Human Molecular Genetics – biotechnology genetics Journal Guide for Researchers

Why Researchers Choose Human Molecular Genetics for High-Impact Publications

Human Molecular Genetics stands as a cornerstone in the field of biotechnology genetics, offering researchers a premier platform to disseminate cutting-edge discoveries in human genetics and molecular biology. Published by Oxford University Press since 1992, this journal has built a reputation for excellence by focusing on the molecular basis of human disease, genetic variation, and functional genomics. With an impact factor of 5.1, it attracts submissions from top global institutions, ensuring that published work reaches a wide audience of geneticists, biologists, and clinicians.

The journal's scope encompasses a broad spectrum of topics, from gene regulation and epigenetics to population genetics and disease modeling. Researchers value its rigorous peer-review process, which upholds the highest standards of scientific integrity. Articles in Human Molecular Genetics often feature innovative methodologies, such as CRISPR-based editing and single-cell sequencing, contributing to advancements in personalized medicine and therapeutic development. Its hybrid publication model allows authors to choose open access, enhancing visibility and citation potential.

Over the years, Human Molecular Genetics has chronicled pivotal shifts in the field, including the integration of big data in genomics and the ethical implications of genetic research. This makes it an essential resource for staying abreast of trends in biotechnology genetics. For those navigating academic careers, publishing here signals expertise and can open doors to collaborations and funding opportunities. Explore related resources like genetics faculty positions to advance your professional journey.

In an era where interdisciplinary approaches dominate, Human Molecular Genetics bridges basic science with clinical applications, fostering discoveries that translate into real-world health benefits. Whether investigating rare genetic disorders or common complex traits, the journal provides a forum for high-quality, impactful research. Its editorial board, comprising renowned experts, ensures that only the most novel and reliable studies see publication.

As biotechnology genetics evolves rapidly, submitting to Human Molecular Genetics offers researchers the chance to contribute to landmark findings. The journal's commitment to rapid dissemination— with accepted manuscripts available online shortly after revision—keeps pace with the field's dynamism. For aspiring authors, understanding its guidelines can streamline the process, increasing chances of success. Delve deeper into academic timelines with our academic calendar to plan submissions effectively.

Overview & History

Human Molecular Genetics was launched in 1992 by Oxford University Press to address the growing need for a dedicated outlet in human genetics research. Initially focusing on mapping and cloning genes associated with inherited diseases, it quickly expanded to include functional studies and genomic technologies. By the early 2000s, as the Human Genome Project concluded, the journal shifted emphasis toward post-genomic analyses, such as transcriptomics and proteomics.

Today, it remains a vital publication, with over 200 articles per volume covering diverse subfields. Its evolution mirrors the biotechnology genetics landscape, from Mendelian disorders to polygenic risk scores. Key milestones include special issues on epigenetics in 2010 and CRISPR applications in 2018, which garnered significant citations. The journal's United Kingdom base underscores its international scope, with contributions from authors worldwide.

Scope and Disciplines Covered

DisciplineDescription
GeneticsStudies on gene structure, function, and inheritance in humans.
Molecular BiologyMechanisms of gene expression, regulation, and protein interactions.
GenomicsGenome-wide analyses, sequencing, and variant discovery.
BiotechnologyApplications of genetic tools in disease modeling and therapy.
EpigeneticsHeritable changes in gene activity without DNA sequence alterations.

These disciplines highlight the journal's interdisciplinary approach, welcoming manuscripts that integrate computational biology with experimental genetics.

Key Journal Metrics

MetricValueSource
Impact Factor (2022)5.1Clarivate Journal Citation Reports
CiteScore (2022)8.7Scopus
Acceptance RateNot publicly disclosedPublisher
Time to First Decision4 weeksJournal Data
Articles per Year~300Publisher

These metrics position Human Molecular Genetics as a competitive venue in biotechnology genetics.

Indexing and Abstracting

Human Molecular Genetics is indexed in major databases, ensuring broad discoverability. It appears in PubMed/MEDLINE for biomedical relevance, Web of Science for citation tracking, and Scopus for global metrics. Additional coverage includes Embase, Google Scholar, and Biological Abstracts. This indexing supports researchers in biotech research positions, facilitating literature reviews and grant applications.

Visit the official journal homepage for indexing details.

