Molecular Genetics & Genomic Medicine

Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care.Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.Molecular Genetics & Genomic Medicine is a Wiley Open Access journal, one of a series of peer reviewed titles publishing quality research with speed and efficiency. Authors of accepted papers pay an Article Publication Charge and their papers are published under a Creative Commons license. With Creative Commons licenses, the author retains copyright and the public is allowed to reuse the content.

《分子遗传学与基因组医学》是一本同行评议的杂志，旨在快速传播与人类、分子遗传学和医学遗传学动态发展领域相关的高质量研究。该杂志发表的原始研究文章涵盖了表型、分子、生物学和基因组方面的发现，包括基因组变异、遗传性疾病和出生缺陷。广泛出版的分子遗传学和基因组医学包括罕见和常见的疾病，从诊断到治疗。适当的文章包括新疾病基因的报告、遗传变异的功能研究、深入的基因型-表型研究、遗传疾病的基因组分析、分子诊断方法、医学生物信息学、伦理、法律和社会影响(ELSI)以及临床诊断方法。分子遗传学和基因组医学为下一代罕见和常见疾病的测序研究提供了一个科学的家，这将使这一迷人的领域的研究容易和快速进入科学界。这将作为将下一代测序研究转化为个性化诊断和治疗的基础，用于日常医疗。分子遗传学和基因组医学出版原始的研究文章，评论，和研究方法论文，连同邀请的社论和评论。原始研究论文必须报告进行良好的研究，并给出数据支持的结论。《分子遗传学与基因组医学》是一份威利开放获取期刊，是一系列同行评议的期刊之一，出版质量高、速度快、效率高。被接受论文的作者需要支付文章发表费，他们的论文是在知识共享许可下发表的。有了知识共享许可，作者保留版权，公众可以重用内容。