Nenad Sestan - Publications

Affiliations: 
Yale University, New Haven, CT 

127 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Duy PQ, Weise SC, Marini C, Li XJ, Liang D, Dahl PJ, Ma S, Spajic A, Dong W, Juusola J, Kiziltug E, Kundishora AJ, Koundal S, Pedram MZ, Torres-Fernández LA, ... ... Sestan N, et al. Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus. Nature Neuroscience. PMID 35379995 DOI: 10.1038/s41593-022-01043-3  0.697
2022 Duy PQ, Rakic P, Alper SL, Butler WE, Walsh CA, Sestan N, Geschwind DH, Jin SC, Kahle KT. Brain ventricles as windows into brain development and disease. Neuron. 110: 12-15. PMID 34990576 DOI: 10.1016/j.neuron.2021.12.009  0.643
2021 Franjic D, Skarica M, Ma S, Arellano JI, Tebbenkamp ATN, Choi J, Xu C, Li Q, Morozov YM, Andrijevic D, Vrselja Z, Spajic A, Santpere G, Li M, Zhang S, ... ... Sestan N, et al. Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells. Neuron. PMID 34798047 DOI: 10.1016/j.neuron.2021.10.036  0.716
2021 Shibata M, Pattabiraman K, Muchnik SK, Kaur N, Morozov YM, Cheng X, Waxman SG, Sestan N. Hominini-specific regulation of CBLN2 increases prefrontal spinogenesis. Nature. PMID 34599306 DOI: 10.1038/s41586-021-03952-y  0.738
2021 Shibata M, Pattabiraman K, Lorente-Galdos B, Andrijevic D, Kim SK, Kaur N, Muchnik SK, Xing X, Santpere G, Sousa AMM, Sestan N. Regulation of prefrontal patterning and connectivity by retinoic acid. Nature. PMID 34599305 DOI: 10.1038/s41586-021-03953-x  0.75
2021 Girskis KM, Stergachis AB, DeGennaro EM, Doan RN, Qian X, Johnson MB, Wang PP, Sejourne GM, Nagy MA, Pollina EA, Sousa AMM, Shin T, Kenny CJ, Scotellaro JL, Debo BM, ... ... Sestan N, et al. Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions. Neuron. PMID 34478631 DOI: 10.1016/j.neuron.2021.08.005  0.647
2021 Taylor SR, Santpere G, Weinreb A, Barrett A, Reilly MB, Xu C, Varol E, Oikonomou P, Glenwinkel L, McWhirter R, Poff A, Basavaraju M, Rafi I, Yemini E, Cook SJ, ... ... Sestan N, et al. Molecular topography of an entire nervous system. Cell. PMID 34237253 DOI: 10.1016/j.cell.2021.06.023  0.313
2021 Runge K, Mathieu R, Bugeon S, Lafi S, Beurrier C, Sahu S, Schaller F, Loubat A, Herault L, Gaillard S, Pallesi-Pocachard E, Montheil A, Bosio A, Rosenfeld JA, Hudson E, ... ... Sestan N, et al. Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons. Molecular Psychiatry. PMID 34188164 DOI: 10.1038/s41380-021-01179-x  0.34
2021 Hu B, Won H, Mah W, Park RB, Kassim B, Spiess K, Kozlenkov A, Crowley CA, Pochareddy S, Li Y, Dracheva S, Sestan N, Akbarian S, Geschwind DH. Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders. Nature Communications. 12: 3968. PMID 34172755 DOI: 10.1038/s41467-021-24243-0  0.371
2021 Tsyporin J, Tastad D, Ma X, Nehme A, Finn T, Huebner L, Liu G, Gallardo D, Makhamreh A, Roberts JM, Katzman S, Sestan N, McConnell SK, Yang Z, Qiu S, et al. Transcriptional repression by FEZF2 restricts alternative identities of cortical projection neurons. Cell Reports. 35: 109269. PMID 34161768 DOI: 10.1016/j.celrep.2021.109269  0.338
2021 Aldinger KA, Thomson Z, Phelps IG, Haldipur P, Deng M, Timms AE, Hirano M, Santpere G, Roco C, Rosenberg AB, Lorente-Galdos B, Gulden FO, O'Day D, Overman LM, Lisgo SN, ... ... Sestan N, et al. Spatial and cell type transcriptional landscape of human cerebellar development. Nature Neuroscience. PMID 34140698 DOI: 10.1038/s41593-021-00872-y  0.319
2020 Li Z, Tyler WA, Zeldich E, Santpere Baró G, Okamoto M, Gao T, Li M, Sestan N, Haydar TF. Transcriptional priming as a conserved mechanism of lineage diversification in the developing mouse and human neocortex. Science Advances. 6. PMID 33158872 DOI: 10.1126/sciadv.abd2068  0.717
2020 Kaur N, Han W, Li Z, Madrigal MP, Shim S, Pochareddy S, Gulden FO, Li M, Xu X, Xing X, Takeo Y, Li Z, Lu K, Imamura Kawasawa Y, Ballester-Lurbe B, ... ... Sestan N, et al. Neural Stem Cells Direct Axon Guidance via Their Radial Fiber Scaffold. Neuron. PMID 32707082 DOI: 10.1016/J.Neuron.2020.06.035  0.798
2020 Pattabiraman K, Muchnik SK, Sestan N. The evolution of the human brain and disease susceptibility. Current Opinion in Genetics & Development. 65: 91-97. PMID 32629339 DOI: 10.1016/J.Gde.2020.05.004  0.699
2020 Micali N, Kim SK, Diaz-Bustamante M, Stein-O'Brien G, Seo S, Shin JH, Rash BG, Ma S, Wang Y, Olivares NA, Arellano JI, Maynard KR, Fertig EJ, Cross AJ, Bürli RW, ... ... Sestan N, et al. Variation of Human Neural Stem Cells Generating Organizer States In Vitro before Committing to Cortical Excitatory or Inhibitory Neuronal Fates. Cell Reports. 31: 107599. PMID 32375049 DOI: 10.1016/J.Celrep.2020.107599  0.831
