| Year |
Citation |
Score |
| 2024 |
Fan R, Zhang D, Rodríguez-Kirby L, Lin Y, Song M, Wang L, Wang L, Kanatani S, Jimenez-Beristain T, Dang Y, Zhong M, Kukanja P, Wang S, Chen X, Gao F, ... ... Sestan N, et al. Spatial dynamics of mammalian brain development and neuroinflammation by multimodal tri-omics mapping. Research Square. PMID 39184075 DOI: 10.21203/rs.3.rs-4814866/v1 |
0.31 |
|
| 2024 |
Zhang D, Rubio Rodríguez-Kirby LA, Lin Y, Song M, Wang L, Wang L, Kanatani S, Jimenez-Beristain T, Dang Y, Zhong M, Kukanja P, Wang S, Chen XL, Gao F, Wang D, ... ... Sestan N, et al. Spatial dynamics of mammalian brain development and neuroinflammation by multimodal tri-omics mapping. Biorxiv : the Preprint Server For Biology. PMID 39091821 DOI: 10.1101/2024.07.28.605493 |
0.31 |
|
| 2024 |
Mato-Blanco X, Kim SK, Jourdon A, Ma S, Tebbenkamp ATN, Liu F, Duque A, Vaccarino FM, Sestan N, Colantuoni C, Rakic P, Santpere G, Micali N. Early Developmental Origins of Cortical Disorders Modeled in Human Neural Stem Cells. Biorxiv : the Preprint Server For Biology. PMID 38915580 DOI: 10.1101/2024.06.14.598925 |
0.8 |
|
| 2024 |
Emani PS, Liu JJ, Clarke D, Jensen M, Warrell J, Gupta C, Meng R, Lee CY, Xu S, Dursun C, Lou S, Chen Y, Chu Z, Galeev T, Hwang A, ... ... Sestan N, et al. Single-cell genomics and regulatory networks for 388 human brains. Science (New York, N.Y.). 384: eadi5199. PMID 38781369 DOI: 10.1126/science.adi5199 |
0.66 |
|
| 2024 |
Wen C, Margolis M, Dai R, Zhang P, Przytycki PF, Vo DD, Bhattacharya A, Matoba N, Tang M, Jiao C, Kim M, Tsai E, Hoh C, Aygün N, Walker RL, ... ... Sestan N, et al. Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain. Science (New York, N.Y.). 384: eadh0829. PMID 38781368 DOI: 10.1126/science.adh0829 |
0.372 |
|
| 2024 |
Emani PS, Liu JJ, Clarke D, Jensen M, Warrell J, Gupta C, Meng R, Lee CY, Xu S, Dursun C, Lou S, Chen Y, Chu Z, Galeev T, Hwang A, ... ... Sestan N, et al. Single-cell genomics and regulatory networks for 388 human brains. Biorxiv : the Preprint Server For Biology. PMID 38562822 DOI: 10.1101/2024.03.18.585576 |
0.657 |
|
| 2024 |
Fleck K, Luria V, Garag N, Karger A, Hunter T, Marten D, Phu W, Nam KM, Sestan N, O'Donnell-Luria AH, Erceg J. Functional associations of evolutionarily recent human genes exhibit sensitivity to the 3D genome landscape and disease. Biorxiv : the Preprint Server For Biology. PMID 38559085 DOI: 10.1101/2024.03.17.585403 |
0.731 |
|
| 2024 |
Sonthalia S, Li G, Blanco XM, Casella A, Liu J, Stein-O'Brien G, Caffo B, Adkins RS, Orvis J, Hertzano R, Mahurkar A, Gillis J, Werner J, Ma S, Micali N, ... Sestan N, et al. transcriptome dissection of neocortical excitatory neurogenesis via joint matrix decomposition and transfer learning. Biorxiv : the Preprint Server For Biology. PMID 38464021 DOI: 10.1101/2024.02.26.581612 |
0.781 |
|
| 2023 |
Singh AK, Allington G, Viviano S, McGee S, Kiziltug E, Ma S, Zhao S, Mekbib KY, Shohfi JP, Duy PQ, DeSpenza T, Furey CG, Reeves BC, Smith H, Sousa AMM, ... ... Sestan N, et al. A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus. Brain : a Journal of Neurology. PMID 38128548 DOI: 10.1093/brain/awad405 |
0.666 |
|
| 2023 |
Klarić TS, Gudelj I, Santpere G, Novokmet M, Vučković F, Ma S, Doll HM, Risgaard R, Bathla S, Karger A, Nairn AC, Luria V, Bečeheli I, Sherwood CC, Ely JJ, ... ... Sestan N, et al. Human-specific features and developmental dynamics of the brain N-glycome. Science Advances. 9: eadg2615. PMID 38055821 DOI: 10.1126/sciadv.adg2615 |
0.798 |
|
| 2023 |
Garrison MA, Jang Y, Bae T, Cherskov A, Emery SB, Fasching L, Jones A, Moldovan JB, Molitor C, Pochareddy S, Peters MA, Shin JH, Wang Y, Yang X, Akbarian S, ... ... Sestan N, et al. Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases. Scientific Data. 10: 813. PMID 37985666 DOI: 10.1038/s41597-023-02645-7 |
0.515 |
|
| 2023 |
Duan D, Lyu W, Chai P, Ma S, Wu K, Wu C, Xiong Y, Sestan N, Zhang K, Koleske AJ. Abl2 repairs microtubules and phase separates with tubulin to promote microtubule nucleation. Current Biology : Cb. PMID 37858340 DOI: 10.1016/j.cub.2023.09.018 |
0.606 |
|
| 2023 |
Micali N, Ma S, Li M, Kim SK, Mato-Blanco X, Sindhu SK, Arellano JI, Gao T, Shibata M, Gobeske KT, Duque A, Santpere G, Sestan N, Rakic P. Molecular programs of regional specification and neural stem cell fate progression in macaque telencephalon. Science (New York, N.Y.). 382: eadf3786. PMID 37824652 DOI: 10.1126/science.adf3786 |
0.774 |
|
| 2023 |
Singh AK, Viviano S, Allington G, McGee S, Kiziltug E, Mekbib KY, Shohfi JP, Duy PQ, DeSpenza T, Furey CG, Reeves BC, Smith H, Ma S, Sousa AMM, Cherskov A, ... ... Sestan N, et al. A novel -mutant BAFopathy implicates epigenetic dysregulation of neural progenitors in hydrocephalus. Medrxiv : the Preprint Server For Health Sciences. PMID 36993720 DOI: 10.1101/2023.03.19.23287455 |
0.608 |
|
| 2023 |
Wen C, Margolis M, Dai R, Zhang P, Przytycki PF, Vo DD, Bhattacharya A, Kim M, Matoba N, Tsai E, Hoh C, Jiao C, Aygun N, Walker RL, Chatzinakos C, ... ... Sestan N, et al. Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain. Medrxiv : the Preprint Server For Health Sciences. PMID 36945630 DOI: 10.1101/2023.03.03.23286706 |
0.352 |
|
| 2023 |
Luria V, Ma S, Shibata M, Pattabiraman K, Sestan N. Molecular and cellular mechanisms of human cortical connectivity. Current Opinion in Neurobiology. 80: 102699. PMID 36921362 DOI: 10.1016/j.conb.2023.102699 |
0.832 |
|
| 2023 |
Klarić TS, Gudelj I, Santpere G, Sousa AMM, Novokmet M, Vučković F, Ma S, Bečeheli I, Sherwood CC, Ely JJ, Hof PR, Josić D, Lauc G, Sestan N. Human-specific features and developmental dynamics of the brain N-glycome. Biorxiv : the Preprint Server For Biology. PMID 36711977 DOI: 10.1101/2023.01.11.523525 |
0.659 |
|
| 2022 |
Duffy EE, Finander B, Choi G, Carter AC, Pritisanac I, Alam A, Luria V, Karger A, Phu W, Sherman MA, Assad EG, Pajarillo N, Khitun A, Crouch EE, Ganesh S, ... ... Sestan N, et al. Developmental dynamics of RNA translation in the human brain. Nature Neuroscience. PMID 36171426 DOI: 10.1038/s41593-022-01164-9 |
0.787 |
|
| 2022 |
Duy PQ, Rakic P, Alper SL, Robert SM, Kundishora AJ, Butler WE, Walsh CA, Sestan N, Geschwind DH, Jin SC, Kahle KT. A neural stem cell paradigm of pediatric hydrocephalus. Cerebral Cortex (New York, N.Y. : 1991). PMID 36097331 DOI: 10.1093/cercor/bhac341 |
0.61 |
|
| 2022 |
