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Items: 1 to 20 of 417


Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations.

Gouder L, Vitrac A, Goubran-Botros H, Danckaert A, Tinevez JY, André-Leroux G, Atanasova E, Lemière N, Biton A, Leblond CS, Poulet A, Boland A, Deleuze JF, Benchoua A, Delorme R, Bourgeron T, Cloëz-Tayarani I.

Sci Rep. 2019 Jan 14;9(1):94. doi: 10.1038/s41598-018-36993-x.


The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders.

Ang CE, Ma Q, Wapinski OL, Fan S, Flynn RA, Lee QY, Coe B, Onoguchi M, Olmos VH, Do BT, Dukes-Rimsky L, Xu J, Tanabe K, Wang L, Elling U, Penninger JM, Zhao Y, Qu K, Eichler EE, Srivastava A, Wernig M, Chang HY.

Elife. 2019 Jan 10;8. pii: e41770. doi: 10.7554/eLife.41770. [Epub ahead of print]


Blood chimerism in twins.

Tavares L, Da Costa DC, Batschauer APB, Jobim LFJ, Ewald GM, de Mello C, Velazquez ESA, Geraldo A.

Immunohematology. 2018 Dec;34(4):151-157.


White Matter Tract Changes Associated with Clinical Improvement in an Open-Label Trial Assessing Autologous Umbilical Cord Blood for Treatment of Young Children with Autism.

Carpenter KLH, Major S, Tallman C, Chen LW, Franz L, Sun J, Kurtzberg J, Song A, Dawson G.

Stem Cells Transl Med. 2019 Jan 8. doi: 10.1002/sctm.18-0251. [Epub ahead of print]


Pathological priming causes developmental gene network heterochronicity in autistic subject-derived neurons.

Schafer ST, Paquola ACM, Stern S, Gosselin D, Ku M, Pena M, Kuret TJM, Liyanage M, Mansour AA, Jaeger BN, Marchetto MC, Glass CK, Mertens J, Gage FH.

Nat Neurosci. 2019 Jan 7. doi: 10.1038/s41593-018-0295-x. [Epub ahead of print]


Neuron-Glia Interactions Increase Neuronal Phenotypes in Tuberous Sclerosis Complex Patient iPSC-Derived Models.

Nadadhur AG, Alsaqati M, Gasparotto L, Cornelissen-Steijger P, van Hugte E, Dooves S, Harwood AJ, Heine VM.

Stem Cell Reports. 2019 Jan 8;12(1):42-56. doi: 10.1016/j.stemcr.2018.11.019. Epub 2018 Dec 20.


Association of HLA alleles with autism.

Sayad A, Akbari MT, Noroozi R, Omrani MD, Inoko H, Taheri M, Ghafouri-Fard S.

Neuropsychiatr Dis Treat. 2018 Nov 27;14:3259-3265. doi: 10.2147/NDT.S186673. eCollection 2018.


Aberrant Expression of Long Non-coding RNAs in Peripheral Blood of Autistic Patients.

Sayad A, Omrani MD, Fallah H, Taheri M, Ghafouri-Fard S.

J Mol Neurosci. 2018 Dec 18. doi: 10.1007/s12031-018-1240-x. [Epub ahead of print]


Widespread RNA editing dysregulation in brains from autistic individuals.

Tran SS, Jun HI, Bahn JH, Azghadi A, Ramaswami G, Van Nostrand EL, Nguyen TB, Hsiao YE, Lee C, Pratt GA, Martínez-Cerdeño V, Hagerman RJ, Yeo GW, Geschwind DH, Xiao X.

Nat Neurosci. 2019 Jan;22(1):25-36. doi: 10.1038/s41593-018-0287-x. Epub 2018 Dec 17.


Autism in India: a case-control study to understand the association between socio-economic and environmental risk factors.

Geetha B, Sukumar C, Dhivyadeepa E, Reddy JK, Balachandar V.

Acta Neurol Belg. 2018 Dec 15. doi: 10.1007/s13760-018-01057-4. [Epub ahead of print]


Transcriptome and epigenome landscape of human cortical development modeled in organoids.

