Pelagia Deriziotis

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2017
Publications (10 Years): 1

Top Topics

Regulatory T Cells

Ejection Fraction

Dendritic Cells

Intellectual Disability

Top Venues

University of Oxford

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Oxford Nov 30 2009 - Nov 29 2011

United Kingdom

Postdoctoral researcher :: Wellcome Trust Centre for Human Genetics

Publications

Elliot Sollis, Pelagia Deriziotis, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto, Mariette J V Hoffer, Claudia A L Ruivenkamp, Mariëlle Alders, Nobuhiko Okamoto, Emilia K Bijlsma, Astrid S Plomp, Simon E Fisher
Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Human mutation 38 (11) (2017)