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Alisa R. Gutman, Ph.D. - Publications

Affiliations: 
2009 Biological and Biomedical Sciences Emory University, Atlanta, GA 
Area:
Behavior
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5/25 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
2011 Wrenn GL, Wingo AP, Moore R, Pelletier T, Gutman AR, Bradley B, Ressler KJ. The effect of resilience on posttraumatic stress disorder in trauma-exposed inner-city primary care patients. Journal of the National Medical Association. 103: 560-6. PMID 21999030 DOI: 10.1016/S0027-9684(15)30381-3  0.447
2010 Wingo AP, Wrenn G, Pelletier T, Gutman AR, Bradley B, Ressler KJ. Moderating effects of resilience on depression in individuals with a history of childhood abuse or trauma exposure. Journal of Affective Disorders. 126: 411-4. PMID 20488545 DOI: 10.1016/J.Jad.2010.04.009  0.405
2009 Chhatwal JP, Gutman AR, Maguschak KA, Bowser ME, Yang Y, Davis M, Ressler KJ. Functional interactions between endocannabinoid and CCK neurotransmitter systems may be critical for extinction learning. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 34: 509-21. PMID 18580872 DOI: 10.1038/Npp.2008.97  0.477
2008 Gutman AR, Yang Y, Ressler KJ, Davis M. The role of neuropeptide Y in the expression and extinction of fear-potentiated startle. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 12682-90. PMID 19036961 DOI: 10.1523/Jneurosci.2305-08.2008  0.518
2005 Nair HP, Gutman AR, Davis M, Young LJ. Central oxytocin, vasopressin, and corticotropin-releasing factor receptor densities in the basal forebrain predict isolation potentiated startle in rats. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 11479-88. PMID 16339041 DOI: 10.1523/Jneurosci.2524-05.2005  0.422
Low-probability matches (unlikely to be authored by this person)
2016 Weine SM, Stone A, Saeed A, Shanfield S, Beahrs J, Gutman A, Mihajlovic A. Violent Extremism, Community-Based Violence Prevention, and Mental Health Professionals. The Journal of Nervous and Mental Disease. PMID 27977500 DOI: 10.1097/Nmd.0000000000000634  0.215
2021 Caroff SN, Gutman AR, Northrop J, Leong SH, Berkowitz RM, Campbell EC. Effect of Varenicline on Tardive Dyskinesia: A Pilot Study. Clinical Psychopharmacology and Neuroscience : the Official Scientific Journal of the Korean College of Neuropsychopharmacology. 19: 355-360. PMID 33888664 DOI: 10.9758/cpn.2021.19.2.355  0.2
2017 Weiss KJ, Gutman AR. Testifying About Trauma: A Call for Science and Civility. The Journal of the American Academy of Psychiatry and the Law. 45: 2-6. PMID 28270455  0.134
2006 Gutman DA, Gutman AR, Owens MJ, Nemeroff CB. Stress neurobiology and corticotropin-releasing factor Psychiatric Times. 23: 91-95.  0.124
2007 Korman SH, Jakobs C, Darmin PS, Gutman A, van der Knaap MS, Ben-Neriah Z, Dweikat I, Wexler ID, Salomons GS. Glutaric aciduria type 1: clinical, biochemical and molecular findings in patients from Israel. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 11: 81-9. PMID 17188916 DOI: 10.1016/j.ejpn.2006.11.006  0.09
2004 Korman SH, Boneh A, Ichinohe A, Kojima K, Sato K, Ergaz Z, Gomori JM, Gutman A, Kure S. Persistent NKH with transient or absent symptoms and a homozygous GLDC mutation. Annals of Neurology. 56: 139-43. PMID 15236413 DOI: 10.1002/ana.20159  0.074
2002 Raas-Rothschild A, Wanders RJ, Mooijer PA, Gootjes J, Waterham HR, Gutman A, Suzuki Y, Shimozawa N, Kondo N, Eshel G, Espeel M, Roels F, Korman SH. A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents. American Journal of Human Genetics. 70: 1062-8. PMID 11873320 DOI: 10.1086/339766  0.061
2004 Korman SH, Gutman A, Brooks R, Sinnathamby T, Gregersen N, Andresen BS. Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic status. Molecular Genetics and Metabolism. 82: 121-9. PMID 15171999 DOI: 10.1016/j.ymgme.2004.03.002  0.056
2007 Zeharia A, Ebberink MS, Wanders RJ, Waterham HR, Gutman A, Nissenkorn A, Korman SH. A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C. Journal of Human Genetics. 52: 599-606. PMID 17534573 DOI: 10.1007/s10038-007-0157-y  0.055
2014 Gutman AR, Sadoff RL. Patient privilege and dangerousness: Should duty to warn affect confidentiality? Journal of the American Academy of Psychiatry and the Law. 42: 245-247.  0.05
2004 Korman SH, Gutman A. N-acetyl tyrosyluria caused by parenteral or enteral administration of N-acetyl-L-tyrosine: differentiation from hereditary and acquired tyrosinemias. Journal of Pediatric Gastroenterology and Nutrition. 39: 95-100. PMID 15187789  0.045
2002 Korman SH, Gutman A. Pitfalls in the diagnosis of glycine encephalopathy (non-ketotic hyperglycinemia). Developmental Medicine and Child Neurology. 44: 712-20. PMID 12418798  0.04
2006 Korman SH, Wexler ID, Gutman A, Rolland MO, Kanno J, Kure S. Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutation. Annals of Neurology. 59: 411-5. PMID 16404748 DOI: 10.1002/ana.20759  0.036
2005 Korman SH, Waterham HR, Gutman A, Jakobs C, Wanders RJ. Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency. Molecular Genetics and Metabolism. 86: 337-43. PMID 16146704 DOI: 10.1016/j.ymgme.2005.07.022  0.034
2006 Korman SH, Pitt JJ, Boneh A, Dweikat I, Zater M, Meiner V, Gutman A, Brivet M. A novel SLC25A20 splicing mutation in patients of different ethnic origin with neonatally lethal carnitine-acylcarnitine translocase (CACT) deficiency. Molecular Genetics and Metabolism. 89: 332-8. PMID 16919490 DOI: 10.1016/j.ymgme.2006.06.009  0.032
2021 Weiss KJ, Gutman AR. Balancing Vulnerability and Resilience in Damage Prognostication. The Journal of the American Academy of Psychiatry and the Law. PMID 33542144 DOI: 10.29158/JAAPL.200108-20  0.031
2004 Korman SH, Gutman A, Stemmer E, Kay BS, Ben-Neriah Z, Zeigler M. Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis. Prenatal Diagnosis. 24: 857-60. PMID 15565656 DOI: 10.1002/pd.1000  0.017
2005 Korman SH, Andresen BS, Zeharia A, Gutman A, Boneh A, Pitt JJ. 2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation. Clinical Chemistry. 51: 610-7. PMID 15615815 DOI: 10.1373/clinchem.2004.043265  0.014
2004 Korman SH, Kanazawa N, Abu-Libdeh B, Gutman A, Tsujino S. Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family. Journal of the Neurological Sciences. 218: 53-8. PMID 14759633 DOI: 10.1016/j.jns.2003.10.017  0.011
2002 Korman SH, Raas-Rothschild A, Elpeleg O, Gutman A. Hypocarnitinemia in lysinuric protein intolerance. Molecular Genetics and Metabolism. 76: 81-3. PMID 12175786  0.01
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