Associate Professor of Psychiatry, University of Chicago Medicine
Psychiatry
Dr. Judith Badner, MD
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Dr. Judith Badner is an expert in the field of Psychiatry. He studied medicine at University of Pittsburgh School of Medicine. He received awards:"CMS Meaningful Use Stage 1 Certification". Judith Badner is a published doctor and has 91 publications published. The lastest was: 'Optimal ascertainment strategies to detect linkage to common disease alleles.' Judith Badner is registered with Medicare and accepts Medicare payments.
Publications
- Rare variants in neuronal excitability genes influence risk for bipolar Disorder.
- Pharmacogenetic associations of the type-3 metabotropic glutamate receptor (GRM3) gene with working memory and clinical symptom response to antipsychotics in first-epi...
- Two gene co-expression modules differentiate psychotics and controls.
- Heritability and linkage analysis of personality in bipolar Disorder.
- Genome-wide association study implicates NDST3 in schizophrenia and bipolar Disorder.
- Heritability and genome-wide SNP linkage analysis of temperament in bipolar Disorder.
- Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar Disorder susceptibility variants.
- Use of exact and adjusted liability scores to detect genes affecting common traits.
- No association of trace amine receptor genes with bipolar Disorder.
- Genome-wide linkage scan of 98 Bipolar pedigrees and analysis of clinical covariates.
- Progress toward discovery of susceptibility genes for Bipolar manic-depressive illness and schizophrenia.
- Family-based association study of DAT1 and DRD4 polymorphism in Korean children with ADHD.
- Family-based association study of the serotonin transporter gene polymorphisms in Korean ADHD trios.
- Genome-wide association study of bipolar Disorder in European American and African American individuals.
- Association between ADORA2A and DRD2 polymorphisms and caffeine-induced Anxiety.
- Genome-wide association in Bipolar.
- Whole-genome association mapping of gene expression in the human prefrontal cortex.
- Meta-analysis of whole-genome linkage scans of bipolar Disorder and schizophrenia.
- Linkage analysis of schizophrenia to chromosome 15.
- Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.
- Comparison of novel and existing methods for detection of linkage disequilibrium using parent-child trios in the GAW12 genetic isolate simulated data.
- Linkage of bipolar Disorder to chromosome 18q and the validity of bipolar II Disorder.
- Fine mapping supports previous linkage evidence for a bipolar Disorder susceptibility locus on 13q32.
- Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.
- Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective Disorder pedigrees.
- Meta-analysis of linkage studies.
- A high-density genome scan detects evidence for a bipolar-Disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.
- Optimal ascertainment strategies to detect linkage to common disease alleles.
- Serotonin transporter (5-HTT) gene and bipolar affective Disorder.
- Closing in on genes for manic-Depressive illness and schizophrenia.
- Bipolar Disorder and chromosome 18: an analysis of multiple data sets.
- Lack of linkage between the corticotropin-releasing hormone (CRH) gene and bipolar affective Disorder.
- Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees.
- Initial genome scan of the NIMH genetics initiative Bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.
- DNA pooling and affected sib pair analysis.
- No abnormality in the gene for the G protein stimulatory alpha subunit in patients with bipolar Disorder.
- Maternal inheritance and chromosome 18 allele sharing in unilineal Bipolar illness pedigrees.
- Detection of linkage to affective Disorders in the catalogued Amish pedigrees: a reply to Pauls et al.
- Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar Disorder, on 21q.
- Multipoint genetic linkage analysis of the m2 human muscarinic receptor gene.
- A test of nonrandom segregation.
- Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores.
- Linkage analysis between Huntington disease and the G8 marker locus.
- A genetic study of Hirschsprung disease.
- Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
- Mutation screening of two candidate genes from 13q32 in families affected with Bipolar Disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5).
- A pharmacogenetic study of uridine diphosphate-glucuronosyltransferase 2B7 in patients receiving morphine.
- Removing batch effects in analysis of expression microarray data: an evaluation of six batch Adjustment methods.
- Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.
- Incorporation of molecular data and redefinition of phenotype: new approaches to genetic epidemiology of Bipolar manic depressive illness and schizophrenia.
- Large-scale genome-wide association analysis of bipolar Disorder identifies a new susceptibility locus near ODZ4.
- Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes.
- A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum Disorders.
- Genome-wide association study of personality traits in Bipolar patients.
- Family-based association testing of glutamate transporter genes in autism.
- Strategies to identify genes for complex Disorders: a focus on bipolar Disorder and chromosome 16p.
- Genome scan meta-analysis of schizophrenia and bipolar Disorder, part III: Bipolar Disorder.
- Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar Disorder in two independent pedigree series.
- Additional, physically ordered markers increase linkage signal for bipolar Disorder on chromosome 18q22.
- A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective Disorder in a small family.
- Can long-range microsatellite data be used to predict short-range linkage disequilibrium?
- An evaluation of the assembly of an approximately 15-Mb region on human chromosome 13q32-q33 linked to bipolar Disorder and schizophrenia.
- Genetic control of individual differences in gene-specific methylation in human brain.
- Allelic association of G72/G30 with schizophrenia and bipolar Disorder: a comprehensive meta-analysis.
- Susceptibility loci involved in cisplatin-induced cytotoxicity and apoptosis.
- Clock genes may influence bipolar Disorder susceptibility and dysfunctional circadian rhythm.
- Recurrent 16p11.2 microdeletions in autism.
- Association and mutation analyses of 16p11.2 autism candidate genes.
- Common and rare variants of DAOA in bipolar Disorder.
- Whole-genome approach implicates CD44 in cellular resistance to carboplatin.
- Identification of genomic regions contributing to etoposide-induced cytotoxicity.
- Further evidence for an association of G72/G30 with schizophrenia in Chinese.
- Genome-wide parametric linkage analyses of 644 Bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20.
- Association study of Wnt signaling pathway genes in bipolar Disorder.
- PDLIM5 and susceptibility to bipolar Disorder: a family-based association study and meta-analysis.
- Neurotransmission and bipolar Disorder: a systematic family-based association study.
- Novel submicroscopic chromosomal abnormalities detected in autism spectrum Disorder.
- Familial variation in episode frequency in bipolar affective Disorder.
- Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar Disorder.
- Linkage disequilibrium of the brain-derived neurotrophic factor Val66Met polymorphism in children with a prepubertal and early adolescent bipolar Disorder phenotype.
- Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective Disorder in the national institute of mental health genetics initiative pedigrees.
- Heritability and linkage analysis of sensitivity to cisplatin-induced cytotoxicity.
- Genome-wide scan and conditional analysis in bipolar Disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar ...
- No evidence for association between 19 cholinergic genes and bipolar Disorder.
- Attempted suicide in bipolar Disorder pedigrees: evidence for linkage to 2p12.
- Are the arginine vasopressin V1a receptor microsatellites related to hypersexuality in children with a prepubertal and early adolescent bipolar Disorder phenotype?
- Sequence variation in DOCK9 and heterogeneity in bipolar Disorder.
- Mapping genes that contribute to daunorubicin-induced cytotoxicity.
- No association detected between a D3 receptor gene-expressed variant and schizophrenia.
- Analysis of DRPLA trinucleotide repeats in schizophrenia.
Schools
Univ Of Pittsburgh Sch Of Med
McLean Hospital
Procedures Preformed
- Psychiatric Evaluation
Conditions Treated
- Adjustment Disorder
- Alcoholism (Alcohol Dependence)
- Anxiety
- Bipolar Disorder
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Doctors Specialties
- Psychiatry
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Card PPO
- Blue Cross Blue Shield of Illinois PPO
- Cofinity PPO
- First Health (Coventry Health Care) PPO
- HealthLink PPO
- MultiPlan PPO
- PHCS Network PPO
- Sagamore Plus
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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National Institutes of Health Clinical Center -
University of Pittsburgh School of Medicine
Hospital
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Mercy Hospital and Medical Center -
University of Chicago Medical Center
Drug Facts
| NPI NUMBER | 1154449544 | |
| NPPES Provider LastName | BADNER | |
| NPPES Provider FirstName | JUDITH | |
| NPPES Provider ZIPCode | 606371447 | |
| NPPES Provider State | IL | |
| Specialty Description | Psychiatry | |
| Total Claim Count | 226.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1154449544 |
| Last Name Of The Provider | BADNER |
| First Name Of The Provider | JUDITH |
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