2020 Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G, Sousa AMM, Tebbenkamp ATN, Kaur N, Gulden FO, Breen MS, Liang L, ... ... Sestan N, et al. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Reports. 31: 107489. PMID 32268104 DOI: 10.1016/J.Celrep.2020.03.053  0.78
2020 Shin J, Ma S, Hofer E, Patel Y, Vosberg DE, Tilley S, Roshchupkin GV, Sousa AMM, Jian X, Gottesman R, Mosley TH, Fornage M, Saba Y, Pirpamer L, Schmidt R, ... ... Sestan N, et al. Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. Cerebral Cortex (New York, N.Y. : 1991). PMID 32198502 DOI: 10.1093/Cercor/Bhaa035  0.526
2020 Pattabiraman K, Shibata M, Lorente Galdos B, Andrijevic D, Sestan N. Regulation of Prefrontal Patterning, Connectivity and Synaptogenesis by Retinoic Acid Biological Psychiatry. 87: S132. DOI: 10.1016/J.Biopsych.2020.02.354  0.62
2019 Muchnik SK, Lorente-Galdos B, Santpere G, Sestan N. Modeling the Evolution of Human Brain Development Using Organoids. Cell. 179: 1250-1253. PMID 31778651 DOI: 10.1016/j.cell.2019.10.041  0.424
2019 Yang H, Kim J, Kim Y, Jang SW, Sestan N, Shim S. Cux2 expression regulated by Lhx2 in the upper layer neurons of the developing cortex. Biochemical and Biophysical Research Communications. PMID 31708105 DOI: 10.1016/j.bbrc.2019.11.004  0.42
2019 Molnár Z, Clowry GJ, Šestan N, Alzu'bi A, Bakken T, Hevner RF, Hüppi PS, Kostović I, Rakic P, Anton ES, Edwards D, Garcez P, Hoerder-Suabedissen A, Kriegstein A. New insights into the development of the human cerebral cortex. Journal of Anatomy. PMID 31373394 DOI: 10.1111/Joa.13055  0.845
2019 Vrselja Z, Daniele SG, Silbereis J, Talpo F, Morozov YM, Sousa AMM, Tanaka BS, Skarica M, Pletikos M, Kaur N, Zhuang ZW, Liu Z, Alkawadri R, Sinusas AJ, Latham SR, ... ... Sestan N, et al. Restoration of brain circulation and cellular functions hours post-mortem. Nature. 568: 336-343. PMID 30996318 DOI: 10.1038/S41586-019-1099-1  0.796
2019 Miller DJ, Bhaduri A, Sestan N, Kriegstein A. Shared and derived features of cellular diversity in the human cerebral cortex. Current Opinion in Neurobiology. 56: 117-124. PMID 30677551 DOI: 10.1016/j.conb.2018.12.005  0.427
2019 Werling D, Pochareddy S, Choi J, An J, Sheppard B, Peng M, Santpere G, Gulden F, Breen M, Talkowski M, Roeder K, State M, Devlin B, Sanders S, Sestan N. 29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX European Neuropsychopharmacology. 29: S75-S76. DOI: 10.1016/J.Euroneuro.2019.07.170  0.596
2019 An J, Lin K, Zhu L, Werling D, Dong S, Brand H, Wang H, Zhao X, Sestan N, State M, Willsey J, Talkowski M, Devlin B, Roeder K, Sanders S. INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING European Neuropsychopharmacology. 29: S36. DOI: 10.1016/J.Euroneuro.2019.07.073  0.554
2018 Meng Q, Wang K, Brunetti T, Xia Y, Jiao C, Dai R, Fitzgerald D, Thomas A, Jay L, Eckart H, Grennan K, Imamura-Kawasawa Y, Li M, Sestan N, White KP, et al. The long noncoding RNA may regulate expression of several schizophrenia-related genes. Science Translational Medicine. PMID 30545965 DOI: 10.1126/Scitranslmed.Aat6912  0.449
2018 Wang D, Liu S, Warrell J, Won H, Shi X, Navarro FCP, Clarke D, Gu M, Emani P, Yang YT, Xu M, Gandal MJ, Lou S, Zhang J, Park JJ, ... ... Sestan N, et al. Comprehensive functional genomic resource and integrative model for the human brain. Science (New York, N.Y.). 362. PMID 30545857 DOI: 10.1126/Science.Aat8464  0.421
2018 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, et al. Spatiotemporal transcriptomic divergence across human and macaque brain development. Science (New York, N.Y.). 362. PMID 30545855 DOI: 10.1126/Science.Aat8077  0.676
2018 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, ... ... Sestan N, et al. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science (New York, N.Y.). 362. PMID 30545854 DOI: 10.1126/Science.Aat7615  0.822
2018 Amiri A, Coppola G, Scuderi S, Wu F, Roychowdhury T, Liu F, Pochareddy S, Shin Y, Safi A, Song L, Zhu Y, Sousa AMM, Gerstein M, Crawford GE, ... Sestan N, et al. Transcriptome and epigenome landscape of human cortical development modeled in organoids. Science (New York, N.Y.). 362. PMID 30545853 DOI: 10.1126/Science.Aat6720  0.676
2018 An JY, Lin K, Zhu L, Werling DM, Dong S, Brand H, Wang HZ, Zhao X, Schwartz GB, Collins RL, Currall BB, Dastmalchi C, Dea J, Duhn C, Gilson MC, ... ... Sestan N, et al. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362. PMID 30545852 DOI: 10.1126/Science.Aat6576  0.67
