Works matching IS 15524841 AND DT 2016 AND VI 171B AND IP 6
Results: 19
FKBP5 genotype interacts with early life trauma to predict heavy drinking in college students.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 879, doi. 10.1002/ajmg.b.32460
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Whole-gene sequencing investigation of SAT1 in attempted suicide.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 888, doi. 10.1002/ajmg.b.32462
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Common variants in CACNA1C and MDD susceptibility: A comprehensive meta-analysis.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 896, doi. 10.1002/ajmg.b.32466
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Multimarker analysis suggests the involvement of BDNF signaling and microRNA biosynthesis in suicidal behavior.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 763, doi. 10.1002/ajmg.b.32433
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An examination of the language construct in NIMH's research domain criteria: Time for reconceptualization!
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 904, doi. 10.1002/ajmg.b.32438
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15q13.3 duplication in two patients with childhood-onset schizophrenia.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 777, doi. 10.1002/ajmg.b.32439
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Transcriptome analysis of genes and gene networks involved in aggressive behavior in mouse and zebrafish.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 827, doi. 10.1002/ajmg.b.32451
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PARK16 is associated with PD in the Malaysian population.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 839, doi. 10.1002/ajmg.b.32454
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The role of protein intrinsic disorder in major psychiatric disorders.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 848, doi. 10.1002/ajmg.b.32455
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The ANK3 gene and facial affect processing: An ERP study.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 861, doi. 10.1002/ajmg.b.32456
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Preliminary examination of microRNA expression profiling in bipolar disorder I patients during antipsychotic treatment.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 867, doi. 10.1002/ajmg.b.32457
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Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 875, doi. 10.1002/ajmg.b.32458
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Cover Image, Volume 171B, Number 6, September 2016.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. i, doi. 10.1002/ajmg.b.32490
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Issue Information - TOC.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 761, doi. 10.1002/ajmg.b.32371
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- Article
COMT genotype is associated with differential expression of muscarinic M1 receptors in human cortex.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 784, doi. 10.1002/ajmg.b.32440
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Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 790, doi. 10.1002/ajmg.b.32441
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Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 797, doi. 10.1002/ajmg.b.32444
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Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 806, doi. 10.1002/ajmg.b.32445
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Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 815, doi. 10.1002/ajmg.b.32446
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