AHI1 gene

Known as: Jouberin, ORF1, AHI1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1997-2018
0246819972018

Papers overview

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Highly Cited
2010
Highly Cited
2010
Degeneration of photoreceptors is a common feature of ciliopathies, owing to the importance of the specialized ciliary structure… (More)
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2010
2010
In previous studies, we identified a locus for schizophrenia on 6q23.3 and proposed the Abelson helper integration site 1 (AHI1… (More)
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2008
2008
It has been suggested that autism, like other complex genetic disorders, may benefit from the study of rare or Mendelian variants… (More)
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2007
2007
Recently, markers in the Abelson Helper Integration Site 1 (AHI1) region were shown to be associated with schizophrenia in a… (More)
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2006
2006
OBJECTIVE Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative… (More)
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2006
2006
Schizophrenia, a severe neuropsychiatric disorder, is believed to involve multiple genetic factors. A significant body of… (More)
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2006
2006
BACKGROUND Joubert syndrome (JS) is an autosomal recessive disorder characterised by hypotonia, ataxia, mental retardation… (More)
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2005
2005
Joubert syndrome (JBTS) is an autosomal recessive multisystem disease characterized by cerebellar vermis aplasia, mental… (More)
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Highly Cited
2004
Highly Cited
2004
Joubert syndrome is a congenital brain malformation of the cerebellar vermis and brainstem with abnormalities of axonal… (More)
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1997
1997
Recently, to reduce the costs of polysomnography, split-night studies have been introduced into routine practice: the first part… (More)
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