Associate Professor of Psychiatry, University Chicago-Pritzker School of Medicine
Psychiatry
Dr. Edwin J. Cook, DO
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Edwin Cook works in the field of Psychiatry. He has 1 awards "Super Doctor". Dr. Edwin J. Cook, DO has written publications. He has 98 publications published with PubMed. The lastest publication is: 'Separating Family-Level and Direct Exposure Effects of Smoking During Pregnancy on Offspring Externalizing Symptoms: Bridging the Behavior Genetic and Behavior Teratol...' Dr. Edwin J. Cook, DO accepts Medicare.
Publications
- Separating Family-Level and Direct Exposure Effects of Smoking During Pregnancy on Offspring Externalizing Symptoms: Bridging the Behavior Genetic and Behavior Teratol...
- The phenotypic Manifestations of rare genic CNVs in autism spectrum disorder.
- CYP2A6 Longitudinal Effects in Young Smokers.
- Loss of δ-catenin function in severe autism.
- Feedforward and feedback motor control abnormalities implicate cerebellar dysfunctions in autism spectrum disorder.
- Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice.
- Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
- A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
- Preliminary evidence for the interaction of the oxytocin receptor gene (oxtr) and face processing in differentiating prenatal smoking patterns.
- Synaptic, transcriptional and chromatin genes disrupted in autism.
- A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?
- Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
- A framework for the interpretation of de novo mutation in human Disease.
- Cognitive Set Shifting Deficits and Their Relationship to Repetitive Behaviors in Autism Spectrum Disorder.
- Convergence of genes and cellular pathways dysregulated in autism spectrum Disorders.
- Dopamine Transporter Genotype and Stimulant Dose-Response in Youth With Attention-Deficit/Hyperactivity Disorder.
- Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2.
- Environmental and state-level regulatory factors affect the incidence of autism and intellectual disability.
- A survey of seizures and current treatments in 15q duplication syndrome.
- Association of the CHRNA4 Neuronal Nicotinic Receptor Subunit Gene With Frequency of Binge Drinking in Young Adults.
- De novo mutation in the dopamine transporter gene associates dopamine dysfunction With autism spectrum disorder.
- Drosophila melanogaster: a novel animal model for the behavioral characterization of autism-associated mutations in the dopamine transporter gene.
- Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait.
- Training of child and adolescent psychiatry fellows in autism and intellectual disability.
- Measuring Anxiety as a Treatment Endpoint in Youth With Autism Spectrum Disorder.
- Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
- Do dopamine gene variants and prenatal smoking interactively predict youth externalizing behavior?
- Effect of Neuronal Nicotinic Acetylcholine Receptor Genes (CHRN) on Longitudinal Cigarettes per Day in Adolescents and Young Adults.
- Parental Broader Autism Subphenotypes in ASD Affected Families: Relationship to Gender, Child's Symptoms, SSRI Treatment, and Platelet Serotonin.
- Genome-wide association study of obsessive-compulsive disorder.
- Intellectual Disability Is Associated With Increased Runs of Homozygosity in Simplex Autism.
- Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1.
- Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls.
- Co-occurrence of autism, childhood psychosis, and intellectual disability associated With a de novo 3q29 microdeletion.
- Reduced behavioral flexibility in autism spectrum Disorders.
- Rare complete knockouts in humans: population distribution and significant role in autism spectrum Disorders.
- Rare inherited A2BP1 deletion in a proband With autism and developmental hemiparesis.
- A Multisite Study of the Clinical Diagnosis of Different Autism Spectrum Disorders.
- A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
- Mitochondrial small RNAs that are up-regulated in hippocampus during olfactory discrimination training in mice.
- Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
- Repetitive behavior profiles: Consistency across autism spectrum disorder cohorts and divergence from Prader-Willi syndrome.
- Identification of genetic Loci underlying the phenotypic constructs of autism spectrum Disorders.
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated With Autism.
- A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum Disorders.
- A genotype resource for postmortem brain samples from the Autism Tissue Program.
- De novo autosomal dominant mutation in SYNGAP1.
- Parent-of-origin effects of the serotonin transporter gene associated With autism.
- Interactions between early parenting and a polymorphism of the child's dopamine transporter gene in predicting future child conduct disorder symptoms.
- Effect of dopamine transporter genotype on caudate volume in childhood ADHD and controls.
- Endogenous siRNAs and noncoding RNA-derived small RNAs are expressed in adult mouse hippocampus and are up-regulated in olfactory discrimination training.