Ma S, Skarica M, Li Q, Xu C, Risgaard RD, Tebbenkamp ATN, Mato-Blanco X, Kovner R, Krsnik Ž, de Martin X, Luria V, Martí-Pérez X, Liang D, Karger A, Schmidt DK, ... ... Sestan N, et al. Molecular and cellular evolution of the primate dorsolateral prefrontal cortex. Science (New York, N.Y.). eabo7257. PMID 36007006 DOI: 10.1126/science.abo7257 |
0.782 |
|
| 2022 |
Andrijevic D, Vrselja Z, Lysyy T, Zhang S, Skarica M, Spajic A, Dellal D, Thorn SL, Duckrow RB, Ma S, Duy PQ, Isiktas AU, Liang D, Li M, Kim SK, ... ... Sestan N, et al. Cellular recovery after prolonged warm ischaemia of the whole body. Nature. PMID 35922506 DOI: 10.1038/s41586-022-05016-1 |
0.618 |
|
| 2022 |
Stutz B, Waterson MJ, Šestan-Peša M, Dietrich MO, Škarica M, Sestan N, Racz B, Magyar A, Sotonyi P, Liu ZW, Gao XB, Matyas F, Stoiljkovic M, Horvath TL. AgRP neurons control structure and function of the medial prefrontal cortex. Molecular Psychiatry. PMID 35906488 DOI: 10.1038/s41380-022-01691-8 |
0.309 |
|
| 2022 |
Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Pattni R, Chahine Y, Yeh R, ... ... Sestan N, et al. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability. Science (New York, N.Y.). 377: 511-517. PMID 35901164 DOI: 10.1126/science.abm6222 |
0.813 |
|
| 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 |
0.756 |
|
| 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 |
0.64 |
|
| 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 |
0.778 |
|
| 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 |
0.816 |
|
| 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 |
0.79 |
|
| 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 |
0.534 |
|
| 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 |
0.314 |
|
| 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 |
0.333 |
|
| 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 |
0.374 |
|
| 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 |
0.343 |
|
| 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 |
0.325 |
|
| 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 |
0.713 |
|
| 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 |
0.773 |
|
| 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 |
0.796 |
|
| 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 |
0.833 |
|
| 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 |
0.739 |
|
| 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 |
0.658 |
|
| 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 |
0.74 |
|
| 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 |
0.434 |
|
| 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 |
0.423 |
|
| 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 |
0.852 |
|
| 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 |
0.8 |
|
| 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 |
0.444 |
|
| 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 |
0.599 |
|
| 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 |
0.547 |
|
| 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 |
0.448 |
|
| 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 |
0.565 |
|
| 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 |
0.827 |
|
| 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 |
0.563 |
|
| 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 |
0.665 |
|
| 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 |
0.628 |
|
| 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 |
0.781 |
|
| 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 |
0.753 |
|
| 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 |
0.393 |
|
| 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 |
0.578 |
|
| 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 |
0.663 |
|
| 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 |
0.364 |
|
| 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 |
0.751 |
|
| 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 |
0.518 |
|
| 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 |
0.811 |
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| 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 |
0.813 |
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| 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 |
0.835 |
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| 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 |
0.435 |
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| 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 |
0.714 |
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| 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 |
0.8 |
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| 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 |
0.43 |
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| 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 |
0.794 |
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| 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 |
0.828 |
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| 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 |
0.781 |
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| 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 |
0.403 |
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| 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 |
0.453 |
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| 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 |
0.792 |
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| 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 |
0.498 |
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| 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 |
0.423 |
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| 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 |
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| 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 |
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| 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 |
0.782 |
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| 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 |
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| 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 |
0.419 |
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| 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 |
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| 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 |
0.816 |
