Allan Thomas Højland (Allan T Højland)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 3

Top Topics

Transcription Factor

Intellectual Disability

Top Venues

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

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

Publications

Inger Norlyk Sheyanth, Allan Thomas Højland, Henrik Okkels, Ihab Lolas, Christian Thorup, Michael Bjørn Petersen
First reported CABP2-related non-syndromic hearing loss in Northern Europe. Molecular genetics & genomic medicine 9 (4) (2021)
Allan Thomas Højland, Lisse J M Tavernier, Isabelle Schrauwen, Manou Sommen, Vedat Topsakal, Isabelle Schatteman, Ingeborg Johanna Maria Dhooge, Alexander M Huber, Diego Zanetti, Henricus P M Kunst, Alexander Hoischen, Michael Bjørn Petersen, Guy Van Camp, Erik Fransen
A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis. Human genetics (2021)
Allan Thomas Højland, Ihab Lolas, Henrik Okkels, Charlotte K Lautrup, Birgitte R Diness, Michael B Petersen, Irene K Nielsen
First reported adult patient with TARP syndrome: A case report. American journal of medical genetics. Part A 176 (12) (2018)