Author

Jeremy McRae

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 Carmel Moo· 1 shared Christina M. HultmaniD· 1 shared Conrad Iyegbe· 1 shared Daniel Geschwind· 1 shared David Collier· 1 shared

Activity by Year

2016-2016 · peak 1/yr

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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

GenomicsbioRxivJan 12, 2016

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

Tarjinder Singh, Mitja I. Kurki, David Curtis…·Carmel Moo

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

DOI 10.1038/nn.4267

humanwhole-exome sequencing

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