GENETIC EPIDEMIOLOGY

Scope & Guideline

Connecting Genetic Discoveries to Public Health Solutions

Introduction

Delve into the academic richness of GENETIC EPIDEMIOLOGY 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
ISSN0741-0395
PublisherWILEY
Support Open AccessNo
CountryUnited States
TypeJournal
Convergefrom 1984 to 2024
AbbreviationGENET EPIDEMIOL / Genet. Epidemiol.
Frequency8 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
Address111 RIVER ST, HOBOKEN 07030-5774, NJ

Aims and Scopes

The journal 'Genetic Epidemiology' aims to bridge the gap between genetics and epidemiology, focusing on the genetic determinants of health and disease across populations. It emphasizes the integration of genetic data with epidemiological methods to enhance our understanding of disease etiology, risk factors, and the interplay between genetic and environmental influences.
  1. Genetic Association Studies:
    The journal publishes research on genetic association studies that identify genetic variants associated with various diseases and traits, often utilizing genome-wide association studies (GWAS) to explore genetic risk factors.
  2. Mendelian Randomization:
    A significant focus is placed on Mendelian randomization techniques, which use genetic variants as instrumental variables to infer causal relationships between exposures (like lifestyle factors) and outcomes (such as diseases).
  3. Genetic Epidemiology of Complex Traits:
    Research in this area investigates the genetic architecture of complex traits, including polygenic risk scores, gene-environment interactions, and the heritability of traits across diverse populations.
  4. Integration of Multi-Omics Data:
    The journal emphasizes studies that integrate genetic data with other omics data (e.g., transcriptomics, proteomics) to gain a comprehensive understanding of biological pathways influencing health.
  5. Population Diversity and Genetics:
    Research that addresses genetic diversity among populations, including studies on admixed populations and transancestry analyses, is a core area, reflecting the journal's commitment to inclusivity in genetic research.
  6. Ethical, Legal, and Social Implications (ELSI):
    The journal also explores the ethical, legal, and social implications of genetic research, particularly in the context of gene-environment interactions and public health.
The journal has observed several emerging themes reflecting the evolving landscape of genetic epidemiology. These trends highlight the integration of advanced methodologies and interdisciplinary approaches to address complex health issues.
  1. Machine Learning and AI in Genetic Research:
    There is a growing trend towards utilizing machine learning and artificial intelligence techniques to analyze genetic data, enhance predictive models, and identify novel genetic associations.
  2. Gene-Environment Interactions:
    Research on gene-environment interactions is gaining prominence, reflecting an increased interest in understanding how environmental factors and genetic predispositions jointly influence health outcomes.
  3. Polygenic Risk Scores and Predictive Modeling:
    The development and application of polygenic risk scores for predicting disease risk across diverse populations are trending, enabling personalized medicine approaches.
  4. Integration of Genomic and Clinical Data:
    There is an emerging focus on integrating genomic data with electronic health records and biobanking resources to enhance the understanding of genetic underpinnings of diseases in real-world settings.
  5. Ethical Considerations in Genetic Research:
    Research addressing the ethical implications of genetic studies, particularly in diverse populations and regarding data privacy, is becoming increasingly relevant.
  6. Longitudinal and Multi-Omics Studies:
    There is a trend towards longitudinal studies that incorporate multi-omics data to uncover the dynamics of genetic influence over time, providing deeper insights into disease progression and risk.

Declining or Waning

While 'Genetic Epidemiology' continues to thrive in various research areas, certain themes appear to be declining in prominence. These waning scopes may reflect shifts in research focus or advancements in methodologies that render previous approaches less relevant.
  1. Traditional Statistical Methods:
    There seems to be a decline in the use of traditional statistical methods for genetic association analysis, as more sophisticated machine learning and Bayesian approaches gain traction.
  2. Single Phenotype Studies:
    Research focusing exclusively on single phenotypes is becoming less common, with a notable shift towards multi-phenotype analyses that capture the complexity of genetic interactions and their impact on health.
  3. Basic Genetic Mapping Techniques:
    Basic genetic mapping techniques are waning in favor of more advanced methods that incorporate multi-omics data and sophisticated computational frameworks, leading to a decrease in publications centered on conventional mapping.
  4. Clinical Trials Focused Solely on Genetic Factors:
    Studies that focus exclusively on the genetic factors of diseases without considering environmental or social determinants are less frequently published, indicating a broader understanding of health determinants.

Similar Journals

Genetics Research

Fostering Global Collaboration in Genetic Research
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.

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.

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.

PLoS Genetics

Connecting the dots in genetics for transformative research.
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.

JOURNAL OF MEDICAL GENETICS

Exploring the Intersection of Genetics and Medicine.
Publisher: BMJ PUBLISHING GROUPISSN: 0022-2593Frequency: 12 issues/year

JOURNAL OF MEDICAL GENETICS, published by the BMJ PUBLISHING GROUP, stands as a premier platform in the field of genetics, focusing on both fundamental genetic research and its clinical applications. With a distinctive legacy dating back to 1965 and a significant role in advancing the understanding of genetic disorders, this journal has established itself in the top tiers with a commendable Q1 category ranking in both Genetics and Clinical Genetics as of 2023. The journal's impact is underscored by its Scopus rankings, placing it among the leading journals in the fields of medicine and genetics. Researchers and practitioners are drawn to its rigorous peer-review process and its commitment to disseminating high-quality research findings, critical reviews, and innovative clinical practices. While it is not an open-access journal, the insights provided are invaluable for anyone looking to deepen their knowledge or contribute to the burgeoning field of medical genetics.

