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Results: 1 to 20 of 87

1.

White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: Associations with medication, neuropsychological function, and prodromal symptoms of psychosis.

Kates WR, Olszewski AK, Gnirke MH, Kikinis Z, Nelson J, Antshel KM, Fremont W, Radoeva PD, Middleton FA, Shenton ME, Coman IL.

Schizophr Res. 2014 Jul 24. pii: S0920-9964(14)00367-3. doi: 10.1016/j.schres.2014.07.010. [Epub ahead of print]

PMID:
25066496
[PubMed - as supplied by publisher]
2.

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.

Melhem NM, Lu C, Dresbold C, Middleton FA, Klei L, Wood S, Faraone SV, Vinogradov S, Tiobech J, Yano V, Roeder K, Byerley W, Myles-Worsley M, Devlin B.

Am J Med Genet B Neuropsychiatr Genet. 2014 Sep;165B(6):521-30. doi: 10.1002/ajmg.b.32255. Epub 2014 Jul 1.

PMID:
24980794
[PubMed - in process]
3.

Autism-related behavioral phenotypes in an inbred rat substrain.

Zhang-James Y, Yang L, Middleton FA, Yang L, Patak J, Faraone SV.

Behav Brain Res. 2014 Aug 1;269:103-14. doi: 10.1016/j.bbr.2014.04.035. Epub 2014 Apr 26.

PMID:
24780868
[PubMed - in process]
4.

White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis.

Perlstein MD, Chohan MR, Coman IL, Antshel KM, Fremont WP, Gnirke MH, Kikinis Z, Middleton FA, Radoeva PD, Shenton ME, Kates WR.

Schizophr Res. 2014 Jan;152(1):117-23. doi: 10.1016/j.schres.2013.11.015. Epub 2013 Dec 8.

PMID:
24321711
[PubMed - indexed for MEDLINE]
5.

Genetic architecture of Wistar-Kyoto rat and spontaneously hypertensive rat substrains from different sources.

Zhang-James Y, Middleton FA, Faraone SV.

Physiol Genomics. 2013 Jul 2;45(13):528-38. doi: 10.1152/physiolgenomics.00002.2013. Epub 2013 May 14.

PMID:
23673728
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family.

Myles-Worsley M, Tiobech J, Browning SR, Korn J, Goodman S, Gentile K, Melhem N, Byerley W, Faraone SV, Middleton FA.

Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):87-95. doi: 10.1002/ajmg.b.32125. Epub 2013 Jan 22.

PMID:
23341099
[PubMed - indexed for MEDLINE]
7.

Functional and biochemical characterization of soleus muscle in Down syndrome mice: insight into the muscle dysfunction seen in the human condition.

Cowley PM, Keslacy S, Middleton FA, DeRuisseau LR, Fernhall B, Kanaley JA, DeRuisseau KC.

Am J Physiol Regul Integr Comp Physiol. 2012 Dec 15;303(12):R1251-60. doi: 10.1152/ajpregu.00312.2012. Epub 2012 Oct 31.

PMID:
23115123
[PubMed - indexed for MEDLINE]
8.

Evaluation of cell proliferation, apoptosis, and DNA-repair genes as potential biomarkers for ethanol-induced CNS alterations.

Hicks SD, Lewis L, Ritchie J, Burke P, Abdul-Malak Y, Adackapara N, Canfield K, Shwarts E, Gentile K, Meszaros ZS, Middleton FA.

BMC Neurosci. 2012 Oct 25;13:128. doi: 10.1186/1471-2202-13-128.

PMID:
23095216
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Transcriptomic analysis of postmortem brain identifies dysregulated splicing events in novel candidate genes for schizophrenia.

Cohen OS, Mccoy SY, Middleton FA, Bialosuknia S, Zhang-James Y, Liu L, Tsuang MT, Faraone SV, Glatt SJ.

Schizophr Res. 2012 Dec;142(1-3):188-99. doi: 10.1016/j.schres.2012.09.015. Epub 2012 Oct 9.

PMID:
23062752
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Hierarchical clustering of gene expression patterns in the Eomes + lineage of excitatory neurons during early neocortical development.

Cameron DA, Middleton FA, Chenn A, Olson EC.

BMC Neurosci. 2012 Aug 1;13:90. doi: 10.1186/1471-2202-13-90.

