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The Choline Acetyltransferase (CHAT) Gene is Associated with Parahippocampal and Hippocampal Structure and Short-term Memory Span.

Zhu B, Chen C, Moyzis RK, Dong Q, Lin C.

Neuroscience. 2018 Jan 15;369:261-268. doi: 10.1016/j.neuroscience.2017.11.021. Epub 2017 Nov 21.


Family-based association study of DRD4 gene in methylphenidate-responded Attention Deficit/Hyperactivity Disorder.

Leung PW, Chan JK, Chen LH, Lee CC, Hung SF, Ho TP, Tang CP, Moyzis RK, Swanson JM.

PLoS One. 2017 Mar 10;12(3):e0173748. doi: 10.1371/journal.pone.0173748. eCollection 2017.


Associations between the CNTNAP2 gene, dorsolateral prefrontal cortex, and cognitive performance on the Stroop task.

Zhu B, Chen C, Xue G, Lei X, Wang Y, Li J, Moyzis RK, Li J, Dong Q, Lin C.

Neuroscience. 2017 Feb 20;343:21-29. doi: 10.1016/j.neuroscience.2016.11.021. Epub 2016 Dec 1.


Striatum-Centered Fiber Connectivity Is Associated with the Personality Trait of Cooperativeness.

Lei X, Chen C, Chen C, He Q, Moyzis RK, Xue G, Dong Q.

PLoS One. 2016 Oct 18;11(10):e0162160. doi: 10.1371/journal.pone.0162160. eCollection 2016.


Gender Interacts with Opioid Receptor Polymorphism A118G and Serotonin Receptor Polymorphism -1438 A/G on Speed-Dating Success.

Wu K, Chen C, Moyzis RK, Greenberger E, Yu Z.

Hum Nat. 2016 Sep;27(3):244-60. doi: 10.1007/s12110-016-9257-8.


Genetic variations in the serotonergic system contribute to amygdala volume in humans.

Li J, Chen C, Wu K, Zhang M, Zhu B, Chen C, Moyzis RK, Dong Q.

Front Neuroanat. 2015 Oct 9;9:129. doi: 10.3389/fnana.2015.00129. eCollection 2015.


Increased brain activity to unpleasant stimuli in individuals with the 7R allele of the DRD4 gene.

Gehricke JG, Swanson JM, Duong S, Nguyen J, Wigal TL, Fallon J, Caburian C, Muftuler LT, Moyzis RK.

Psychiatry Res. 2015 Jan 30;231(1):58-63. doi: 10.1016/j.pscychresns.2014.10.021. Epub 2014 Nov 4.


The GABRB1 gene is associated with thalamus volume and modulates the association between thalamus volume and intelligence.

Zhu B, Chen C, Xue G, Lei X, Li J, Moyzis RK, Dong Q, Lin C.

Neuroimage. 2014 Nov 15;102 Pt 2:756-63. doi: 10.1016/j.neuroimage.2014.08.048. Epub 2014 Sep 2.


Preadoption adversity, MAOA, and behavioral adjustment in internationally adopted Chinese girls.

Li J, Tan TX, Camras LA, Chen C, Moyzis RK.

Psychiatr Genet. 2014 Oct;24(5):211-7. doi: 10.1097/YPG.0000000000000049.


The SEMA5A gene is associated with hippocampal volume, and their interaction is associated with performance on Raven's Progressive Matrices.

Zhu B, Chen C, Xue G, Moyzis RK, Dong Q, Chen C, Li J, He Q, Lei X, Wang Y, Lin C.

Neuroimage. 2014 Mar;88:181-7. doi: 10.1016/j.neuroimage.2013.11.035. Epub 2013 Nov 27.


True but not false memories are associated with the HTR2A gene.

Zhu B, Chen C, Loftus EF, Moyzis RK, Dong Q, Lin C.

Neurobiol Learn Mem. 2013 Nov;106:204-9. doi: 10.1016/j.nlm.2013.09.004. Epub 2013 Sep 17.


Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene.

Luo XJ, Li M, Huang L, Steinberg S, Mattheisen M, Liang G, Donohoe G, Shi Y, Chen C, Yue W, Alkelai A, Lerer B, Li Z, Yi Q, Rietschel M, Cichon S, Collier DA, Tosato S, Suvisaari J, Rujescu D, Golimbet V, Silagadze T, Durmishi N, Milovancevic MP, Stefansson H, Schulze TG, Nöthen MM, Chen C, Lyne R, Morris DW, Gill M, Corvin A, Zhang D, Dong Q, Moyzis RK, Stefansson K, Sigurdsson E, Hu F; MooDS SCZ Consortium, Su B, Gan L.

Mol Psychiatry. 2014 Jul;19(7):774-83. doi: 10.1038/mp.2013.103. Epub 2013 Aug 20.


