Hong LE - Search Results

1

P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans.

Kochunov P, Glahn DC, Hong LE, Lancaster J, Curran JE, Johnson MP, Winkler AM, Holcomb HH, Kent JW Jr, Mitchell B, Kochunov V, Olvera RL, Cole SA, Dyer TD, Moses EK, Goring H, Almasy L, Duggirala R, Blangero J. Kochunov P, et al. Among authors: hong le. Front Genet. 2012 May 1;3:65. doi: 10.3389/fgene.2012.00065. eCollection 2012. Front Genet. 2012. PMID: 22558002 Free PMC article.

2

Specific motion processing pathway deficit during eye tracking in schizophrenia: a performance-matched functional magnetic resonance imaging study.

Hong LE, Tagamets M, Avila M, Wonodi I, Holcomb H, Thaker GK. Hong LE, et al. Biol Psychiatry. 2005 Apr 1;57(7):726-32. doi: 10.1016/j.biopsych.2004.12.015. Biol Psychiatry. 2005. PMID: 15820229

3

Dihydropyrimidinase-related protein 2 (DRP-2) gene and association to deficit and nondeficit schizophrenia.

Hong LE, Wonodi I, Avila MT, Buchanan RW, McMahon RP, Mitchell BD, Stine OC, Carpenter WT Jr, Thaker GK. Hong LE, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):8-11. doi: 10.1002/ajmg.b.30181. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15858820

4

Familial aggregation of eye-tracking endophenotypes in families of schizophrenic patients.

Hong LE, Mitchell BD, Avila MT, Adami H, McMahon RP, Thaker GK. Hong LE, et al. Arch Gen Psychiatry. 2006 Mar;63(3):259-64. doi: 10.1001/archpsyc.63.3.259. Arch Gen Psychiatry. 2006. PMID: 16520430

5

Lack of association between COMT gene and deficit/nondeficit schizophrenia.

Wonodi I, Mitchell BD, Stine OC, Hong LE, Elliott A, Kirkpatrick B, Carpenter WT Jr, Thaker GK, Buchanan RW. Wonodi I, et al. Among authors: hong le. Behav Brain Funct. 2006 Dec 15;2:42. doi: 10.1186/1744-9081-2-42. Behav Brain Funct. 2006. PMID: 17173666 Free PMC article.

6

Evidence of missense mutations on the neuregulin 1 gene affecting function of prepulse inhibition.

Hong LE, Wonodi I, Stine OC, Mitchell BD, Thaker GK. Hong LE, et al. Biol Psychiatry. 2008 Jan 1;63(1):17-23. doi: 10.1016/j.biopsych.2007.05.011. Epub 2007 Jul 12. Biol Psychiatry. 2008. PMID: 17631867 Free PMC article.

7

Dopamine transporter polymorphism modulates oculomotor function and DAT1 mRNA expression in schizophrenia.

Wonodi I, Hong LE, Stine OC, Mitchell BD, Elliott A, Roberts RC, Conley RR, McMahon RP, Thaker GK. Wonodi I, et al. Among authors: hong le. Am J Med Genet B Neuropsychiatr Genet. 2009 Mar 5;150B(2):282-9. doi: 10.1002/ajmg.b.30811. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18553389 Free PMC article.

8

Sensory gating endophenotype based on its neural oscillatory pattern and heritability estimate.

Hong LE, Summerfelt A, Mitchell BD, McMahon RP, Wonodi I, Buchanan RW, Thaker GK. Hong LE, et al. Arch Gen Psychiatry. 2008 Sep;65(9):1008-16. doi: 10.1001/archpsyc.65.9.1008. Arch Gen Psychiatry. 2008. PMID: 18762587 Free PMC article.

9

Downregulated kynurenine 3-monooxygenase gene expression and enzyme activity in schizophrenia and genetic association with schizophrenia endophenotypes.

Wonodi I, Stine OC, Sathyasaikumar KV, Roberts RC, Mitchell BD, Hong LE, Kajii Y, Thaker GK, Schwarcz R. Wonodi I, et al. Among authors: hong le. Arch Gen Psychiatry. 2011 Jul;68(7):665-74. doi: 10.1001/archgenpsychiatry.2011.71. Arch Gen Psychiatry. 2011. PMID: 21727251 Free PMC article.

10

A shared low-frequency oscillatory rhythm abnormality in resting and sensory gating in schizophrenia.

Hong LE, Summerfelt A, Mitchell BD, O'Donnell P, Thaker GK. Hong LE, et al. Clin Neurophysiol. 2012 Feb;123(2):285-92. doi: 10.1016/j.clinph.2011.07.025. Epub 2011 Sep 8. Clin Neurophysiol. 2012. PMID: 21862398 Free PMC article. Clinical Trial.

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