Charles Glatt - Publications

University of California, Los Angeles, Los Angeles, CA 

49 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
2016 Gee DG, Fetcho RN, Jing D, Li A, Glatt CE, Drysdale AT, Cohen AO, Dellarco DV, Yang RR, Dale AM, Jernigan TL, Lee FS, Casey BJ. Individual differences in frontolimbic circuitry and anxiety emerge with adolescent changes in endocannabinoid signaling across species. Proceedings of the National Academy of Sciences of the United States of America. PMID 27001846 DOI: 10.1073/pnas.1600013113  1
2015 Casey BJ, Glatt CE, Lee FS. Treating the Developing versus Developed Brain: Translating Preclinical Mouse and Human Studies. Neuron. 86: 1358-68. PMID 26087163 DOI: 10.1016/j.neuron.2015.05.020  1
2015 Dincheva I, Drysdale AT, Hartley CA, Johnson DC, Jing D, King EC, Ra S, Gray JM, Yang R, DeGruccio AM, Huang C, Cravatt BF, Glatt CE, Hill MN, Casey BJ, et al. FAAH genetic variation enhances fronto-amygdala function in mouse and human. Nature Communications. 6: 6395. PMID 25731744 DOI: 10.1038/ncomms7395  1
2015 Glatt CE, Lee FS. Common Polymorphisms in the Age of Research Domain Criteria (RDoC): Integration and Translation. Biological Psychiatry. PMID 25680673 DOI: 10.1016/j.biopsych.2014.12.020  1
2014 Milrod B, Markowitz JC, Gerber AJ, Cyranowski J, Altemus M, Shapiro T, Hofer M, Glatt C. Childhood separation anxiety and the pathogenesis and treatment of adult anxiety. The American Journal of Psychiatry. 171: 34-43. PMID 24129927 DOI: 10.1176/appi.ajp.2013.13060781  1
2014 King EC, Pattwell SS, Glatt CE, Lee FS. Sensitive periods in fear learning and memory. Stress (Amsterdam, Netherlands). 17: 13-21. PMID 23611461 DOI: 10.3109/10253890.2013.796355  1
2013 King EC, Pattwell SS, Sun A, Glatt CE, Lee FS. Nonlinear developmental trajectory of fear learning and memory. Annals of the New York Academy of Sciences. 1304: 62-9. PMID 24176014 DOI: 10.1111/nyas.12280  1
2013 Yoon Y, McKenna MC, Rollins DA, Song M, Nuriel T, Gross SS, Xu G, Glatt CE. Anxiety-associated alternative polyadenylation of the serotonin transporter mRNA confers translational regulation by hnRNPK. Proceedings of the National Academy of Sciences of the United States of America. 110: 11624-9. PMID 23798440 DOI: 10.1073/pnas.1301485110  1
2013 Riddle MC, McKenna MC, Yoon YJ, Pattwell SS, Santos PM, Casey BJ, Glatt CE. Caloric restriction enhances fear extinction learning in mice. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 38: 930-7. PMID 23303073 DOI: 10.1038/npp.2012.268  1
2013 Casey BJ, Pattwell SS, Glatt CE, Lee FS. Treating the developing brain: implications from human imaging and mouse genetics. Annual Review of Medicine. 64: 427-39. PMID 23190151 DOI: 10.1146/annurev-med-052611-130408  1
2012 Glatt CE. Biology trumps statistics in the postgenomic era. The Behavioral and Brain Sciences. 35: 366-7. PMID 23095387 DOI: 10.1017/S0140525X12001008  1
2012 Gunnar MR, Wenner JA, Thomas KM, Glatt CE, McKenna MC, Clark AG. The brain-derived neurotrophic factor Val66Met polymorphism moderates early deprivation effects on attention problems. Development and Psychopathology. 24: 1215-23. PMID 23062292 DOI: 10.1017/S095457941200065X  1
