BMC Medical Genomics

Scope & Guideline

Exploring the Genetic Blueprint of Disease and Treatment

Introduction

Delve into the academic richness of BMC Medical Genomics 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
ISSN-
PublisherBMC
Support Open AccessNo
Country-
Type-
Converge-
AbbreviationBMC MED GENOMICS / BMC Med. Genomics
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

BMC Medical Genomics focuses on advancing the understanding of genomic medicine through comprehensive analyses of genetic and genomic data across various medical conditions. The journal aims to publish high-quality research that employs cutting-edge methodologies to explore the genetic underpinnings of diseases, with a strong emphasis on translational applications in clinical settings.
  1. Genetic and Genomic Analysis:
    The journal emphasizes studies that utilize genetic and genomic analysis, including whole-exome sequencing and genome-wide association studies (GWAS), to identify variants associated with diseases.
  2. Bioinformatics and Computational Biology:
    BMC Medical Genomics publishes papers that apply bioinformatics and computational biology methods for analyzing large genomic datasets, facilitating the identification of key biomarkers and therapeutic targets.
  3. Translational Research:
    Research that bridges the gap between laboratory findings and clinical applications is a core focus, aiming at improving diagnostics, prognostics, and treatment strategies based on genomic insights.
  4. Molecular Mechanisms of Disease:
    The journal covers studies investigating the molecular mechanisms underlying various diseases, including cancer, genetic disorders, and metabolic diseases, highlighting how genetic variations impact disease pathology.
  5. Personalized Medicine:
    A strong emphasis is placed on research that contributes to the field of personalized medicine, utilizing genomic data to tailor medical treatment to individual patients.
BMC Medical Genomics has witnessed a surge in interest in several emerging themes that reflect the evolving landscape of genomic research. These trends highlight the journal's commitment to addressing contemporary challenges in genomics and medicine.
  1. Machine Learning Applications in Genomics:
    There is an increasing trend in the application of machine learning techniques to analyze genomic data, aiming to enhance predictive modeling and improve understanding of complex diseases.
  2. Long Non-Coding RNAs (lncRNAs):
    Research focusing on lncRNAs and their roles in gene regulation and disease mechanisms is gaining traction, reflecting a broader recognition of their importance in genomics.
  3. Integration of Multi-Omics Data:
    Studies that integrate genomic, transcriptomic, proteomic, and metabolomic data are on the rise, enabling a more comprehensive understanding of biological processes and disease pathways.
  4. Genomic Medicine and Personalized Healthcare:
    There is a growing emphasis on research that directly contributes to genomic medicine and personalized healthcare, focusing on how genomic insights can guide treatment decisions and patient management.
  5. Immunogenomics:
    Research exploring the interactions between the immune system and genetic factors, particularly in the context of cancer immunotherapy and autoimmune diseases, is increasingly prominent.

Declining or Waning

While BMC Medical Genomics continues to thrive in various research areas, certain themes have shown signs of declining prominence in recent years. This may reflect shifts in research focus or advancements in methodologies that render previous approaches less relevant.
  1. Traditional Genetic Mapping:
    Research focused solely on traditional genetic mapping techniques has decreased as more advanced methodologies, such as next-generation sequencing and whole-genome sequencing, become prevalent.
  2. Cohort Studies with Limited Genomic Insight:
    Papers that present cohort studies without substantial genomic analysis or insights into genetic variants are less frequently published, as the field moves towards more integrative approaches.
  3. Single-Locus Studies:
    There is a waning interest in studies that focus on single-locus associations, as multi-locus and polygenic approaches are increasingly favored for their ability to capture complex genetic interactions.
  4. General Population Studies:
    Research that addresses genetic factors in general populations without a specific focus on clinical applications or translational impact has seen a decline, reflecting a shift towards more targeted and clinically relevant investigations.

Similar Journals

CURRENT GENOMICS

Unraveling the complexities of genomics for a healthier future.
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.

BMC Genomic Data

Shaping the future of genomic data dissemination.
Publisher: BMCISSN: Frequency: 1 issue/year

BMC Genomic Data is a pioneering open-access journal dedicated to the dynamic field of genomics and health informatics, published by BMC, a renowned leader in scientific publishing based in the United Kingdom. Since its inception in 2021, the journal has established itself as a valuable resource for researchers, professionals, and students, providing a platform for the dissemination of high-quality genomic data research. With a focus on advancing knowledge in both genetics and health informatics, BMC Genomic Data holds a Q3 ranking in both categories as of 2023, indicating its growing influence and relevance in the scientific community. The journal has an impressive entry into the competitive landscape of academia, ranking #55 in the Medicine & Health Informatics category and #173 in Biochemistry, Genetics and Molecular Biology, reflecting its commitment to publishing impactful research. By offering an open-access model, researchers are encouraged to disseminate their findings widely, contributing to the ongoing dialogue in genomics. For those looking to stay at the forefront of genomic research and data analysis, BMC Genomic Data is an essential resource that promotes innovation and collaboration across disciplines.

