Feil Family Brain & Mind Research Institute

Publications

Found 414 results
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2019
Krusche P, Trigg L, Boutros PC, Mason CE, De La Vega FM, Moore BL, Gonzalez-Porta M, Eberle MA, Tezak Z, Lababidi S et al..  2019.  Best practices for benchmarking germline small-variant calls in human genomes.. Nat Biotechnol.
Chang A, Ricci B, Grory BMac, Cutting S, Burton T, Dakay K, Jayaraman M, Merkler A, Reznik M, Lerario MP et al..  2019.  Cardiac Biomarkers Predict Large Vessel Occlusion in Patients with Ischemic Stroke.. J Stroke Cerebrovasc Dis.
Chaker S, Al-Dasuqi K, Baradaran H, Demetres M, Delgado D, Nehmeh S, Osborne JR, Christos PJ, Kamel H, Gupta A.  2019.  Carotid Plaque Positron Emission Tomography Imaging and Cerebral Ischemic Disease.. Stroke. :STROKEAHA118023987.
Chaker S, Al-Dasuqi K, Baradaran H, Demetres M, Delgado D, Nehmeh S, Osborne JR, Christos PJ, Kamel H, Gupta A.  2019.  Carotid Plaque Positron Emission Tomography Imaging and Cerebral Ischemic Disease.. Stroke. :STROKEAHA118023987.
Linden JR, Flores C, Schmidt EF, Uzal FA, Michel AO, Valenzuela M, Dobrow S, Vartanian T.  2019.  Clostridium perfringens epsilon toxin induces blood brain barrier permeability via caveolae-dependent transcytosis and requires expression of MAL.. PLoS Pathog. 15(11):e1008014.
McIntyre ABR, Ounit R, Afshinnekoo E, Prill RJ, Hénaff E, Alexander N, Minot SS, Danko D, Foox J, Ahsanuddin S et al..  2019.  Correction to: Comprehensive benchmarking and ensemble approaches for metagenomic classifiers.. Genome Biol. 20(1):72.
Dubin MJ, Ilieva IP, De Deng Z-, Thomas J, Cochran A, Kravets K, Brody BD, Christos PJ, Kocsis JH, Liston C et al..  2019.  A double-blind pilot dosing study of low field magnetic stimulation (LFMS) for treatment-resistant depression (TRD).. J Affect Disord. 249:286-293.
Dubin MJ, Ilieva IP, De Deng Z-, Thomas J, Cochran A, Kravets K, Brody BD, Christos PJ, Kocsis JH, Liston C et al..  2019.  A double-blind pilot dosing study of low field magnetic stimulation (LFMS) for treatment-resistant depression (TRD).. J Affect Disord. 249:286-293.
Hung P, Finn C, Chen M, Knight-Greenfield A, Baradaran H, Patel P, Díaz I, Kamel H, Gupta A.  2019.  Effect of Clinical History on Interpretation of Computed Tomography for Acute Stroke.. Neurohospitalist. 9(3):140-143.
Waters EM, Mazid S, Dodos M, Puri R, Janssen WG, Morrison JH, McEwen BS, Milner TA.  2019.  Effects of estrogen and aging on synaptic morphology and distribution of phosphorylated Tyr1472 NR2B in the female rat hippocampus.. Neurobiol Aging. 73:200-210.
Grosenick L, Shi TC, Gunning FM, Dubin MJ, Downar J, Liston C.  2019.  Functional and Optogenetic Approaches to Discovering Stable Subtype-Specific Circuit Mechanisms in Depression.. Biol Psychiatry Cogn Neurosci Neuroimaging. 4(6):554-566.
Grosenick L, Shi TC, Gunning FM, Dubin MJ, Downar J, Liston C.  2019.  Functional and Optogenetic Approaches to Discovering Stable Subtype-Specific Circuit Mechanisms in Depression.. Biol Psychiatry Cogn Neurosci Neuroimaging. 4(6):554-566.
Duan ZRan S, Che A, Chu P, Modol L, Bollmann Y, Babij R, Fetcho RN, Otsuka T, Fuccillo MV, Liston C et al..  2019.  GABAergic Restriction of Network Dynamics Regulates Interneuron Survival in the Developing Cortex.. Neuron.
Strandwitz P, Kim KHyun, Terekhova D, Liu JK, Sharma A, Levering J, McDonald D, Dietrich D, Ramadhar TR, Lekbua A et al..  2019.  GABA-modulating bacteria of the human gut microbiota.. Nat Microbiol. 4(3):396-403.
Strandwitz P, Kim KHyun, Terekhova D, Liu JK, Sharma A, Levering J, McDonald D, Dietrich D, Ramadhar TR, Lekbua A et al..  2019.  GABA-modulating bacteria of the human gut microbiota.. Nat Microbiol. 4(3):396-403.
Demertzi A, Tagliazucchi E, Dehaene S, Deco G, Barttfeld P, Raimondo F, Martial C, Fernández-Espejo D, Rohaut B, Voss HU et al..  2019.  Human consciousness is supported by dynamic complex patterns of brain signal coordination.. Sci Adv. 5(2):eaat7603.
Demertzi A, Tagliazucchi E, Dehaene S, Deco G, Barttfeld P, Raimondo F, Martial C, Fernández-Espejo D, Rohaut B, Voss HU et al..  2019.  Human consciousness is supported by dynamic complex patterns of brain signal coordination.. Sci Adv. 5(2):eaat7603.
Demertzi A, Tagliazucchi E, Dehaene S, Deco G, Barttfeld P, Raimondo F, Martial C, Fernández-Espejo D, Rohaut B, Voss HU et al..  2019.  Human consciousness is supported by dynamic complex patterns of brain signal coordination.. Sci Adv. 5(2):eaat7603.
Doria JW, Forgacs PB.  2019.  Incidence, Implications, and Management of Seizures Following Ischemic and Hemorrhagic Stroke.. Curr Neurol Neurosci Rep. 19(7):37.
Dunlop K, Talishinsky A, Liston C.  2019.  Intrinsic Brain Network Biomarkers of Antidepressant Response: a Review.. Curr Psychiatry Rep. 21(9):87.
Agirre X, Meydan C, Jiang Y, Garate L, Doane AS, Li Z, Verma A, Paiva B, Martín-Subero JI, Elemento O et al..  2019.  Long non-coding RNAs discriminate the stages and gene regulatory states of human humoral immune response.. Nat Commun. 10(1):821.
Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D et al..  2019.  Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.. Acta Neuropathol.
Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D et al..  2019.  Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.. Acta Neuropathol.
Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D et al..  2019.  Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.. Acta Neuropathol.
Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D et al..  2019.  Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.. Acta Neuropathol.