2012 Pattwell SS, Duhoux S, Hartley CA, Johnson DC, Jing D, Elliott MD, Ruberry EJ, Powers A, Mehta N, Yang RR, Soliman F, Glatt CE, Casey BJ, Ninan I, Lee FS. Altered fear learning across development in both mouse and human. Proceedings of the National Academy of Sciences of the United States of America. 109: 16318-23. PMID 22988092 DOI: 10.1073/pnas.1206834109  1
2012 Hartley CA, McKenna MC, Salman R, Holmes A, Casey BJ, Phelps EA, Glatt CE. Serotonin transporter polyadenylation polymorphism modulates the retention of fear extinction memory. Proceedings of the National Academy of Sciences of the United States of America. 109: 5493-8. PMID 22431634 DOI: 10.1073/pnas.1202044109  1
2012 Dincheva I, Glatt CE, Lee FS. Impact of the BDNF Val66Met polymorphism on cognition: implications for behavioral genetics. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 18: 439-51. PMID 22367929 DOI: 10.1177/1073858411431646  1
2011 Casey BJ, Ruberry EJ, Libby V, Glatt CE, Hare T, Soliman F, Duhoux S, Frielingsdorf H, Tottenham N. Transitional and translational studies of risk for anxiety. Depression and Anxiety. 28: 18-28. PMID 21225849 DOI: 10.1002/da.20783  1
2011 Kanellopoulos D, Gunning FM, Morimoto SS, Hoptman MJ, Murphy CF, Kelly RE, Glatt C, Lim KO, Alexopoulos GS. Hippocampal volumes and the brain-derived neurotrophic factor val66met polymorphism in geriatric major depression. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. 19: 13-22. PMID 21218562 DOI: 10.1097/JGP.0b013e3181f61d62  1
2010 Casey BJ, Soliman F, Bath KG, Glatt CE. Imaging genetics and development: challenges and promises. Human Brain Mapping. 31: 838-51. PMID 20496375 DOI: 10.1002/hbm.21047  1
2010 Alexopoulos GS, Glatt CE, Hoptman MJ, Kanellopoulos D, Murphy CF, Kelly RE, Morimoto SS, Lim KO, Gunning FM. BDNF val66met polymorphism, white matter abnormalities and remission of geriatric depression. Journal of Affective Disorders. 125: 262-8. PMID 20346518 DOI: 10.1016/j.jad.2010.02.115  1
2010 Lin Z, Zhao Y, Chung CY, Zhou Y, Xiong N, Glatt CE, Isacson O. High regulatability favors genetic selection in SLC18A2, a vesicular monoamine transporter essential for life. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 24: 2191-200. PMID 20181938 DOI: 10.1096/fj.09-140368  1
2010 Soliman F, Glatt CE, Bath KG, Levita L, Jones RM, Pattwell SS, Jing D, Tottenham N, Amso D, Somerville LH, Voss HU, Glover G, Ballon DJ, Liston C, Teslovich T, et al. A genetic variant BDNF polymorphism alters extinction learning in both mouse and human. Science (New York, N.Y.). 327: 863-6. PMID 20075215 DOI: 10.1126/science.1181886  1
2010 Gyawali S, Subaran R, Weissman MM, Hershkowitz D, McKenna MC, Talati A, Fyer AJ, Wickramaratne P, Adams PB, Hodge SE, Schmidt CJ, Bannon MJ, Glatt CE. Association of a polyadenylation polymorphism in the serotonin transporter and panic disorder. Biological Psychiatry. 67: 331-8. PMID 19969287 DOI: 10.1016/j.biopsych.2009.10.015  1
2009 Alexopoulos GS, Murphy CF, Gunning-Dixon FM, Glatt CE, Latoussakis V, Kelly RE, Kanellopoulos D, Klimstra S, Lim KO, Young RC, Hoptman MJ. Serotonin transporter polymorphisms, microstructural white matter abnormalities and remission of geriatric depression. Journal of Affective Disorders. 119: 132-41. PMID 19375170 DOI: 10.1016/j.jad.2009.03.004  1
