Associated Papers
A pharmacogenetic study of perampanel: association between rare variants of glutamate receptor genes and outcomes.
Lin CH et al.
Frontiers in Genetics, 2023
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia.
Dong W et al.
Journal of Lipid Research, 2022
35460704 (PubMed )
Supplement: mmc1.pdf
A Functional Variant Rs492554 Associated With Congenital Heart Defects Modulates SESN2 Expression Through POU2F1.
Yang W et al.
Frontiers in Cell and Developmental Biology, 2021
34249922 (PubMed )
Supplement: Table_1.xls › MQ1-2-3
Hardy-Weinberg Equilibrium in the Large Scale Genomic Sequencing Era.
Abramovs N et al.
Frontiers in Genetics, 2020
32231685 (PubMed )
Supplement: Data_Sheet_1.xlsx › Supplementary_Table_1
Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.
Hammer MF et al.
Plos One, 2017
28686619 (PubMed )
Supplement: pone.0180485.s008.xlsx › Sheet1
The contribution of rare and common variants in 30 genes to risk nicotine dependence.
Yang J et al.
Molecular Psychiatry, 2015
Whole genome/exome sequencing in mood and psychotic disorders.
Kato T
Psychiatry and Clinical Neurosciences, 2015
A population-specific uncommon variant in GRIN3A associated with schizophrenia.
Takata A et al.
Biological Psychiatry, 2013
Exomic sequencing of the ionotropic glutamate receptor N-methyl-D-aspartate 3A gene (GRIN3A) reveals no association with schizophrenia.
Shen YC et al.
Schizophrenia Research, 2009
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