Author

GROUP Investigators

Maastricht University Medical Centre

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

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Genetics· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Assay:whole-exome sequencing· 2 Assay:electronic health records· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alexander L. RichardsiD· 2 shared Andrew J. PocklingtoniD· 2 shared Antonio F. PardiñasiD· 2 shared Elliott ReesiD· 2 shared George KiroviD· 2 shared James WaltersiD· 2 shared Joanne MorganiD· 2 shared Michael C. O’DonovaniD· 2 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Alexander L. RichardsORCID

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3 papers

Recent·Most cited

Phenome-wide and Genome-wide Analyses of Quality of Life in Schizophrenia

Raha Pazoki, Bochao Danae Lin, Kristel R. van Eijk, Dick Schijven, Sonja M. C. de Zwarte, GROUP Investigators, Sinan Gülöksüz, Jurjen Justin Luykx

The paper identifies nine clinical phenotypes and polygenic risk scores associated with quality of life in schizophrenia patients and their relatives.

BJPsych Open · Dec 9, 2020Peer-reviewedGenetics

Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

Elliott Rees, Jun Han, Joanne Morgan, Noa Carrera, Valentina Escott‐Price, Andrew J. Pocklington, Madeleine Duffield, Lynsey S. Hall, Sophie E. Legge, Antonio F. Pardiñas, Alexander L. Richards, Julian Roth, Tatyana Lezheiko, Nikolay V. Kondratyev, Вера Евгеньевна Голимбет, , Michael John Owen

The paper analyzes rare and common alleles in schizophrenia trios, identifying rare missense variants in SLC6A1 and confirming the role of neurodevelopmental disorder genes.

bioRxiv · Apr 18, 2019 · PreprintGenetics

Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

Elliott Rees, Noa Carrera, Joanne Morgan, Kirsty Hambridge, Valentina Escott‐Price, Andrew J. Pocklington, Alexander L. Richards, Antonio F. Pardiñas, GROUP Investigators, Colm McDonald, Gary J Donohoe, Derek W. Morris, Elaine M. Kenny, Eric Kelleher, Michael Gill, , Michael C. O’Donovan

The paper identifies an excess of rare loss-of-function and missense mutations in voltage-gated sodium channels and synaptic genes associated with schizophrenia using large-scale sequencing and meta-analysis.

bioRxiv · Jan 12, 2018 · PreprintGenetics