ANNALS OF HUMAN GENETICS

Scope & Guideline

Navigating the Complexities of Human Genetics

Introduction

Explore the comprehensive scope of ANNALS OF HUMAN GENETICS 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 ANNALS OF HUMAN GENETICS in depth and align your research initiatives with current academic trends.
LanguageEnglish
ISSN0003-4800
PublisherWILEY
Support Open AccessNo
CountryUnited Kingdom
TypeJournal
Convergefrom 1954 to 2024
AbbreviationANN HUM GENET / Ann. Hum. Genet.
Frequency6 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
Address111 RIVER ST, HOBOKEN 07030-5774, NJ

Aims and Scopes

The Annals of Human Genetics is a leading journal dedicated to the advancement of knowledge in human genetics, focusing on the genetic basis of human disease, population genetics, and the implications of genetic research on health and disease. The journal publishes original research, reviews, and case studies, contributing to a deeper understanding of genetic variations and their impact on human health.
  1. Genetic Epidemiology:
    The journal emphasizes the study of genetic factors in human populations, exploring the heritability of diseases and traits through various statistical methodologies.
  2. Molecular Genetics:
    Research on the molecular mechanisms underlying genetic disorders, including the identification of genetic variants and their functional implications, is a core focus.
  3. Population Genetics:
    The journal examines the genetic diversity within and between populations, utilizing advanced genomic techniques to understand human evolution and migration patterns.
  4. Clinical Genetics:
    A significant aim of the journal is to bridge the gap between genetic research and clinical practice, facilitating the application of genetic findings in diagnostic and therapeutic settings.
  5. Ethical, Legal, and Social Implications (ELSI) of Genetics:
    The journal addresses the broader implications of genetic research, including ethical considerations, public health policies, and the social impact of genetic discoveries.
Recent publications in the Annals of Human Genetics reflect a dynamic evolution of research themes, with certain topics gaining momentum. This section outlines emerging areas of interest that are increasingly featured in the journal, highlighting their relevance and potential significance in the field of human genetics.
  1. Genomic Medicine and Precision Health:
    There is a growing emphasis on the application of genomic information to personalize medical treatment and health management, reflecting the trend towards precision medicine.
  2. CRISPR and Gene Editing Technologies:
    Research exploring the implications and applications of CRISPR technology in treating genetic disorders is rapidly gaining traction, indicating a shift towards innovative therapeutic approaches.
  3. Mendelian Randomization Studies:
    The use of Mendelian randomization to infer causal relationships between genetic variants and complex traits or diseases is becoming increasingly prominent in genetic epidemiology.
  4. Interdisciplinary Approaches to Genetics:
    There is a notable trend towards integrating genetics with other fields such as bioinformatics, epidemiology, and social sciences to address complex health issues.
  5. Ethical Considerations in Genetic Research:
    As genetic technologies advance, there is an increasing focus on the ethical implications of genetic testing and data sharing, reflecting broader societal concerns.

Declining or Waning

As the field of human genetics evolves, certain themes within the Annals of Human Genetics have shown a decline in prominence. This section highlights topics that have become less frequent in recent publications, indicating a potential shift in research focus or emerging priorities within the field.
  1. Traditional Genetic Mapping Studies:
    While genetic mapping has been foundational in genetics, the rise of high-throughput sequencing and more sophisticated analytical techniques has led to a decrease in traditional mapping studies.
  2. Single Gene Disorders Focus:
    Research specifically centered on single-gene disorders appears to be waning as the field moves towards understanding complex polygenic traits and multifactorial diseases.
  3. Basic Genetic Variants Studies:
    The exploration of genetic variants without functional or clinical implications is becoming less prevalent, as the focus shifts towards variants with clear health impacts.

Similar Journals

Genetic Testing and Molecular Biomarkers

Exploring the Frontiers of Genomic Medicine.
Publisher: MARY ANN LIEBERT, INCISSN: 1945-0265Frequency: 12 issues/year

Genetic Testing and Molecular Biomarkers, an esteemed journal published by MARY ANN LIEBERT, INC, serves as a pivotal platform for advancing the field of genetic research and its applications in medicine. Focused on the innovative intersections of genetics and biomarker discovery, this journal has consistently contributed meaningful insights since its inception in 2009, with its scope evolving through 2024. With an ISSN of 1945-0265 and an E-ISSN of 1945-0257, it offers both traditional and open access options to cater to a broad audience of researchers, professionals, and students. Despite its current classification in the Q4 and Q3 quartiles for Genetics (clinical) and Medicine (miscellaneous) respectively, the journal remains committed to publishing high-quality, peer-reviewed articles that push the boundaries of knowledge in the field. As the landscape of genomic medicine continues to expand, Genetic Testing and Molecular Biomarkers is positioned as a crucial resource for disseminating cutting-edge discoveries and fostering interdisciplinary collaboration.

