Dr. Andrew Paul Feinberg M.D.
Internist
1800 Orleans St Baltimore MD, 21287About
Dr. Andrew Feinberg is an internist practicing in Baltimore, MD. Dr. Feinberg specializes in the medical treatment of adults. Internists can act as a primary physician or a consultant to a primary physician. They manage both common and rare diseases. Dr. Feinberg provides comprehensive care and manages treatment with surgeons as well. Internists establish long-term relationships with their patients and incorporate disease prevention and mental health care into their practice.
Education and Training
Johns Hopkins Univ Sch of Med, Baltimore Md 1976
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.
- Mendel stayed home. Genomic imprinting and environmental disease susceptibility, National Institute of Environmental Health Sciences and Duke University Medical Center, Durham, NC, USA, 8-10 October 1998.
- Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: an introduction.
- Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.
- LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.
- Mosaic allelic insulin-like growth factor 2 expression patterns reveal a link between Wilms' tumorigenesis and epigenetic heterogeneity.
- DNA methylation, genomic imprinting and cancer.
- Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios.
- The two-domain hypothesis in Beckwith-Wiedemann syndrome.
- Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain.
- Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice.
- Methylation meets genomics.
- Cancer epigenetics takes center stage.
- Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site.
- Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor.
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