2009 Casey BJ, Glatt CE, Tottenham N, Soliman F, Bath K, Amso D, Altemus M, Pattwell S, Jones R, Levita L, McEwen B, Magariños AM, Gunnar M, Thomas KM, Mezey J, et al. Brain-derived neurotrophic factor as a model system for examining gene by environment interactions across development. Neuroscience. 164: 108-20. PMID 19358879 DOI: 10.1016/j.neuroscience.2009.03.081  1
2007 Wahner AD, Glatt CE, Bronstein JM, Ritz B. Glutathione S-transferase mu, omega, pi, and theta class variants and smoking in Parkinson's disease. Neuroscience Letters. 413: 274-8. PMID 17194543 DOI: 10.1016/j.neulet.2006.11.053  1
2006 Glatt C, Almonte M, Taylor T, Edwards RH, Freimer N, Tanner C. Structural variants in the vesicular monoamine transporter do not contribute to sporadic Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 426-7. PMID 16450345 DOI: 10.1002/mds.20798  1
2006 Glatt CE, Wahner AD, White DJ, Ruiz-Linares A, Ritz B. Gain-of-function haplotypes in the vesicular monoamine transporter promoter are protective for Parkinson disease in women. Human Molecular Genetics. 15: 299-305. PMID 16339215 DOI: 10.1093/hmg/ddi445  1
2005 Glatt CE, Carlson E, Taylor TR, Risch N, Reus VI, Schaefer CA. Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16. Neuron. 48: 704-5; author reply . PMID 16337902 DOI: 10.1016/j.neuron.2005.11.019  1
2005 Zhou Z, Peters EJ, Hamilton SP, McMahon F, Thomas C, McGrath PJ, Rush J, Trivedi MH, Charney DS, Roy A, Wisniewski S, Lipsky R, Goldman D, Van Den Bogaert A, De Zutter S, ... ... Glatt CE, et al. Response to Zhang et al. (2005) loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16 [2] (multiple letters) Neuron. 48: 702-706. PMID 16337901 DOI: 10.1016/j.neuron.2005.11.018  1
2004 Burman J, Tran CH, Glatt C, Freimer NB, Edwards RH. The effect of rare human sequence variants on the function of vesicular monoamine transporter 2. Pharmacogenetics. 14: 587-94. PMID 15475732 DOI: 10.1097/00008571-200409000-00003  1
2004 Breidenthal SE, White DJ, Glatt CE. Identification of genetic variants in the neuronal form of tryptophan hydroxylase (TPH2). Psychiatric Genetics. 14: 69-72. PMID 15167691 DOI: 10.1097/01.ypg.0000107929.32051.58  1
2004 Glatt CE, Tampilic M, Christie C, DeYoung J, Freimer NB. Re-screening serotonin receptors for genetic variants identifies population and molecular genetic complexity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 124: 92-100. PMID 14681923 DOI: 10.1002/ajmg.b.20056  1
2003 Glatt CE, Reus VI. Pharmacogenetics of monoamine transporters. Pharmacogenomics. 4: 583-96. PMID 12943466 DOI: 10.1517/phgs.4.5.583.23789  1
2003 Shu Y, Leabman MK, Feng B, Mangravite LM, Huang CC, Stryke D, Kawamoto M, Johns SJ, DeYoung J, Carlson E, Ferrin TE, Herskowitz I, Giacomini KM. Evolutionary conservation predicts function of variants of the human organic cation transporter, OCT1. Proceedings of the National Academy of Sciences of the United States of America. 100: 5902-7. PMID 12719534 DOI: 10.1073/pnas.0730858100  1
2003 Leabman MK, Huang CC, DeYoung J, Carlson EJ, Taylor TR, de la Cruz M, Johns SJ, Stryke D, Kawamoto M, Urban TJ, Kroetz DL, Ferrin TE, Clark AG, Risch N, Herskowitz I, et al. Natural variation in human membrane transporter genes reveals evolutionary and functional constraints. Proceedings of the National Academy of Sciences of the United States of America. 100: 5896-901. PMID 12719533 DOI: 10.1073/pnas.0730857100  1
