations but also disseminates significant research findings that aid in understanding the implications for public health and safety. Operating from Amsterdam, Netherlands, it serves as a pivotal platform for researchers, professionals, and students, fostering an informed community keen on evolving the parameters of genetic research. Although it currently does not offer open access, the journal's commitment to high-quality peer-reviewed content ensures substantial contributions to the academic literature, enhancing our comprehension of mutagenic processes and their environmental triggers.

JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES

Unraveling the Complexities of Toxicology and Health
Publisher: TAYLOR & FRANCIS INCISSN: 1528-7394Frequency: 24 issues/year

JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, published by Taylor & Francis Inc, stands as a key resource in the interdisciplinary field of toxicology and environmental health. Operating under the ISSN 1528-7394 and E-ISSN 1087-2620, this journal maintains a strong presence with a Q2 category ranking in Health, Toxicology and Mutagenesis and a Q3 ranking in Toxicology as of 2023. It aims to disseminate critical findings that address contemporary issues in toxicology and environmental health, emphasizing the implications of environmental agents on human health. The journal offers both subscription and open access options, making cutting-edge research accessible to a diverse readership. With coverage of key topics from 1998 to 2024, it is an essential platform for academics, professionals, and students seeking to stay at the forefront of environmental health sciences.

Epigenomics

Unraveling the Epigenetic Mysteries of Health and Disease.
Publisher: FUTURE MEDICINE LTDISSN: 1750-1911Frequency: 24 issues/year

Epigenomics is a leading journal in the realms of Cancer Research and Genetics, published by Future Medicine Ltd in the United Kingdom. With an ISSN of 1750-1911 and an E-ISSN of 1750-192X, the journal has been an integral part of the scientific community since its inception in 2009, and is set to converge its impactful research publications through 2024. The journal occupies a significant position in its category quartiles as evidenced by its ranking—Q3 in Cancer Research and Q2 in Genetics as of 2023. With Scopus rankings of #138/347 in Genetics and #113/230 in Cancer Research, it demonstrates scholarly excellence and is recognized for its contributions to understanding the role of epigenetic modifications in health and disease. While Epigenomics operates under traditional subscription models, it remains a vital resource for researchers, professionals, and students eager to explore the complex interplay between genes and the epigenome. The journal's innovative approach to epigenetics and its impact on cancer research makes it essential reading for those at the forefront of biomedical research.

Human Gene

Connecting Discoveries in Genetics and Clinical Applications
Publisher: ELSEVIERISSN: 2773-0441Frequency: 4 issues/year

Human Gene is an innovative open access journal published by ELSEVIER, dedicated to the ever-evolving field of genetics. Established in 2022, this journal serves as a vital resource for researchers, professionals, and students alike, aiming to facilitate the dissemination of groundbreaking research and advancements in both basic and clinical genetics. With an ISSN of 2773-0441, Human Gene focuses on providing a platform for high-quality studies that investigate genetic mechanisms, their implications in health and disease, and novel therapeutic strategies. The journal currently holds a Q4 ranking in both Genetics and Clinical Genetics categories, reflecting its emerging status within the scientific community, and strives to enhance its impact to better serve an engaged audience. With its base in Amsterdam, Netherlands, Human Gene is committed to making research accessible through its open access model, inviting contributions that advance our understanding of human genetics and foster collaboration across disciplines.

Cancer Epidemiology

Exploring the Frontiers of Cancer Research
Publisher: ELSEVIER SCI LTDISSN: 1877-7821Frequency: 6 issues/year

Cancer Epidemiology, published by ELSEVIER SCI LTD, serves as a premier platform for disseminating innovative research in the areas of cancer epidemiology and oncology. Operating from the Netherlands, this journal provides a critical insight into the factors influencing cancer incidence, including genetic, environmental, and lifestyle variables. With an impact factor reflecting its significance in the field, it holds a respectable Q2 ranking in Cancer Research, Epidemiology, and Oncology. The journal spans a wide range of topics and publishes studies that aim to bridge gaps in existing literature through rigorous research methodologies. Researchers and professionals interested in acquiring the latest insights and contributing to the evolving discourse on cancer epidemiology will find this journal an invaluable resource. Access to articles may be available through open access options, ensuring the widest dissemination of knowledge.

GENOMICS

Exploring the Depths of Genomic Discovery
Publisher: ACADEMIC PRESS INC ELSEVIER SCIENCEISSN: 0888-7543Frequency: 6 issues/year

GENOMICS is a prestigious journal published by Academic Press Inc Elsevier Science, dedicated to advancing the field of genetic research and molecular biology. With an impressive impact factor, this journal is recognized for its rigorous peer-review process and high-quality publications that cover a wide range of topics within the genomics discipline. Operating from the United States, GENOMICS has established itself as a vital resource for researchers, professionals, and students alike, standing at Q2 in the Genetics category according to the latest rankings. With a rich history dating back to 1987 and convergence extending to 2024, the journal highlights cutting-edge discoveries and methodologies, ensuring that its readership remains at the forefront of genetic advancements. Although currently not an open-access journal, articles published within its pages are often accessible through various academic platforms, enhancing worldwide reach and dissemination. For those engaged in the fields of biochemistry, genetics, and molecular biology, GENOMICS serves as an indispensable platform for impactful research and collaborative initiatives.

Reports of Biochemistry and Molecular Biology

Unlocking the secrets of biochemical processes.
Publisher: VARASTEGAN INST MEDICAL SCIENCESISSN: 2322-3480Frequency: 2 issues/year

Reports of Biochemistry and Molecular Biology, published by VARASTEGAN INST MEDICAL SCIENCES, is a distinguished open access journal dedicated to advancing the fields of biochemistry and molecular biology. Since its inception in 2012, the journal has fostered a platform for researchers and professionals to disseminate their findings, contributing to a richer understanding of biochemical processes and molecular mechanisms. With a focus on innovative research and technology, the journal has established itself as a significant resource within its field, being classified in the Q3 category for Biochemistry and Molecular Biology by 2023. Notably, it has achieved respectable Scopus rankings, including a rank of #40/72 in Biochemistry (medical) as well as a common ground across multiple related categories. The journal’s commitment to open access ensures that its valuable content is freely available to the global scientific community, facilitating knowledge sharing among students, researchers, and professionals alike. Located in Mashhad, Iran, Reports of Biochemistry and Molecular Biology serves as a bridge between cutting-edge research and practical applications in the biochemistry and molecular biology domains.

FOLIA BIOLOGICA

Nurturing Scholarly Dialogue in Molecular Biology
Publisher: CHARLES UNIV PRAGUE, FIRST FACULTY MEDICINEISSN: 0015-5500Frequency: 6 issues/year

FOLIA BIOLOGICA, published by Charles University Prague, First Faculty of Medicine, is an esteemed academic journal that has been contributing to the fields of Biochemistry, Cell Biology, Developmental Biology, Genetics, Immunology, and Molecular Biology since its inception in 1961. With an ISSN of 0015-5500, this journal serves as a vital platform for researchers and professionals to disseminate their findings and advance knowledge within these disciplines. Despite its current Category Quartiles ranking in the lower tiers (Q3 and Q4), FOLIA BIOLOGICA continues to provide valued insights and foster scholarly dialogue, particularly in its paralleled fields. The journal is headquartered in Prague, Czech Republic, and operates without Open Access options, which emphasizes its focus on curated, peer-reviewed content essential for academicians and students. By bridging theoretical and practical knowledge, FOLIA BIOLOGICA remains committed to enriching the scientific community and serving as a cornerstone for future research innovations.

Human Genomics

Empowering Research in Health and Disease
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.