S. Brandenburg

发表

Comprehensive high-throughput arrays for relative methylation (CHARM).

Rafael A Irizarry, Andrew P Feinberg, Christine Ladd-Acosta, 2008, Genome research.

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.

A. Feinberg, Victor V Lobanenkov, E. Niemitz, 2001, Cancer research.

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.

Andrew P Feinberg, Maxwell P Lee, A. Feinberg, 2002, American journal of human genetics.

Loss of imprinting of insulin growth factor II gene: a potential heritable biomarker for colon neoplasia predisposition.

A. Feinberg, N. Powe, H. Cui, 2004, Gastroenterology.

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.

A. Feinberg, G. Landes, M. Adams, 1999, Human molecular genetics.

Loss of IGF2 Imprinting: A Potential Marker of Colorectal Cancer Risk

A. Feinberg, N. Powe, H. Cui, 2003, Science.

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.

A. Feinberg, A. Schmitt, T. Connors, 1998, Cancer research.

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice.

A. Feinberg, P. Argani, R. Berger, 2000, The Journal of clinical investigation.

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.

A. Feinberg, K. Mitsuya, M. Oshimura, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2.

A. Feinberg, C. Hsieh, P. Onyango, 2002, Cancer research.

Distinct effects on gene expression of chemical and genetic manipulation of the cancer epigenome revealed by a multimodality approach.

James B. Mitchell, A. Feinberg, P. Munson, 2004, Cancer cell.

Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.

A. Feinberg, M. DeBaun, E. Niemitz, 2005, American journal of human genetics.

Mutations of CTCF or Its Binding Site Tumor Commonly Involves Altered Methylation but not Loss of Imprinting of Insulin-like Growth Factor-II in Wilms'

A. Feinberg, Victor V Lobanenkov, E. Niemitz, 2001 .

Somatic Mutation of TSSC 5 , a Novel Imprinted Gene from Human Chromosome llplS . 51

A. Feinberg, A. Schmitt, T. Connors, 2006 .