2018 Sestan N, State MW. Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder. Neuron. 100: 406-423. PMID 30359605 DOI: 10.1016/J.Neuron.2018.10.015  0.632
2018 Tebbenkamp ATN, Varela L, Choi J, Paredes MI, Giani AM, Song JE, Sestan-Pesa M, Franjic D, Sousa AMM, Liu ZW, Li M, Bichsel C, Koch M, Szigeti-Buck K, Liu F, ... ... Sestan N, et al. The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development. Cell. PMID 30318146 DOI: 10.1016/J.Cell.2018.09.014  0.789
2018 Dell'Anno MT, Wang X, Onorati M, Li M, Talpo F, Sekine Y, Ma S, Liu F, Cafferty WBJ, Sestan N, Strittmatter SM. Human neuroepithelial stem cell regional specificity enables spinal cord repair through a relay circuit. Nature Communications. 9: 3419. PMID 30143638 DOI: 10.1038/S41467-018-05844-8  0.649
2018 Carlyle BC, Kitchen RR, Zhang J, Wilson R, Lam TT, Rozowsky JS, Williams KR, Sestan N, Gerstein M, Nairn AC. Isoform level interpretation of high-throughput proteomic data enabled by deep integration with RNA-seq. Journal of Proteome Research. PMID 30125121 DOI: 10.1021/Acs.Jproteome.8B00310  0.335
2018 Hammarlund M, Hobert O, Miller DM, Sestan N. The CeNGEN Project: The Complete Gene Expression Map of an Entire Nervous System. Neuron. 99: 430-433. PMID 30092212 DOI: 10.1016/J.Neuron.2018.07.042  0.394
2018 Willsey AJ, Morris MT, Wang S, Willsey HR, Sun N, Teerikorpi N, Baum TB, Cagney G, Bender KJ, Desai TA, Srivastava D, Davis GW, Doudna J, Chang E, Sohal V, ... ... Sestan N, et al. The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders. Cell. 174: 505-520. PMID 30053424 DOI: 10.1016/J.Cell.2018.06.016  0.584
2018 Werling DM, Brand H, An JY, Stone MR, Zhu L, Glessner JT, Collins RL, Dong S, Layer RM, Markenscoff-Papadimitriou E, Farrell A, Schwartz GB, Wang HZ, Currall BB, Zhao X, ... ... Sestan N, et al. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics. PMID 29700473 DOI: 10.1038/S41588-018-0107-Y  0.668
2018 Farahany NA, Greely HT, Hyman S, Koch C, Grady C, Pașca SP, Sestan N, Arlotta P, Bernat JL, Ting J, Lunshof JE, Iyer EPR, Hyun I, Capestany BH, Church GM, et al. The ethics of experimenting with human brain tissue. Nature. 556: 429-432. PMID 29691509 DOI: 10.1038/D41586-018-04813-X  0.358
2018 Castiglioni V, Faedo A, Onorati M, Bocchi VD, Li Z, Iennaco R, Vuono R, Bulfamante GP, Muzio L, Martino G, Sestan N, Barker RA, Cattaneo E. Dynamic and Cell-Specific DACH1 Expression in Human Neocortical and Striatal Development. Cerebral Cortex (New York, N.Y. : 1991). PMID 29688344 DOI: 10.1093/Cercor/Bhy092  0.755
2018 Mi D, Li Z, Lim L, Li M, Moissidis M, Yang Y, Gao T, Hu TX, Pratt T, Price DJ, Sestan N, Marín O. Early emergence of cortical interneuron diversity in the mouse embryo. Science (New York, N.Y.). PMID 29472441 DOI: 10.1126/Science.Aar6821  0.521
2017 Bae T, Tomasini L, Mariani J, Zhou B, Roychowdhury T, Franjic D, Pletikos M, Pattni R, Chen BJ, Venturini E, Riley-Gillis B, Sestan N, Urban AE, Abyzov A, Vaccarino FM. Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. Science (New York, N.Y.). PMID 29217587 DOI: 10.1126/Science.Aan8690  0.807
2017 Carlyle BC, Kitchen RR, Kanyo JE, Voss EZ, Pletikos M, Sousa AMM, Lam TT, Gerstein MB, Sestan N, Nairn AC. A multiregional proteomic survey of the postnatal human brain. Nature Neuroscience. 20: 1787-1795. PMID 29184206 DOI: 10.1038/S41593-017-0011-2  0.809
2017 Sousa AMM, Zhu Y, Raghanti MA, Kitchen RR, Onorati M, Tebbenkamp ATN, Stutz B, Meyer KA, Li M, Kawasawa YI, Liu F, Perez RG, Mele M, Carvalho T, Skarica M, ... ... Sestan N, et al. Molecular and cellular reorganization of neural circuits in the human lineage. Science (New York, N.Y.). 358: 1027-1032. PMID 29170230 DOI: 10.1126/Science.Aan3456  0.825
2017 Ecker JR, Geschwind DH, Kriegstein AR, Ngai J, Osten P, Polioudakis D, Regev A, Sestan N, Wickersham IR, Zeng H. The BRAIN Initiative Cell Census Consortium: Lessons Learned toward Generating a Comprehensive Brain Cell Atlas. Neuron. 96: 542-557. PMID 29096072 DOI: 10.1016/J.Neuron.2017.10.007  0.431
2017 Zhang M, Chen D, Xia J, Han W, Cui X, Neuenkirchen N, Hermes G, Sestan N, Lin H. Post-transcriptional regulation of mouse neurogenesis by Pumilio proteins. Genes & Development. PMID 28794184 DOI: 10.1101/Gad.298752.117  0.75
2017 Gu Z, Kalamboglas J, Yoshioka S, Han W, Li Z, Kawasawa YI, Pochareddy S, Li Z, Liu F, Xu X, Wijeratne S, Ueno M, Blatz E, Salomone J, Kumanogoh A, ... ... Sestan N, et al. Control of species-dependent cortico-motoneuronal connections underlying manual dexterity. Science (New York, N.Y.). 357: 400-404. PMID 28751609 DOI: 10.1126/Science.Aan3721  0.795
