Search Results - "KELSOE, JOHN R"
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Polygenic Polarity in Bipolar Disorder
Published in The American journal of psychiatry (01-03-2023)“…The polygenic risk score (PRS) was created in order to capture the overall polygenic contribution to genetic heritability. This is accomplished by summing all…”
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2
High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
Published in Neuron (Cambridge, Mass.) (22-12-2011)“…While it is known that rare copy-number variants (CNVs) contribute to risk for some neuropsychiatric disorders, the role of CNVs in bipolar disorder is…”
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Toward a Valid Animal Model of Bipolar Disorder: How the Research Domain Criteria Help Bridge the Clinical-Basic Science Divide
Published in Biological psychiatry (1969) (2016)“…Abstract Bipolar disorder is a diagnostically heterogeneous disorder, although mania emerges as a distinct phenotype characterized by elevated mood and…”
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Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate
Published in PLoS genetics (01-04-2013)“…Several lines of evidence suggest that genome-wide association studies (GWAS) have the potential to explain more of the "missing heritability" of common…”
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A survey of genomic studies supports association of circadian clock genes with bipolar disorder spectrum illnesses and lithium response
Published in PloS one (22-02-2012)“…Circadian rhythm abnormalities in bipolar disorder (BD) have led to a search for genetic abnormalities in circadian "clock genes" associated with BD. However,…”
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Circadian rhythms in bipolar disorder patient-derived neurons predict lithium response: preliminary studies
Published in Molecular psychiatry (01-07-2021)“…A bstract Bipolar disorder (BD) is a neuropsychiatric illness defined by recurrent episodes of mania/hypomania, depression and circadian rhythm abnormalities…”
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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
Published in Nature (London) (24-03-2011)“…Rare copy number variants (CNVs) have a prominent role in the aetiology of schizophrenia and other neuropsychiatric disorders. Substantial risk for…”
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All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs
Published in PLoS genetics (01-04-2013)“…Recent results indicate that genome-wide association studies (GWAS) have the potential to explain much of the heritability of common complex phenotypes, but…”
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Analysis of 94 Candidate Genes and 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia
Published in American Journal of Psychiatry (01-09-2011)“…Genes affecting glutamate neurotransmission featured prominently in associations between 94 genes and 12 inherited physiological or cognitive characteristics…”
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10
Differentiation of Inflammation-Responsive Astrocytes from Glial Progenitors Generated from Human Induced Pluripotent Stem Cells
Published in Stem cell reports (06-06-2017)“…Astrocyte dysfunction and neuroinflammation are detrimental features in multiple pathologies of the CNS. Therefore, the development of methods that produce…”
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Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice
Published in Translational psychiatry (24-11-2020)“…Previously, we reported a family in which bipolar disorder (BD) co-segregates with a Mendelian kidney disorder linked to 1q22. The causative renal gene was…”
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Common and rare variant analysis in early-onset bipolar disorder vulnerability
Published in PloS one (11-08-2014)“…Bipolar disorder is one of the most common and devastating psychiatric disorders whose mechanisms remain largely unknown. Despite a strong genetic contribution…”
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13
CRY2 is associated with depression
Published in PloS one (24-02-2010)“…Abnormalities in the circadian clockwork often characterize patients with major depressive and bipolar disorders. Circadian clock genes are targets of interest…”
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14
Pharmacogenetics of lithium response in bipolar disorder
Published in Pharmacogenomics (01-10-2010)“…Bipolar disorder (BD) is a serious mental illness with well-established, but poorly characterized genetic risk. Lithium is among the best proven mood…”
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Effect of the Type and Number of Adverse Childhood Experiences and the Timing of Adverse Experiences on Clinical Outcomes in Individuals with Bipolar Disorder
Published in Brain sciences (27-04-2020)“…Studies have reported an association between adverse childhood experiences (ACEs) and the clinical outcomes of bipolar disorder (BD). However, these studies…”
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Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective Disorders
Published in EBioMedicine (01-08-2015)“…Psychiatric disorders are common mental disorders without a pathological biomarker. Classic genetic studies found that an extra X chromosome frequently causes…”
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TEMPS-A: validation of a short version of a self-rated instrument designed to measure variations in temperament
Published in Journal of affective disorders (01-03-2005)“…Objective: To validate a short English-language version of the Temperament Evaluation of Memphis, Pisa, Paris and San Diego-autoquestionnaire version…”
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A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder
Published in Journal of affective disorders (20-02-2013)“…Abstract Objective The use of subphenotypes may be an effective approach for genetic studies of complex diseases. Manic episodes with a seasonal pattern may…”
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RNA sequencing of transcriptomes in human brain regions: protein-coding and non-coding RNAs, isoforms and alleles
Published in BMC genomics (23-11-2015)“…We used RNA sequencing to analyze transcript profiles of ten autopsy brain regions from ten subjects. RNA sequencing techniques were designed to detect both…”
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Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene
Published in Genomics (San Diego, Calif.) (01-11-2003)“…We have attempted to identify regions involved in the transcriptional regulation of the DAT1 (HUGO approved symbol SLC6A3) gene that may harbor functional…”
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