Author

Lottie D. Morison

Murdoch Children's Research InstituteORCID 0000-0003-2822-6522Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Angela Tamsin MorganiD· 2 shared David J. AmoriD· 2 shared Himanshu GoeliD· 2 shared Ruth O. BradeniD· 2 shared Simon E. FisheriD· 2 shared Adam P. VogeliD· 1 shared Amber BoysiD· 1 shared Angelika Rieß· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Angela Tamsin MorganORCID

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2 papers

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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Genetic & Genomic MedicinemedRxivPreprintJun 1, 2022

Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

Lottie D. Morison, Elisabeth Meffert, Miriam Stampfer…·Angela Tamsin Morgan

This study characterizes 29 individuals with FOXP2 variants, showing high prevalence of speech disorders and language impairments, with relatively specific phenotypes compared to other monogenic conditions.

DOI 10.1101/2022.06.01.22275851

humanstatistical model

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