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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
2014
Highly Cited
2014
Casanova and colleagues discuss the importance of single-patient genetic studies in the discovery of novel primary… Expand
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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… Expand
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Highly Cited
2013
Highly Cited
2013
Single crystals of novel orthorhombic (space group Pnnm) iron tetraboride FeB4 were synthesized at pressures above 8 GPa and high… Expand
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Highly Cited
2011
Highly Cited
2011
PURPOSE Whirlin is the causative gene for Usher syndrome type IID (USH2D), a condition manifested as both retinitis pigmentosa… Expand
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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… Expand
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Highly Cited
2008
Highly Cited
2008
We investigate the relationship between black hole mass and host galaxy properties for active galaxies with the lowest black hole… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes… Expand