E. Niemitz

发表

Ras pathway activation in breast cancer

E. Niemitz, 2013, Nature Genetics.

ADAM10 and Alzheimer's disease

E. Niemitz, 2013, Nature Genetics.

Oncogenic chimeric transcript

E. Niemitz, 2014, Nature Genetics.

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19.

Andrew P Feinberg, A. Feinberg, M. DeBaun, 2003, American journal of human genetics.

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.

Parent-of-origin effects

E. Niemitz, 2014, Nature Genetics.

AID mistargeting to enhancers

E. Niemitz, 2015, Nature Genetics.

Mapping 5-hydroxylmethylcytosine

E. Niemitz, 2012, Nature Genetics.

Cohesin and chromosome loops

E. Niemitz, 2014, Nature Genetics.

Dynamic enhancer usage during development

E. Niemitz, 2014, Nature Genetics.

Embryonic epigenetic chimerism

E. Niemitz, 2013, Nature Genetics.

Interpretation of regulatory polymorphism

E. Niemitz, 2012, Nature Genetics.

Epigenetics and assisted reproductive technology: a call for investigation.

A. Feinberg, E. Niemitz, 2004, American journal of human genetics.

BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma

J. J. Breen, A. Feinberg, Victor V Lobanenkov, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Functional Interactions between DrosophilabHLH/PAS, Sox, and POU Transcription Factors Regulate CNS Midline Expression of the slit Gene

W. A. Johnson, A. Mukherjee, E. Niemitz, 2000, The Journal of Neuroscience.

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.

A. Feinberg, M. Oshimura, M. DeBaun, 2004, American journal of human genetics.

Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor.

A. Feinberg, K. Broman, D. Haber, 2001, Journal of the National Cancer Institute.

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 .

SETD2 and mismatch repair

E. Niemitz, 2013, Nature Genetics.

Gene regulatory functions of Drosophila Fish-hook, a high mobility group domain Sox protein

M. Fujioka, T. Goto, E. Niemitz, 1998, Mechanisms of Development.

Are you my mother?: Genomic imprinting

E. Niemitz, 2005 .

Modeling NOTCH1 haploinsufficiency

E. Niemitz, 2015, Nature Genetics.

Kabuki syndrome and HDAC inhibitors

E. Niemitz, 2014, Nature Genetics.

Transgenerational epigenetic inheritance and piRNAs

E. Niemitz, 2012, Nature Genetics.

Quantitative trait loci modulate neutrophil infiltration in the liver during LPS‐induced inflammation

E. Niemitz, R. Reeves, L. Matesic, 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.