Medizinische Genetik

Scope & Guideline

Fostering Collaboration in Genetic Science.

Introduction

Explore the comprehensive scope of Medizinische Genetik through our detailed guidelines, including its aims and scope. Stay updated with trending and emerging topics, and delve into declining areas to understand shifts in academic interest. Our guidelines also showcase highly cited topics, featuring influential research making a significant impact. Additionally, discover the latest published papers and those with high citation counts, offering a snapshot of current scholarly conversations. Use these guidelines to explore Medizinische Genetik in depth and align your research initiatives with current academic trends.
LanguageGerman
ISSN0936-5931
PublisherWALTER DE GRUYTER GMBH
Support Open AccessNo
CountryGermany
TypeJournal
Convergefrom 1994 to 2024
AbbreviationMED GENET-BERLIN / Med. Genet.
Frequency4 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
AddressGENTHINER STRASSE 13, D-10785 BERLIN, GERMANY

Aims and Scopes

The journal 'Medizinische Genetik' aims to provide a platform for the dissemination of knowledge and advancements in the field of medical genetics. It focuses on the integration of genetic insights into clinical practice, the implications of genetic research for patient care, and the evolving methodologies in genetic diagnostics and counseling.
  1. Clinical Genetics and Diagnostics:
    The journal emphasizes the application of genetic knowledge in clinical settings, including diagnostic methodologies, genetic testing, and the role of genetics in various diseases.
  2. Research on Genetic Disorders:
    A core focus is on understanding genetic disorders, their mechanisms, and implications for treatment and management, with attention to both rare and common genetic conditions.
  3. Genetic Counseling and Ethical Considerations:
    The journal addresses the importance of genetic counseling, exploring ethical issues, patient perspectives, and the evolving role of genetic counselors in healthcare.
  4. Technological Advances in Genetics:
    It highlights innovations in genetic technologies, including next-generation sequencing, liquid biopsies, and bioinformatics, and their impacts on research and clinical practice.
  5. Multidisciplinary Approaches:
    The journal promotes interdisciplinary research that integrates genetics with other fields such as psychiatry, oncology, and reproductive health, reflecting the multifaceted nature of genetic issues.
The journal has shown a dynamic shift in focus, embracing new themes and areas of research that reflect current trends in the field of medical genetics.
  1. Non-invasive Prenatal Testing (NIPT):
    There is an increasing emphasis on NIPT, reflecting its growing relevance in prenatal care and discussions around its implications for maternal and fetal health.
  2. Liquid Biopsies and Cancer Genomics:
    Research on liquid biopsies has surged, highlighting their potential for minimally invasive cancer diagnostics and monitoring, as well as their role in understanding tumor genetics.
  3. Psychiatric Genomics:
    The integration of genetics in psychiatry is gaining momentum, with a focus on understanding the genetic basis of psychiatric disorders and the implications for treatment.
  4. Ethics and Policy in Genetic Testing:
    Emerging discussions around the ethical implications and policy frameworks for genetic testing, particularly concerning consent and incidental findings, are increasingly prominent.
  5. Genomic Medicine and Public Health:
    The journal is placing more emphasis on the intersection of genomics and public health, particularly in areas such as newborn screening and population genetics, reflecting a broader societal impact of genetic research.

Declining or Waning

While 'Medizinische Genetik' continues to cover a broad range of topics, certain themes appear to be diminishing in frequency or relevance as the field evolves.
  1. Historical Perspectives in Genetics:
    Papers focusing on the historical development of genetics and its methodologies have become less common, indicating a shift towards contemporary issues and applications.
  2. Basic Genetic Mechanisms without Clinical Context:
    There is a noticeable decline in publications centered solely on basic genetic mechanisms without direct application to clinical scenarios, as the journal increasingly prioritizes translational research.
  3. Niche Genetic Disorders:
    Research on very specific or niche genetic disorders appears to be waning, possibly as the journal focuses more on broadly impactful genetic diseases and common conditions.
  4. Traditional Genetic Counseling Models:
    As the field adapts to new technologies and methodologies, traditional models of genetic counseling are being less frequently discussed, indicating a shift towards more innovative and integrated approaches.
  5. Stand-alone Genetic Studies:
    The frequency of standalone studies focusing solely on genetic variants without linking them to clinical implications or patient outcomes has decreased, reflecting a trend towards more applied research.

