Thomas S Scerri

5PUBLICATIONS
42CO-AUTHORS
Medical infection agents (incl. prions)Child language acquisitionDevelopmental genetics (incl. sex determination)NeurogeneticsMedical mycology
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Publications (5)

|Jun 21, 2020
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction.

Joanne M Hildebrand, Maria Kauppi, Ian J Majewski

|Apr 30, 2020
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation.

Michael S Hildebrand, Victoria E Jackson, Thomas S Scerri

|May 01, 2019
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.

Kamal Khan, Michael Zech, Angela T Morgan

|Feb 22, 2018
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.

Else Eising, Amaia Carrion-Castillo, Arianna Vino

|Mar 03, 2017
Genome-wide analyses identify common variants associated with macular telangiectasia type 2.

Thomas S Scerri, Anna Quaglieri, Carolyn Cai

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