2017 Sousa AMM, Meyer KA, Santpere G, Gulden FO, Sestan N. Evolution of the Human Nervous System Function, Structure, and Development. Cell. 170: 226-247. PMID 28708995 DOI: 10.1016/j.cell.2017.06.036  0.579
2017 Feng L, Jeon T, Yu Q, Ouyang M, Peng Q, Mishra V, Pletikos M, Sestan N, Miller MI, Mori S, Hsiao S, Liu S, Huang H. Population-averaged macaque brain atlas with high-resolution ex vivo DTI integrated into in vivo space. Brain Structure & Function. PMID 28634624 DOI: 10.1007/S00429-017-1463-6  0.792
2017 McConnell MJ, Moran JV, Abyzov A, Akbarian S, Bae T, Cortes-Ciriano I, Erwin JA, Fasching L, Flasch DA, Freed D, Ganz J, Jaffe AE, Kwan KY, Kwon M, Lodato MA, ... ... Sestan N, et al. Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science (New York, N.Y.). 356. PMID 28450582 DOI: 10.1126/Science.Aal1641  0.829
2017 Diao Y, Cui L, Chen Y, Burbridge TJ, Han W, Wirth B, Sestan N, Crair MC, Zhang J. Reciprocal Connections Between Cortex and Thalamus Contribute to Retinal Axon Targeting to Dorsal Lateral Geniculate Nucleus. Cerebral Cortex (New York, N.Y. : 1991). 1-15. PMID 28334242 DOI: 10.1093/Cercor/Bhx028  0.784
2017 Sgourdou P, Mishra-Gorur K, Saotome I, Henagariu O, Tuysuz B, Campos C, Ishigame K, Giannikou K, Quon JL, Sestan N, Caglayan AO, Gunel M, Louvi A. Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly. Scientific Reports. 7: 43708. PMID 28272472 DOI: 10.1038/Srep43708  0.408
2017 Meyer KA, Marques-Bonet T, Sestan N. Differential Gene Expression in the Human Brain Is Associated with Conserved, but not Accelerated, Noncoding Sequences. Molecular Biology and Evolution. PMID 28204568 DOI: 10.1093/Molbev/Msx076  0.447
2017 Akins MR, Berk-Rauch HE, Kwan KY, Mitchell ME, Shepard KA, Korsak LI, Stackpole EE, Warner-Schmidt JL, Sestan N, Cameron HA, Fallon JR. Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains. Human Molecular Genetics. PMID 28082376 DOI: 10.1093/Hmg/Ddw381  0.774
2017 Scuderi S, Amiri A, Coppola G, Wu F, Franjic D, Sestan N, Gerstein M, Weissman S, Abyzov A, Vaccarino FM. Comparative transcriptome and gene regulation in human iPSC-derived organoids and donor-identical brain tissue Italian Journal of Anatomy and Embryology. 122: 196. DOI: 10.13128/Ijae-21588  0.494
2016 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. Simultaneous dimension reduction and adjustment for confounding variation. Proceedings of the National Academy of Sciences of the United States of America. PMID 27930330 DOI: 10.1073/Pnas.1617317113  0.435
2016 Ataman B, Boulting GL, Harmin DA, Yang MG, Baker-Salisbury M, Yap EL, Malik AN, Mei K, Rubin AA, Spiegel I, Durresi E, Sharma N, Hu LS, Pletikos M, Griffith EC, ... ... Sestan N, et al. Evolution of Osteocrin as an activity-regulated factor in the primate brain. Nature. 539: 242-247. PMID 27830782 DOI: 10.1038/Nature20111  0.829
2016 Caubit X, Gubellini P, Andrieux J, Roubertoux PL, Metwaly M, Jacq B, Fatmi A, Had-Aissouni L, Kwan KY, Salin P, Carlier M, Liedén A, Rudd E, Shinawi M, Vincent-Delorme C, ... ... Sestan N, et al. TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons. Nature Genetics. PMID 27668656 DOI: 10.1038/Ng.3681  0.826
2016 Onorati M, Li Z, Liu F, Sousa AM, Nakagawa N, Li M, Dell'Anno MT, Gulden FO, Pochareddy S, Tebbenkamp AT, Han W, Pletikos M, Gao T, Zhu Y, Bichsel C, ... ... Sestan N, et al. Zika Virus Disrupts Phospho-TBK1 Localization and Mitosis in Human Neuroepithelial Stem Cells and Radial Glia. Cell Reports. PMID 27568284 DOI: 10.1016/J.Celrep.2016.08.038  0.775
2016 Ding SL, Royall JJ, Sunkin SM, Ng L, Facer BA, Lesnar P, Guillozet-Bongaarts A, McMurray B, Szafer A, Dolbeare TA, Stevens A, Tirrell L, Benner T, Caldejon S, Dalley RA, ... ... Sestan N, et al. Comprehensive cellular-resolution atlas of the adult human brain. The Journal of Comparative Neurology. PMID 27418273 DOI: 10.1002/Cne.24080  0.39
2016 Kawasawa YI, Salzberg AC, Li M, Sestan N, Greer CA, Imamura F. RNA-seq analysis of developing olfactory bulb projection neurons. Molecular and Cellular Neurosciences. PMID 27073125 DOI: 10.1016/j.mcn.2016.03.009  0.418
2016 Lin Z, Li M, Sestan N, Zhao H. A Markov random field-based approach for joint estimation of differentially expressed genes in mouse transcriptome data. Statistical Applications in Genetics and Molecular Biology. PMID 26926866 DOI: 10.1515/sagmb-2015-0070  0.383