HUMAN HEREDITY

Pioneering Studies in Human Genetic Diversity
Publisher: KARGERISSN: 0001-5652Frequency: 4 issues/year

HUMAN HEREDITY is a peer-reviewed journal published by KARGER, dedicated to advancing the understanding of genetics and inherited traits in human populations. Established in 1950, this journal has become a vital resource for researchers, professionals, and students in the fields of genetics and clinical genetics, currently categorized in the third quartile (Q3) for both general and clinical genetics as of 2023. With an ISSN of 0001-5652, HUMAN HEREDITY provides rigorous academic content that analyzes heredity patterns and genetic variations, aiming to illuminate the complexities of human genetic inheritance. Although it does not operate on an open access model, the journal offers a comprehensive collection of studies and insights that are crucial for genetic research and clinical applications. Situated in Basel, Switzerland, HUMAN HEREDITY contributes to the global dialogue in genetics, making it an essential platform for those seeking to enrich their understanding of human heredity in a rapidly evolving scientific landscape.

Twin Research and Human Genetics

Pioneering Insights into Genetic Influences on Health and Behavior
Publisher: CAMBRIDGE UNIV PRESSISSN: 1832-4274Frequency: 6 issues/year

Twin Research and Human Genetics, published by Cambridge University Press, is a leading academic journal that focuses on the vital intersections of genetics, human development, and twin studies. With an ISSN of 1832-4274 and E-ISSN 1839-2628, this journal serves as a critical resource for researchers, healthcare professionals, and students interested in advancing their understanding of genetic influences on human health and behavior. In its dedication to disseminating high-quality research, Twin Research and Human Genetics holds impressive category quartile rankings, including Q2 in Pediatrics, Perinatology, and Child Health, and Q3 in both Genetics (Clinical) and Obstetrics and Gynecology as of 2023. The journal has a converged publication timeline from 2005 to 2024, providing a longstanding platform for rigorous scientific inquiry and discussion in its specialized fields. As an open-access title, it fosters accessibility to vital findings and promotes collaboration among scholars worldwide, ensuring that groundbreaking research reaches a broader audience. Positioned within a challenging and competitive landscape, this journal stands out for its commitment to excellence and its pivotal role in shaping the future of genetic research and its implications for health across the lifespan.

HUMAN MOLECULAR GENETICS

Exploring the genetic blueprint of health and disease.
Publisher: OXFORD UNIV PRESSISSN: 0964-6906Frequency: 26 issues/year

HUMAN MOLECULAR GENETICS, published by Oxford University Press, is a premier journal in the field of genetics, with an established reputation since its inception in 1992. With an impressive Q1 ranking in various categories, including Genetics, Clinical Genetics, and Molecular Biology, this journal engages a diverse readership by reporting significant advances in our understanding of the genetic basis of human health and disease. The journal has achieved notable rankings within Scopus, particularly in Clinical Genetics, making it a key resource for professionals and researchers aiming to stay at the forefront of genetic research. Although it operates under a traditional access model, it remains committed to disseminating high-quality research that informs clinical practice and enhances knowledge in the genetic field. The journal's impact factor signifies its crucial role in shaping contemporary genetic research and its application in medicine. As the field continues to evolve, HUMAN MOLECULAR GENETICS serves not only as an academic repository but also as a vital platform for innovation and discussion among students, researchers, and clinicians.

THEORETICAL AND APPLIED GENETICS

Connecting theoretical frameworks with practical solutions in genetics.
Publisher: SPRINGERISSN: 0040-5752Frequency: 12 issues/year

THEORETICAL AND APPLIED GENETICS, published by Springer, is a premier journal that has significantly contributed to the fields of Agronomy, Crop Science, Biotechnology, and Genetics since its inception in 1933. With a solid reputation reflected in its Q1 ranking across multiple disciplines for 2023, this journal provides a vital platform for the dissemination of high-quality research that advances our understanding of genetic principles and their applications in agriculture and biology. The journal's indexed status and high impact factor indicate its vital role in shaping contemporary genetic research, marking it as an essential resource for researchers, professionals, and students seeking to stay at the forefront of these dynamic fields. Although it currently does not offer Open Access options, the journal ensures that quality studies are accessible through institutional subscriptions, supporting an informed community of scientists dedicated to innovation in genetics and applied biological sciences.

GENETICS SELECTION EVOLUTION

Leading the Charge in Evolutionary Genetics Research
Publisher: BMCISSN: 0999-193XFrequency: 1 issue/year

GENETICS SELECTION EVOLUTION is a prominent open-access journal published by BMC since 1989, situated in the United Kingdom. With a focus on evolutionary genetics and the mechanisms of selection, this journal serves as a pivotal platform for researchers, professionals, and students in the fields of Animal Science, Ecology, and Genetics. Notably, it has achieved remarkable rankings, being categorized in Q1 for various disciplines, reflecting its high impact and contribution to scientific discourse. The journal boasts an impressive recognition in the Scopus rankings, sitting at the 94th percentile in Animal Science and Zoology, and 86th percentile in Ecology and Evolution, underscoring its influence in these domains. Offering open access since its inception, it ensures broad dissemination of knowledge, allowing critical research findings to reach a wider audience. As we converge into its upcoming issues, the journal continues to foster the exploration of innovative genetic research and selection processes, shaping the future of evolutionary studies.