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ADGRV1 gene

Known as: KIAA0686, G PROTEIN-COUPLED RECEPTOR 98, MONOGENIC AUDIOGENIC SEIZURE SUSCEPTIBILITY 1, MOUSE, HOMOLOG OF 
National Institutes of Health

Papers overview

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Highly Cited
2020
Highly Cited
2020
Supplemental Digital Content is available in the text. Background: Dilated cardiomyopathy (DCM) is genetically heterogeneous… 
Review
2015
Review
2015
The Adhesion family forms a large branch of the pharmacologically important superfamily of G protein–coupled receptors (GPCRs… 
Highly Cited
2014
Highly Cited
2014
Casanova and colleagues discuss the importance of single-patient genetic studies in the discovery of novel primary… 
Highly Cited
2014
Highly Cited
2014
We report the design of a targeted resequencing panel for monogenic dyslipidemias, LipidSeq, for the purpose of replacing Sanger… 
Review
2009
Review
2009
  • R. Hegele
  • Nature reviews genetics
  • 2009
  • Corpus ID: 10224444
Susceptibility to the growing global public health problem of cardiovascular disease is associated with levels of plasma lipids… 
Highly Cited
2006
Highly Cited
2006
Sensory hair bundles in the inner ear are composed of stereocilia that can be interconnected by a variety of different link types… 
Highly Cited
2006
Highly Cited
2006
Mutations in the DFNB31 gene encoding the PDZ scaffold protein whirlin are causative for hearing loss in man and mouse. Whirlin… 
Highly Cited
2005
Highly Cited
2005
Usher syndrome (USH) is the most frequent cause of combined deaf-blindness in man. USH is clinically and genetically… 
Highly Cited
2004
Highly Cited
2004
Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes… 
Highly Cited
2002
Highly Cited
2002
A naturally occurring mutation of the mass1 (monogenic audiogenic seizure‐susceptible) gene recently has been reported in the…