| De novo mutations revealed by whole-exome sequencing are strongly associated with autism SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ... Nature 485 (7397), 237-241, 2012 | 2327 | 2012 |
| Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ... Neuron 70 (5), 863-885, 2011 | 1471 | 2011 |
| Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons K Griesi-Oliveira, A Acab, AR Gupta, DY Sunaga, T Chailangkarn, X Nicol, ... Molecular psychiatry 20 (11), 1350-1365, 2015 | 215 | 2015 |
| Recent developments in the genetics of autism spectrum disorders JD Murdoch, MW State Current opinion in genetics & development 23 (3), 310-315, 2013 | 171 | 2013 |
| Endophilin-A Deficiency Induces the Foxo3a-Fbxo32 Network in the Brain and Causes Dysregulation of Autophagy and the Ubiquitin-Proteasome System JDM , CM Rostosky, S Gowrisankaran, AS Arora, SF Soukup, R Vidal, V Capece ... Cell Reports 17 (4), 1071-1086, 2016 | 117 | 2016 |
| Worldwide Population Variation and Haplotype Analysis at the Serotonin Transporter Gene SLC6A4 and Implications for Association Studies JD Murdoch, WC Speed, AJ Pakstis, CE Heffelfinger, KK Kidd Biological psychiatry 74 (12), 879-889, 2013 | 76 | 2013 |
| 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 … JD Murdoch, AR Gupta, SJ Sanders, MF Walker, J Keaney, TV Fernandez, ... PLoS Genet 11 (1), e1004852, 2015 | 51 | 2015 |
| Rare deleterious mutations of the gene EFR3A in autism spectrum disorders AR Gupta, M Pirruccello, F Cheng, HJ Kang, TV Fernandez, JM Baskin, ... Molecular autism 5 (1), 31, 2014 | 30 | 2014 |
| EndophilinAs regulate endosomal sorting of BDNF-TrkB to mediate survival signaling in hippocampal neurons K Burk, JD Murdoch, S Freytag, M Koenig, V Bharat, R Markworth, ... Scientific Reports 7 (1), 2149, 2017 | 27 | 2017 |
| Reducing Artifactual EGFR T790M Mutations in DNA from Formalin-Fixed Paraffin-Embedded Tissue by Use of Thymine-DNA Glycosylase H Do, R Molania, PL Mitchell, R Vaiskunaite, JD Murdoch, A Dobrovic Clinical Chemistry, clinchem. 2017.271932, 2016 | 17 | 2016 |
| Synaptic Proteins JD Murdoch, MF Walker Encyclopedia of Autism Spectrum Disorders, 3058-3060, 2013 | | 2013 |
| SHANK 3 JD Murdoch, MF Walker Encyclopedia of Autism Spectrum Disorders, 2849-2850, 2013 | | 2013 |
| Recessive Genes JD Murdoch, MF Walker Encyclopedia of Autism Spectrum Disorders, 2529-2530, 2013 | | 2013 |
| Multilocus Genetic Models JD Murdoch Encyclopedia of Autism Spectrum Disorders, 1954-1957, 2013 | | 2013 |
| Contactin-Associated Protein 2 JD Murdoch Encyclopedia of Autism Spectrum Disorders, 796-799, 2013 | | 2013 |
| Multiple Approaches to Characterizing Variation in the Neuropsychiatric Candidate Genes SLC6A4, the Contactins, and the Contactin-associated Proteins JD Murdoch Yale University, 2012 | | 2012 |