2016 Olmos-Serrano JL, Kang HJ, Tyler WA, Silbereis JC, Cheng F, Zhu Y, Pletikos M, Jankovic-Rapan L, Cramer NP, Galdzicki Z, Goodliffe J, Peters A, Sethares C, Delalle I, Golden JA, ... ... Sestan N, et al. Down Syndrome Developmental Brain Transcriptome Reveals Defective Oligodendrocyte Differentiation and Myelination. Neuron. PMID 26924435 DOI: 10.1016/J.Neuron.2016.01.042  0.815
2016 Silbereis JC, Pochareddy S, Zhu Y, Li M, Sestan N. The Cellular and Molecular Landscapes of the Developing Human Central Nervous System. Neuron. 89: 248-68. PMID 26796689 DOI: 10.1016/J.Neuron.2015.12.008  0.495
2015 Mishra-Gorur K, Çağlayan AO, Schaffer AE, Chabu C, Henegariu O, Vonhoff F, Akgümüş GT, Nishimura S, Han W, Tu S, Baran B, Gümüş H, Dilber C, Zaki MS, Hossni HAA, et al. Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors. Neuron. 85: 228. PMID 29654772 DOI: 10.1016/J.Neuron.2014.12.046  0.77
2015 Lin Z, Sanders SJ, Li M, Sestan N, State MW, Zhao H. A MARKOV RANDOM FIELD-BASED APPROACH TO CHARACTERIZING HUMAN BRAIN DEVELOPMENT USING SPATIAL-TEMPORAL TRANSCRIPTOME DATA. The Annals of Applied Statistics. 9: 429-451. PMID 26877824 DOI: 10.1214/14-Aoas802  0.636
2015 D'Gama AM, Pochareddy S, Li M, Jamuar SS, Reiff RE, Lam AT, Sestan N, Walsh CA. Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms. Neuron. 88: 910-7. PMID 26637798 DOI: 10.1016/J.Neuron.2015.11.009  0.504
2015 Akbarian S, Liu C, Knowles JA, Vaccarino FM, Farnham PJ, Crawford GE, Jaffe AE, Pinto D, Dracheva S, Geschwind DH, Mill J, Nairn AC, Abyzov A, Pochareddy S, Prabhakar S, ... ... Sestan N, et al. The PsychENCODE project. Nature Neuroscience. 18: 1707-1712. PMID 26605881 DOI: 10.1038/Nn.4156  0.66
2015 Nishimura S, Bilgüvar K, Ishigame K, Sestan N, Günel M, Louvi A. Functional synergy between cholecystokinin receptors CCKAR and CCKBR in mammalian brain development. Plos One. 10: e0124295. PMID 25875176 DOI: 10.1371/Journal.Pone.0124295  0.376
2015 Lun MP, Johnson MB, Broadbelt KG, Watanabe M, Kang YJ, Chau KF, Springel MW, Malesz A, Sousa AM, Pletikos M, Adelita T, Calicchio ML, Zhang Y, Holtzman MJ, Lidov HG, ... Sestan N, et al. Spatially heterogeneous choroid plexus transcriptomes encode positional identity and contribute to regional CSF production. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 4903-16. PMID 25810521 DOI: 10.1523/Jneurosci.3081-14.2015  0.793
2015 Cotney J, Muhle RA, Sanders SJ, Liu L, Willsey AJ, Niu W, Liu W, Klei L, Lei J, Yin J, Reilly SK, Tebbenkamp AT, Bichsel C, Pletikos M, Sestan N, et al. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment. Nature Communications. 6: 6404. PMID 25752243 DOI: 10.1038/Ncomms7404  0.806
2015 Shibata M, Gulden FO, Sestan N. From trans to cis: transcriptional regulatory networks in neocortical development. Trends in Genetics : Tig. 31: 77-87. PMID 25624274 DOI: 10.1016/j.tig.2014.12.004  0.352
2015 Ouyang A, Jeon T, Sunkin SM, Pletikos M, Sedmak G, Sestan N, Lein ES, Huang H. Spatial mapping of structural and connectional imaging data for the developing human brain with diffusion tensor imaging. Methods (San Diego, Calif.). 73: 27-37. PMID 25448302 DOI: 10.1016/J.Ymeth.2014.10.025  0.799
2015 Ercan-Sencicek AG, Jambi S, Franjic D, Nishimura S, Li M, El-Fishawy P, Morgan TM, Sanders SJ, Bilguvar K, Suri M, Johnson MH, Gupta AR, Yuksel Z, Mane S, Grigorenko E, et al. Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. European Journal of Human Genetics : Ejhg. 23: 165-72. PMID 24781755 DOI: 10.1038/Ejhg.2014.82  0.658
2015 Lin Z, Sanders SJ, Li M, Sestan N, State MW, Zhao H. A markov random field-based approach to characterizing human brain development using spatial–temporal transcriptome data Annals of Applied Statistics. 9: 429-451. DOI: 10.1214/14-AOAS802  0.562
2014 Mishra-Gorur K, Ça?layan AO, Schaffer AE, Chabu C, Henegariu O, Vonhoff F, Akgümü? GT, Nishimura S, Han W, Tu S, Baran B, Gümü? H, Dilber C, Zaki MS, Hossni HA, et al. Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors. Neuron. 84: 1226-39. PMID 25521378 DOI: 10.1016/J.Neuron.2014.12.014  0.812
2014 Caglayan AO, Baranoski JF, Aktar F, Han W, Tuysuz B, Guzel A, Guclu B, Kaymakcalan H, Aktekin B, Akgumus GT, Murray PB, Erson-Omay EZ, Caglar C, Bakircioglu M, Sakalar YB, et al. Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutations. Pediatric Neurology. 51: 806-813.e8. PMID 25456301 DOI: 10.1016/J.Pediatrneurol.2014.08.025  0.317
2014 Gulden FO, Šestan N. Neurobiology: building a bigger brain. Nature. 515: 206-7. PMID 25391958 DOI: 10.1038/515206a  0.518