AMERICAN JOURNAL OF HUMAN GENETICS

Elevating Genetic Insights for a Brighter Future
Publisher: CELL PRESSISSN: 0002-9297Frequency: 12 issues/year

The American Journal of Human Genetics, published by Cell Press, stands at the forefront of the genetics field, serving as an invaluable resource for researchers, clinicians, and students alike. With ISSN 0002-9297 and E-ISSN 1537-6605, this esteemed journal has been a cornerstone of genetic research since its inception in 1950 and continues to shape the landscape of human genetics as it evolves through 2024. Recognized for its exceptional quality, it holds a prestigious Q1 ranking in both genetics and clinical genetics, highlighting its significance and impact in the scientific community. With Scopus rankings placing it 5th out of 99 in clinical genetics and 20th out of 347 in biochemistry, genetics, and molecular biology, the journal attracts cutting-edge research and groundbreaking discoveries. While the journal maintains a subscription-only model for access, its contributions are critical in advancing our understanding of human genetics, making it a must-read for those dedicated to pushing the boundaries of knowledge in this dynamic field.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Transforming Genetic Research into Clinical Solutions
Publisher: WILEYISSN: 1552-4825Frequency: 12 issues/year

American Journal of Medical Genetics Part A, published by Wiley, is a vital resource for those immersed in the field of medical genetics. Established as a premier platform for interdisciplinary scholarship, this journal offers insights into the latest advances in genetic research, specifically focusing on clinical applications. With an ISSN of 1552-4825 and an E-ISSN of 1552-4833, it is recognized in the academic community with a noteworthy Q2 ranking in Genetics and Q3 in Clinical Genetics for 2023, reflecting its significant contribution to the field. The journal encompasses a broad scope of topics, from genetic disorders to the implications of genetic findings in clinical practice, and it has consistently attracted high-quality research submissions. Researchers and professionals can freely access its articles due to open access options, promoting the dissemination of knowledge globally. As it converges from its historical foundation established from 1996 to 1999 and 2001, continuing through to 2024, the American Journal of Medical Genetics Part A remains a crucial conduit for new scientific knowledge necessary for advancing genetic medicine.

CLINICAL GENETICS

Unlocking the potential of genetic research.
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.

Annual Review of Genetics

Elevating Understanding in the Evolving World of Genetics.
Publisher: ANNUAL REVIEWSISSN: 0066-4197Frequency: 1 issue/year

The Annual Review of Genetics is a premier academic journal dedicated to advancing the field of genetics through critical, comprehensive reviews that synthesize current research and highlight future directions. Published by Annual Reviews, this esteemed journal boasts an impressive impact factor, ranking in the Q1 category for Genetics, and holds a distinguished position as 14th out of 347 journals in the Scopus ranking for Genetics, placing it in the 96th percentile among its peers. With its convergence of knowledge from 1970 to 2023, the journal serves as an essential resource for researchers, professionals, and students alike, facilitating a deeper understanding of genetic principles and their applications. Although the journal is not open access, it remains a vital platform for disseminating high-quality, peer-reviewed content that shapes the conversation in genetics, making it a must-read for those seeking to stay at the forefront of this dynamic field.

Egyptian Journal of Medical Human Genetics

Advancing knowledge in medical genetics for a healthier tomorrow.
Publisher: SPRINGERNATUREISSN: 1110-8630Frequency: 1 issue/year

The Egyptian Journal of Medical Human Genetics is a distinguished Open Access journal published by SPRINGER NATURE, dedicated to advancing the field of medical human genetics. With an ISSN of 1110-8630 and an E-ISSN of 2090-2441, this journal serves as a vital platform for researchers, professionals, and students who are committed to the exploration of genetic implications on human health. Since its inception in 2010, it has become a growing repository of knowledge, significantly contributing to the discourse in clinical genetics, despite currently being ranked in the Q4 quartile of its category in 2023. The journal embraces an open access model, ensuring widespread visibility and accessibility of published research, thereby fostering collaboration and innovation in the field. The journal is not only aimed at disseminating findings but also at encouraging the dialogue around genetic research developments, making it an essential resource for anyone interested in the nuances of genetics and its impact on medicine.

GENETICS AND MOLECULAR BIOLOGY

Unveiling discoveries in genetics and molecular biology.
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.

GENETIC EPIDEMIOLOGY

Transforming Health Outcomes with Genetic Insights
Publisher: WILEYISSN: 0741-0395Frequency: 8 issues/year

GENETIC EPIDEMIOLOGY is a pioneering journal published by Wiley that bridges the fields of genetics and epidemiology to advance our understanding of the genetic underpinnings of health and disease. Established in 1984 and converging into its 40th year of impactful research in 2024, this journal offers a key platform for the dissemination of innovative research findings, statistical methods, and applications in both clinical genetics and epidemiological practices. With a robust presence in Scopus, ranking in the second quartile (Q2) for both epidemiology and clinical genetics, it enjoys a significant reputation among its peers. The journal does not currently offer open access, but it is vital for researchers, professionals, and students committed to exploring the evolving landscape of genetic influences on population health. Its rich repository of studies not only enhances knowledge but also informs public health policies and clinical practices worldwide, making it an indispensable resource for those seeking to innovate and apply genetic research in the quest for better health outcomes.

JOURNAL OF GENETICS

Advancing the Frontiers of Genetic Research
Publisher: INDIAN ACAD SCIENCESISSN: 0022-1333Frequency: 1 issue/year

JOURNAL OF GENETICS, published by the Indian Academy of Sciences, is a pivotal platform for researchers and scholars in the field of genetics. With its long-standing history dating back to 1910, this journal has consistently contributed to the academic discourse through the rigorous publication of original research, reviews, and case studies. Despite its current classification in the Q4 quartile for the 2023 metrics in Genetics, the journal plays a critical role in advancing our understanding of genetic principles, experimental methodologies, and innovations. Spanning a diverse array of topics, the journal aims to foster scholarly exchange and collaboration within the global genetics community. For researchers aiming to publish their work, accessing the journal’s comprehensive archives, which include publications from as early as 1910 to the present day, offers a valuable perspective on the evolution of genetic research. As it continues to adapt to the changing landscape of scientific inquiry, JOURNAL OF GENETICS remains a significant resource for students, professionals, and academics dedicated to exploring the complexities of genetics.

Frontiers in Genetics

Innovative Research, Global Impact
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.