Genome Medicine

Scope & Guideline

Pioneering Innovations in Genomic Medicine

Introduction

Welcome to the Genome Medicine information hub, where our guidelines provide a wealth of knowledge about the journal’s focus and academic contributions. This page includes an extensive look at the aims and scope of Genome Medicine, highlighting trending and emerging areas of study. We also examine declining topics to offer insight into academic interest shifts. Our curated list of highly cited topics and recent publications is part of our effort to guide scholars, using these guidelines to stay ahead in their research endeavors.
LanguageEnglish
ISSN1756-994x
PublisherBMC
Support Open AccessYes
CountryUnited Kingdom
TypeJournal
Convergefrom 2009 to 2024
AbbreviationGENOME MED / Genome Med.
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

Genome Medicine is dedicated to advancing the integration of genomic and molecular data into clinical practice and public health. The journal emphasizes innovative research that bridges the gap between laboratory findings and their application in medicine, particularly focusing on the implications of genomic research in understanding disease mechanisms, diagnostics, and therapeutic strategies.
  1. Genomic Medicine and Diagnostics:
    The journal highlights research that explores the role of genomic information in diagnosing various diseases, including rare genetic disorders and cancers, emphasizing the clinical utility of whole genome sequencing and targeted genetic testing.
  2. Precision Medicine and Therapeutics:
    A core focus is on the development of precision medicine approaches, including the identification of genetic variants that influence treatment responses and the exploration of personalized therapeutic strategies based on genomic data.
  3. Public Health Genomics:
    Research addressing the implications of genomics in public health, including the genetic epidemiology of diseases and the role of genomics in infectious disease surveillance and control.
  4. Multi-Omics Integration:
    The journal promotes studies that utilize multi-omics approaches (genomics, transcriptomics, proteomics, metabolomics) to provide a comprehensive understanding of disease mechanisms and treatment responses.
  5. Ethics and Policy in Genomics:
    Genome Medicine also considers the ethical implications and policy issues surrounding genetic research and its application in clinical settings, including data sharing and patient consent.
Recent publications in Genome Medicine reflect evolving trends and emerging themes that are shaping the future of genomic research and its application in medicine. These trends highlight the journal's responsiveness to current scientific needs and societal challenges.
  1. Integration of AI and Machine Learning:
    There is a rising trend in the application of artificial intelligence and machine learning techniques to enhance genomic analysis, improve diagnostic accuracy, and predict treatment responses, showcasing the intersection of technology and genomics.
  2. Focus on Health Disparities and Ancestry:
    Recent studies increasingly address genetic diversity and health disparities among different populations, emphasizing the importance of considering ancestry in genomic research and clinical applications.
  3. Microbiome Research in Disease Contexts:
    The exploration of the human microbiome's role in health and disease is gaining traction, with studies linking microbiome profiles to various conditions, including cancer and metabolic disorders.
  4. Liquid Biopsy and Non-Invasive Testing:
    Emerging research focuses on non-invasive techniques, such as liquid biopsies, for cancer detection and monitoring, reflecting a shift towards more patient-friendly diagnostic methods.
  5. Spatial and Single-Cell Omics:
    Advancements in spatial transcriptomics and single-cell genomics are becoming prominent, enabling researchers to explore cellular heterogeneity and the tumor microenvironment in unprecedented detail.

Declining or Waning

While Genome Medicine continues to evolve and adapt to emerging research areas, certain themes have seen a decline in prominence over recent years. These waning scopes reflect shifts in research focus and funding priorities in the field of genomics and medicine.
  1. Traditional Genetic Association Studies:
    The journal has seen a decrease in papers focused solely on traditional genetic association studies without integrating genomic data with other omics or clinical features. This shift indicates a move towards more comprehensive approaches that incorporate multiple layers of biological data.
  2. Single-Method Approaches:
    There is a noticeable decline in the publication of studies relying on single-method approaches, such as single-nucleotide polymorphism (SNP) analyses, as researchers increasingly favor integrative techniques that combine various methodologies for richer insights.
  3. Basic Science Without Clinical Relevance:
    Research that lacks direct implications for clinical practice or public health has become less common, suggesting a growing expectation for studies to demonstrate translational potential.

