Works matching AU Sestan, Nenad


Results: 33
    1

    Higher dopamine D1 receptor expression in prefrontal parvalbumin neurons underlies higher distractibility in marmosets versus macaques.

    Published in:
    Communications Biology, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s42003-025-08297-0
    By:
    • Joyce, Mary Kate P.;
    • Ivanov, Tsvetoslav G.;
    • Krienen, Fenna M.;
    • Mitchell, Jude F.;
    • Ma, Shaojie;
    • Inoue, Wataru;
    • Nandy, Anirvan S.;
    • Datta, Dibyadeep;
    • Duque, Alvaro;
    • Arellano, Jon I.;
    • Gupta, Rahul;
    • Gonzalez-Burgos, Guillermo;
    • Lewis, David A.;
    • Sestan, Nenad;
    • McCarroll, Steven A.;
    • Martinez-Trujillo, Julio;
    • Froudist-Walsh, Seán;
    • Arnsten, Amy F. T.
    Publication type:
    Article
    2

    New insights into the development of the human cerebral cortex.

    Published in:
    Journal of Anatomy, 2019, v. 235, n. 3, p. 432, doi. 10.1111/joa.13055
    By:
    • Molnár, Zoltán;
    • Clowry, Gavin J.;
    • Šestan, Nenad;
    • Alzu'bi, Ayman;
    • Bakken, Trygve;
    • Hevner, Robert F.;
    • Hüppi, Petra S.;
    • Kostović, Ivica;
    • Rakic, Pasko;
    • Anton, E. S.;
    • Edwards, David;
    • Garcez, Patricia;
    • Hoerder‐Suabedissen, Anna;
    • Kriegstein, Arnold
    Publication type:
    Article
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    Spatially Heterogeneous Choroid Plexus Transcriptomes Encode Positional Identity and Contribute to Regional CSF Production.

    Published in:
    Journal of Neuroscience, 2015, v. 35, n. 12, p. 4903, doi. 10.1523/JNEUROSCI.3081-14.2015
    By:
    • Lun, Melody P.;
    • Johnson, Matthew B.;
    • Broadbelt, Kevin G.;
    • Watanabe, Momoko;
    • Young-jin Rang;
    • Chau, Kevin F.;
    • Springel, Mark W.;
    • Malesz, Alexandra;
    • Sousa, André M.M.;
    • Pletikos, Mihovil;
    • Adelita, Tai;
    • Calicchio, Monica L.;
    • Yong Zhang;
    • Holtzman, Michael J.;
    • Lidov, Hart G.W.;
    • Sestan, Nenad;
    • Steen, Hanno;
    • Monuki, Edwin S.;
    • Lehtinen, Maria K.
    Publication type:
    Article
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    Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.

    Published in:
    European Journal of Human Genetics, 2015, v. 23, n. 2, p. 165, doi. 10.1038/ejhg.2014.82
    By:
    • Ercan-Sencicek, A Gulhan;
    • Jambi, Samira;
    • Franjic, Daniel;
    • Nishimura, Sayoko;
    • Li, Mingfeng;
    • El-Fishawy, Paul;
    • Morgan, Thomas M;
    • Sanders, Stephan J;
    • Bilguvar, Kaya;
    • Suri, Mohnish;
    • Johnson, Michele H;
    • Gupta, Abha R;
    • Yuksel, Zafer;
    • Mane, Shrikant;
    • Grigorenko, Elena;
    • Picciotto, Marina;
    • Alberts, Arthur S;
    • Gunel, Murat;
    • Šestan, Nenad;
    • State, Matthew W
    Publication type:
    Article
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    Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

    Published in:
    Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-31
    By:
    • Gupta, Abha R.;
    • Pirruccello, Michelle;
    • Feng Cheng;
    • Hyo Jung Kang;
    • Fernandez, Thomas V.;
    • Baskin, Jeremy M.;
    • Murim Choi;
    • Li Liu;
    • Ercan-Sencicek, Adife Gulhan;
    • Murdoch, John D.;
    • Klei, Lambertus;
    • Neale, Benjamin M.;
    • Franjic, Daniel;
    • Daly, Mark J.;
    • Lifton, Richard P.;
    • De Camilli, Pietro;
    • Hongyu Zhao;
    • Šestan, Nenad;
    • State, Matthew W.
    Publication type:
    Article
    13

    DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.

    Published in:
    Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-22
    By:
    • Li Liu;
    • Jing Lei;
    • Sanders, Stephan J.;
    • Willsey, Arthur Jeremy;
    • Yan Kou;
    • Cicek, Abdullah Ercument;
    • Klei, Lambertus;
    • Cong Lu;
    • Xin He;
    • Mingfeng Li;
    • Muhle, Rebecca A.;
    • Ma'ayan, Avi;
    • Noonan, James P.;
    • Sestan, Nenad;
    • McFadden, Kathryn A.;
    • State, Matthew W.;
    • Buxbaum, Joseph D.;
    • Devlin, Bernie;
    • Roeder, Kathryn
    Publication type:
    Article
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    The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.

    Published in:
    Nature Communications, 2015, v. 6, n. 3, p. 6404, doi. 10.1038/ncomms7404
    By:
    • Cotney, Justin;
    • Muhle, Rebecca A.;
    • Sanders, Stephan J.;
    • Liu, Li;
    • Willsey, A. Jeremy;
    • Niu, Wei;
    • Liu, Wenzhong;
    • Klei, Lambertus;
    • Lei, Jing;
    • Yin, Jun;
    • Reilly, Steven K.;
    • Tebbenkamp, Andrew T.;
    • Bichsel, Candace;
    • Pletikos, Mihovil;
    • Sestan, Nenad;
    • Roeder, Kathryn;
    • State, Matthew W.;
    • Devlin, Bernie;
    • Noonan, James P.
    Publication type:
    Article
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    The DGCR5 long noncoding RNA may regulate expression of several schizophrenia-related genes.

    Published in:
    Science Translational Medicine, 2018, v. 10, n. 472, p. N.PAG, doi. 10.1126/scitranslmed.aat6912
    By:
    • Meng, Qingtuan;
    • Wang, Kangli;
    • Brunetti, Tonya;
    • Xia, Yan;
    • Jiao, Chuan;
    • Dai, Rujia;
    • Fitzgerald, Dominic;
    • Thomas, Amber;
    • Jay, Lindsey;
    • Eckart, Heather;
    • Grennan, Kay;
    • Imamura-Kawasawa, Yuka;
    • Li, Mingfeng;
    • Sestan, Nenad;
    • White, Kevin P.;
    • Chen, Chao;
    • Liu, Chunyu
    Publication type:
    Article
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    A neural stem cell paradigm of pediatric hydrocephalus.

    Published in:
    Cerebral Cortex, 2023, v. 33, n. 8, p. 4262, doi. 10.1093/cercor/bhac341
    By:
    • Duy, Phan Q;
    • Rakic, Pasko;
    • Alper, Seth L;
    • Robert, Stephanie M;
    • Kundishora, Adam J;
    • Butler, William E;
    • Walsh, Christopher A;
    • Sestan, Nenad;
    • Geschwind, Daniel H;
    • Jin, Sheng Chih;
    • Kahle, Kristopher T
    Publication type:
    Article
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