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SVETLANA CHERNY, M.D.
M.D.
Family Medicine Physician
NPI: 1942473350Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
Research & Publications (20)
Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.
PMID 19367581·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Elevated plasma level of soluble F11 receptor/junctional adhesion molecule-A (F11R/JAM-A) in hypertension.
PMID 19214165·Am J Hypertens·2009
8-other
Novel sib pair selection strategy increases power in quantitative association analysis.
PMID 19568925·Behav Genet·2009
8-other
Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci.
PMID 19127410·Genetica·2009
6-review
A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma.
PMID 19176457·J Natl Cancer Inst·2009
5-case
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
PMID 19196962·Proc Natl Acad Sci U S A·2009
8-other
Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications.
PMID 18712713·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Diabetes prevalence and therapeutic target achievement in the United States, 1999 to 2006.
PMID 19375554·Am J Med·2009
4-observational
Association of a polymorphism in the lipin 1 gene with systolic blood pressure in men.
PMID 18437145·Am J Hypertens·2008
8-other
Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds.
PMID 18481795·Genet Epidemiol·2008
8-other
Mutational analysis of SHH and GLI3 in anorectal malformations.
PMID 18655123·Birth Defects Res A Clin Mol Teratol·2008
8-other
Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins.
PMID 18779828·Int J Obes (Lond)·2008
4-observational
A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis.
PMID 18081025·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays.
PMID 19117518·BMC Genomics·2008
8-other
Association of F11 receptor gene polymorphisms with central obesity and blood pressure.
PMID 18067551·J Intern Med·2008
8-other
The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset.
PMID 17181545·Ann Hum Genet·2007
8-other
Testing for maternal cell contamination in prenatal samples: a comprehensive survey of current diagnostic practices in 35 molecular diagnostic laboratories.
PMID 17591939·J Mol Diagn·2007
4-observational
Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins.
PMID 17903110·Twin Res Hum Genet·2007
4-observational
A genome-wide scan in forty large pedigrees with multiple sclerosis.
PMID 18000641·J Hum Genet·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6539 N DRAKE AVE
LINCOLNWOOD, IL 60712 - Phone
- (312) 576-2958
Quick Facts
- NPI
- 1942473350
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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