PMID:
22852769
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Differential expression of SLC9A9 and interacting molecules in the hippocampus of rat models for attention deficit/hyperactivity disorder.

Zhang-James Y, Middleton FA, Sagvolden T, Faraone SV.

Dev Neurosci. 2012;34(2-3):218-27. Epub 2012 Jul 6.

PMID:
22777493
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Molecular substrates of social avoidance seen following prenatal ethanol exposure and its reversal by social enrichment.

Middleton FA, Varlinskaya EI, Mooney SM.

Dev Neurosci. 2012;34(2-3):115-28. Epub 2012 May 8.

PMID:
22572756
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Genetic overlap of schizophrenia and bipolar disorder in a high-density linkage survey in the Portuguese Island population.

Fanous AH, Middleton FA, Gentile K, Amdur RL, Maher BS, Zhao Z, Sun J, Medeiros H, Carvalho C, Ferreira SR, Macedo A, Knowles JA, Azevedo MH, Pato MT, Pato CN.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jun;159B(4):383-91. doi: 10.1002/ajmg.b.32041. Epub 2012 Mar 27.

PMID:
22461138
[PubMed - indexed for MEDLINE]
14.

Increased promoter methylation of the immune regulatory gene SHP-1 in leukocytes of multiple sclerosis subjects.

Kumagai C, Kalman B, Middleton FA, Vyshkina T, Massa PT.

J Neuroimmunol. 2012 May 15;246(1-2):51-7. doi: 10.1016/j.jneuroim.2012.03.003. Epub 2012 Mar 27.

PMID:
22458980
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.

Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, Frackelton EC, Chiavacci RM, Sakurai T, Rabin C, Middleton FA, Thomas KA, Garris M, Mentch F, Freitag CM, Steinhausen HC, Todorov AA, Reif A, Rothenberger A, Franke B, Mick EO, Roeyers H, Buitelaar J, Lesch KP, Banaschewski T, Ebstein RP, Mulas F, Oades RD, Sergeant J, Sonuga-Barke E, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Meyer J, Pálmason H, Seitz C, Loo SK, Smalley SL, Biederman J, Kent L, Asherson P, Anney RJ, Gaynor JW, Shaw P, Devoto M, White PS, Grant SF, Buxbaum JD, Rapoport JL, Williams NM, Nelson SF, Faraone SV, Hakonarson H.

Nat Genet. 2011 Dec 4;44(1):78-84. doi: 10.1038/ng.1013.

PMID:
22138692
[PubMed - indexed for MEDLINE]
16.

Transcriptome-wide gene expression in a rat model of attention deficit hyperactivity disorder symptoms: rats developmentally exposed to polychlorinated biphenyls.

Sazonova NA, DasBanerjee T, Middleton FA, Gowtham S, Schuckers S, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):898-912. doi: 10.1002/ajmg.b.31230. Epub 2011 Sep 14.

PMID:
21919189
[PubMed - indexed for MEDLINE]
17.

SLC9A9 mutations, gene expression, and protein-protein interactions in rat models of attention-deficit/hyperactivity disorder.

Zhang-James Y, DasBanerjee T, Sagvolden T, Middleton FA, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):835-43. doi: 10.1002/ajmg.b.31229. Epub 2011 Aug 19.

PMID:
21858920
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Accuracy of self-reported medical problems in patients with alcohol dependence and co-occurring schizophrenia or schizoaffective disorder.

Meszaros ZS, Dimmock JA, Ploutz-Snyder R, Chauhan SV, Abdul-Malak Y, Middleton FA, Batki SL.

Schizophr Res. 2011 Nov;132(2-3):190-3. doi: 10.1016/j.schres.2011.07.033. Epub 2011 Aug 17.

PMID:
21852074
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Familial transmission of schizophrenia in Palau: A 20-year genetic epidemiological study in three generations.

Myles-Worsley M, Tiobech J, Blailes F, Middleton FA, Vinogradov S, Byerley W, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2011 Apr;156B(3):247-54. doi: 10.1002/ajmg.b.31171. Epub 2011 Feb 3.

PMID:
21294248
[PubMed - indexed for MEDLINE]
20.

Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder.

Mick E, McGough JJ, Middleton FA, Neale B, Faraone SV.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):466-72. doi: 10.1016/j.pnpbp.2010.11.037. Epub 2010 Dec 2.

PMID:
21130132
[PubMed - indexed for MEDLINE]

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