MAMMALIAN GENOME

Scope & Guideline

Pioneering research in mammalian evolutionary genetics.

Introduction

Welcome to the MAMMALIAN GENOME 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 MAMMALIAN GENOME, 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
ISSN0938-8990
PublisherSPRINGER
Support Open AccessNo
CountryUnited States
TypeJournal
Convergefrom 1991 to 2024
AbbreviationMAMM GENOME / Mamm. Genome
Frequency12 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressONE NEW YORK PLAZA, SUITE 4600 , NEW YORK, NY 10004, UNITED STATES

Aims and Scopes

The journal 'Mammalian Genome' focuses on the genetic and genomic research of mammals, with an emphasis on providing insights into mammalian evolution, development, and disease mechanisms. It serves as a platform for the dissemination of novel findings related to mammalian genetics, resources, and methodologies.
  1. Mammalian Genetics and Genomics:
    The journal covers a wide range of topics related to the genetics of various mammalian species, including the identification of genetic variants, genomic mapping, and the role of specific genes in health and disease.
  2. Model Organisms and Disease Models:
    A significant focus is placed on the use of mouse models and other mammalian species to explore disease mechanisms, develop therapeutic strategies, and understand genetic disorders.
  3. Comparative Genomics:
    Research that compares genomes across different mammalian species to uncover evolutionary relationships and functional conservation is a key area of interest.
  4. Functional Genomics and Phenotyping:
    The journal includes studies on high-throughput phenotyping, transcriptomic analyses, and the functional characterization of genes and non-coding RNAs.
  5. Resource Development:
    Mammalian Genome serves as a hub for the development and sharing of genomic resources, including databases, biobanks, and repositories for mutant and genetically altered mouse models.
The journal has been adapting to the evolving landscape of mammalian genetics and genomics, highlighting several emerging themes that reflect current research trends and technological advancements.
  1. Network Medicine Approaches:
    There is an increasing interest in network medicine, which integrates genomic data with other biological and clinical information to identify disease mechanisms and potential therapeutic targets.
  2. Epigenetics and Non-Coding RNAs:
    Research on epigenetic modifications and the role of non-coding RNAs in gene regulation and disease is gaining traction, indicating a shift towards understanding complex regulatory networks.
  3. Systems Biology and Integrative Genomics:
    Emerging themes include systems biology approaches that combine genomic, transcriptomic, and phenotypic data to provide comprehensive insights into mammalian biology.
  4. High-Throughput Genomic Technologies:
    The utilization of advanced genomic technologies such as CRISPR, whole-genome sequencing, and high-throughput phenotyping is on the rise, facilitating deeper exploration of genetic functions and interactions.
  5. Comparative and Evolutionary Genomics:
    There is a growing trend towards comparative genomics that seeks to understand evolutionary relationships and functional conservation across species, particularly in relation to disease susceptibility.

Declining or Waning

While the journal continues to advance in various areas, some themes have seen a decline in prominence over recent years. This may indicate a shift in research focus or the maturation of certain fields.
  1. Microbiome Studies:
    Research specifically focused on the gut microbiome in relation to mammalian health and disease appears to have diminished, possibly as the field has matured or integrated into broader studies of mammalian biology.
  2. Basic Gene Expression Studies:
    There is a noticeable decline in papers focusing solely on basic gene expression without the context of functional or disease-related studies, indicating a shift towards more applied genetic research.
  3. Traditional Phenotyping Methods:
    Papers that rely on traditional, lower-throughput phenotyping techniques seem to be less frequent, as the field moves towards high-throughput and integrated approaches.
  4. Single Species Studies:
    Research focusing exclusively on a single mammalian species, particularly those that do not contribute to translational insights or comparative analysis, has been less common, reflecting a trend towards more comparative and integrative studies.