Fiber connectivity between the striatum and cortical and subcortical regions is associated with temperaments in Chinese males.

Lei X, Chen C, Xue F, He Q, Chen C, Liu Q, Moyzis RK, Xue G, Cao Z, Li J, Li H, Zhu B, Liu Y, Hsu AS, Li J, Dong Q.

Neuroimage. 2014 Apr 1;89:226-34. doi: 10.1016/j.neuroimage.2013.04.043. Epub 2013 Apr 22.


DRD4 genotype predicts longevity in mouse and human.

Grady DL, Thanos PK, Corrada MM, Barnett JC Jr, Ciobanu V, Shustarovich D, Napoli A, Moyzis AG, Grandy D, Rubinstein M, Wang GJ, Kawas CH, Chen C, Dong Q, Wang E, Volkow ND, Moyzis RK.

J Neurosci. 2013 Jan 2;33(1):286-91. doi: 10.1523/JNEUROSCI.3515-12.2013.


The DOPA decarboxylase (DDC) gene is associated with alerting attention.

Zhu B, Chen C, Moyzis RK, Dong Q, Chen C, He Q, Li J, Li J, Lei X, Lin C.

Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jun 3;43:140-5. doi: 10.1016/j.pnpbp.2012.12.020. Epub 2012 Dec 29.


The NTSR1 gene modulates the association between hippocampal structure and working memory performance.

Li J, Chen C, Lei X, Wang Y, Chen C, He Q, Moyzis RK, Xue G, Zhu B, Cao Z, Dong Q.

Neuroimage. 2013 Jul 15;75:79-86. doi: 10.1016/j.neuroimage.2012.09.077. Epub 2012 Oct 27.


COMT Val158Met polymorphism interacts with stressful life events and parental warmth to influence decision making.

He Q, Xue G, Chen C, Lu ZL, Chen C, Lei X, Liu Y, Li J, Zhu B, Moyzis RK, Dong Q, Bechara A.

Sci Rep. 2012;2:677. Epub 2012 Sep 20.


Sex determines which section of the SLC6A4 gene is linked to obsessive-compulsive symptoms in normal Chinese college students.

Lei X, Chen C, He Q, Chen C, Moyzis RK, Xue G, Chen X, Cao Z, Li J, Li H, Zhu B, Chun Hsu AS, Li S, Li J, Dong Q.

J Psychiatr Res. 2012 Sep;46(9):1153-60. doi: 10.1016/j.jpsychires.2012.05.002. Epub 2012 Jun 22.


Genetic variations in the dopamine system and facial expression recognition in healthy chinese college students.

Zhu B, Chen C, Moyzis RK, Dong Q, Chen C, He Q, Stern HS, Li H, Li J, Li J, Lessard J, Lin C.

Neuropsychobiology. 2012;65(2):83-9. doi: 10.1159/000329555. Epub 2012 Jan 5.


Gene-environment interaction in problematic substance use: interaction between DRD4 and insecure attachments.

Olsson CA, Moyzis RK, Williamson E, Ellis JA, Parkinson-Bates M, Patton GC, Dwyer T, Romaniuk H, Moore EE.

Addict Biol. 2013 Jul;18(4):717-26. doi: 10.1111/j.1369-1600.2011.00413.x. Epub 2011 Nov 29.


Neurotensin receptor 1 gene (NTSR1) polymorphism is associated with working memory.

Li J, Chen C, Chen C, He Q, Li H, Li J, Moyzis RK, Xue G, Dong Q.

PLoS One. 2011 Mar 4;6(3):e17365. doi: 10.1371/journal.pone.0017365.


Whole-genome genetic diversity in a sample of Australians with deep Aboriginal ancestry.

McEvoy BP, Lind JM, Wang ET, Moyzis RK, Visscher PM, van Holst Pellekaan SM, Wilton AN.

Am J Hum Genet. 2010 Aug 13;87(2):297-305. doi: 10.1016/j.ajhg.2010.07.008.


Serotonin transporter gene-linked polymorphic region (5-HTTLPR) influences decision making under ambiguity and risk in a large Chinese sample.

He Q, Xue G, Chen C, Lu Z, Dong Q, Lei X, Ding N, Li J, Li H, Chen C, Li J, Moyzis RK, Bechara A.

Neuropharmacology. 2010 Nov;59(6):518-26. doi: 10.1016/j.neuropharm.2010.07.008. Epub 2010 Jul 24.


Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm.

Saccone SF, Bierut LJ, Chesler EJ, Kalivas PW, Lerman C, Saccone NL, Uhl GR, Li CY, Philip VM, Edenberg HJ, Sherry ST, Feolo M, Moyzis RK, Rutter JL.

