Author

Georg Kirov

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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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Conrad Iyegbe· 2 shared Daniel Geschwind· 2 shared Aarno Palotie· 1 shared Alison Foster· 1 shared Andrew M. McIntosh· 1 shared Andrew M. McIntoshiD· 1 shared Andrew McQuilliniD· 1 shared Carmel Moo· 1 shared

Activity by Year

2016-2016 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Conrad Iyegbe

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2 papers

Recent·Most cited

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

Tarjinder Singh, James T. R. Walters, Mandy Johnstone, David Curtis, Jaana Suvisaari, Minna Torniainen, Elliott Rees, Conrad Iyegbe, Douglas Blackwood, Andrew M. McIntosh, Georg Kirov, Daniel Geschwind, Robin M. Murray, Marta Di Forti, Elvira Bramon, , Jeffrey C. Barrett

This study identifies rare schizophrenia risk variants enriched in genes shared with neurodevelopmental disorders through meta-analysis of exome and copy number variant data.

bioRxiv · Aug 16, 2016 · PreprintGenetics

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