Hildegard Kehrer-Sawatzki

发表

Encyclopedia of Life Sciences. www.els.net. Continuously updated electronic encyclopedia.

Wf Bynum, David Neil Cooper, Pj Delves, 2014 .

PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies

Eric Legius, Kristian Helin, Hildegard Kehrer-Sawatzki, 2014, Nature.

On the sequence‐directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease

David N Cooper, Hildegard Kehrer-Sawatzki, D. Cooper, 2011, Human mutation.

Wide genome comparisons reveal the origins of the human X chromosome.

Horst Hameister, Hildegard Kehrer-Sawatzki, J. Graves, 2004, Trends in genetics : TIG.

Handbook of human molecular evolution

Hildegard Kehrer-Sawatzki, David Neil Cooper, 2008 .

Evolutionary History and Genome Organization of DUF1220 Protein Domains

C. Michael Dickens, Gerald J. Wyckoff, James M. Sikela, 2012, G3: Genes | Genomes | Genetics.

Reconstruction of the ancestral ferungulate karyotype by electronic chromosome painting (E-painting)

Horst Hameister, Josef Högel, Hildegard Kehrer-Sawatzki, 2006, Chromosome Research.

Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome

Xavier Estivill, David N. Cooper, Horst Hameister, 2006, Human Genetics.

Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

Michael Krawczak, Constantin Polychronakos, David N. Cooper, 2013, Human Genetics.

Encyclopedia of life sciences

Peter Delves, William F. Bynum, Gerry Melino, 2009 .

Segmental duplication associated with the human-specific inversion of chromosome 18: a further example of the impact of segmental duplications on karyotype and genome evolution in primates

Horst Hameister, Hildegard Kehrer-Sawatzki, H. Hameister, 2004, Human Genetics.

Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes)

Matthias Platzer, Horst Hameister, David N Cooper, 2005, Human mutation.

Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17.

Matthias Platzer, Horst Hameister, Hildegard Kehrer-Sawatzki, 2002, American journal of human genetics.

Cruciform-forming inverted repeats appear to have mediated many of the microinversions that distinguish the human and chimpanzee genomes

David N. Cooper, Nadia A. Chuzhanova, Josef Högel, 2009, Chromosome Research.

Genomic rearrangements in inherited disease and cancer.

George P Patrinos, David N Cooper, Hildegard Kehrer-Sawatzki, 2010, Seminars in cancer biology.