Published in Genomics on July 01, 2001
Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene. Mamm Genome (2004) 1.39
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Mapping a mouse limbic seizure susceptibility locus on chromosome 10. Epilepsia (2011) 0.81
Susceptibility to seizure-induced excitotoxic cell death is regulated by an epistatic interaction between Chr 18 (Sicd1) and Chr 15 (Sicd2) loci in mice. PLoS One (2014) 0.80
Quantitative trait locus on distal chromosome 1 regulates the occurrence of spontaneous spike-wave discharges in DBA/2 mice. Epilepsia (2012) 0.80
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A potassium channel is associated with resistance to epilepsy. Epilepsy Curr (2005) 0.75
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The functional mu opioid receptor (OPRM1) Asn40Asp variant predicts short-term response to nicotine replacement therapy in a clinical trial. Pharmacogenomics J (2004) 1.74
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Human G(olf) gene polymorphisms and vulnerability to bipolar disorder. Psychiatr Genet (1998) 1.47
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Evidence for a susceptibility gene for anorexia nervosa on chromosome 1. Am J Hum Genet (2002) 1.17
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Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy. Epilepsy Res (2005) 1.10
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The effect of electrode configuration and duration of deafness on threshold and selectivity of responses to intracochlear electrical stimulation. J Acoust Soc Am (2001) 1.10
Alternative transcripts and evidence of imprinting of GNAL on 18p11.2. Mol Psychiatry (2005) 1.09
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A biallelic RFLP of the human alpha 2-C4 adrenergic receptor gene (ADRA2RL2) localized on the short arm of chromosome 4 and encoding the putative alpha 2B receptor is identified with Bsu 36 I, using a 1.5 kb probe (p ADRA2RL2). Nucleic Acids Res (1989) 1.06
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Plasticity in central representations in the inferior colliculus induced by chronic single- vs. two-channel electrical stimulation by a cochlear implant after neonatal deafness. Hear Res (2000) 1.00
Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder. Am J Med Genet B Neuropsychiatr Genet (2005) 0.99
A novel allelic variant of the human serotonin transporter gene regulatory polymorphism. Cytogenet Cell Genet (1997) 0.99
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Linkage analysis of fifty-seven microsatellite loci to bipolar disorder. Neuropsychopharmacology (1993) 0.98
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Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa. Mol Psychiatry (2003) 0.97
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Potentiation of kainic acid epileptogenicity and sparing from neuronal damage by an NMDA receptor antagonist. Epilepsy Res (1989) 0.96
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Strengthening individual and community capacity to prevent disease and promote health: in search of relevant theories and principles. Health Educ Q (1995) 0.95
Uptake of horseradish peroxidase from perilymph by cochlear hair cells. Hear Res (1987) 0.95
Interaction between variation in the D2 dopamine receptor (DRD2) and the neuronal calcium sensor-1 (FREQ) genes in predicting response to nicotine replacement therapy for tobacco dependence. Pharmacogenomics J (2006) 0.94
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Differential susceptibility to seizures induced by systemic kainic acid treatment in mature DBA/2J and C57BL/6J mice. Epilepsia (1995) 0.94
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Chronic intracochlear electrical stimulation in neonatally deafened cats: effects of intensity and stimulating electrode location. Hear Res (1992) 0.93
SPARC is expressed by mesangial cells in experimental mesangial proliferative nephritis and inhibits platelet-derived-growth-factor-medicated mesangial cell proliferation in vitro. Am J Pathol (1996) 0.93
Changes in the cat cochlear nucleus following neonatal deafening and chronic intracochlear electrical stimulation. Hear Res (1994) 0.93
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Consequences of chronic extracochlear electrical stimulation in neonatally deafened cats. Hear Res (1995) 0.91
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Acute cocaine-induced seizures: differential sensitivity of six inbred mouse strains. Neuropsychopharmacology (2001) 0.90