Similar Journals

Asian Biomedicine

Championing Cutting-edge Research in Medicine
Publisher: WALTER DE GRUYTER GMBHISSN: 1905-7415Frequency: 6 issues/year

Asian Biomedicine, published by WALTER DE GRUYTER GMBH, serves as a crucial platform for disseminating pioneering research in the field of biomedical sciences. Established in 2008, this journal has carved its niche in the landscape of academic publishing, concentrating on a diverse array of topics within biochemistry, genetics, and molecular biology, as well as medicine. Though it currently holds a Q4 ranking in its category, it is dedicated to fostering academic discussions and advancing knowledge among researchers, professionals, and students alike. While the journal features a variety of access options, it is committed to ensuring that its content remains relevant and impactful, with an emphasis on the latest developments and research trends. The editorial board encourages submissions that address pressing biomedical issues, thus empowering contributors to engage meaningfully with the scientific community. With a broad international scope and a focus on quality, Asian Biomedicine is poised to play an increasingly important role in the advancement of biomedical research in Asia and beyond.

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.

EUROPEAN JOURNAL OF HUMAN GENETICS

Fostering Collaboration in Human Genetic Studies
Publisher: SPRINGERNATUREISSN: 1018-4813Frequency: 12 issues/year

The EUROPEAN JOURNAL OF HUMAN GENETICS, published by SpringerNature, stands as a preeminent platform in the field of genetics and clinical genetics. Established in 1993, this prestigious journal, with an ISSN of 1018-4813 and an E-ISSN of 1476-5438, has consistently maintained its position in the Q1 quartile for both Genetics and Clinical Genetics categories as of 2023, reflecting its significant contributions to the field. Its impact is further underscored by its impressive Scopus rankings, placing it in the 92nd percentile among clinical genetics journals. The journal aims to disseminate cutting-edge research, case studies, and reviews that advance our understanding of human genetics, promoting collaboration and innovation among researchers, professionals, and students alike. While it does not currently offer open access, the journal provides substantial value through its rigorous peer review process and commitment to quality. As it continues to shape the future of genetic research through 2024 and beyond, the EUROPEAN JOURNAL OF HUMAN GENETICS remains an essential resource for those dedicated to exploring the complexities of human heredity.

Byulleten Sibirskoy Meditsiny

Connecting Innovators in Biomedical Sciences
Publisher: SIBERIAN STATE MEDICAL UNIVISSN: 1682-0363Frequency: 6 issues/year

Byulleten Sibirskoy Meditsiny, published by the Siberian State Medical University, is a pivotal open-access journal in the field of Molecular Medicine, with its current edition indexed under the ISSN 1682-0363. Since its transition to open access in 2013, the journal aims to disseminate high-quality research and advancements in biomedical sciences, particularly focusing on molecular mechanisms and therapeutic interventions. Despite its relatively recent recognition in Molecular Medicine, where it ranks in the 6th percentile, the journal is dedicated to fostering knowledge exchange and collaboration among researchers, professionals, and students alike. With a modest impact factor and quarterly publication, Byulleten Sibirskoy Meditsiny is positioned to serve as a valuable resource for those engaged in the intricate realms of molecular biology, biochemistry, and general medicine, contributing to the broader scientific discourse in the Russian Federation and beyond.

Frontiers in Genetics

Transforming Genetic Discoveries into Solutions
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.

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.

