Author

Gabriel Dabscheck

Royal Children's HospitalORCID 0000-0002-8186-6628Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amber BoysiD· 1 shared Angela Tamsin MorganiD· 1 shared Antony KaspiiD· 1 shared Bronwyn Parry‐Fielder· 1 shared David J. AmoriD· 1 shared David John ComaniD· 1 shared Emma K. BakeriD· 1 shared Erandee RobertsoniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amber BoysORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineMolecular PsychiatryPeer-reviewedSep 18, 2022

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

Antony Kaspi, Michael S. Hildebrand, Victoria E. Jackson…·Angela Tamsin Morgan

This study identifies 18 high-confidence genetic variants in 26% of childhood apraxia of speech cases, expanding the list of candidate genes and highlighting shared pathways with other neurodevelopmental disorders.

40 citationstop 3%

humanwhole-exome sequencing

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