Amiri A, Coppola G, Scuderi S, Wu F, Roychowdhury T, Liu F, Pochareddy S, Shin Y, Safi A, Song L, Zhu Y, Sousa AMM; PsychENCODE Consortium, Gerstein M, Crawford GE, Sestan N, Abyzov A, Vaccarino FM.

Science. 2018 Dec 14;362(6420). pii: eaat6720. doi: 10.1126/science.aat6720.


Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk.

Rajarajan P, Borrman T, Liao W, Schrode N, Flaherty E, Casiño C, Powell S, Yashaswini C, LaMarca EA, Kassim B, Javidfar B, Espeso-Gil S, Li A, Won H, Geschwind DH, Ho SM, MacDonald M, Hoffman GE, Roussos P, Zhang B, Hahn CG, Weng Z, Brennand KJ, Akbarian S.

Science. 2018 Dec 14;362(6420). pii: eaat4311. doi: 10.1126/science.aat4311.


Altered Global mRNA Expressions of Pain and Aggression Related Genes in the Blood of Children with Autism Spectrum Disorders.

Sener EF, Taheri S, Sahin MC, Bayramov KK, Marasli MK, Zararsiz G, Mehmetbeyoglu E, Oztop DB, Canpolat M, Canatan H, Ozkul Y.

J Mol Neurosci. 2018 Dec 5. doi: 10.1007/s12031-018-1213-0. [Epub ahead of print]


Prenatal Progestin Exposure Is Associated With Autism Spectrum Disorders.

Li L, Li M, Lu J, Ge X, Xie W, Wang Z, Li X, Li C, Wang X, Han Y, Wang Y, Zhong L, Xiang W, Huang X, Chen H, Yao P.

Front Psychiatry. 2018 Nov 19;9:611. doi: 10.3389/fpsyt.2018.00611. eCollection 2018.


Intranasal administration of exosomes derived from mesenchymal stem cells ameliorates autistic-like behaviors of BTBR mice.

Perets N, Hertz S, London M, Offen D.

Mol Autism. 2018 Nov 21;9:57. doi: 10.1186/s13229-018-0240-6. eCollection 2018.


JIP2 haploinsufficiency contributes to neurodevelopmental abnormalities in human pluripotent stem cell-derived neural progenitors and cortical neurons.

Roessler R, Goldmann J, Shivalila C, Jaenisch R.

Life Sci Alliance. 2018 Jun 25;1(4):e201800094. doi: 10.26508/lsa.201800094. eCollection 2018 Aug.


Self-injurious behaviours in rhesus macaques: Potential glial mechanisms.

Ramsey J, Martin EC, Purcell OM, Lee KM, MacLean AG.

J Intellect Disabil Res. 2018 Dec;62(12):1008-1017. doi: 10.1111/jir.12558.


WDR68 is essential for the transcriptional activation of the PRC1-AUTS2 complex and neuronal differentiation of mouse embryonic stem cells.

Wang Q, Geng Z, Gong Y, Warren K, Zheng H, Imamura Y, Gao Z.

Stem Cell Res. 2018 Dec;33:206-214. doi: 10.1016/j.scr.2018.10.023. Epub 2018 Nov 12.


Next-Generation Sequencing in Autism Spectrum Disorder.

Sanders SJ.

Cold Spring Harb Perspect Med. 2018 Nov 12. pii: a026872. doi: 10.1101/cshperspect.a026872. [Epub ahead of print]


Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a.

Cheng Y, Wang ZM, Tan W, Wang X, Li Y, Bai B, Li Y, Zhang SF, Yan HL, Chen ZL, Liu CM, Mi TW, Xia S, Zhou Z, Liu A, Tang GB, Liu C, Dai ZJ, Wang YY, Wang H, Wang X, Kang Y, Lin L, Chen Z, Xie N, Sun Q, Xie W, Peng J, Chen D, Teng ZQ, Jin P.

Nat Neurosci. 2018 Dec;21(12):1689-1703. doi: 10.1038/s41593-018-0261-7. Epub 2018 Nov 5.


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