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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia.
Not available
S-EPMC3204930
|
biostudies-literature
Cite
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.
Not available
S-EPMC2925262
|
biostudies-literature
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Selected rapporteur summaries from the XX World Congress of Psychiatric Genetics, Hamburg, Germany, October 14-18, 2012.
Not available
S-EPMC4090768
|
biostudies-literature
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De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.
Not available
S-EPMC2867875
|
biostudies-literature
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Lithium Treatment in the Prevention of Repeat Suicide-Related Outcomes in Veterans With Major Depression or Bipolar Disorder: A Randomized Clinical Trial.
Not available
S-EPMC8600458
|
biostudies-literature
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The 3rd Schizophrenia International Research Society Conference, 14-18 April 2012, Florence, Italy: summaries of oral sessions.
Not available
S-EPMC3877922
|
biostudies-literature
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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Not available
S-EPMC2990633
|
biostudies-literature
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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.
Not available
S-EPMC1180588
|
biostudies-literature
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Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia, Bipolar Disorder, and Depression Among Adults in the US Veterans Affairs Health Care System.
Not available
S-EPMC9475441
|
biostudies-literature
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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Not available
S-EPMC2847896
|
biostudies-literature
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