Rare coding variants in ten genes confer substantial risk for schizophrenia
Author:
Singh TarjinderORCID, Poterba Timothy, Curtis David, Akil Huda, Al Eissa Mariam, Barchas Jack D., Bass Nicholas, Bigdeli Tim B., Breen Gerome, Bromet Evelyn J., Buckley Peter F., Bunney William E., Bybjerg-Grauholm Jonas, Byerley William F., Chapman Sinéad B., Chen Wei J., Churchhouse Claire, Craddock Nicholas, Cusick Caroline M., DeLisi Lynn, Dodge Sheila, Escamilla Michael A., Eskelinen Saana, Fanous Ayman H., Faraone Stephen V., Fiorentino Alessia, Francioli Laurent, Gabriel Stacey B., Gage Diane, Gagliano Taliun Sarah A., Ganna Andrea, Genovese Giulio, Glahn David C., Grove Jakob, Hall Mei-Hua, Hämäläinen Eija, Heyne Henrike O., Holi Matti, Hougaard David M., Howrigan Daniel P., Huang Hailiang, Hwu Hai-Gwo, Kahn René S., Kang Hyun Min, Karczewski Konrad J., Kirov George, Knowles James A., Lee Francis S., Lehrer Douglas S., Lescai Francesco, Malaspina Dolores, Marder Stephen R., McCarroll Steven A., McIntosh Andrew M., Medeiros Helena, Milani Lili, Morley Christopher P., Morris Derek W., Mortensen Preben Bo, Myers Richard M., Nordentoft Merete, O’Brien Niamh L., Olivares Ana Maria, Ongur Dost, Ouwehand Willem H., Palmer Duncan S., Paunio Tiina, Quested Digby, Rapaport Mark H., Rees Elliott, Rollins Brandi, Satterstrom F. Kyle, Schatzberg Alan, Scolnick Edward, Scott Laura J., Sharp Sally I., Sklar Pamela, Smoller Jordan W., Sobell Janet L., Solomonson Matthew, Stahl Eli A., Stevens Christine R., Suvisaari Jaana, Tiao Grace, Watson Stanley J., Watts Nicholas A., Blackwood Douglas H., Børglum Anders D., Cohen Bruce M., Corvin Aiden P., Esko Tõnu, Freimer Nelson B., Glatt Stephen J., Hultman Christina M., McQuillin Andrew, Palotie Aarno, Pato Carlos N., Pato Michele T., Pulver Ann E., St. Clair David, Tsuang Ming T., Vawter Marquis P., Walters James T., Werge Thomas M., Ophoff Roel A., Sullivan Patrick F., Owen Michael J., Boehnke Michael, O’Donovan Michael C., Neale Benjamin M.ORCID, Daly Mark J.ORCID
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Reference41 articles.
1. Satterstrom, F. K. et al. Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism. Cell 180, 568–584 (2020). 2. Kaplanis, J. et al. Evidence for 28 genetic disorders discovered by combining healthcare and research data. Nature 586, 757–762 (2020). 3. Trubetskoy, V. et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature https://doi.org/10.1038/s41586-022-04434-5 (2022). 4. McGrath, J., Saha, S., Chant, D. & Welham, J. Schizophrenia: a concise overview of incidence, prevalence, and mortality. Epidemiol. Rev. 30, 67–76 (2008). 5. Hjorthøj, C., Stürup, A. E., McGrath, J. J. & Nordentoft, M. Years of potential life lost and life expectancy in schizophrenia: a systematic review and meta-analysis. Lancet Psychiat. 4, 295–301 (2017).
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