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Author Details
Full Name
Sevilla D Detera-Wadleigh
Affiliation
National Institute of Mental Health Intramural Research Program
ORCID
Career Start Year
1979
Papers
130
H Index
49
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33558674
Deep transcriptome sequencing of subgenual anterior cingulate cortex reveals cross-diagnostic and diagnosis-specific RNA expression changes in major psychiatric disorders.
Neuropsychopharmacology
2021
30135510
Sodium valproate rescues expression of TRANK1 in iPSC-derived neural cells that carry a genetic variant associated with serious mental illness.
Mol Psychiatry
2019
25730879
Rare variants in neuronal excitability genes influence risk for bipolar disorder.
Proc Natl Acad Sci U S A
2015
24393808
RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms and GTPase binding in bipolar disorder.
Mol Psychiatry
2014
23840348
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report.
PLoS One
2013
21383773
Interaction networks of lithium and valproate molecular targets reveal a striking enrichment of apoptosis functional clusters and neurotrophin signaling.
Pharmacogenomics J
2012
21547870
A systems approach to the biology of mood disorders through network analysis of candidate genes.
Pharmacopsychiatry
2011
22242126
Ablation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice.
PLoS One
2011
22373213
Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives.
BMC Proc
2011
20081856
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
Nat Genet
2010
20453537
The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment.
Neuropsychobiology
2010
19214142
Association study of phosphodiesterase genes in the Sequenced Treatment Alternatives to Relieve Depression sample.
Pharmacogenet Genomics
2009
19461657
Analysis of a t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia.
J Hum Genet
2009
19088739
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder.
Mol Psychiatry
2009
19194963
Common and rare variants of DAOA in bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
2009
17486107
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
Mol Psychiatry
2008
18246526
Glucocorticoid receptor gene polymorphisms in premenopausal women with major depression.
Horm Metab Res
2008
18197083
SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder.
Psychiatr Genet
2008
18197079
Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder.
Psychiatr Genet
2008
17671966
Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
Am J Med Genet B Neuropsychiatr Genet
2008
16806105
Nested association between genetic variation in tryptophan hydroxylase II, bipolar affective disorder, and suicide attempts.
Biol Psychiatry
2007
17728666
Sequence variation in DOCK9 and heterogeneity in bipolar disorder.
Psychiatr Genet
2007
17380209
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.
J Clin Invest
2007
17453059
Rare plus common SERT variants in obsessive-compulsive disorder.
Mol Psychiatry
2007
16996484
Haplotype analysis and a novel allele-sharing method refines a chromosome 4p locus linked to bipolar affective disorder.
Biol Psychiatry
2007
17251911
A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription.
Neuropsychopharmacology
2007
16205735
Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3.
Mol Psychiatry
2006
16859551
Common variations in ALG9 are not associated with bipolar I disorder: a family-based study.
Behav Brain Funct
2006
16487942
Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression.
Biol Psychiatry
2006
16581030
G72/G30 in schizophrenia and bipolar disorder: review and meta-analysis.
Biol Psychiatry
2006
15635705
Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
2005
14699445
Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
Mol Psychiatry
2004
16194763
Genetic association studies in mood disorders: issues and promise.
Int Rev Psychiatry
2004
15219468
Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees.
Biol Psychiatry
2004
14706423
Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders.
Biol Psychiatry
2004
12802785
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
Am J Hum Genet
2003
14643094
Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.
Biol Psychiatry
2003
14653307
Experimental gene interaction studies with SERT mutant mice as models for human polygenic and epistatic traits and disorders.
Genes Brain Behav
2003
12618287
Analysis of a cluster of polymorphisms in AKT1 gene in bipolar pedigrees: a family-based association study.
Neurosci Lett
2003
12647258
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series.
Am J Hum Genet
2003
12627459
Distribution of haplotypes derived from three common variants of the NR4A2 gene in Japanese patients with schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
2003
12809987
Genetic analysis of a functional GRIN2A promoter (GT)n repeat in bipolar disorder pedigrees in humans.
Neurosci Lett
2003
11986976
Map of candidate genes and STSs on 18p11.2, a bipolar disorder and schizophrenia susceptibility region.
Mol Psychiatry
2002
12176134
Expression of the smoothelin gene is mediated by alternative promoters.
Cardiovasc Res
2002
12399948
Association between serotonin 4 receptor gene polymorphisms and bipolar disorder in Japanese case-control samples and the NIMH Genetics Initiative Bipolar Pedigrees.
Mol Psychiatry
2002
12392603
Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5).
BMC Genomics
2002
12030331
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family.
Neurogenetics
2002
12082561
Association analysis of adenylate cyclase type 9 gene using pedigree disequilibrium test in bipolar disorder.
Mol Psychiatry
2002
11405549
Lithium-related genetics of bipolar disorder.
Ann Med
2001
11317223
Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samples.
Mol Psychiatry
2001
1 - 50 of 130
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University of Michigan ann arbor
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James B Potash
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Sven Cichon
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