Similar Journals

npj Genomic Medicine

Bridging Science and Healthcare through Genomics
Publisher: NATURE PORTFOLIOISSN: Frequency: 1 issue/year

npj Genomic Medicine is a leading open-access journal published by NATURE PORTFOLIO, specializing in the rapidly evolving areas of genomic medicine, including genetics, molecular biology, and clinical applications. Launched in 2016, the journal has quickly established itself within the academic community, boasting a prestigious Q1 ranking in multiple categories, including Genetics and Molecular Biology, with remarkable positions in both Scopus ranks and percentiles. With an emphasis on innovative genomic research that bridges the gap between laboratory findings and clinical implementation, npj Genomic Medicine aims to provide a platform for researchers, professionals, and students to share significant advancements and insights. Being an open-access journal enhances accessibility to cutting-edge research, ensuring that vital discoveries in genomics can benefit a global audience and facilitate interdisciplinary collaboration. The journal continues to contribute to the forefront of genomic research, impacting both academic scholarship and practical healthcare solutions.

CYTOGENETIC AND GENOME RESEARCH

Empowering discoveries in clinical genetics through open access.
Publisher: KARGERISSN: 1424-8581Frequency: 12 issues/year

CYTOGENETIC AND GENOME RESEARCH is a pivotal journal dedicated to the exploration of cytogenetics, genomics, and their applications within clinical genetics and molecular biology. Published by KARGER in Switzerland, this journal aims to foster comprehensive discussions and disseminate impactful research from diverse fields related to genetics. It operates under an open access model, ensuring that researchers, professionals, and students can easily access and contribute to the latest findings. With coverage spanning from 1962 to 2024, CYTOGENETIC AND GENOME RESEARCH continues to serve as a vital resource, despite its current categorization in the Q4 quartile across Genetics and Molecular Biology. It provides an avenue for advancing the understanding of genomic mechanisms and their implications for human health. The journal encourages submissions that delve into cutting-edge methodologies, data interpretation, and theoretical frameworks, thereby playing a crucial role in the advancement of genetic research and its clinical applications.

JOURNAL OF MAMMALIAN EVOLUTION

Innovating Understanding in Mammalian Ecology and Behavior
Publisher: SPRINGERISSN: 1064-7554Frequency: 4 issues/year

JOURNAL OF MAMMALIAN EVOLUTION, published by SPRINGER, stands at the forefront of the field of mammalian evolutionary research since its inception in 1993. Renowned for its scholarly rigor, this journal covers an extensive range of topics within ecology, evolution, behavior, and systematics, achieving a prestigious Q1 rank in its category, according to the latest metrics. With an ISSN of 1064-7554 and E-ISSN of 1573-7055, it offers critical insights into the diverse adaptations and evolutionary processes of mammals, making it an invaluable resource for researchers, professionals, and students alike. The journal maintains a significant impact factor, reflecting its relevance in shaping current discourse and discoveries within the biological sciences, particularly in mammalogy. Access to its rich repository of articles aids in fostering scientific collaborations and advancing knowledge in the evolutionary sciences, thus solidifying its role as a critical platform for cutting-edge research.

GENETICS AND MOLECULAR BIOLOGY

Bridging theory and practice in genetic science.
Publisher: SOC BRASIL GENETICAISSN: 1415-4757Frequency: 4 issues/year

GENETICS AND MOLECULAR BIOLOGY, published by the SOC BRASIL GENETICA, is a prominent journal dedicated to the advancement of knowledge in the fields of genetics and molecular biology. Since its inception in 1998, this Open Access journal has served as a vital platform for researchers, professionals, and students to disseminate their findings and engage with the latest innovations and discoveries. With an impact factor that reflects its growing influence, GENETICS AND MOLECULAR BIOLOGY ranks in the Q3 category for both genetics and molecular biology as of 2023, indicating its position within the academic community. The journal is indexed in Scopus, highlighting its commitment to maintaining rigorous peer-review standards while providing wide-reaching access to quality research. Operating out of Ribeirão Preto, Brazil, it fosters a collaborative environment for academic discourse and research development not only in Brazil but also globally. The journal encourages submissions that explore a wide range of topics in genetics and molecular biology, making it an essential resource for anyone involved in these dynamic fields.

Genome Medicine

Unlocking the Secrets of Genetic Disorders
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.

