Genetic Testing and Molecular Biomarkers

Scope & Guideline

Advancing the Future of Genetic Research.

Introduction

Welcome to your portal for understanding Genetic Testing and Molecular Biomarkers, 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
ISSN1945-0265
PublisherMARY ANN LIEBERT, INC
Support Open AccessNo
CountryUnited States
TypeJournal
Convergefrom 2009 to 2024
AbbreviationGENET TEST MOL BIOMA / Genet. Test. Mol. Biomark.
Frequency12 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
Address140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801

Aims and Scopes

The journal 'Genetic Testing and Molecular Biomarkers' primarily focuses on the integration of genetic testing technologies and molecular biomarkers in the context of disease diagnosis, treatment, and prognosis. It serves as a platform for disseminating research that bridges the gap between molecular genetics and clinical application.
  1. Genetic Testing Applications:
    The journal emphasizes various applications of genetic testing in clinical settings, including but not limited to, cancer genetics, hereditary diseases, and pharmacogenomics. It explores how genetic tests can inform treatment decisions and patient management.
  2. Molecular Biomarkers Discovery:
    A core area of focus is the identification and validation of molecular biomarkers that can serve as diagnostic, prognostic, or therapeutic targets in various diseases. This includes studies on gene expression, epigenetics, and non-coding RNAs.
  3. Population Genetics and Ethnic Variability:
    Research addressing genetic diversity across different populations is a prominent theme. The journal publishes studies that investigate genetic polymorphisms and their implications for disease susceptibility and treatment responses in diverse ethnic groups.
  4. Innovative Methodologies in Genetic Research:
    The journal highlights advancements in genetic research methodologies, including next-generation sequencing, CRISPR technology, and bioinformatics tools, which enhance the understanding of genetic contributions to diseases.
  5. Clinical Implications and Ethical Considerations:
    A unique contribution of this journal is its exploration of the clinical implications of genetic testing and biomarkers, including discussions on ethical, legal, and social implications (ELSI) surrounding genetic research and testing.
The journal reflects the evolving landscape of genetic testing and molecular biomarkers, with several emerging themes gaining traction in recent publications. These trends indicate a shift towards more complex and integrated approaches to genetics in medicine.
  1. Integrative Genomics and Multi-Omics Approaches:
    Recent studies are increasingly utilizing integrative genomic methods, combining data from genomics, transcriptomics, and proteomics to provide a more holistic understanding of disease mechanisms and therapeutic targets.
  2. Liquid Biopsy and Non-Invasive Diagnostics:
    There is a growing emphasis on liquid biopsy techniques for cancer diagnostics, which allow for non-invasive collection of biomarkers from body fluids, enhancing patient comfort and accessibility to testing.
  3. Role of Non-Coding RNAs:
    The investigation of non-coding RNAs, such as microRNAs and long non-coding RNAs, as potential biomarkers and therapeutic targets is emerging as a hot topic, reflecting their significant role in gene regulation and disease progression.
  4. Pharmacogenomics and Personalized Medicine:
    An increasing number of studies focus on pharmacogenomics, which examines how genetic variations affect individual responses to drugs, paving the way for personalized medicine approaches that optimize treatment efficacy and minimize adverse effects.
  5. Ethical and Social Implications of Genetic Testing:
    There is a noticeable rise in publications addressing the ethical, legal, and social implications of genetic testing and biomarker discovery, emphasizing the importance of responsible practices in genetic research.

Declining or Waning

While the journal continues to thrive in many research areas, certain themes are witnessing a decline in prominence. This shift may reflect changing research priorities or advancements in technology that render some topics less relevant.
  1. Traditional Genetic Screening Methods:
    There is a noticeable decline in studies focusing on conventional genetic screening methods, as newer technologies such as whole-genome sequencing and advanced bioinformatics approaches gain favor.
  2. Single Gene Studies:
    Research concentrating solely on single-gene mutations or polymorphisms is becoming less frequent. The trend is moving towards more comprehensive studies that consider multiple genes and their interactions, reflecting a shift to systems biology.
  3. Invasive Diagnostic Techniques:
    The journal has seen fewer publications related to invasive diagnostic techniques, such as tissue biopsies, as non-invasive methods like liquid biopsy and other biomarker-based diagnostics become more prevalent.
  4. Generalized Cancer Genetics:
    There seems to be a waning interest in generalized studies of cancer genetics without a specific focus on molecular pathways or targeted therapies. The emphasis is now on personalized medicine approaches that cater to specific patient subgroups.

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