Author

Carmel Moo

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alison Foster· 1 shared Andrew M. McIntoshiD· 1 shared Andrew McQuilliniD· 1 shared Christina M. HultmaniD· 1 shared Conrad Iyegbe· 1 shared Daniel Geschwind· 1 shared David Collier· 1 shared David CurtisiD· 1 shared

Activity by Year

2016-2016 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Alison Foster

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1 paper

Recent·Most cited

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

Tarjinder Singh, Mitja I. Kurki, David Curtis, Shaun M. Purcell, Lucy Crooks, Jeremy McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen, Olli Pietilainen, Sebastian S. Gerety, Muhammad Ayub, Moira Blyth, Trevor Cole, , Carmel Moo

The paper identifies rare loss-of-function variants in KMT2F associated with schizophrenia and developmental disorders, showing their role in neurodevelopmental conditions.

bioRxiv · Jan 12, 2016Genomics