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Author Details
Full Name
Judith A Badner
Affiliation
Rush University Medical College
ORCID
Career Start Year
1984
Papers
109
H Index
43
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35546635
Rare variants implicate NMDA receptor signaling and cerebellar gene networks in risk for bipolar disorder.
Mol Psychiatry
2022
34080073
Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation.
Arch Sex Behav
2021
30503783
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.
Eur Neuropsychopharmacol
2019
31530798
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.
Transl Psychiatry
2019
30415424
Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.
Int J Bipolar Disord
2018
30545964
The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders.
Sci Transl Med
2018
29217827
Genome-Wide Association Study of Male Sexual Orientation.
Sci Rep
2017
26905411
Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes.
Transl Psychiatry
2016
27867939
A Rare Variant in <i>CACNA1D</i> Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree.
Mol Neuropsychiatry
2016
27329760
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Hum Mol Genet
2016
25096017
Pharmacogenetic associations of the type-3 metabotropic glutamate receptor (GRM3) gene with working memory and clinical symptom response to antipsychotics in first-episode schizophrenia.
Psychopharmacology (Berl)
2015
26481615
Pursuit eye movements as an intermediate phenotype across psychotic disorders: Evidence from the B-SNIP study.
Schizophr Res
2015
25832558
Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies.
Am J Med Genet B Neuropsychiatr Genet
2015
25730879
Rare variants in neuronal excitability genes influence risk for bipolar disorder.
Proc Natl Acad Sci U S A
2015
25399360
Genome-wide scan demonstrates significant linkage for male sexual orientation.
Psychol Med
2015
23979604
A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain.
Mol Psychiatry
2014
22212596
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
Mol Psychiatry
2013
24253340
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.
Nat Commun
2013
23933821
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Nat Genet
2013
23972719
Heritability and linkage analysis of personality in bipolar disorder.
J Affect Disord
2013
23759419
Heritability and genome-wide SNP linkage analysis of temperament in bipolar disorder.
J Affect Disord
2013
23147385
Two gene co-expression modules differentiate psychotics and controls.
Mol Psychiatry
2013
21769101
Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.
Mol Psychiatry
2012
23010768
Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.
Transl Psychiatry
2012
23038240
Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin.
Am J Med Genet B Neuropsychiatr Genet
2012
22633946
Genome-wide linkage analysis of obsessive-compulsive disorder implicates chromosome 1p36.
Biol Psychiatry
2012
22591576
Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci.
Mol Autism
2012
20453718
Strategies to identify genes for complex disorders: a focus on bipolar disorder and chromosome 16p.
Psychiatr Genet
2011
21609426
A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders.
Mol Autism
2011
21691774
Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.
Hum Genet
2011
21738484
Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.
PLoS Genet
2011
21368711
Genome-wide association study of personality traits in bipolar patients.
Psychiatr Genet
2011
21386892
Removing batch effects in analysis of expression microarray data: an evaluation of six batch adjustment methods.
PLoS One
2011
21085054
Family-based association testing of glutamate transporter genes in autism.
Psychiatr Genet
2011
20351726
Whole-genome association mapping of gene expression in the human prefrontal cortex.
Mol Psychiatry
2010
20215007
Genetic control of individual differences in gene-specific methylation in human brain.
Am J Hum Genet
2010
18775646
Further evidence for an association of G72/G30 with schizophrenia in Chinese.
Schizophr Res
2009
19488044
Genome-wide association study of bipolar disorder in European American and African American individuals.
Mol Psychiatry
2009
19089452
Identification of genomic regions contributing to etoposide-induced cytotoxicity.
Hum Genet
2009
19164090
Whole-genome approach implicates CD44 in cellular resistance to carboplatin.
Hum Genomics
2009
19242545
Association and mutation analyses of 16p11.2 autism candidate genes.
PLoS One
2009
19194963
Common and rare variants of DAOA in bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
2009
18084308
Genome-wide association in bipolar.
Mol Psychiatry
2008
18496208
PDLIM5 and susceptibility to bipolar disorder: a family-based association study and meta-analysis.
Psychiatr Genet
2008
18606951
Association study of Wnt signaling pathway genes in bipolar disorder.
Arch Gen Psychiatry
2008
18628681
Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20.
Psychiatr Genet
2008
18305461
Association between ADORA2A and DRD2 polymorphisms and caffeine-induced anxiety.
Neuropsychopharmacology
2008
18300947
Susceptibility loci involved in cisplatin-induced cytotoxicity and apoptosis.
Pharmacogenet Genomics
2008
18228528
Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm.
Am J Med Genet B Neuropsychiatr Genet
2008
18374305
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Biol Psychiatry
2008
1 - 50 of 109
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Tatiana Foroud
Indiana University School of Medicine
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John P Rice
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Jay Raymond DePaulo
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Thomas G Schulze
SUNY Upstate Medical University
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Lynn R Goldin
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David W Craig
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