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| 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 |
0.49 |
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| 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 |
0.741 |
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| 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 |
0.633 |
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| 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 |
0.501 |
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| 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 |
0.653 |
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| 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 |
0.373 |
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| 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 |
0.797 |
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| 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 |
0.812 |
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| 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 |
0.35 |
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| 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 |
0.802 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
0.311 |
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| 2014 |
Gulden FO, Šestan N. Neurobiology: building a bigger brain. Nature. 515: 206-7. PMID 25391958 DOI: 10.1038/515206a |
0.526 |
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| 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 |
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| 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 |
0.618 |
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| 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 |
0.582 |
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| 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 |
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| 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 |
0.842 |
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| 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 |
0.614 |
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| 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 |
0.831 |
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| 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 |
0.806 |
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| 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 |
0.679 |
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| 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 |
0.799 |
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| 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 |
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| 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 |
0.74 |
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| 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 |
0.829 |
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| 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 |
0.822 |
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| 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 |
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| 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 |
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| 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 |
0.818 |
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| 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 |
0.616 |
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| 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 |
0.572 |
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| 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 |
0.823 |
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| 2012 |
Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, Rašin 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 |
0.811 |
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| 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 |
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| 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 |
0.817 |
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| 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 |
0.815 |
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| 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 |
0.826 |
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| 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 |
0.79 |
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| 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 |
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| 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 |
0.762 |
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| 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 |
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| 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 |
0.821 |
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| 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 |
0.833 |
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| 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 |
0.81 |
|
| 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 |
0.808 |
|
| 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 |
0.814 |
|
| 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 |
0.775 |
|
| 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 |
0.788 |
|
| 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 |
0.767 |
|
| 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 |
0.764 |
|
| 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 |
0.778 |
|
| 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 |
0.806 |
|
| 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 |
0.788 |
|
| 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 |
0.674 |
|
| 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 |
0.357 |
|
| 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 |
0.608 |
|
| 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 |
0.649 |
|
| 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 |
0.658 |
|
| 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 |
0.724 |
|
| 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 |
0.591 |
|
| 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 |
0.33 |
|
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