Associated Papers
A mutation in CCDC91, Homo sapiens coiled-coil domain containing 91 protein, cause autosomal-dominant acrokeratoelastoidosis.
Zhu Y et al.
European Journal of Human Genetics : Ejhg, 2024
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Association between N-methyl-D-aspartate Receptor Subunit 2B Gene Polymorphisms and Personality Traits in a Young Japanese Population.
Narita S et al.
East Asian Archives of Psychiatry : Official Journal of the Hong Kong College of Psychiatrists = Dong Ya Jing Shen Ke Xue Zhi : Xianggang Jing Shen Ke Yi Xue Yuan Qi Kan, 2018
Integrative genomic and functional analysis of human oral squamous cell carcinoma cell lines reveals synergistic effects of FAT1 and CASP8 inactivation.
Hayes TF et al.
Cancer Letters, 2016
Association of genetic variants of GRIN2B with autism.
Pan Y et al.
Scientific Reports, 2015
Polymorphisms in microRNA target sites influence susceptibility to schizophrenia by altering the binding of miRNAs to their targets.
Gong Y et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, 2013
Genetic variation of GRIN1 confers vulnerability to methamphetamine-dependent psychosis in a Thai population.
Chanasong R et al.
Neuroscience Letters, 2013
Genetic association studies of glutamate, GABA and related genes in schizophrenia and bipolar disorder: a decade of advance.
Cherlyn SY et al.
Neuroscience and Biobehavioral Reviews, 2010
Association study between the NMDA receptor 2B subunit gene (GRIN2B) and schizophrenia: a HuGE review and meta-analysis.
Li D et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2007
An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray.
Qin S et al.
European Journal of Human Genetics : Ejhg, 2005
Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia.
Ohtsuki T et al.
Molecular Psychiatry, 2001
Pharmacogenetics of Ketamine-Induced Emergence Phenomena: A Pilot Study.
Aroke EN et al.
Nursing Research, 0