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1958 1
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16 results

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Page 1
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Günel M, Roeder K, Geschwind DH, Devlin B, State MW. Sanders SJ, et al. Among authors: murdoch jd. Nature. 2012 Apr 4;485(7397):237-41. doi: 10.1038/nature10945. Nature. 2012. PMID: 22495306 Free PMC article.
A SNP resource for studying North American moose.
Kalbfleisch TS, Murdoch BM, Smith TPL, Murdoch JD, Heaton MP, McKay SD. Kalbfleisch TS, et al. Among authors: murdoch jd. F1000Res. 2018 Jan 10;7:40. doi: 10.12688/f1000research.13501.1. eCollection 2018. F1000Res. 2018. PMID: 29479424 Free PMC article.
Wildlife resistance and protection in a changing New England landscape.
Pearman-Gillman SB, Duveneck MJ, Murdoch JD, Donovan TM. Pearman-Gillman SB, et al. Among authors: murdoch jd. PLoS One. 2020 Sep 24;15(9):e0239525. doi: 10.1371/journal.pone.0239525. eCollection 2020. PLoS One. 2020. PMID: 32970736 Free PMC article.
HYSTEROGRAPHY AFTER CAESAREAN SECTION.
ENDE S, HALL GS, LIANG DY, MURDOCH JD. ENDE S, et al. Among authors: murdoch jd. Br J Radiol. 1963 Oct;36:720-4. doi: 10.1259/0007-1285-36-430-720. Br J Radiol. 1963. PMID: 14067654 No abstract available.
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons.
Griesi-Oliveira K, Acab A, Gupta AR, Sunaga DY, Chailangkarn T, Nicol X, Nunez Y, Walker MF, Murdoch JD, Sanders SJ, Fernandez TV, Ji W, Lifton RP, Vadasz E, Dietrich A, Pradhan D, Song H, Ming GL, Gu X, Haddad G, Marchetto MC, Spitzer N, Passos-Bueno MR, State MW, Muotri AR. Griesi-Oliveira K, et al. Among authors: murdoch jd. Mol Psychiatry. 2015 Nov;20(11):1350-65. doi: 10.1038/mp.2014.141. Epub 2014 Nov 11. Mol Psychiatry. 2015. PMID: 25385366 Free PMC article.
Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.
Gupta AR, Pirruccello M, Cheng F, Kang HJ, Fernandez TV, Baskin JM, Choi M, Liu L, Ercan-Sencicek AG, Murdoch JD, Klei L, Neale BM, Franjic D, Daly MJ, Lifton RP, De Camilli P, Zhao H, Sestan N, State MW. Gupta AR, et al. Among authors: murdoch jd. Mol Autism. 2014 Apr 29;5:31. doi: 10.1186/2040-2392-5-31. eCollection 2014. Mol Autism. 2014. PMID: 24860643 Free PMC article.
16 results