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NANCY CAMP, MD
MD
Emergency Medicine Physician
NPI: 1336167659Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
204935-1(NY)
Research & Publications (20)
Identifying rarer genetic variants for common complex diseases: diseased versus neutral discovery panels.
PMID 19132978·Ann Hum Genet·2009
4-observational
Identification of a major susceptibility locus for lethal graft-versus-host disease in MHC-matched mice.
PMID 19525392·J Immunol·2009
7-preclinical
Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource.
PMID 19092775·Eur J Hum Genet·2009
8-other
The sumLINK statistic for genetic linkage analysis in the presence of heterogeneity.
PMID 19217022·Genet Epidemiol·2009
8-other
Replication of the 10q11 and Xp11 prostate cancer risk variants: results from a Utah pedigree-based study.
PMID 19336566·Cancer Epidemiol Biomarkers Prev·2009
8-other
Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21.
PMID 19155440·Cancer Epidemiol Biomarkers Prev·2009
4-observational
No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees.
PMID 19476645·BMC Res Notes·2009
8-other
Bruton's tyrosine kinase revealed as a negative regulator of Wnt-beta-catenin signaling.
PMID 19471023·Sci Signal·2009
7-preclinical
Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium.
PMID 19423537·Cancer Epidemiol Biomarkers Prev·2009
4-observational
Polygenic model for predicting breast cancer risk via genome-wide polymorphisms.
PMID 18999159·AMIA Annu Symp Proc·2008
8-other
Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration.
PMID 18207215·Vision Res·2008
8-other
Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.
PMID 19033013·Am Heart J·2008
8-other
Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.
PMID 18093282·Ann Hum Genet·2008
4-observational
A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease.
PMID 18547558·Comput Biol Med·2008
8-other
hapConstructor: automatic construction and testing of haplotypes in a Monte Carlo framework.
PMID 18653522·Bioinformatics·2008
8-other
10q26 is associated with increased risk of age-related macular degeneration in the Utah population.
PMID 18188952·Adv Exp Med Biol·2008
8-other
Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease.
PMID 17512363·J Am Coll Cardiol·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
- 153 W 11TH ST, SAINT VINCENT'S MEDICAL CENTER
NEW YORK, NY 10011 - Phone
- (212) 604-7000
Quick Facts
- NPI
- 1336167659
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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