Similar Journals

Journal of Pediatric Genetics

Illuminating Genetic Pathways in Pediatric Medicine
Publisher: GEORG THIEME VERLAG KGISSN: 2146-4596Frequency: 4 issues/year

Journal of Pediatric Genetics, published by GEORG THIEME VERLAG KG, is an essential resource in the field of pediatric medicine and genetics. With a focus on the genetic determinants of health and disease in children, this journal aims to advance the knowledge and application of genetic research in pediatric care. Although it has faced challenges in its indexing in recent years, it provides an important platform for practitioners and researchers dedicated to understanding the complexities of pediatric genetics. As evidenced by its position in Scopus ranks—ranked #209 in Pediatrics and #87 in Clinical Genetics—the journal serves a niche yet critical audience seeking to explore the interplay between genetic factors and childhood health outcomes. The Journal of Pediatric Genetics invites scholars and professionals to delve into its rich content, contributing to the ongoing discourse in this vital field, while the absence of open access highlights the journal’s curation of high-quality, peer-reviewed articles that are valued across academia and clinical practices.

Application of Clinical Genetics

Elevating Standards in Clinical Genetics Scholarship
Publisher: DOVE MEDICAL PRESS LTDISSN: Frequency: 1 issue/year

Application of Clinical Genetics is a premier open-access journal published by Dove Medical Press Ltd., dedicated to advancing the field of clinical genetics since its inception in 2008. Based in New Zealand, this journal has established itself as a significant resource for researchers, clinicians, and students alike, contributing to the body of knowledge in both genetic medicine and clinical applications. With an impact factor reflecting its contributions to the field, the journal holds positions in the Q2 and Q3 quartiles of the 2023 Genetics categories, showcasing its relevance and scientific merit. Furthermore, it ranks #43 out of 99 in Clinical Genetics and #153 out of 347 in Biochemistry, Genetics, and Molecular Biology, indicating robust performance amongst its peers. The journal’s broad scope, encompassing various aspects of clinical genetics, ensures that it remains at the forefront of critical discussions, innovative research, and applications essential for the progression of personalized medicine. Researchers and professionals are encouraged to explore its openly accessible content that fosters collaboration and the sharing of knowledge in this dynamic and rapidly evolving field.

AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Advancing the Frontiers of Medical Genetics.
Publisher: WILEYISSN: 1552-4868Frequency: 4 issues/year

AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS is a premier peer-reviewed journal published by Wiley, focusing on the intricate and evolving field of medical genetics. With its ISSN 1552-4868 and E-ISSN 1552-4876, the journal has established itself as a significant resource for researchers, professionals, and students alike, addressing cutting-edge developments in genetic research and clinical practice. Ranked in the top quartile (Q2) in both Genetics and clinical Genetics categories for 2023, it maintains an impressive Scopus ranking, positioning it within the 75th and 71st percentiles for Medicine and Genetics respectively. The journal encourages open access to its content, promoting wider dissemination of knowledge and fostering collaboration among medical genetics experts. From its inaugural issues in 1980 to its ongoing publications, the journal aims to bridge the gap between genetics research and its clinical applications, providing insights that reflect the latest advancements in the field. As it continues to serve the global medical community, the AMERICAN JOURNAL OF MEDICAL GENETICS PART C remains a vital source for those seeking to understand the complexities of genetic disorders and their implications for health and disease.

CLINICAL GENETICS

Innovating solutions for genetic challenges.
Publisher: WILEYISSN: 0009-9163Frequency: 12 issues/year

CLINICAL GENETICS is a premier journal in the field of genetics, published by Wiley, and is renowned for advancing the understanding of genetic disorders and their clinical applications. With a notable impact factor and ranking in the top quartile (Q1) in both general genetics and clinical genetics as of 2023, this journal is instrumental for researchers, professionals, and students seeking to explore groundbreaking studies and developments in genetics. Since its inception in 1970, CLINICAL GENETICS has continued to publish high-quality, rigorously peer-reviewed research that pushes the boundaries of knowledge in clinical genetics. The journal maintains a strong reputation in its field, currently holding significant positions in Scopus rankings, including 30th out of 99 in clinical genetics, underscoring its relevance and impact in the field. For those interested, the journal's website provides comprehensive access options for current and archived research, making it an essential resource for anyone involved in genetic research and its clinical application.

Gene Reports

Empowering Researchers with Open Access Genetics
Publisher: ELSEVIERISSN: Frequency: 4 issues/year

Gene Reports is a prominent academic journal published by Elsevier that focuses on the rapidly evolving field of genetics. Launched in 2015, this journal serves as a pivotal platform for the dissemination of cutting-edge research, bridging the gap between basic and applied genetics studies. Although it currently holds a Q4 ranking in the Genetics category and stands at the 248th position out of 347 in Scopus rankings, its potential for growth is significant given the increasing interest in genetic research across various disciplines. With an E-ISSN of 2452-0144, Gene Reports aims to provide open access to original research articles, reviews, and short communications that advance the collective understanding of genetic mechanisms and their applications. As a publication that continues to shape the future of genetics, it is an essential resource for researchers, professionals, and students seeking to stay informed about the latest developments in this crucial field.

