Erika L. Nurmi, Ph.D. - Publications

Affiliations: 
2003 Vanderbilt University, Nashville, TN 
Area:
Genetics, Neuroscience Biology, Molecular Biology, Pathology

22 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
2015 Brandl EJ, Tiwari AK, Zai CC, Nurmi EL, Chowdhury NI, Arenovich T, Sanches M, Goncalves VF, Shen JJ, Lieberman JA, Meltzer HY, Kennedy JL, Müller DJ. Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample. The Pharmacogenomics Journal. PMID 26323598 DOI: 10.1038/tpj.2015.59  0.32
2015 Kohno M, Nurmi EL, Laughlin CP, Morales AM, Gail EH, Hellemann GS, London ED. Functional Genetic Variation in Dopamine Signaling Moderates Prefrontal Cortical Activity During Risky Decision Making. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 26119471 DOI: 10.1038/npp.2015.192  0.32
2015 Qin H, Samuels JF, Wang Y, Zhu Y, Grados MA, Riddle MA, Greenberg BD, Knowles JA, Fyer AJ, McCracken JT, Murphy DL, Rasmussen SA, Cullen BA, Piacentini J, Geller D, ... ... Nurmi EL, et al. Whole-genome association analysis of treatment response in obsessive-compulsive disorder. Molecular Psychiatry. PMID 25824302 DOI: 10.1038/mp.2015.32  0.32
2015 Pouget JG, Gonçalves VF, Nurmi EL, P Laughlin C, Mallya KS, McCracken JT, Aman MG, McDougle CJ, Scahill L, Misener VL, Tiwari AK, Zai CC, Brandl EJ, Felsky D, Leung AQ, et al. Investigation of TSPO variants in schizophrenia and antipsychotic treatment outcomes. Pharmacogenomics. 16: 5-22. PMID 25560467 DOI: 10.2217/pgs.14.158  0.32
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Nurmi E, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/appi.ajp.2014.13101306  0.32
2015 Mattheisen M, Samuels JF, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, McLaughlin NC, Nurmi EL, Askland KD, et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Molecular Psychiatry. 20: 337-44. PMID 24821223 DOI: 10.1038/mp.2014.43  0.32
2014 Davis MC, Horan WP, Nurmi EL, Rizzo S, Li W, Sugar CA, Green MF. Associations between oxytocin receptor genotypes and social cognitive performance in individuals with schizophrenia. Schizophrenia Research. 159: 353-7. PMID 25244972 DOI: 10.1016/j.schres.2014.09.006  0.32
2014 McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Nurmi E, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/j.jaac.2014.04.022  0.32
2014 O'Neill J, Tobias MC, Hudkins M, Oh EY, Hellemann GS, Nurmi EL, London ED. Thalamic glutamate decreases with cigarette smoking. Psychopharmacology. 231: 2717-24. PMID 24535652 DOI: 10.1007/s00213-014-3441-5  0.32
2014 McCracken JT, Badashova KK, Posey DJ, Aman MG, Scahill L, Tierney E, Arnold LE, Vitiello B, Whelan F, Chuang SZ, Davies M, Shah B, McDougle CJ, Nurmi EL. Positive effects of methylphenidate on hyperactivity are moderated by monoaminergic gene variants in children with autism spectrum disorders Pharmacogenomics Journal. 14: 295-302. PMID 23856854 DOI: 10.1038/tpj.2013.23  0.32
2013 Nurmi EL, Spilman SL, Whelan F, Scahill LL, Aman MG, McDougle CJ, Arnold LE, Handen B, Johnson C, Sukhodolsky DG, Posey DJ, Lecavalier L, Stigler KA, Ritz L, Tierney E, et al. Moderation of antipsychotic-induced weight gain by energy balance gene variants in the RUPP autism network risperidone studies Translational Psychiatry. 3. PMID 23799528 DOI: 10.1038/tp.2013.26  0.32
2013 Mehta SQ, Nurmi EL. Genetic pathways to autism spectrum disorders Neuropsychiatry. 3: 193-207. DOI: 10.2217/npy.13.16  0.32
2012 Payer DE, Nurmi EL, Wilson SA, McCracken JT, London ED. Effects of methamphetamine abuse and serotonin transporter gene variants on aggression and emotion-processing neurocircuitry. Translational Psychiatry. 2: e80. PMID 22832817 DOI: 10.1038/tp.2011.73  0.32
2012 Sakolsky DJ, McCracken JT, Nurmi EL. Genetics of pediatric anxiety disorders. Child and Adolescent Psychiatric Clinics of North America. 21: 479-500. PMID 22800990 DOI: 10.1016/j.chc.2012.05.010  0.32
2004 McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS. A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 131: 51-9. PMID 15389768 DOI: 10.1002/ajmg.b.30038  0.32
2003 Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Molecular Psychiatry. 8: 624-34, 570. PMID 12851639 DOI: 10.1038/sj.mp.4001283  0.32
2003 Nurmi EL, Dowd M, Tadevosyan-Leyfer O, Haines JL, Folstein SE, Sutcliffe JS. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13. Journal of the American Academy of Child and Adolescent Psychiatry. 42: 856-63. PMID 12819446 DOI: 10.1097/01.CHI.0000046868.56865.0F  0.32
2003 Sutcliffe JS, Han MK, Amin T, Kesterson RA, Nurmi EL. Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures. Bmc Genomics. 4: 15. PMID 12720574 DOI: 10.1186/1471-2164-4-15  0.32
2003 Sutcliffe JS, Nurmi EL, Lombroso PJ. Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism. Journal of the American Academy of Child and Adolescent Psychiatry. 42: 253-6. PMID 12544187 DOI: 10.1097/00004583-200302000-00021  0.32
2003 Matsumura M, Kubota T, Hidaka E, Wakui K, Kadowaki S, Ueta I, Shimizu T, Ueno I, Yamauchi K, Herzing LB, Nurmi EL, Sutcliffe JS, Fukushima Y, Katsuyama T. 'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation. Clinical Genetics. 63: 79-81. PMID 12519378 DOI: 10.1034/j.1399-0004.2003.630114.x  0.32
2003 Nurmi EL, Amin T, Olson LM, Jacob MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism Molecular Psychiatry. 8: 570. DOI: 10.1038/sj.mp.4001361  0.32
2001 Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, et al. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics. 77: 105-13. PMID 11543639 DOI: 10.1006/geno.2001.6617  0.32
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