Lukas Soellner

Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans

Louise E Docherty, Faisal I. Rezwan, Rebecca Poole et al. · Nature Communications · 2015 · 187 citations · Full text

Paternally Inherited<i>IGF2</i>Mutation and Growth Restriction

Matthias Begemann, Birgit Zirn, Gijs W.E. Santen et al. · New England Journal of Medicine · 2015 · 186 citations · Full text

Family Members, Human Growth, Genetics +22

EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome

Katja Eggermann, Jet Bliek, Frédéric Brioude et al. · European Journal of Human Genetics · 2016 · 81 citations · Full text

Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself

R. Scheuvens, Matthias Begemann, Lukas Soellner et al. · Clinical Genetics · 2016 · 74 citations

Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith–Wiedemann syndrome and ovarian steroid cell tumour

Magdalena Gogiel, Matthias Begemann, Sabrina Spengler et al. · European Journal of Human Genetics · 2012 · 54 citations · Full text

Cytogenetics, Genetic Disorder, Genetics +9