Work

Genome-wide methylation analysis in Silver–Russell syndrome patients

Year: 2015

Type: article

Study design: Observational Study

Source: Human Genetics

DOI: 10.1007/s00439-014-1526-1

Authors: A. R. Prickett, M. Ishida, S. Böhm, J. M. Frost, W. Puszyk, S. Abu-Amero, P. Stanier, R. Schulz, G. E. Moore, R. J. Oakey

Institutions: Guy's Hospital, King's College London, University College London, University of California, Berkeley, University of Florida

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Wellcome Trust, NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research, National Institute for Health and Care Research, British Heart Foundation, National Institutes of Health, Medical Research Council, Engineering and Physical Sciences Research Council

Awards: Characterisation of the endocardial epigenome for identification of therapeutic regenerative strategies, Defining the features of minimal imprinted loci generated by retrotransposition., A genome-wide approach to the characterisation of human and murine DNA methylation mutants., A genome-wide approach to the characterisation of human and murine DNA methylation mutants, G5172690410

OpenAlex ID: W2019393142

FWCI: 2.733

Cites: 66

Cited by: 35

Related to: 10