INTERNATIONAL JOURNAL OF HUMAN GENETICS

Bridging Gaps in Human Genetic Understanding
Publisher: KAMLA-RAJ ENTERPRISESISSN: 0972-3757Frequency: 4 issues/year

INTERNATIONAL JOURNAL OF HUMAN GENETICS is a distinguished publication dedicated to advancing knowledge in the fields of genetics and molecular biology. Published by KAMLA-RAJ ENTERPRISES, this journal explores critical developments and research findings from 2008 to 2016, though its coverage in Scopus has since been discontinued. With an ISSN of 0972-3757 and an E-ISSN of 2456-6330, the journal aimed to foster scholarly dialogue and serve as a resource for researchers, professionals, and students engaged in human genetics. While the journal holds a modest ranking in categories such as Biochemistry and Genetics, it remains a vital source for exploring niche topics within the realm of human genetics. Researchers interested in genetic screening, gene therapy, and clinical genetics will find valuable insights herein. Despite its pause in indexing, the journal continues to contribute to the academic discourse by disseminating critical research that bridges gaps in understanding human genetics.

Biomedical Reports

Connecting disciplines to unlock biomedical breakthroughs.
Publisher: SPANDIDOS PUBL LTDISSN: 2049-9434Frequency: 6 issues/year

Biomedical Reports, published by SPANDIDOS PUBL LTD in Greece, is a distinguished open-access journal that focuses on the dynamic fields of biochemistry, genetics, molecular biology, medicine, pharmacology, and neuroscience. Established in 2014, the journal has rapidly gained recognition, securing Q2 and Q3 rankings in several categories for 2023, including a notable ranking of #125/636 in General Medicine, placing it in the 80th percentile amongst its peers. The journal continually aims to disseminate innovative research findings that advance the understanding of complex biomedical issues, making it an invaluable resource for researchers, professionals, and students alike. Its multidisciplinary approach not only reflects the interconnectivity of modern biomedical sciences but also promotes collaborative discourse among diverse fields, ensuring ongoing relevance and impact within the scientific community.

Precision Clinical Medicine

Shaping tomorrow's healthcare, today.
Publisher: OXFORD UNIV PRESSISSN: 2096-5303Frequency: 4 issues/year

Precision Clinical Medicine, published by Oxford University Press, is an esteemed open-access journal that has been at the forefront of clinical research since its inception in 2018. With an ISSN of 2096-5303, this journal specializes in the rapidly evolving field of precision medicine, which aims to tailor healthcare to individual patient characteristics, needs, and preferences. As a testament to its influence, Precision Clinical Medicine holds a remarkable rank of #34 out of 636 in the General Medicine category on Scopus, placing it within the 94th percentile of its field and earning a prestigious Q1 rating in 2023. Based in the United Kingdom, the journal not only provides open access content, ensuring that groundbreaking research is widely disseminated, but also serves as a crucial platform for innovations and discussions that shape modern medical practices. Researchers, professionals, and students alike will find valuable insights and influential studies that drive the future of personalized healthcare within its pages.

TRENDS IN MOLECULAR MEDICINE

Catalyzing Research in Molecular Medicine
Publisher: CELL PRESSISSN: 1471-4914Frequency: 12 issues/year

TRENDS IN MOLECULAR MEDICINE, published by CELL PRESS, is a premier journal that stands at the forefront of the rapidly evolving fields of molecular biology and molecular medicine. With a distinguished Q1 ranking in both categories and an impressive Scopus standing—ranked #12 out of 410 in Molecular Biology and #6 out of 178 in Molecular Medicine—this journal is a vital source of high-impact research and insights for researchers, professionals, and students alike. The journal, which has been published consistently since 2000, promotes the dissemination of groundbreaking discoveries that bridge the gap between molecular biology and therapeutic applications. Furthermore, TRENDS IN MOLECULAR MEDICINE embraces modern accessibility options, engaging a global audience eager to explore pioneering advancements in human health. Set against the backdrop of the United Kingdom, this esteemed publication not only informs but also inspires ongoing research and innovation in molecular sciences, making it an essential resource for those shaping the future of medicine.