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Sabrina Böhm
Ms
77
Citations
Overview
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Research output
(3)
Similar Profiles
(6)
Research output
3
Article
Research output per year
Research output per year
3 results
Publication Year, Title
(descending)
Publication Year, Title
(ascending)
Title
Type
Search results
2015
Genome-wide methylation analysis in Silver-Russell syndrome patients
Prickett, A. R.
,
Ishida, M.
,
Böhm, S.
,
Frost, J. M.
,
Puszyk, W.
,
Abu-Amero, S.
,
Stanier, P.
,
Schulz, R.
,
Moore, G. E.
&
Oakey, R. J.
,
Mar 2015
,
In:
Human Genetics.
134
,
3
,
p. 317-32
16 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
Methylation
100%
Epimutation
100%
Gene
33%
DNA Hypomethylation
16%
Uniparental Disomy
16%
21
Citations (Scopus)
2012
Epigenetic control of alternative mRNA processing at the imprinted Herc3/Nap1l5 locus
Cowley, M.
,
Wood, A. J.
,
Böhm, S.
,
Schulz, R.
&
Oakey, R. J.
,
Oct 2012
,
In:
Nucleic Acids Research.
40
,
18
,
p. 8917-8926
10 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
Epigenetics
100%
Polyadenylation
100%
Epigenetic Mechanism
28%
Gene
28%
Isoform
14%
42
Citations (Scopus)
2010
Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities
Frost, A. R.
,
Böhm, S. V.
,
Sewduth, R. N.
,
Josifova, D.
,
Ogilvie, C. M.
,
Izatt, L.
&
Roberts, R. G.
,
Jul 2010
,
In:
European Journal of Human Genetics.
18
,
7
,
p. 852 - 855
4 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
Muscle Disorder
100%
White Matter
100%
Hypotonia
100%
Gene
100%
Protein
60%
14
Citations (Scopus)