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RUSSELL KOOY, M.D.
M.D.
Surgery Physician
NPI: 1770567596Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
23993(MN)
Research & Publications (20)
The complexity of the GABAA receptor shapes unique pharmacological profiles.
PMID 19576998·Drug Discov Today·2009
6-review
Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS).
PMID 19070606·Brain Res·2009
7-preclinical
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
PMID 18159213·Eur J Hum Genet·2008
8-other
Effect of genetic background on acoustic startle response in fragile X knockout mice.
PMID 18840308·Genet Res (Camb)·2008
7-preclinical
CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1.
PMID 17236128·Am J Hum Genet·2007
8-other
FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis.
PMID 17083330·Genes Brain Behav·2007
4-observational
The GABAA receptor: a novel target for treatment of fragile X?
PMID 17590448·Trends Neurosci·2007
6-review
Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiency.
PMID 17994567·Am J Med Genet A·2007
5-case
Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation.
PMID 16991117·Hum Mutat·2007
8-other
The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior.
PMID 17236142·Am J Hum Genet·2007
8-other
Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse model.
PMID 16199166·Neurobiol Dis·2006
4-observational
Decreased expression of the GABAA receptor in fragile X syndrome.
PMID 17046729·Brain Res·2006
7-preclinical
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
PMID 16906164·Nat Genet·2006
4-observational
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
PMID 16773126·Eur J Hum Genet·2006
7-preclinical
Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.
PMID 16451137·Clin Genet·2006
5-case
Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods.
PMID 15880643·Hum Mutat·2005
4-observational
Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).
PMID 15876460·Behav Brain Res·2005
4-observational
Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype.
PMID 15822126·Am J Med Genet A·2005
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1000 1ST DR NW
AUSTIN, MN 55912 - Phone
- (507) 434-1092
Quick Facts
- NPI
- 1770567596
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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