- Family-based association testing of glutamate transporter genes in autism.
- Dopamine transporter gene variation modulates activation of striatum in youth With ADHD.
- Neural response to working memory load varies by dopamine transporter genotype in children.
- Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.
- A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications.
- Autism spectrum disorder: unbroken mirror neurons; rare copy number variants.
- A pharmacogenetic study of escitalopram in autism spectrum Disorders.
- Reduction of increased repetitive self-grooming in ASD mouse model by metabotropic 5 glutamate receptor antagonism; randomized controlled trial of Early Start Denver M...
- Literature review: gastrointestinal symptoms in ASD, brain structure of identical twins With ASD.
- Serotonin rising.
- Dopamine transporter genotype and stimulant side effect factors in youth diagnosed With attention-deficit/hyperactivity disorder.
- Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
- Association and mutation analyses of 16p11.2 autism candidate genes.
- The impact of individual and methodological factors in the variability of response to methylphenidate in ADHD pharmacogenetic studies from four different continents.
- Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
- Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
- It is time to take a stand for medical research and against terrorism targeting medical scientists.
- Interactions between integrin alphaIIbbeta3 and the serotonin transporter regulate serotonin transport and platelet aggregation in mice and humans.
- Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample.
- Pharmacogenetics of minimal residual disease response in children with B-precursor Acute lymphoblastic leukemia: a report from the Children's Oncology Group.
- Heterogeneous association between engrailed-2 and autism in the CPEA network.
- GAD1 single nucleotide polymorphism is in linkage disequilibrium With a child bipolar I disorder phenotype.
- Molecular genetics of the platelet serotonin system in first-degree relatives of patients With autism.
- A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
- Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines.
- Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder.
- Norepinephrine transporter gene variation modulates Acute response to D-amphetamine.
- Ancestry and pharmacogenetics of antileukemic drug toxicity.
- Association of dopamine transporter genotype with disruptive behavior Disorders in an eight-year longitudinal study of children and adolescents.
- Using the autism diagnostic interview--revised to increase phenotypic homogeneity in genetic studies of autism.
- Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder.
- Genetic studies of stuttering in a founder population.
- 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism.
- A prospective, open-label trial of memantine in the treatment of cognitive, behavioral, and memory dysfunction in pervasive developmental Disorders.
- An association study of the brain-derived neurotrophic factor Val66Met polymorphism and amphetamine response.
- Combining information from multiple sources in the diagnosis of autism spectrum Disorders.
- Serotonin transporter genotype and Acute subjective response to amphetamine.
- Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
- Association between the casein kinase 1 epsilon gene region and subjective response to D-amphetamine.
- New complexities in the genetics of stuttering: significant sex-specific linkage signals.
- Interindividual variation in anxiety response to amphetamine: possible role for adenosine A2A receptor gene variants.
- A double-blind, placebo-controlled study of valproate for aggression in youth with pervasive developmental Disorders.
- Dopamine transporter genotype and methylphenidate dose response in children With ADHD.
- Pharmacogenetics of outcome in children with Acute lymphoblastic leukemia.
- An open-label trial of escitalopram in pervasive developmental Disorders.
- EPS or stereotypies?
Schools
Chicago College Of Osteopathic Medicine Of Midwestern University Midwestern University
Chicago Osteo Hosps and M C
Cleveland Clinic Fndn
Detroit Osteo Hospital
Procedures Preformed
- Hemodialysis
- Peritoneal Dialysis
Conditions Treated
- Acidosis
- Acute Kidney Failure
- Calcium Metabolism Disorders
- Chronic Kidney Diseases
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Doctors Specialties
- Nephrology
- Psychiatry
Accepted Insurances
Awards
- Super Doctor
Hospital
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University of Illinois Hospital & Health Sciences System
Drug Facts
| NPI NUMBER | 1508952011 | |
| NPPES Provider LastName | COOK | |
| NPPES Provider FirstName | EDWIN | |
| NPPES Provider ZIPCode | 60461 | |
| NPPES Provider State | IL | |
| Specialty Description | Nephrology | |
| Total Claim Count | 2303.0 | |
| Distinct Opioid Count | 1.0 | |
| Opioid Claim Count | 14.0 | |
| Percent Opioid Claims | 0.61 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1508952011 |
| Last Name Of The Provider | COOK |
| First Name Of The Provider | EDWIN |
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