PLoS One. 2009;4(4):e5225. doi: 10.1371/journal.pone.0005225. Epub 2009 Apr 21.


Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

Langley K, Fowler TA, Grady DL, Moyzis RK, Holmans PA, van den Bree MB, Owen MJ, O'Donovan MC, Thapar A.

Eur Child Adolesc Psychiatry. 2009 Jan;18(1):26-32. doi: 10.1007/s00787-008-0698-4. Epub 2008 Jun 18.


Recent acceleration of human adaptive evolution.

Hawks J, Wang ET, Cochran GM, Harpending HC, Moyzis RK.

Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20753-8. Epub 2007 Dec 17.


Effects of source of DNA on genotyping success rates and allele percentages in the Preschoolers with Attention-Deficit/Hyperactivity Disorder Treatment Study (PATS).

Swanson JM, Moyzis RK, McGough JJ, McCracken JT, Riddle MA, Kollins SH, Greenhill LL, Abikoff HB, Wigal T, Wigal SB, Posner K, Skrobala AM, Davies M, Ghuman JK, Cunningham C, Vitiello B, Stehli A, Smalley SL, Grady D.

J Child Adolesc Psychopharmacol. 2007 Oct;17(5):635-46.


Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens".

Yu F, Hill RS, Schaffner SF, Sabeti PC, Wang ET, Mignault AA, Ferland RJ, Moyzis RK, Walsh CA, Reich D.

Science. 2007 Apr 20;316(5823):370.


Genetic evidence for ongoing balanced selection at human DNA repair genes ERCC8, FANCC, and RAD51C.

Wang ET, Moyzis RK.

Mutat Res. 2007 Mar 1;616(1-2):165-74. Epub 2007 Jan 25.


Global landscape of recent inferred Darwinian selection for Homo sapiens.

Wang ET, Kodama G, Baldi P, Moyzis RK.

Proc Natl Acad Sci U S A. 2006 Jan 3;103(1):135-40. Epub 2005 Dec 21.


Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific.

Grady DL, Harxhi A, Smith M, Flodman P, Spence MA, Swanson JM, Moyzis RK.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):33-5.


The sequence and analysis of duplication-rich human chromosome 16.

Martin J, Han C, Gordon LA, Terry A, Prabhakar S, She X, Xie G, Hellsten U, Chan YM, Altherr M, Couronne O, Aerts A, Bajorek E, Black S, Blumer H, Branscomb E, Brown NC, Bruno WJ, Buckingham JM, Callen DF, Campbell CS, Campbell ML, Campbell EW, Caoile C, Challacombe JF, Chasteen LA, Chertkov O, Chi HC, Christensen M, Clark LM, Cohn JD, Denys M, Detter JC, Dickson M, Dimitrijevic-Bussod M, Escobar J, Fawcett JJ, Flowers D, Fotopulos D, Glavina T, Gomez M, Gonzales E, Goodstein D, Goodwin LA, Grady DL, Grigoriev I, Groza M, Hammon N, Hawkins T, Haydu L, Hildebrand CE, Huang W, Israni S, Jett J, Jewett PB, Kadner K, Kimball H, Kobayashi A, Krawczyk MC, Leyba T, Longmire JL, Lopez F, Lou Y, Lowry S, Ludeman T, Manohar CF, Mark GA, McMurray KL, Meincke LJ, Morgan J, Moyzis RK, Mundt MO, Munk AC, Nandkeshwar RD, Pitluck S, Pollard M, Predki P, Parson-Quintana B, Ramirez L, Rash S, Retterer J, Ricke DO, Robinson DL, Rodriguez A, Salamov A, Saunders EH, Scott D, Shough T, Stallings RL, Stalvey M, Sutherland RD, Tapia R, Tesmer JG, Thayer N, Thompson LS, Tice H, Torney DC, Tran-Gyamfi M, Tsai M, Ulanovsky LE, Ustaszewska A, Vo N, White PS, Williams AL, Wills PL, Wu JR, Wu K, Yang J, Dejong P, Bruce D, Doggett NA, Deaven L, Schmutz J, Grimwood J, Richardson P, Rokhsar DS, Eichler EE, Gilna P, Lucas SM, Myers RM, Rubin EM, Pennacchio LA.

Nature. 2004 Dec 23;432(7020):988-94.


The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.

Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, Grady DL, Ryder OA, Spence MA, Swanson JM, Moyzis RK.

Am J Hum Genet. 2004 May;74(5):931-44. Epub 2004 Apr 9.


High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.

Grady DL, Chi HC, Ding YC, Smith M, Wang E, Schuck S, Flodman P, Spence MA, Swanson JM, Moyzis RK.

Mol Psychiatry. 2003 May;8(5):536-45.


Evidence of positive selection acting at the human dopamine receptor D4 gene locus.

