Genetic variability in the regulation of gene expression in ten regions of the human brain

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18. Genetic Variants and Multiple Sclerosis Risk Gene SLC9A9 Expression in Distinct Human Brain Regions
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20. Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment
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26. The Arc Gene Confers Genetic Susceptibility to Alzheimer’s Disease in Han Chinese
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27. A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus
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28. Exome sequencing of healthy phenotypic extremes links TROVE2 to emotional memory and PTSD
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30. Disease status affects the association between rs4813620 and the expression of Alzheimer’s disease susceptibility gene TRIB3
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31. Sex-stratified genome-wide association meta-analysis of major depressive disorder
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32. Genome-Wide Variants Shared Between Smoking Quantity and Schizophrenia on 15q25 Are Associated With CHRNA5 Expression in the Brain
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35. Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
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36. Morphometric dis-similarity between cortical and subcortical areas underlies cognitive function and psychiatric symptomatology: a preadolescence study from ABCD
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37. Genetic risk mechanisms of posttraumatic stress disorder in the human brain
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38. NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis
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41. RNA sequencing of transcriptomes in human brain regions: protein-coding and non-coding RNAs, isoforms and alleles
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43. The genetic architecture of language functional connectivity
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51. Genome-Wide Association Study of Over 427,000 Individuals Establishes Executive Functioning as a Neurocognitive Basis of Psychiatric Disorders Influenced by GABAergic Processes
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75. Genetic architectures of cerebral ventricles and their overlap with neuropsychiatric traits
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83. SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed
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84. Genomic approaches to the assessment of human spina bifida risk
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85. A new locus regulating MICALL2 expression was identified for association with executive inhibition in children with attention deficit hyperactivity disorder
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86. Genetic loci for alcohol-related life events and substance-induced affective symptoms: indexing the “dark side” of addiction
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88. Genomewide Gene-by-Sex Interaction Scans Identify ADGRV1 for Sex Differences in Opioid Dependent African Americans
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89. Unique Allelic eQTL Clusters in Human MHC Haplotypes
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90. Genome-Wide Association Study of Opioid Cessation
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91. Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination
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92. A comprehensive analysis of NDST3 for schizophrenia and bipolar disorder in Han Chinese
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93. Genetic regulation of gene expression in the epileptic human hippocampus
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95. Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population
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96. Estimating contribution of rare non‐coding variants to neuropsychiatric disorders
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97. MYORG -related disease is associated with central pontine calcifications and atypical parkinsonism
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98. A Comprehensive Analysis of the Effect of SIRT1 Variation on the Risk of Schizophrenia and Depressive Symptoms
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99. Predictability of polygenic risk score for progression to dementia and its interaction with APOE ε4 in mild cognitive impairment
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100. Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health
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