Neurology-Genetics

Transforming Understanding of Neurological and Genetic Disorders.
Publisher: LIPPINCOTT WILLIAMS & WILKINSISSN: 2376-7839Frequency: 6 issues/year

Neurology-Genetics, an esteemed journal published by LIPPINCOTT WILLIAMS & WILKINS, is at the forefront of advancing the fields of neurology and genetics. With a dedicated Open Access model since 2015, this journal ensures that cutting-edge research is readily available to researchers, professionals, and students worldwide. Operating from the United States, Neurology-Genetics has established a reputable position within the scientific community, as reflected by its impressive rankings in Scopus; it holds a Q1 ranking in clinical neurology and a Q2 ranking in clinical genetics, showcasing its dual commitment to these intertwined fields. With an impact factor that continues to grow alongside its reach, the journal encourages the dissemination of novel findings, innovative methodologies, and critical reviews that contribute to the understanding and treatment of neurological and genetic disorders. Researchers and practitioners are invited to engage with the latest discoveries and discussions, making Neurology-Genetics an essential resource for anyone involved in these dynamic areas of study.

PSYCHIATRIC GENETICS

Exploring the Intersection of Genes and Psychiatry
Publisher: LIPPINCOTT WILLIAMS & WILKINSISSN: 0955-8829Frequency: 6 issues/year

PSYCHIATRIC GENETICS, published by LIPPINCOTT WILLIAMS & WILKINS, is a pivotal journal dedicated to the interdisciplinary study of genetic factors in psychiatric disorders, bridging the fields of genetics, psychiatry, and neuroscience. With a commitment to advancing research from its inception in 1990 and continuing through 2024, the journal provides a platform for innovative studies and findings that explore the genetic underpinnings of mental health. Although not currently an Open Access publication, it reaches a wide audience concerned with the complex interplay between genetics and psychiatric conditions, contributing to its Q3 and Q2 quartile rankings across multiple relevant categories in 2023. The importance of this journal cannot be understated; it serves as a crucial resource for researchers, clinicians, and students eager to uncover insights that could lead to more effective interventions and treatments in the realm of mental health.

TRENDS IN GENETICS

Pioneering Insights in the World of Genetics
Publisher: CELL PRESSISSN: 0168-9525Frequency: 12 issues/year

TRENDS IN GENETICS, published by CELL PRESS, is a leading journal in the field of genetics, recognized for its significant impact on research and advancements in the discipline. With an impressive Scopus ranking of #10 out of 347 in the category of Genetics and a 97th percentile ranking, this journal stands as a premier platform for publishing innovative, high-quality articles that shape the future of genetic research. Since its inception in 1985, TRENDS IN GENETICS has been at the forefront of the genetic sciences, continuously disseminating crucial findings while maintaining a strong commitment to scientific rigor and integrity. Although it does not currently offer open access options, its rigorous peer-review process ensures that only the most relevant and groundbreaking studies make it to publication. Scholars and practitioners in genetics will find this journal to be an invaluable resource for keeping abreast of the latest developments, trends, and methodologies that drive the field forward.

Molecular Genetics & Genomic Medicine

Fostering global dialogue in molecular biology.
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.

GENES & GENETIC SYSTEMS

Shaping the Future of Genetic Science and Medicine
Publisher: GENETICS SOC JAPANISSN: 1341-7568Frequency: 6 issues/year

GENES & GENETIC SYSTEMS, an esteemed journal published by the Genetics Society of Japan, serves as a vital platform for the dissemination of innovative research within the fields of genetics, molecular biology, and medicine. Established in 1996 and based in Mishima, Shizuoka, Japan, this journal has actively contributed to the academic community, fostering collaboration and knowledge sharing among researchers and professionals. The journal’s impact can be seen through its category quartiles, which reflect its position in Genetics, Molecular Biology, and Medicine, and while it currently ranks in Q4 in Genetics and Q3 in Medicine (miscellaneous), it is poised for growth as it continues to publish pivotal studies. With a commitment to open access, GENES & GENETIC SYSTEMS ensures that research findings are freely accessible to the global scientific community, promoting a more inclusive approach to knowledge distribution. This journal is essential for students, researchers, and professionals seeking to stay informed of advancements in genetic research and its implications for the broader field of medicine.