Identification of loci associated with schizophrenia by genome-wide association and follow-up
By M. O’Donovan, N. Craddock, N. Norton, H. Williams, T. Peirce, V. Moskvina, I. Nikolov, M. Hamshere, L. Carroll, L. Georgieva and 38 more. Nature Genetics, 2008
1,107 citations recorded by the source corpus.
Subfields: Genetics
View Paper: https://www.semanticscholar.org/paper/270c9c8075ca0dee2c73d8235cf27afbb4b2beae
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- Peter M. Visscher
- Naomi R. Wray
- Ian J. Deary
- Jordan W. Smoller
- D. Liewald
- Henrik Walter
- Patrick F. Sullivan
- Paul M. Thompson
Citations in the corpus
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014, positive): “A variant within ZNF804A was the first genome-wide significant SNP associated with risk for schizophrenia (O’Donovan et al. 2008).”
- Social Cognitive Neuroscience of Empathy: Concepts, Circuits, and Genes (2012, background): “This variant was the first that was shown to have a genome-wide significant association with schizophrenia and bipolar disorder (O’Donovan et al., 2008), a finding that has now been replicated several times (Steinberg et al., 2011).”
- Common polygenic variation contributes to risk of schizophrenia and bipolar disorder (2009, background): “In conclusion, our molecular genetic data strongly support a polygenic basis to schizophrenia that (1) involves common SNPs, (2) explains at least one-third of the total variation in liability, (3) is substantially shared with bipolar disorder, and (4) is largely not shared with several non-psychiat”