Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies

出版年份 2020 全文链接

标题

作者

关键词

electronic medical records, Human Phenotype Ontology, childhood epilepsies, neurogenetic disorders, developmental and epileptic encephalopathies, whole-exome sequencing, computational phenotypes

出版物

AMERICAN JOURNAL OF HUMAN GENETICS

Volume 107, Issue 4, Pages 683-697

出版商

Elsevier BV

发表日期

2020-08-26

DOI

10.1016/j.ajhg.2020.08.003

向作者/读者发起求助以获取更多资源

Protocol

在线求助

Reagent

在线求助

Reprint

联系作者

Find the ideal target journal for your manuscript

Explore over 38,000 international journals covering a vast array of academic fields.

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started