-Edwin H Cook Researcher Activity Profile

Research Author Detailed Information 

Edwin H Cook Publication Rate By Year

Edwin H Cook has published 5 paper(s) in 2006, 16 paper(s) in 2007, 7 paper(s) in 2008, for a total of 28 research publications in total.

Edwin H Eh Cook Author Information

LAST NAME: cook

FIRST NAME: Edwin H

INITIALS: eh

AFFILIATION:

Papers

Edwin H Cook's Publication Record

1. Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Year Published: 2007
Institute for Juvenile Research, Department of Psychiatry, University of Illinois at Chicago, 1747 West Roosevelt Road, Chicago, IL 60608, USA. sjacob@psych.uic.edu
2. ITGB3 shows genetic and expression interaction with SLC6A4. Year Published: 2006
Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA. laweiss@chgr.mgh.harvard.edu
3. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. Year Published: 2006
Department of Human Genetics, The University of Chicago, Chicago, IL, USA.
4. Serotonin transporter genotype and acute subjective response to amphetamine. Year Published: 2006
Linden Oaks Hospital at Edward, Naperville, Illinois, USA. dlott@jhu.edu
5. A prospective, open-label trial of memantine in the treatment of cognitive, behavioral, and memory dysfunction in pervasive developmental disorders. Year Published: 2006
University of Illinois at Chicago, Department of Psychiatry, Institute for Juvenile Research, Chicago, Illinois 60608, USA. towley@psych.uic.edu
6. 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism. Year Published: 2006
Institute for Juvenile Research, Department of Psychiatry (M/C 747), University of Illinois at Chicago, 1747 West Roosevelt Rd., Rm. 155, Chicago, IL 60608, USA.
7. Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder. Year Published: 2007
Institute of Juvenile Research, Department of Psychiatry, University of Illinois at Chicago, Chicago, Illinois, USA.
8. Using the autism diagnostic interview--revised to increase phenotypic homogeneity in genetic studies of autism. Year Published: 2007
University of Michigan Autism and Communication Disorders Center, Ann Arbor, Michigan, USA.
9. Genetic studies of stuttering in a founder population. Year Published: 2007
Department of Human Genetics, The University of Chicago, Chicago, IL 60637, United States.
10. Association of dopamine transporter genotype with disruptive behavior disorders in an eight-year longitudinal study of children and adolescents. Year Published: 2007
Department of Psychology, University of California, Los Angeles, California 90095-1563, USA. stevelee@psych.ucla.edu
11. Norepinephrine transporter gene variation modulates acute response to D-amphetamine. Year Published: 2007
12. Between a ROC and a hard place: decision making and making decisions about using the SCQ. Year Published: 2007
University of California, San Diego, USA. ccorsello@ucsd.edu
13. Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder. Year Published: 2007
Department of Psychiatry, University of Michigan, Ann Arbor, Michigan 48105, USA. ghanna@umich.edu
14. Relationship of EGFR Mutations, Expression, Amplification, and Polymorphisms to Epidermal Growth Factor Receptor Inhibitors in the NCI60 Cell Lines. Year Published: 2007
Authors' Affiliations: Departments of Medicine and Human Genetics, Committee on Clinical Pharmacology and Pharmacogenomics, and Cancer Research Center, The University of Chicago.
15. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Year Published: 2007
1Pritzker School of Medicine, University of Chicago, Chicago, IL, USA.
16. Between a ROC and a hard place: decision making and making decisions about using the SCQ. Year Published: 2007
University of California, San Diego, USA. ccorsello@ucsd.edu
17. Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines. Year Published: 2007
Department of Medicine, The University of Chicago, 5841 South Maryland Avenue, Chicago, IL 60637, USA.
18. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Year Published: 2007
Pritzker School of Medicine, University of Chicago, Chicago, IL, USA.
19. A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. Year Published: 2008
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
20. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Year Published: 2008
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
21. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Year Published: 2008
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
22. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Year Published: 2007
Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.
23. Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines. Year Published: 2007
Department of Medicine, The University of Chicago, 5841 South Maryland Avenue, Chicago, IL 60637, USA.
24. Recurrent 16p11.2 microdeletions in autism. Year Published: 2008
25. Recurrent 16p11.2 microdeletions in autism. Year Published: 2008
Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
26. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Year Published: 2007
Pritzker School of Medicine, University of Chicago, Chicago, IL, USA.
27. GAD1 single nucleotide polymorphism is in linkage disequilibrium with a child bipolar I disorder phenotype. Year Published: 2008
Department of Psychiatry, Washington University in St. Louis, 660 South Euclid Avenue, St. Louis, MO 63110, USA. gellerb@medicine.wustl.edu
28. It is time to take a stand for medical research and against terrorism targeting medical scientists. Year Published: 2008
Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA. john.krystal@yale.edu