2014 Lennington JB, Coppola G, Kataoka-Sasaki Y, Fernandez TV, Palejev D, Li Y, Huttner A, Pletikos M, Sestan N, Leckman JF, Vaccarino FM. Transcriptome Analysis of the Human Striatum in Tourette Syndrome. Biological Psychiatry. PMID 25199956 DOI: 10.1016/J.Biopsych.2014.07.018  0.785
2014 Zhu Y, Li M, Sousa AM, Sestan N. XSAnno: a framework for building ortholog models in cross-species transcriptome comparisons. Bmc Genomics. 15: 343. PMID 24884593 DOI: 10.1186/1471-2164-15-343  0.559
2014 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, ... ... Sestan N, et al. Rare deleterious mutations of the gene EFR3A in autism spectrum disorders. Molecular Autism. 5: 31. PMID 24860643 DOI: 10.1186/2040-2392-5-31  0.59
2014 Carlyle BC, Nairn AC, Wang M, Yang Y, Jin LE, Simen AA, Ramos BP, Bordner KA, Craft GE, Davies P, Pletikos M, Šestan N, Arnsten AF, Paspalas CD. cAMP-PKA phosphorylation of tau confers risk for degeneration in aging association cortex. Proceedings of the National Academy of Sciences of the United States of America. 111: 5036-41. PMID 24707050 DOI: 10.1073/Pnas.1322360111  0.791
2014 Miller JA, Ding SL, Sunkin SM, Smith KA, Ng L, Szafer A, Ebbert A, Riley ZL, Royall JJ, Aiona K, Arnold JM, Bennet C, Bertagnolli D, Brouner K, Butler S, ... ... Sestan N, et al. Transcriptional landscape of the prenatal human brain. Nature. 508: 199-206. PMID 24695229 DOI: 10.1038/Nature13185  0.836
2014 Liu L, Lei J, Sanders SJ, Willsey AJ, Kou Y, Cicek AE, Klei L, Lu C, He X, Li M, Muhle RA, Ma'ayan A, Noonan JP, Sestan N, McFadden KA, et al. DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics. Molecular Autism. 5: 22. PMID 24602502 DOI: 10.1186/2040-2392-5-22  0.618
2014 Tebbenkamp AT, Willsey AJ, State MW, Sestan N. The developmental transcriptome of the human brain: implications for neurodevelopmental disorders. Current Opinion in Neurology. 27: 149-56. PMID 24565942 DOI: 10.1097/Wco.0000000000000069  0.828
2014 Fertuzinhos S, Li M, Kawasawa YI, Ivic V, Franjic D, Singh D, Crair M, Sestan N. Laminar and temporal expression dynamics of coding and noncoding RNAs in the mouse neocortex. Cell Reports. 6: 938-50. PMID 24561256 DOI: 10.1016/J.Celrep.2014.01.036  0.803
2014 Bae BI, Tietjen I, Atabay KD, Evrony GD, Johnson MB, Asare E, Wang PP, Murayama AY, Im K, Lisgo SN, Overman L, Šestan N, Chang BS, Barkovich AJ, Grant PE, et al. Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning. Science (New York, N.Y.). 343: 764-8. PMID 24531968 DOI: 10.1126/Science.1244392  0.681
2014 Robichaux MA, Chenaux G, Ho HY, Soskis MJ, Dravis C, Kwan KY, Šestan N, Greenberg ME, Henkemeyer M, Cowan CW. EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding. Proceedings of the National Academy of Sciences of the United States of America. 111: 2188-93. PMID 24453220 DOI: 10.1073/Pnas.1324215111  0.78
2014 Pletikos M, Sousa AM, Sedmak G, Meyer KA, Zhu Y, Cheng F, Li M, Kawasawa YI, Sestan N. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron. 81: 321-32. PMID 24373884 DOI: 10.1016/J.Neuron.2013.11.018  0.809
2013 Han W, Sestan N. Cortical projection neurons: sprung from the same root. Neuron. 80: 1103-5. PMID 24314721 DOI: 10.1016/J.Neuron.2013.11.016  0.77
2013 Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, ... ... Sestan N, et al. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell. 155: 997-1007. PMID 24267886 DOI: 10.1016/J.Cell.2013.10.020  0.821
2013 Li H, Fertuzinhos S, Mohns E, Hnasko TS, Verhage M, Edwards R, Sestan N, Crair MC. Laminar and columnar development of barrel cortex relies on thalamocortical neurotransmission. Neuron. 79: 970-86. PMID 24012009 DOI: 10.1016/J.Neuron.2013.06.043  0.817
2013 Ruusuvuori E, Huebner AK, Kirilkin I, Yukin AY, Blaesse P, Helmy M, Kang HJ, El Muayed M, Hennings JC, Voipio J, Šestan N, Hübner CA, Kaila K. Neuronal carbonic anhydrase VII provides GABAergic excitatory drive to exacerbate febrile seizures. The Embo Journal. 32: 2275-86. PMID 23881097 DOI: 10.1038/Emboj.2013.160  0.315
2013 Radmanesh F, Caglayan AO, Silhavy JL, Yilmaz C, Cantagrel V, Omar T, Rosti B, Kaymakcalan H, Gabriel S, Li M, Sestan N, Bilguvar K, Dobyns WB, Zaki MS, Gunel M, et al. Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities. American Journal of Human Genetics. 92: 468-74. PMID 23472759 DOI: 10.1016/J.Ajhg.2013.02.005  0.611
