Lethal phenotypes in Mendelian disorders-Reference-Cited by-同舟云学术

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Lethal phenotypes in Mendelian disorders

Published:2024-07 Issue:7 Volume:26 Page:101141
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Cacheiro Pilar^ORCID,Lawson Samantha^ORCID,Van den Veyver Ignatia B.^ORCID,Marengo Gabriel^ORCID,Zocche David^ORCID,Murray Stephen A.^ORCID,Duyzend Michael^ORCID,Robinson Peter N.^ORCID,Smedley Damian^ORCID

Funder

NIH

Publisher

Elsevier BV

Reference80 articles.

1. High-throughput discovery of novel developmental phenotypes;Dickinson;Nature,2016

2. Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families;Shamseldin;Genome Biol,2015

3. Causal genetic variants in stillbirth;Stanley;N Engl J Med,2020

4. An estimate of the average number of recessive lethal mutations carried by humans;Gao;Genetics,2015

5. Human and mouse essentiality screens as a resource for disease gene discovery;Cacheiro;Nat Commun,2020

Cited by 1 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. Computational identification of disease models through cross-species phenotype comparison;Disease Models & Mechanisms;2024-06-01

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