自引率: 5.8%
被引量: 13045
通过率: 暂无数据
审稿周期: 1
版面费用: 暂无数据
国人发稿量: 4
投稿须知/期刊简介:
Published by Lippincott Williams and Wilkins. ISSN: 1098-3600.<br /><br />As a respected part of the genetics community, Genetics in Medicine is a must read for all those applying new genetic findings to their practice. Genetics in Medicine is devoted to the broad clinical application of genetics, and outstanding editorial content and uniqueness make it a necessary acquisition for all clinicians and institutional libraries. Topics covered in the journal include clinical genetics, biochemical genetics, cytogenetics, molecular genetics, common disease genetics, genetic counseling and legal updates and genetics legacies.
期刊描述简介:
Genetics in Medicine, the official peer-reviewed journal of the American College of Medical Genetics and Genomics, aims to enhance the knowledge and practice of medical genetics. We publish original articles relevant to the broad aspects of medical genetics and genomics including manuscripts in clinical genetics/genomics; biochemical genetics and inherited metabolic disease; genetic disease therapeutics; cancer genetics, cytogenetics; laboratory genetics and genomics; molecular genetics; public health genetics; health services and implementation; genetic epidemiology/statistical genetics, genetic counseling, reproductive genetics, genetics and genomics education, economics and precision medicine, and ethical, legal and social implications of genetics and genomics. Innovation and influence on research and practice, as well as quality, methodology and impact on the delivery of genetic medicine will be considered during the review process. Genetics in Medicine does not publish case reports. Submitted manuscripts should not contain previously published material.
-
Evaluation of a Master's in Genomic Medicine framework: a national, multi-professional programme to educate healthcare professionals in NHS England.
被引量:- 发表:1970
-
Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder.
被引量:- 发表:1970
-
Severe Neurodevelopmental Phenotype, Diagnostic and Treatment Challenges in Patients with SECISBP2 Deficiency.
被引量:- 发表:1970
-
The Role of Double Heterozygotes of SLC3A1 and SLC7A9 in the Prevalence of Cystine Stones.
被引量:- 发表:1970
-
Group-based medical mistrust in genomic medicine: Associations with patient and provider perceptions of a specialty clinical encounter.
被引量:- 发表:1970