Ding YC, Chi HC, Grady DL, Morishima A, Kidd JR, Kidd KK, Flodman P, Spence MA, Schuck S, Swanson JM, Zhang YP, Moyzis RK.

Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):309-14. Epub 2001 Dec 26.


A sequence-ready map of the human chromosome 1q telomere.

Xiang Z, Morse E, Hu XL, Flint J, Chi HC, Grady DL, Moyzis RK, Riethman HC.

Genomics. 2001 Feb 15;72(1):105-7.


Integration of telomere sequences with the draft human genome sequence.

Riethman HC, Xiang Z, Paul S, Morse E, Hu XL, Flint J, Chi HC, Grady DL, Moyzis RK.

Nature. 2001 Feb 15;409(6822):948-51.


An integrated physical map for the short arm of human chromosome 5.

Peterson ET, Sutherland R, Robinson DL, Chasteen L, Gersh M, Overhauser J, Deaven LL, Moyzis RK, Grady DL.

Genome Res. 1999 Dec;9(12):1250-67.


Reduced telomere DNA content is correlated with genomic instability and metastasis in invasive human breast carcinoma.

Griffith JK, Bryant JE, Fordyce CA, Gilliland FD, Joste NE, Moyzis RK.

Breast Cancer Res Treat. 1999 Mar;54(1):59-64.


Inhibition of human telomerase by a retrovirus expressing telomeric antisense RNA.

Bisoffi M, Chakerian AE, Fore ML, Bryant JE, Hernandez JP, Moyzis RK, Griffith JK.

Eur J Cancer. 1998 Jul;34(8):1242-9.


Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3.

Centola M, Chen X, Sood R, Deng Z, Aksentijevich I, Blake T, Ricke DO, Chen X, Wood G, Zaks N, Richards N, Krizman D, Mansfield E, Apostolou S, Liu J, Shafran N, Vedula A, Hamon M, Cercek A, Kahan T, Gumucio D, Callen DF, Richards RI, Moyzis RK, Doggett NA, Collins FS, Liu PP, Fischel-Ghodsian N, Kastner DL.

Genome Res. 1998 Nov;8(11):1172-91.


Construction of human chromosome 16- and 5-specific circular YAC/BAC libraries by in vivo recombination in yeast (TAR cloning).

Kouprina N, Campbell M, Graves J, Campbell E, Meincke L, Tesmer J, Grady DL, Doggett NA, Moyzis RK, Deaven LL, Larionov V.

Genomics. 1998 Oct 1;53(1):21-8.


Integrated physical and transcript map of 5q31.3-qter.

Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U.

Eur J Hum Genet. 1998 May-Jun;6(3):266-74.


Centromeric protein B null mice are viable with no apparent abnormalities.

Perez-Castro AV, Shamanski FL, Meneses JJ, Lovato TL, Vogel KG, Moyzis RK, Pedersen R.

Dev Biol. 1998 Sep 15;201(2):135-43.


Solution structures of the Huntington's disease DNA triplets, (CAG)n.

Mariappan SV, Silks LA 3rd, Chen X, Springer PA, Wu R, Moyzis RK, Bradbury EM, Garcia AE, Gupta G.

J Biomol Struct Dyn. 1998 Feb;15(4):723-44.


Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets.

Chen X, Mariappan SV, Moyzis RK, Bradbury EM, Gupta G.

J Biomol Struct Dyn. 1998 Feb;15(4):745-56.


Cystosine-rich strands of the insulin minisatellite adopt hairpins with intercalated cytosine+.cytosine pairs.

Catasti P, Chen X, Deaven LL, Moyzis RK, Bradbury EM, Gupta G.

J Mol Biol. 1997 Sep 26;272(3):369-82.


A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.

McPherson JD, Apostol B, Wagner-McPherson CB, Hakim S, Del Mastro RG, Aziz N, Baer E, Gonzales G, Krane MC, Markovich R, Masny P, Ortega M, Vu J, Vujicic M, Church DM, Segal A, Grady DL, Moyzis RK, Spence MA, Lovett M, Wasmuth JJ.

Genome Res. 1997 Sep;7(9):897-909.


Measurement of telomeric DNA content in human tissues.

Bryant JE, Hutchings KG, Moyzis RK, Griffith JK.

Biotechniques. 1997 Sep;23(3):476-8, 480, 482, passim.


Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.

Mitchison HM, Munroe PB, O'Rawe AM, Taschner PE, de Vos N, Kremmidiotis G, Lensink I, Munk AC, D'Arigo KL, Anderson JW, Lerner TJ, Moyzis RK, Callen DF, Breuning MH, Doggett NA, Gardiner RM, Mole SE.

Genomics. 1997 Mar 1;40(2):346-50.


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