2002 Glatt CE, Freimer NB. Association analysis of candidate genes for neuropsychiatric disease: the perpetual campaign. Trends in Genetics : Tig. 18: 307-12. PMID 12044360 DOI: 10.1016/S0168-9525(02)02670-7  1
2001 McInnes LA, Service SK, Reus VI, Barnes G, Charlat O, Jawahar S, Lewitzky S, Yang Q, Duong Q, Spesny M, Araya C, Araya X, Gallegos A, Meza L, Molina J, ... ... Glatt CE, et al. Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population. Proceedings of the National Academy of Sciences of the United States of America. 98: 11485-90. PMID 11572994 DOI: 10.1073/pnas.191519098  1
2001 Glatt CE, DeYoung JA, Delgado S, Service SK, Giacomini KM, Edwards RH, Risch N, Freimer NB. Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes. Nature Genetics. 27: 435-8. PMID 11279528 DOI: 10.1038/86948  1
1995 Glatt CE, Snowman AM, Sibley DR, Snyder SH. Clozapine: selective labeling of sites resembling 5HT6 serotonin receptors may reflect psychoactive profile. Molecular Medicine (Cambridge, Mass.). 1: 398-406. PMID 8521297  1
1993 Pieroni JP, Miller D, Premont RT, Iyengar R. Type 5 adenylyl cyclase distribution. Nature. 363: 679-80. PMID 8515810 DOI: 10.1038/363679a0  1
1993 Glatt CE, Snyder SH. Cloning and expression of an adenylyl cyclase localized to the corpus striatum. Nature. 361: 536-8. PMID 8429907 DOI: 10.1038/361536a0  1
1993 Fotuhi M, Sharp AH, Glatt CE, Hwang PM, von Krosigk M, Snyder SH, Dawson TM. Differential localization of phosphoinositide-linked metabotropic glutamate receptor (mGluR1) and the inositol 1,4,5-trisphosphate receptor in rat brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 13: 2001-12. PMID 8386753  1
1993 Verma A, Hirsch DJ, Glatt CE, Ronnett GV, Snyder SH. Carbon monoxide: a putative neural messenger. Science (New York, N.Y.). 259: 381-4. PMID 7678352  1
1992 Hwang PM, Glatt CE, Bredt DS, Yellen G, Snyder SH. A novel K+ channel with unique localizations in mammalian brain: molecular cloning and characterization. Neuron. 8: 473-81. PMID 1550672 DOI: 10.1016/0896-6273(92)90275-I  1
1992 Steiner JP, Dawson TM, Fotuhi M, Glatt CE, Snowman AM, Cohen N, Snyder SH. High brain densities of the immunophilin FKBP colocalized with calcineurin. Nature. 358: 584-7. PMID 1380130 DOI: 10.1038/358584a0  1
1992 Lowenstein CJ, Glatt CS, Bredt DS, Snyder SH. Cloned and expressed macrophage nitric oxide synthase contrasts with the brain enzyme. Proceedings of the National Academy of Sciences of the United States of America. 89: 6711-5. PMID 1379716  1
1991 Bredt DS, Glatt CE, Hwang PM, Fotuhi M, Dawson TM, Snyder SH. Nitric oxide synthase protein and mRNA are discretely localized in neuronal populations of the mammalian CNS together with NADPH diaphorase. Neuron. 7: 615-24. PMID 1718335 DOI: 10.1016/0896-6273(91)90374-9  1
1991 Bredt DS, Hwang PM, Glatt CE, Lowenstein C, Reed RR, Snyder SH. Cloned and expressed nitric oxide synthase structurally resembles cytochrome P-450 reductase. Nature. 351: 714-8. PMID 1712077 DOI: 10.1038/351714a0  1
1989 Ross CA, MacCumber MW, Glatt CE, Snyder SH. Brain phospholipase C isozymes: differential mRNA localizations by in situ hybridization. Proceedings of the National Academy of Sciences of the United States of America. 86: 2923-7. PMID 2468162 DOI: 10.1073/pnas.86.8.2923  1
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