共 440 条
[1]
Kanner AM(2016)Management of psychiatric and neurological comorbidities in epilepsy Nat Rev Neurol 12 106-32
[2]
Ben-Shalom R(2017)Opposing effects on NaV 1.2 function underlie differences between SCN2A variants observed in individuals with autism spectrum disorder or infantile seizures Biol Psychiatry 82 224-51
[3]
Keeshen CM(2017)A recurrent de novo variant in NACC1 causes a syndrome characterized by infantile epilepsy, cataracts, and profound developmental delay Am J Hum Genet 100 343-90
[4]
Berrios KN(2014)A polygenic burden of rare disruptive mutations in schizophrenia Nature 506 185-84
[5]
An JY(2014)De novo mutations in schizophrenia implicate synaptic networks Nature 506 179-41
[6]
Sanders SJ(2016)Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia Nat Neurosci 19 1433-7
[7]
Bender KJ(2016)Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders Nat Neurosci 19 571-9
[8]
Schoch K(2017)Truncating mutations in RBM12 are associated with psychosis Nat Genet 49 1251-92
[9]
Meng L(2009)Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study Lancet 373 234-7
[10]
Szelinger S(2003)Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies Arch Gen Psychiatr 60 1187-52