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WENDY BERGMAN, MD
MD
Internal Medicine Physician
NPI: 1083674451IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
71992(MA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE
Class of 1985
Research & Publications (20)
p16(INK4A)-independence of Epstein-Barr virus-induced cell proliferation and virus latency.
PMID 15166419·J Gen Virol·2004
8-other
[Dermatoscopy: an asset in the clinical assessment of pigmented skin lesions].
PMID 12224479·Ned Tijdschr Geneeskd·2002
6-review
A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes.
PMID 18792098·Int J Cancer·2009
8-other
Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls.
PMID 19359257·Int J Epidemiol·2009
8-other
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families.
PMID 18981015·Clin Cancer Res·2008
8-other
Genetic testing in familial melanoma: uptake and implications.
PMID 18613292·Psychooncology·2008
8-other
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
PMID 18398432·Eur J Hum Genet·2008
8-other
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL).
PMID 18394881·Eur J Cancer·2008
4-observational
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patients.
PMID 17276542·J Am Acad Dermatol·2007
8-other
Is statin use associated with a reduced incidence, a reduced Breslow thickness or delayed metastasis of melanoma of the skin?
PMID 17950596·Eur J Cancer·2007
8-other
Phenotypic variation in familial melanoma: consequences for predictive DNA testing.
PMID 17438187·Arch Dermatol·2007
8-other
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
PMID 16905682·J Med Genet·2007
4-observational
Behavioral and neurochemical alterations in mice lacking the RNA-binding protein translin.
PMID 16495445·J Neurosci·2006
7-preclinical
Hereditary melanoma and predictive genetic testing: why not?
PMID 15744786·Psychooncology·2005
8-other
Extreme difference in rate of mitochondrial and nuclear DNA evolution in a large ectotherm, Galápagos tortoises.
PMID 15062813·Mol Phylogenet Evol·2004
7-preclinical
Familial melanoma: a complex disorder leading to controversy on DNA testing.
PMID 14574160·Fam Cancer·2003
6-review
Pancreatic carcinoma in carriers of a specific 19 base pair deletion of CDKN2A/p16 (p16-leiden).
PMID 14506146·Clin Cancer Res·2003
8-other
Localization of a novel melanoma susceptibility locus to 1p22.
PMID 12844286·Am J Hum Genet·2003
8-other
Homozygous germline mutation of CDKN2A/p16 and glucose-6-phosphate dehydrogenase deficiency in a multiple melanoma case.
PMID 12690301·Melanoma Res·2003
5-case
Analyzing risk factors for late posttraumatic seizures: a prospective, multicenter investigation.
PMID 12638104·Arch Phys Med Rehabil·2003
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 5 NEPONSET ST
WORCESTER, MA 01606 - Phone
- (508) 595-2300
Quick Facts
- NPI
- 1083674451
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 41
- Publications
- 20
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