DNA RESEARCH

Unveiling the secrets of genetics, one article at a time.
Publisher: OXFORD UNIV PRESSISSN: 1340-2838Frequency: 6 issues/year

DNA RESEARCH is a pioneering open-access journal published by Oxford University Press, dedicated to advancing the field of genetics and molecular biology. Since its inception in 1994, the journal has been at the forefront of scientific innovation, providing a global platform for researchers to publish high-quality findings that drive the understanding of DNA and its implications in medicine. With an impactful presence characterized by a Q2 ranking in Genetics, a Q1 ranking in Medicine (miscellaneous), and a Q2 ranking in Molecular Biology as per the latest 2023 assessments, DNA RESEARCH stands as a vital resource for both established scholars and emerging scientists. The journal's diverse range of articles caters to a wide audience, fostering collaboration and the sharing of knowledge. Researchers, professionals, and students alike will find an abundance of cutting-edge research and insights that can inform their work and further their understanding of this critical scientific domain. For more information and to access articles, visit the journal's website at Oxford University Press.

Genes & Genomics

Connecting Researchers with Cutting-Edge Genetic Discoveries
Publisher: SPRINGERISSN: 1976-9571Frequency: 6 issues/year

Genes & Genomics is a prominent academic journal dedicated to the fields of biochemistry, genetics, and molecular biology, published by Springer from South Korea. With an evolving focus on innovative genetic research and its implications, this journal serves as a crucial platform for disseminating knowledge within the scientific community. The journal has been indexed in Scopus and boasts a Q3 quartile ranking in 2023 for its contributions to these disciplines, highlighting its relevance and growing impact. In addition to traditional subscription options, Genes & Genomics supports Open Access, offering broader accessibility for researchers and enthusiasts eager to explore the latest advancements in genetic studies. Since its inception in 2008, the journal has committed to publishing high-quality research that drives forward our understanding of genetics and its applications, making it an essential resource for researchers, professionals, and students alike who are passionate about the complexities and breakthroughs in genomic sciences.

EUROPEAN JOURNAL OF HUMAN GENETICS

Exploring the Complexities of Heredity
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.

RUSSIAN JOURNAL OF THERIOLOGY

Connecting Researchers in Animal Science and Ecology
Publisher: KMK SCIENTIFIC PRESS LTD, MOSCOW STATE UNIVISSN: 1682-3559Frequency: 2 issues/year

RUSSIAN JOURNAL OF THERIOLOGY is a prominent academic journal published by KMK SCIENTIFIC PRESS LTD in collaboration with the esteemed Moscow State University. As a dedicated platform for researchers in the fields of Animal Science and Zoology, Ecology, Evolution, Behavior and Systematics, and Plant Science, this journal strives to advance our understanding of terrestrial ecosystems and their inhabitants. Although it currently holds a Q4 ranking and ranks within the lower percentiles of its respective categories, the journal's consistent publishing output since 2011 showcases a commitment to facilitating scientific discourse and collaboration. Addressed to a diverse audience of researchers, professionals, and students, RUSSIAN JOURNAL OF THERIOLOGY serves as an essential resource for disseminating valuable insights and fostering future advancements in the biological sciences.

G3-Genes Genomes Genetics

Your Gateway to Cutting-Edge Genetic Insights
Publisher: OXFORD UNIV PRESS INCISSN: 2160-1836Frequency: 12 issues/year

G3-Genes Genomes Genetics is a prominent open access journal published by Oxford University Press, Inc., dedicated to advancing the field of genetics and genomics. Since its inception in 2011, the journal has become a vital resource for researchers, professionals, and students, featuring high-quality, peer-reviewed articles that cover a broad spectrum of topics within genetics, including clinical genetics and molecular biology. With an impressive standing reflected in its 2023 Scopus rankings, which positions it in the Q2 category for Genetics (Clinical) and Q1 for Medicine (Miscellaneous), G3 remains at the forefront of scholarly communication in these disciplines. The journal's commitment to open access ensures that cutting-edge research is accessible to a global audience, stimulating collaboration and innovation in the field. For those eager to explore the latest in genetic research, G3 serves as an indispensable platform, inviting contributions that push the boundaries of scientific understanding.