Front & Back Matter

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Human Heredity Pub Date : 2021-05-01 DOI:10.1159/000517133
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引用次数: 0

Abstract

69 49th European Mathematical Genetics Meeting (EMGM) 2021 Génin, E. (Brest) Cover illustration © iStock.com know what matters in karger.com/genetics Genetics K I2 01 67 _g en et ic s_ 28 0 IA 21 03 6_ 21 0x 28 0 Practical e-learning on setting up genetic testing in European hospitals Can my hospital benefi t from next-generation sequencing? This free-to-access, e-learning course has been created for hospital directors and medical managers of European hospitals wishing to improve their genetic testing. It has been compiled by a multidisciplinary team of expert authors from pathology, health economics, and bioinformatics. Students will leave with a solid understanding of the benefi ts of genetic testing, and the practical implications of setting up either an in-house laboratory or outsourced analyses. Authors: Fernando Schmitt; Rhodri Saunders; Stefan Nicolet FREE ENROLLMENT!
正面和背面事项
69第49届欧洲数学遗传学会议(EMGM)2021 Génin,E.(Brest)封面插图©iStock.com know what matters in karger.com/Genetics Genetics K I2 01 67 _G en et ic s_ 28 0 IA 21 03 6_ 21 0x 28 0关于在欧洲医院进行基因检测的实用电子学习我的医院能从下一代测序中受益吗?这门免费的电子学习课程是为希望改进基因检测的欧洲医院院长和医疗经理开设的。它是由一个由病理学、健康经济学和生物信息学专家作者组成的多学科团队编写的。离开时,学生们将对基因检测的好处以及建立内部实验室或外包分析的实际意义有一个坚实的理解。作者:Fernando Schmitt;罗德里·桑德斯;Stefan Nicolet免费注册!
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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