John Daniel Murdoch

2012 Genetics Yale University, New Haven, CT 
"John Murdoch"
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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
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