2013 Huang H, Jeon T, Sedmak G, Pletikos M, Vasung L, Xu X, Yarowsky P, Richards LJ, Kostovic I, Sestan N, Mori S. Coupling diffusion imaging with histological and gene expression analysis to examine the dynamics of cortical areas across the fetal period of human brain development. Cerebral Cortex (New York, N.Y. : 1991). 23: 2620-31. PMID 22933464 DOI: 10.1093/Cercor/Bhs241  0.814
2012 Miller DJ, Duka T, Stimpson CD, Schapiro SJ, Baze WB, McArthur MJ, Fobbs AJ, Sousa AM, Sestan N, Wildman DE, Lipovich L, Kuzawa CW, Hof PR, Sherwood CC. Prolonged myelination in human neocortical evolution. Proceedings of the National Academy of Sciences of the United States of America. 109: 16480-5. PMID 23012402 DOI: 10.1073/Pnas.1117943109  0.541
2012 State MW, Šestan N. Neuroscience. The emerging biology of autism spectrum disorders. Science (New York, N.Y.). 337: 1301-3. PMID 22984058 DOI: 10.1126/Science.1224989  0.578
2012 Shim S, Kwan KY, Li M, Lefebvre V, Sestan N. Cis-regulatory control of corticospinal system development and evolution. Nature. 486: 74-9. PMID 22678282 DOI: 10.1038/nature11094  0.805
2012 Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, RaÅ¡in MR, Sousa AM, Fertuzinhos S, Chen JG, Arellano JI, Chan DW, Pletikos M, Vasung L, Rowitch DH, Huang EJ, ... ... Sestan N, et al. Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex. Cell. 149: 899-911. PMID 22579290 DOI: 10.1016/J.Cell.2012.02.060  0.806
2012 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, ... ... Sestan N, et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 485: 237-41. PMID 22495306 DOI: 10.1038/Nature10945  0.597
2012 Kwan KY, Sestan N, Anton ES. Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex. Development (Cambridge, England). 139: 1535-46. PMID 22492350 DOI: 10.1242/dev.069963  0.799
2011 Kang HJ, Kawasawa YI, Cheng F, Zhu Y, Xu X, Li M, Sousa AM, Pletikos M, Meyer KA, Sedmak G, Guennel T, Shin Y, Johnson MB, Krsnik Z, Mayer S, ... ... Sestan N, et al. Spatio-temporal transcriptome of the human brain. Nature. 478: 483-9. PMID 22031440 DOI: 10.1038/Nature10523  0.807
2011 Barak T, Kwan KY, Louvi A, Demirbilek V, Sayg? S, Tüysüz B, Choi M, Boyac? H, Doerschner K, Zhu Y, Kaymakçalan H, Y?lmaz S, Bak?rc?o?lu M, Ca?layan AO, Oztürk AK, ... ... Sestan N, et al. Recessive LAMC3 mutations cause malformations of occipital cortical development. Nature Genetics. 43: 590-4. PMID 21572413 DOI: 10.1038/Ng.836  0.82
2011 Han W, Kwan KY, Shim S, Lam MM, Shin Y, Xu X, Zhu Y, Li M, Sestan N. TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract. Proceedings of the National Academy of Sciences of the United States of America. 108: 3041-6. PMID 21285371 DOI: 10.1073/Pnas.1016723108  0.789
2010 Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizo?lu D, Tüysüz B, Ca?layan AO, Gökben S, Kaymakçalan H, Barak T, Bakircio?lu M, Yasuno K, Ho W, ... ... Sestan N, et al. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature. 467: 207-10. PMID 20729831 DOI: 10.1038/Nature09327  0.831
2009 Ros H, Sachdev RN, Yu Y, Sestan N, McCormick DA. Neocortical networks entrain neuronal circuits in cerebellar cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 10309-20. PMID 19692605 DOI: 10.1523/Jneurosci.2327-09.2009  0.761
2009 Johnson MB, Kawasawa YI, Mason CE, Krsnik Z, Coppola G, Bogdanovi? D, Geschwind DH, Mane SM, State MW, Sestan N. Functional and evolutionary insights into human brain development through global transcriptome analysis. Neuron. 62: 494-509. PMID 19477152 DOI: 10.1016/J.Neuron.2009.03.027  0.839
2009 Fertuzinhos S, Krsnik Z, Kawasawa YI, Rasin MR, Kwan KY, Chen JG, Judas M, Hayashi M, Sestan N. Selective depletion of molecularly defined cortical interneurons in human holoprosencephaly with severe striatal hypoplasia. Cerebral Cortex (New York, N.Y. : 1991). 19: 2196-207. PMID 19234067 DOI: 10.1093/Cercor/Bhp009  0.813
2009 Stillman AA, Krsnik Z, Sun J, Rasin MR, State MW, Sestan N, Louvi A. Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome. The Journal of Comparative Neurology. 513: 21-37. PMID 19105198 DOI: 10.1002/Cne.21919  0.83
2008 Hashimoto-Torii K, Torii M, Sarkisian MR, Bartley CM, Shen J, Radtke F, Gridley T, Sestan N, Rakic P. Interaction between Reelin and Notch signaling regulates neuronal migration in the cerebral cortex. Neuron. 60: 273-84. PMID 18957219 DOI: 10.1016/J.Neuron.2008.09.026  0.806
2008 Kwan KY, Lam MM, Krsnik Z, Kawasawa YI, Lefebvre V, Sestan N. SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons. Proceedings of the National Academy of Sciences of the United States of America. 105: 16021-6. PMID 18840685 DOI: 10.1073/pnas.0806791105  0.806
