Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 206,121,951 papers from all fields of science
Search
Sign In
Create Free Account
CHADL gene
Known as:
chondroadherin like
, CHONDROADHERIN-LIKE
, CHADL
Expand
National Institutes of Health
Create Alert
Alert
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
Haniel C de Oliveira
,
A. Ibelli
,
+4 authors
M. Ledur
BMC Genetics
2020
Corpus ID: 219183846
Background Bacterial chondronecrosis with osteomyelitis (BCO) develops in the growth plate (GP) of the proximal femur and tibia…
Expand
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
U. Styrkarsdottir
,
S. Lund
,
+26 authors
K. Stefánsson
Nature Genetics
2018
Corpus ID: 53103306
Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we…
Expand
2018
2018
Identification of molecular pathways and candidate genes associated with cocks’ comb size trait by genome-wide transcriptome analysis
Yi-fan Liu
,
Y. Tu
,
+7 authors
Jianmin Zou
Scientific Reports
2018
Corpus ID: 23151669
The comb of the male is an important secondary sexual characteristic. Although quantitative trait loci (QTLs) related to comb…
Expand
Highly Cited
2017
Highly Cited
2017
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
U. Styrkarsdottir
,
H. Helgason
,
+45 authors
K. Stefánsson
Nature Genetics
2017
Corpus ID: 52859781
We performed a genome-wide association study of total hip replacements, based on variants identified through whole-genome…
Expand
2017
2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
U. Styrkarsdottir
,
H. Helgason
,
+46 authors
K. Stefánsson
Nature genetics
2017
Corpus ID: 13728615
Nat. Genet.; doi:10.1038/ng.3816; corrected online 17 April 2017 In the version of this article initially published online, the…
Expand
2017
2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
B. Niu
,
Adam D. Scott
,
+16 authors
L. Ding
Nature Genetics
2017
Corpus ID: 9693097
Unnur Styrkarsdottir, Hannes Helgason, Asgeir Sigurdsson, Gudmundur L Norddahl, Arna B Agustsdottir, Louise N Reynard, Amanda…
Expand
2016
2016
Abstract 12066: TIMP3 and CHADL Mutations Are Common in Turner Syndrome Aortopathy
M. Silberbach
,
Holly Corbitt
,
Diedre Krupp
,
B. O’Roak
,
C. Maslen
2016
Corpus ID: 81721707
Introduction: Turner syndrome (TS) is caused by the loss of the second sex chromosome, which occurs in approximately 1 in 2,000…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
,
Terms of Service
, and
Dataset License
ACCEPT & CONTINUE