Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing-Reference-Cited by-同舟云学术

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Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing

Published:2018-05 Issue:5 Volume:20 Page:486-494
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Bruun Theodora U.J.,DesRoches Caro-Lyne,Wilson Diane,Chau Vann,Nakagawa Tadashi,Yamasaki Masahiro,Hasegawa Shinya,Fukao Toshiyuki,Marshall Christian,Mercimek-Andrews Saadet

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2017129.pdf

Reference40 articles.

Cited by 43 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Causes and Terminology in Neonatal Encephalopathy;Clinics in Perinatology;2024-09

2. Genetic and Congenital Anomalies in Infants With Hypoxic-Ischemic Encephalopathy;Pediatric Neurology;2024-05

3. Early Differential Diagnosis and Restorative Treatment of Patients with Cerebral Palsy;Neuroscience and Behavioral Physiology;2024-05

4. Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic–ischemic encephalopathy: A retrospective analysis;Clinical Genetics;2024-03-28

5. Newly discovered variants in unexplained neonatal encephalopathy;Molecular Genetics & Genomic Medicine;2024-01

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