2008 Britanova O, de Juan Romero C, Cheung A, Kwan KY, Schwark M, Gyorgy A, Vogel T, Akopov S, Mitkovski M, Agoston D, Sestan N, Molnár Z, Tarabykin V. Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex. Neuron. 57: 378-92. PMID 18255031 DOI: 10.1016/J.Neuron.2007.12.028  0.796
2007 Breunig JJ, Silbereis J, Vaccarino FM, Sestan N, Rakic P. Notch regulates cell fate and dendrite morphology of newborn neurons in the postnatal dentate gyrus. Proceedings of the National Academy of Sciences of the United States of America. 104: 20558-63. PMID 18077357 DOI: 10.1073/pnas.0710156104  0.779
2007 Rasin MR, Gazula VR, Breunig JJ, Kwan KY, Johnson MB, Liu-Chen S, Li HS, Jan LY, Jan YN, Rakic P, Sestan N. Numb and Numbl are required for maintenance of cadherin-based adhesion and polarity of neural progenitors. Nature Neuroscience. 10: 819-27. PMID 17589506 DOI: 10.1038/nn1924  0.786
2007 Brandt N, Franke K, Rasin MR, Baumgart J, Vogt J, Khrulev S, Hassel B, Pohl EE, Sestan N, Nitsch R, Schumacher S. The neural EGF family member CALEB/NGC mediates dendritic tree and spine complexity. The Embo Journal. 26: 2371-86. PMID 17431398 DOI: 10.1038/sj.emboj.7601680  0.769
2006 Kuo CT, Mirzadeh Z, Soriano-Navarro M, Rasin M, Wang D, Shen J, Sestan N, Garcia-Verdugo J, Alvarez-Buylla A, Jan LY, Jan YN. Postnatal deletion of Numb/Numblike reveals repair and remodeling capacity in the subventricular neurogenic niche. Cell. 127: 1253-64. PMID 17174898 DOI: 10.1016/J.Cell.2006.10.041  0.766
2006 Smith KM, Ohkubo Y, Maragnoli ME, Rasin MR, Schwartz ML, Sestan N, Vaccarino FM. Midline radial glia translocation and corpus callosum formation require FGF signaling. Nature Neuroscience. 9: 787-97. PMID 16715082 DOI: 10.1038/Nn1705  0.779
2005 Chen JG, Rasin MR, Kwan KY, Sestan N. Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex. Proceedings of the National Academy of Sciences of the United States of America. 102: 17792-7. PMID 16314561 DOI: 10.1073/pnas.0509032102  0.805
2005 Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, ... ... Sestan N, et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science (New York, N.Y.). 310: 317-20. PMID 16224024 DOI: 10.1126/Science.1116502  0.789
2004 Miska EA, Alvarez-Saavedra E, Townsend M, Yoshii A, Sestan N, Rakic P, Constantine-Paton M, Horvitz HR. Microarray analysis of microRNA expression in the developing mammalian brain. Genome Biology. 5: R68. PMID 15345052 DOI: 10.1186/gb-2004-5-9-r68  0.677
2003 Schmid RS, McGrath B, Berechid BE, Boyles B, Marchionni M, Sestan N, Anton ES. Neuregulin 1-erbB2 signaling is required for the establishment of radial glia and their transformation into astrocytes in cerebral cortex. Proceedings of the National Academy of Sciences of the United States of America. 100: 4251-6. PMID 12649319 DOI: 10.1073/pnas.0630496100  0.356
2002 Roncarati R, Sestan N, Scheinfeld MH, Berechid BE, Lopez PA, Meucci O, McGlade JC, Rakic P, D'Adamio L. The gamma-secretase-generated intracellular domain of beta-amyloid precursor protein binds Numb and inhibits Notch signaling. Proceedings of the National Academy of Sciences of the United States of America. 99: 7102-7. PMID 12011466 DOI: 10.1073/Pnas.102192599  0.613
2001 Sestan N, Rakic P, Donoghue MJ. Independent parcellation of the embryonic visual cortex and thalamus revealed by combinatorial Eph/ephrin gene expression. Current Biology : Cb. 11: 39-43. PMID 11166178 DOI: 10.1016/S0960-9822(00)00043-9  0.647
1999 Sestan N, Artavanis-Tsakonas S, Rakic P. Contact-dependent inhibition of cortical neurite growth mediated by notch signaling. Science (New York, N.Y.). 286: 741-6. PMID 10531053 DOI: 10.1126/science.286.5440.741  0.661
1999 Judas M, Sestan N, Kostovi? I. Nitrinergic neurons in the developing and adult human telencephalon: transient and permanent patterns of expression in comparison to other mammals. Microscopy Research and Technique. 45: 401-19. PMID 10402267 DOI: 10.1002/(Sici)1097-0029(19990615)45:6<401::Aid-Jemt7>3.0.Co;2-Q  0.722
1999 Qi H, Rand MD, Wu X, Sestan N, Wang W, Rakic P, Xu T, Artavanis-Tsakonas S. Processing of the notch ligand delta by the metalloprotease Kuzbanian. Science (New York, N.Y.). 283: 91-4. PMID 9872749 DOI: 10.1126/Science.283.5398.91  0.596
1992 Sajin B, Sestan N, Dmitrovi? B. Compartmentalization of NADPH-diaphorase staining in the developing human striatum. Neuroscience Letters. 140: 117-20. PMID 1407689 DOI: 10.1016/0304-3940(92)90695-4  0.32
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