Richard S. Smith, PhD - Publications

Northwestern University, Evanston, IL 
Neurobiology, Ion channels, cortex, sodium channels

20 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
2023 Barão S, Xu Y, Vistein R, Goff L, Nielsen K, Bae BI, Smith RS, Walsh CA, Stein-O'Brien G, Müller U. Transcriptional Control of Neocortical Size and Microcephaly. Biorxiv : the Preprint Server For Biology. PMID 37961182 DOI: 10.1101/2023.11.02.565322  0.547
2023 Akula SK, Chen AY, Neil JE, Shao DD, Mo A, Hylton NK, DiTroia S, Ganesh VS, Smith RS, O'Kane K, Yeh RC, Marciano JH, Kirkham S, Kenny CJ, Song JHT, et al. Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria. Jama Neurology. PMID 37486637 DOI: 10.1001/jamaneurol.2023.2363  0.651
2022 Qian X, DeGennaro EM, Talukdar M, Akula SK, Lai A, Shao DD, Gonzalez D, Marciano JH, Smith RS, Hylton NK, Yang E, Bazan JF, Barrett L, Yeh RC, Hill RS, et al. Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis. Developmental Cell. PMID 36228617 DOI: 10.1016/j.devcel.2022.09.011  0.751
2021 Shao DD, Straussberg R, Ahmed H, Khan A, Tian S, Hill RS, Smith RS, Majmundar AJ, Ameziane N, Neil JE, Yang E, Al Tenaiji A, Jamuar SS, Schlaeger TM, Al-Saffar M, et al. A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33531666 DOI: 10.1038/s41436-021-01097-x  0.678
2020 Krienen FM, Goldman M, Zhang Q, C H Del Rosario R, Florio M, Machold R, Saunders A, Levandowski K, Zaniewski H, Schuman B, Wu C, Lutservitz A, Mullally CD, Reed N, Bien E, ... ... Smith R, et al. Innovations present in the primate interneuron repertoire. Nature. PMID 32999462 DOI: 10.1038/s41586-020-2781-z  0.43
2020 Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Muna Al-Saffar, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, et al. Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32103185 DOI: 10.1038/S41436-020-0758-9  0.679
2020 Smith RS, Walsh CA. Ion Channel Functions in Early Brain Development. Trends in Neurosciences. PMID 31959360 DOI: 10.1016/j.tins.2019.12.004  0.455
2018 Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, et al. Sodium Channel SCN3A (Na1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development. Neuron. PMID 30146301 DOI: 10.1016/J.Neuron.2018.07.052  0.755
2018 Coulter ME, Dorobantu CM, Lodewijk GA, Delalande F, Cianferani S, Ganesh VS, Smith RS, Lim ET, Xu CS, Pang S, Wong ET, Lidov HGW, Calicchio ML, Yang E, Gonzalez DM, et al. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Reports. 24: 973-986.e8. PMID 30044992 DOI: 10.1016/J.Celrep.2018.06.100  0.73
2018 Johnson MB, Sun X, Kodani A, Borges-Monroy R, Girskis KM, Ryu SC, Wang PP, Patel K, Gonzalez DM, Woo YM, Yan Z, Liang B, Smith RS, Chatterjee M, Coman D, et al. Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size. Nature. PMID 29643508 DOI: 10.1038/S41586-018-0035-0  0.699
2015 Smith RS, Hu R, DeSouza A, Eberly CL, Krahe K, Chan W, Araneda RC. Differential Muscarinic Modulation in the Olfactory Bulb. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 10773-85. PMID 26224860 DOI: 10.1523/Jneurosci.0099-15.2015  0.74
2015 Ramaswamy B, Kulkarni SD, Villar PS, Smith RS, Eberly C, Araneda RC, Depireux DA, Shapiro B. Movement of Magnetic Nanoparticles in Brain Tissue: Mechanisms and Safety. Nanomedicine : Nanotechnology, Biology, and Medicine. PMID 26115639 DOI: 10.1016/J.Nano.2015.06.003  0.709
2015 Woodford CR, Frady EP, Smith RS, Morey B, Canzi G, Palida SF, Araneda RC, Kristan WB, Kubiak CP, Miller EW, Tsien RY. Improved PeT molecules for optically sensing voltage in neurons. Journal of the American Chemical Society. 137: 1817-24. PMID 25584688 DOI: 10.1021/Ja510602Z  0.647
2015 Smith RS, Hu R, DeSouza A, Eberly CL, Krahe K, Chan W, Araneda RC. Differential muscarinic modulation in the olfactory bulb Journal of Neuroscience. 35: 10773-10785. DOI: 10.1523/JNEUROSCI.0099-15.2015  0.655
2013 Nunez-Parra A, Maurer RK, Krahe K, Smith RS, Araneda RC. Disruption of centrifugal inhibition to olfactory bulb granule cells impairs olfactory discrimination. Proceedings of the National Academy of Sciences of the United States of America. 110: 14777-82. PMID 23959889 DOI: 10.1073/Pnas.1310686110  0.744
2013 Smith RS, Peterlin Z, Araneda RC. Pharmacology of mammalian olfactory receptors. Methods in Molecular Biology (Clifton, N.J.). 1003: 203-9. PMID 23585044 DOI: 10.1007/978-1-62703-377-0_15  0.675
2013 Zimnik NC, Treadway T, Smith RS, Araneda RC. α(1A)-Adrenergic regulation of inhibition in the olfactory bulb. The Journal of Physiology. 591: 1631-43. PMID 23266935 DOI: 10.1113/jphysiol.2012.248591  0.676
2010 Smith RS, Araneda RC. Cholinergic modulation of neuronal excitability in the accessory olfactory bulb. Journal of Neurophysiology. 104: 2963-74. PMID 20861438 DOI: 10.1152/jn.00446.2010  0.703
2009 Smith RS, Weitz CJ, Araneda RC. Excitatory actions of noradrenaline and metabotropic glutamate receptor activation in granule cells of the accessory olfactory bulb. Journal of Neurophysiology. 102: 1103-14. PMID 19474170 DOI: 10.1152/jn.91093.2008  0.683
2001 Chang B, Smith RS, Peters M, Savinova OV, Hawes NL, Zabaleta A, Nusinowitz S, Martin JE, Davisson ML, Cepko CL, Hogan BL, John SW. Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure. Bmc Genetics. 2: 18. PMID 11722794 DOI: 10.1186/1471-2156-2-18  0.457
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