John Daniel Murdoch
Affiliations: | 2012 | Genetics | Yale University, New Haven, CT |
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"John Murdoch"Mean distance: 18.85 | S | N | B | C | P |
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Sign in to add mentor| Matthew W. State | grad student | 2012 | Yale | |
| (Multiple Approaches to Characterizing Variation in the Neuropsychiatric Candidate Genes SLC6A4, the Contactins, and the Contactin-Associated Proteins.) | ||||
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| Murdoch JD, Gupta AR, Sanders SJ, et al. (2015) No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins. Plos Genetics. 11: e1004852 |
| Griesi-Oliveira K, Acab A, Gupta AR, et al. (2014) Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons. Molecular Psychiatry |
| Gupta AR, Pirruccello M, Cheng F, et al. (2014) Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. Molecular Autism. 5: 31 |
| Murdoch JD, State MW. (2013) Recent developments in the genetics of autism spectrum disorders. Current Opinion in Genetics & Development. 23: 310-5 |
| Murdoch JD, Speed WC, Pakstis AJ, et al. (2013) Worldwide population variation and haplotype analysis at the serotonin transporter gene SLC6A4 and implications for association studies. Biological Psychiatry. 74: 879-89 |
| Sanders SJ, Murtha MT, Gupta AR, et al. (2012) De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 485: 237-41 |
| Sanders SJ, Ercan-Sencicek AG, Hus V, et al. (2011) Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85 |