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VANESSA COLLINS, MD
MD
Surgery Physician
NPI: 1811458201Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
125074059(IL)
Research & Publications (20)
The impact of predictive genetic testing for hereditary nonpolyposis colorectal cancer: three years after testing.
PMID 17505206·Genet Med·2007
8-other
Screening and preventive behaviors one year after predictive genetic testing for hereditary nonpolyposis colorectal carcinoma.
PMID 15948171·Cancer·2005
8-other
Providing services for families with a genetic condition: a contrast between cystic fibrosis and Down syndrome.
PMID 14595065·Pediatrics·2003
4-observational
Cancer worries, risk perceptions and associations with interest in DNA testing and clinic satisfaction in a familial colorectal cancer clinic.
PMID 11149615·Clin Genet·2000
8-other
Utilization of genetic counseling after diagnosis of a birth defect--trends over time and variables associated with utilization.
PMID 19265720·Genet Med·2009
8-other
A wireless recording system that utilizes Bluetooth technology to transmit neural activity in freely moving animals.
PMID 19524612·J Neurosci Methods·2009
7-preclinical
A20 deletion is associated with copy number gain at the TNFA/B/C locus and occurs preferentially in translocation-negative MALT lymphoma of the ocular adnexa and salivary glands.
PMID 19006194·J Pathol·2009
4-observational
Going down a different road: first support and information needs of families with a baby with Down syndrome.
PMID 19236288·Med J Aust·2009
8-other
IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas.
PMID 19435942·Neuro Oncol·2009
8-other
Subclinical rejection in stable positive crossmatch kidney transplant patients: incidence and correlations.
PMID 19538492·Am J Transplant·2009
8-other
Problems assessing uptake of Huntington disease predictive testing and a proposed solution.
PMID 18665196·Eur J Hum Genet·2009
8-other
Novel mechanisms of gene disruption at the medulloblastoma isodicentric 17p11 breakpoint.
PMID 18973140·Genes Chromosomes Cancer·2009
8-other
Real-time quantitative polymerase chain reaction (qPCR) analysis with fluorescence resonance energy transfer (FRET) probes reveals differential expression of the four ERBB4 juxtamembrane region variants between medulloblastoma and pilocytic astrocytoma.
PMID 19017278·Neuropathol Appl Neurobiol·2009
8-other
Has prenatal screening influenced the prevalence of comorbidities associated with Down syndrome and subsequent survival rates?
PMID 19117890·Pediatrics·2009
4-observational
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
PMID 19330029·Nat Genet·2009
8-other
Oncogenic RAF1 rearrangement and a novel BRAF mutation as alternatives to KIAA1549:BRAF fusion in activating the MAPK pathway in pilocytic astrocytoma.
PMID 19363522·Oncogene·2009
7-preclinical
1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas.
PMID 17934521·Oncogene·2008
8-other
'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening.
PMID 18059419·Eur J Hum Genet·2008
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
- 5841 S MARYLAND AVE # MC6040
CHICAGO, IL 60637 - Phone
- (773) 702-1000
Quick Facts
- NPI
- 1811458201
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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