Case Reports in Neurology is a distinguished open-access journal published by KARGER, dedicated to the advancement of knowledge in the field of neurology. Since its inception in 2009, the journal has provided a vital platform for the dissemination of clinical case reports, enhancing the understanding of various neurological disorders and their management. With an ISSN of 1662-680X, it is indexed in Scopus, ranking #295 out of 400 in the neurology (clinical) category for 2023, placing it in the 26th percentile. The journal welcomes contributions from researchers, clinicians, and students alike, offering insights into unique cases and treatment outcomes that can significantly impact clinical practice. Located in Basel, Switzerland, the journal emphasizes the importance of sharing exceptional clinical experiences that can inform future research and evidence-based practices. By promoting open access, Case Reports in Neurology ensures that valuable information is available to the global medical community, further bridging gaps in neurology research and clinical application.

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.

Clinical Pediatric Endocrinology is a prestigious journal dedicated to advancing the field of pediatric endocrinology, published by the Japanese Society of Pediatric Endocrinology. With a respectable ISSN 0918-5739 and E-ISSN 1347-7358, this journal serves as a critical platform for innovative research spanning various aspects of endocrine disorders in children, including diabetes and metabolic conditions. Although it does not currently offer open access, it remains highly relevant in its category, being ranked in Q4 and Q3 tiers across multiple specialties as of 2023. With a publication history that spans from 1992 to 2024, this journal has contributed significantly to the literature, as evidenced by its inclusion in prominent databases. It invites submissions from researchers and practitioners worldwide, aiming to facilitate knowledge sharing and improve clinical practices in pediatric endocrinology. For those dedicated to enhancing care outcomes in children with endocrine disorders, Clinical Pediatric Endocrinology provides essential insights and fosters a community of engaged professionals.

Human Genome Variation, published by SpringerNature, is an esteemed open access journal dedicated to the field of genetic research and exploration. Since its inception in 2014, the journal has been at the forefront of advancing our understanding of human genome diversity and its implications in health and disease. With an E-ISSN of 2054-345X, it features a diverse array of studies that encompass biochemistry, genetics, and molecular biology, making it an invaluable resource for researchers and professionals alike. The journal holds a Q3 ranking in both biochemistry and genetics, and a Q4 ranking in molecular biology, highlighting its growing influence within these disciplines. As the landscape of genomics continues to evolve, Human Genome Variation serves as a platform for the dissemination of high-quality research, fostering collaboration and innovation within the scientific community. Researchers and academics are invited to contribute to this pivotal journal, which not only provides open access to its content since 2014 but also aims to bridge the gap between basic research and clinical applications in genetics.

The JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, published by Walter de Gruyter GmbH, is a reputable peer-reviewed journal dedicated to advancing the field of pediatric endocrinology and metabolism. Since its inception in 1985, this journal has become a vital resource for professionals and researchers, providing insights into the latest advancements, clinical practices, and foundational research in the care of children with endocrine disorders. With a noted Q3 ranking in Endocrinology, Diabetes and Metabolism, and a robust focus on Pediatrics, Perinatology, and Child Health, it addresses important topics such as hormonal imbalances and metabolic syndromes in young populations. Despite its non-open access status, it continues to play an essential role in bridging the knowledge gap within our understanding of children's health and disease, contributing significantly to the progress in this specialized field.

Journal of Clinical Research in Pediatric Endocrinology is a premier open-access journal dedicated to advancing the field of pediatric endocrinology through rigorous research and innovative findings. Published by GALENOS PUBL HOUSE, this journal has established itself as a key resource since its inception in 2008, serving a broad audience of researchers, healthcare professionals, and students in the fields of endocrinology, pediatrics, and child health. With an impact factor reflecting its significance (currently ranked in the Q2 and Q3 quartiles across multiple relevant categories), it provides a platform for high-quality peer-reviewed articles that encompass clinical observations, experimental studies, and reviews. The journal operates under an open-access model, ensuring that findings are accessible to a global audience, fostering collaborative solutions for the challenges in pediatric endocrine disorders. Residing in Turkey, the journal continues to impact the scientific community by disseminating valuable research that promotes better understanding and treatment of hormonal and metabolic disorders in children.

Modern Rheumatology Case Reports, published by Oxford University Press, is an essential platform dedicated to the dissemination of unique clinical cases within the field of rheumatology. Launched in 2017, this journal provides a valuable resource for researchers, clinicians, and students interested in the nuances of rheumatological conditions and their management. With an E-ISSN of 2472-5625, the journal is accessible to a global audience, fostering knowledge exchange and collaborative research. Although currently ranked in the Q4 quartile and positioned 53rd out of 73 in the Scopus Medicine Rheumatology category, the journal is committed to enhancing its impact in the discipline by focusing on innovative case reports that inform clinical practice and contribute to the evolving understanding of rheumatic diseases. This endeavor not only supports the academic community but also aims to inspire new avenues for research and diagnostics. As such, Modern Rheumatology Case Reports is poised to become a significant reference point for those dedicated to advancing rheumatological care.

Congenital Heart Disease, published by TECH SCIENCE PRESS, is a pivotal academic journal focusing on the complexities of congenital heart conditions. With an ISSN of 1747-079X and an E-ISSN of 1747-0803, this journal serves as a crucial platform for researchers and healthcare professionals engaged in cardiology, pediatrics, and related fields. Established in 2006 and continuing through to 2024, it aims to disseminate insightful research findings and reviews that advance the understanding of congenital heart diseases and their management. The journal currently holds a Q4 classification in cardiology and cardiovascular medicine, with rankings in various medical categories highlighting its dedication to emerging research. Although it does not offer open access, its contributions are vital for professionals seeking to explore innovative strategies and collaborative solutions in congenital heart disease management. As it continues to navigate the evolving landscape of pediatric cardiac health, Congenital Heart Disease is committed to fostering a community of knowledge that impacts both clinical practices and academic inquiry.

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.

NATURE MEDICINE, published by NATURE PORTFOLIO, is a premier journal in the fields of medicine and biochemistry, recognized for its rigorous peer-review process and high-impact research contributions. With an impressive Scopus ranking placing it in the top percentile—#3 out of 636 in General Medicine and #2 out of 221 in General Biochemistry, Genetics, and Molecular Biology—it embodies excellence and innovation in biomedical science. The journal has been a vital source of cutting-edge discoveries since its inception in 1995, and it encompasses a wide range of topics including clinical research, translational medicine, and advances in genetic technologies. The journal’s impact factor reflects its significance, making it an essential resource for researchers, professionals, and students aiming to stay at the forefront of medical science. Though the journal follows a subscription model, it remains crucial for disseminating pivotal research findings that shape the future of healthcare and therapeutic strategies worldwide.