Publication Model and Fees

As a hybrid journal, Human Molecular Genetics offers subscription-based access with an open access option via Oxford Open. The article processing charge (APC) for gold open access is £3,430 (approximately $4,500 USD), waivable for low-income countries. No fees apply for traditional subscription publication. This model balances accessibility with sustainability, allowing wide dissemination of biotechnology genetics research.

Authors retain copyright under Creative Commons licenses for OA articles, enhancing reuse in educational settings like those linked to rate my professor resources.

Submission Process and Guidelines

Submissions are handled through the ScholarOne platform. Manuscripts must follow specific formatting: double-spaced text, 5,000-word limit, and figures in TIFF format. Ethical standards require IRB approval for human studies and declaration of conflicts. The process involves initial screening, peer review by 2-3 experts, and revisions. Track progress via the portal, detailed on the publisher guidelines page.

Prepare using tools from our academic calendar for genetics conferences to align with deadlines.

Editorial Board Highlights

The editorial team includes Editor-in-Chief Prof. David Fitzpatrick, a leader in developmental genetics from the University of Edinburgh. Associate Editors cover expertise in neurogenetics (Dr. Evan Eichler, University of Washington) and cancer genomics (Dr. Nazneen Rahman, Institute of Cancer Research). This diverse board ensures balanced, high-quality oversight in biotechnology genetics.

Why Publish in Human Molecular Genetics?

Publishing in Human Molecular Genetics elevates a researcher's profile due to its prestige and readership. With a 5.1 impact factor, articles gain rapid citations, boosting h-index and funding prospects. The journal's focus on translational research appeals to those in clinical genetics, while its open access option amplifies global reach. Compared to peers, it offers faster review times and supportive editorial feedback.

For career growth, consider exploring molecular biology postdoc opportunities post-publication.

Comparison with Similar Journals

JournalImpact FactorPublisherFocus
American Journal of Human Genetics11.0Cell PressPopulation and clinical genetics
Genetics in Medicine8.7Nature PublishingTranslational medical genetics
European Journal of Human Genetics4.6Springer NatureEthical and policy aspects
Human Genetics5.2SpringerBasic human genetic research

Human Molecular Genetics excels in molecular mechanisms, distinguishing it from more clinically oriented peers.

Researcher Tips for Successful Submission

To succeed, ensure novelty by highlighting gaps in current biotechnology genetics knowledge. Use clear visuals and robust statistics. Address reviewer comments thoroughly. Collaborate internationally for diverse perspectives. Finally, proofread for clarity. Leverage genetics faculty reviews for mentorship insights.

Timing submissions around key events via academic calendar can optimize visibility.

Frequently Asked Questions about Human Molecular Genetics

📈What is the current impact factor of Human Molecular Genetics?

The 2022 impact factor is 5.1, according to Clarivate Journal Citation Reports. This metric reflects its influence in biotechnology genetics. For career advancement, check genetics professor roles to leverage such publications.

🔍What is the acceptance rate for submissions?

The acceptance rate is not publicly disclosed by the publisher. It remains selective, prioritizing high-impact work. Researchers can prepare by reviewing guidelines and exploring submission deadlines in our academic calendar.

💰What is the APC and open access policy?

As a hybrid journal, the APC for open access is £3,430. Subscription model has no fees. Policies align with Plan S compliance. For funding tips, visit biotech grants opportunities.

⏱️How long is the average review time?

Initial editorial decision takes about 4 weeks, with full peer review around 8-10 weeks. This efficiency aids timely publication in biotechnology genetics. Plan your timeline using academic calendar.

📝Where do I submit my manuscript?

Use the ScholarOne portal via the official site. Detailed instructions are available there. For preparation, rate experiences with genetics editors on our platform.

📚Which databases index Human Molecular Genetics?

It is indexed in PubMed, Scopus, Web of Science, and Embase. This ensures wide visibility. Enhance your search skills with research librarian positions.

👨‍🔬Who is the Editor-in-Chief?

Prof. David Fitzpatrick from the University of Edinburgh leads as Editor-in-Chief, specializing in developmental genetics. Learn more about leadership via editorial boards ratings.

🚀What career value does publishing here provide?

Publication boosts CVs for tenure-track roles and collaborations in biotechnology genetics. It signals expertise to peers. Explore impacts through academic career advice.

⚖️How does it compare to peer journals?

With a 5.1 IF, it rivals Human Genetics (5.2) but focuses more on molecular aspects than clinical ones like Genetics in Medicine (8.7). Compare scopes using journal comparison events.