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SDCCAG8 gene

Known as: SDCCAG8, SLSN7, NPHP10 
National Institutes of Health

Papers overview

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2019
2019
BackgroundSOX11 is a transcription factor that plays an important role in mantle cell lymphoma development. However, its… Expand
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2016
2016
Recent genome‐wide association studies (GWASs) have identified numerous putative genetic polymorphisms associated with bipolar… Expand
2016
2016
Recessive mutations in the SDCCAG8 gene cause a nephronophthisis-related ciliopathy with Bardet-Biedl syndrome-like features in… Expand
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Highly Cited
2014
Highly Cited
2014
Nephronophthisis-related ciliopathies (NPHP-RCs) are developmental and degenerative kidney diseases that are frequently… Expand
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2014
2014
Mutations of SDCCAG8 are associated with nephronophthisis and Bardet-Biedl syndrome, as well as schizophrenia; however, the… Expand
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2012
2012
Genome‐wide association analyses (GWAS) contributed to the detection of a number of single‐nucleotide polymorphisms (SNPs… Expand
Highly Cited
2011
Highly Cited
2011
Nephronophthisis (NPHP), an autosomal recessive cystic kidney disease, is the most frequent genetic cause for end-stage renal… Expand
Highly Cited
2010
Highly Cited
2010
Nephronophthisis-related ciliopathies (NPHP-RC) are recessive disorders that feature dysplasia or degeneration occurring… Expand
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Highly Cited
2010
Highly Cited
2010
The ciliopathies are an expanding group of disorders caused by mutations in genes implicated in the biogenesis and function of… Expand
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