
doi: 10.1038/nn.4271
pmid: 27021940
A study reports mutations in a histone methyltransferase gene, SETD1A, in schizophrenia patients and demonstrates that tens of thousands of people must be screened to provide robust evidence of a gene's involvement in schizophrenia.
Male, Neurodevelopmental Disorders, Schizophrenia, Genetic Variation, Humans, Female, Histone-Lysine N-Methyltransferase, Genetic Association Studies
Male, Neurodevelopmental Disorders, Schizophrenia, Genetic Variation, Humans, Female, Histone-Lysine N-Methyltransferase, Genetic Association Studies
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 11 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
