Concepedia

Martha V. Koerner

MV

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Publications

12

Citations

1.3K

H-Index

12

Active since

2008

Affiliations

University of Edinburgh(Current)

Wellcome Centre for Cell Biology

CeMM Research Center for Molecular Medicine

Austrian Academy of Sciences

Research Institute of Molecular Pathology

Martha V. Koerner is an author at University of Edinburgh specializing in life sciences, genetics, and mecp2 function.

ORCID

Publications per year

2008–2021

12

Publications

12

<i>Airn</i> Transcriptional Overlap, But Not Its lncRNA Products, Induces Imprinted <i>Igf2r</i> Silencing

Paulina A. Latos, Florian M. Pauler, Martha V. Koerner et al. · Science · 2012 · 538 citations

, , +17

H3K27me3 forms BLOCs over silent genes and intergenic regions and specifies a histone banding pattern on a mouse autosomal chromosome

Florian M. Pauler, Mathew A. Sloane, Ru Huang et al. · Genome Research · 2008 · 244 citations · Full text

, , +16

Radically truncated MeCP2 rescues Rett syndrome-like neurological defects

Rebekah Tillotson, Jim Selfridge, Martha V. Koerner et al. · Nature · 2017 · 162 citations · Full text

, , +7

The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome

Kyla Brown, Jim Selfridge, Sabine Lagger et al. · Human Molecular Genetics · 2015 · 104 citations · Full text

, , +15

An in vitro ES cell imprinting model shows that imprinted expression of the<i>Igf2r</i>gene arises from an allele-specific expression bias

Paulina A. Latos, Stefan H. Stricker, Florian M. Pauler et al. · Development · 2009 · 60 citations · Full text

, , +15

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