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CHADL gene

Known as: chondroadherin like, CHONDROADHERIN-LIKE, CHADL 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
RNA-seq reveals downregulated osteochondral genes potentially related to tibia bacterial chondronecrosis with osteomyelitis in broilers
Background Bacterial chondronecrosis with osteomyelitis (BCO) develops in the growth plate (GP) of the proximal femur and tibia… 
Highly Cited
2018
Highly Cited
2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we… 
2018
2018
Identification of molecular pathways and candidate genes associated with cocks’ comb size trait by genome-wide transcriptome analysis
The comb of the male is an important secondary sexual characteristic. Although quantitative trait loci (QTLs) related to comb… 
Highly Cited
2017
Highly Cited
2017
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
We performed a genome-wide association study of total hip replacements, based on variants identified through whole-genome… 
2017
2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
Nat. Genet.; doi:10.1038/ng.3816; corrected online 17 April 2017 In the version of this article initially published online, the… 
2017
2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
Unnur Styrkarsdottir, Hannes Helgason, Asgeir Sigurdsson, Gudmundur L Norddahl, Arna B Agustsdottir, Louise N Reynard, Amanda… 
2016
2016
Abstract 12066: TIMP3 and CHADL Mutations Are Common in Turner Syndrome Aortopathy
Introduction: Turner syndrome (TS) is caused by the loss of the second sex chromosome, which occurs in approximately 1 in 2,000… 
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