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CHELSEY RUSS, M.D.
M.D.
Obstetrics & Gynecology Physician
NPI: 1699207118IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
067559(CT)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
OTHER
Class of 2017
Research & Publications (20)
DNA sequence analysis of the conserved region around the SOD1 gene locus in recessively inherited ALS.
PMID 19596401·Neurosci Lett·2009
8-other
Quantitative deep sequencing reveals dynamic HIV-1 escape and large population shifts during CCR5 antagonist therapy in vivo.
PMID 19479085·PLoS One·2009
8-other
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
PMID 19251627·Science·2009
7-preclinical
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing.
PMID 19182786·Nat Biotechnol·2009
8-other
High-resolution mapping of copy-number alterations with massively parallel sequencing.
PMID 19043412·Nat Methods·2009
8-other
50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis.
PMID 18608091·Amyotroph Lateral Scler·2008
8-other
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS.
PMID 18574757·Amyotroph Lateral Scler·2008
8-other
Combat related post traumatic stress disorder: a multiple case report using virtual reality graded exposure therapy with physiological monitoring.
PMID 18391367·Stud Health Technol Inform·2008
5-case
Quality scores and SNP detection in sequencing-by-synthesis systems.
PMID 18212088·Genome Res·2008
8-other
SOD1A4V-mediated ALS: absence of a closely linked modifier gene and origination in Asia.
PMID 18055113·Neurosci Lett·2008
8-other
Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
PMID 17721707·Acta Neuropathol·2007
8-other
A familial form of pallidoluysionigral degeneration and amyotrophic lateral sclerosis with divergent clinical presentations.
PMID 17620990·J Neuropathol Exp Neurol·2007
8-other
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells.
PMID 17603471·Nature·2007
7-preclinical
No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approach.
PMID 16546759·Amyotroph Lateral Scler·2006
4-observational
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.
PMID 16501576·Nat Genet·2006
8-other
Association analysis of the glycogen synthase kinase-3beta gene in bipolar disorder.
PMID 16289783·Neurosci Lett·2006
8-other
Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes.
PMID 16174551·Neurosci Lett·2006
4-observational
Rate of progression of cognitive decline in Alzheimer's disease: effect of butyrylcholinesterase K gene variation.
PMID 15834019·J Neurol Neurosurg Psychiatry·2005
8-other
No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS.
PMID 15623718·Neurology·2004
8-other
Functional effects of a tandem duplication polymorphism in the 5'flanking region of the DRD4 gene.
PMID 15522254·Biol Psychiatry·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 491 GOLD STAR HWY STE 100
GROTON, CT 06340 - Phone
- (860) 445-4290
Quick Facts
- NPI
- 1699207118
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 9
- Publications
- 20
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