Genome Medicine

Fostering Collaboration for Genomic Breakthroughs
Publisher: BMCISSN: 1756-994XFrequency: 1 issue/year

Genome Medicine is a prestigious, peer-reviewed journal published by BMC, focusing on the rapidly evolving fields of genetics, molecular biology, and molecular medicine. Established in 2009 and boasting an open-access format, it has become a leading platform for disseminating high-quality research findings that advance our understanding of genetic diseases and therapeutic innovations. With an impressive Q1 ranking across multiple relevant categories—in particular, genetics (clinical), molecular biology, and molecular medicine—this journal is recognized for its substantial impact in the academic community, as evidenced by its exceptional placement in Scopus rankings. By providing unrestricted access to groundbreaking studies, Genome Medicine fosters collaboration and knowledge sharing among researchers, clinicians, and educators, thus playing a vital role in the transition from fundamental genetic research to clinical applications. Researchers are encouraged to contribute their findings and insights, further solidifying the journal’s position as a pivotal resource for those dedicated to advancing genomic medicine.

Frontiers in Genetics

Exploring Genetic Horizons Together
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.

Current Genetic Medicine Reports

Elevating Standards in Genetic Medicine Reporting
Publisher: SPRINGERNATUREISSN: Frequency: 4 issues/year

Current Genetic Medicine Reports, published by SPRINGERNATURE, is a prominent journal dedicated to advancing the field of genetic medicine. With an emphasis on the latest research and advancements, this journal serves as a critical platform for disseminating high-quality original articles, reviews, and reports that focus on the application of genetic information in various medical disciplines. As an open-access journal, it ensures that valuable findings are freely accessible to a global audience, thereby fostering collaboration and innovation among researchers, healthcare professionals, and students alike. Although the journal does not yet have an established impact factor, its commitment to rigorous peer review and its contributions to the understanding and integration of genetic medicine into clinical practice enhance its scholarly significance. The editorial board is comprised of leading experts, encouraging submissions that tackle contemporary issues in genetic research and its clinical applications. Located in London, England, this journal is poised to be a vital resource for those seeking to stay abreast of the rapid changes in the dynamic field of genetic medicine.

GENOME BIOLOGY

Pioneering discoveries in genomics and bioinformatics.
Publisher: BMCISSN: 1474-760XFrequency: 1 issue/year

GENOME BIOLOGY is a premier, peer-reviewed journal published by BMC, focusing on the rapidly evolving fields of genomics, molecular biology, and bioinformatics. Accessible as an Open Access journal since 2000, it aims to disseminate high-quality, cutting-edge research that contributes to our understanding of genome biology's intricate mechanisms. The journal boasts an impressive impact, ranking 8th in Agricultural and Biological Sciences and 9th in Biochemistry, Genetics and Molecular Biology, highlighting its significance among scholars, professionals, and students alike. With a commitment to facilitating the exchange of invaluable scientific knowledge, GENOME BIOLOGY provides an important platform for discussions on evolutionary biology, genetic systems, and cell biology, contributing to the advancement of these dynamic disciplines.

Human Genomics

Shaping the Future of Molecular Biology and Medicine
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.

Molecular Genetics & Genomic Medicine

Transforming discoveries into clinical applications.
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.

ANIMAL GENETICS

Shaping the Future of Animal Science and Conservation
Publisher: WILEYISSN: 0268-9146Frequency: 6 issues/year

ANIMAL GENETICS, published by WILEY, is a leading journal in the fields of Animal Science and Zoology, with a commendable Q1 classification for 2023, reflecting its critical role in advancing research and knowledge in animal genetics. Established in 1986, this journal has become a cornerstone for professionals, researchers, and students alike, providing a platform for innovative research that explores the genetic underpinnings of animal biology. With an ISSN of 0268-9146 and an E-ISSN of 1365-2052, it boasts a significant impact in both agricultural and biological sciences, as indicated by its ranking of #74 out of 490 in its category on Scopus, positioning it in the 85th percentile for Animal Science and Zoology. Readers can access high-quality, peer-reviewed articles that not only illuminate current advancements but also foster future research directions. While currently not an open access journal, ANIMAL GENETICS remains vital for anyone engaged in the exploration of genetics and its applications in medicine and beyond, with a continual commitment to publishing findings that shape the future of animal breeding, conservation, and genetics research.

Global Medical Genetics

Bridging the Gap Between Genetics and Clinical Practice
Publisher: GEORG THIEME VERLAG KGISSN: 2699-9404Frequency: 4 issues/year

Global Medical Genetics is a premier open-access journal dedicated to advancing the field of medical genetics. Published by GEORG THIEME VERLAG KG, this journal has been providing a dynamic platform for disseminating cutting-edge research and clinical findings since its inception in 2020. With the ISSN 2699-9404, it serves as an essential resource for researchers, healthcare professionals, and students who seek to explore the complex interplay between genetics and medicine. The journal aims to foster collaboration and innovation in the genetics community, addressing a diverse range of topics from genetic disorders to the application of genomics in personalized medicine. By providing open access to its content, Global Medical Genetics enhances knowledge sharing and accelerates advancements in healthcare, making it a vital asset for anyone invested in the future of genetics.