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Spatiotemporal transcriptomic divergence across human and macaque brain development.
Zhu Y, Sousa AMM, Gao T, Skarica M, Li M, Santpere G, Esteller-Cucala P, Juan D, Ferrández-Peral L, Gulden FO, Yang M, Miller DJ, Marques-Bonet T, Imamura Kawasawa Y, Zhao H, Sestan N. Zhu Y, et al. Among authors: zhao h. Science. 2018 Dec 14;362(6420):eaat8077. doi: 10.1126/science.aat8077. Epub 2018 Dec 13. Science. 2018. PMID: 30545855 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: zhao h. Mol Autism. 2014 Apr 29;5:31. doi: 10.1186/2040-2392-5-31. eCollection 2014. Mol Autism. 2014. PMID: 24860643 Free PMC article.
Simultaneous dimension reduction and adjustment for confounding variation.
Lin Z, Yang C, Zhu Y, Duchi J, Fu Y, Wang Y, Jiang B, Zamanighomi M, Xu X, Li M, Sestan N, Zhao H, Wong WH. Lin Z, et al. Among authors: zhao h. Proc Natl Acad Sci U S A. 2016 Dec 20;113(51):14662-14667. doi: 10.1073/pnas.1617317113. Epub 2016 Dec 7. Proc Natl Acad Sci U S A. 2016. PMID: 27930330 Free PMC article.
Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
Li M, Santpere G, Imamura Kawasawa Y, Evgrafov OV, Gulden FO, Pochareddy S, Sunkin SM, Li Z, Shin Y, Zhu Y, Sousa AMM, Werling DM, Kitchen RR, Kang HJ, Pletikos M, Choi J, Muchnik S, Xu X, Wang D, Lorente-Galdos B, Liu S, Giusti-Rodríguez P, Won H, de Leeuw CA, Pardiñas AF; BrainSpan Consortium; PsychENCODE Consortium; PsychENCODE Developmental Subgroup; Hu M, Jin F, Li Y, Owen MJ, O'Donovan MC, Walters JTR, Posthuma D, Reimers MA, Levitt P, Weinberger DR, Hyde TM, Kleinman JE, Geschwind DH, Hawrylycz MJ, State MW, Sanders SJ, Sullivan PF, Gerstein MB, Lein ES, Knowles JA, Sestan N. Li M, et al. Science. 2018 Dec 14;362(6420):eaat7615. doi: 10.1126/science.aat7615. Science. 2018. PMID: 30545854 Free PMC article.
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.
Wilson FH, Hariri A, Farhi A, Zhao H, Petersen KF, Toka HR, Nelson-Williams C, Raja KM, Kashgarian M, Shulman GI, Scheinman SJ, Lifton RP. Wilson FH, et al. Among authors: zhao h. Science. 2004 Nov 12;306(5699):1190-4. doi: 10.1126/science.1102521. Epub 2004 Oct 21. Science. 2004. PMID: 15498972 Free PMC article.
33,906 results
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