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Results: 1 to 20 of 26

1.

Addressing the unmet need for visualizing conditional random fields in biological data.

Ray WC, Wolock SL, Callahan NW, Dong M, Li QQ, Liang C, Magliery TJ, Bartlett CW.

BMC Bioinformatics. 2014 Jul 10;15:202. doi: 10.1186/1471-2105-15-202.

PMID:
25000815
[PubMed - in process]
2.

Who is afraid of math? Two sources of genetic variance for mathematical anxiety.

Wang Z, Hart SA, Kovas Y, Lukowski S, Soden B, Thompson LA, Plomin R, McLoughlin G, Bartlett CW, Lyons IM, Petrill SA.

J Child Psychol Psychiatry. 2014 Mar 10. doi: 10.1111/jcpp.12224. [Epub ahead of print]

PMID:
24611799
[PubMed - as supplied by publisher]
3.

A genome scan for loci shared by autism spectrum disorder and language impairment.

Bartlett CW, Hou L, Flax JF, Hare A, Cheong SY, Fermano Z, Zimmerman-Bier B, Cartwright C, Azaro MA, Buyske S, Brzustowicz LM.

Am J Psychiatry. 2014 Jan 1;171(1):72-81. doi: 10.1176/appi.ajp.2013.12081103.

PMID:
24170272
[PubMed - indexed for MEDLINE]
4.

Gene-environment interplay in child psychology and psychiatry--challenges and ways forward.

Petrill SA, Bartlett CW, Blair C.

J Child Psychol Psychiatry. 2013 Oct;54(10):1029. doi: 10.1111/jcpp.12133.

PMID:
24007414
[PubMed - indexed for MEDLINE]
5.

Gene × smoking interactions on human brain gene expression: finding common mechanisms in adolescents and adults.

Wolock SL, Yates A, Petrill SA, Bohland JW, Blair C, Li N, Machiraju R, Huang K, Bartlett CW.

J Child Psychol Psychiatry. 2013 Oct;54(10):1109-19. doi: 10.1111/jcpp.12119. Epub 2013 Aug 2.

PMID:
23909413
[PubMed - indexed for MEDLINE]
6.

Evaluation of a bayesian model integration-based method for censored data.

Hou L, Wang K, Bartlett CW.

Hum Hered. 2012;74(1):1-11. doi: 10.1159/000342707. Epub 2012 Sep 26.

PMID:
23018141
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Gene × gene interaction in shared etiology of autism and specific language impairment.

Bartlett CW, Flax JF, Fermano Z, Hare A, Hou L, Petrill SA, Buyske S, Brzustowicz LM.

Biol Psychiatry. 2012 Oct 15;72(8):692-9. doi: 10.1016/j.biopsych.2012.05.019. Epub 2012 Jun 15.

PMID:
22704665
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

An eQTL biological data visualization challenge and approaches from the visualization community.

Bartlett CW, Cheong SY, Hou L, Paquette J, Lum PY, Jäger G, Battke F, Vehlow C, Heinrich J, Nieselt K, Sakai R, Aerts J, Ray WC.

BMC Bioinformatics. 2012;13 Suppl 8:S8. doi: 10.1186/1471-2105-13-S8-S8. Epub 2012 May 18.

PMID:
22607587
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Defining the genetic architecture of human developmental language impairment.

Li N, Bartlett CW.

Life Sci. 2012 Apr 9;90(13-14):469-75. doi: 10.1016/j.lfs.2012.01.016. Epub 2012 Feb 17. Review.

PMID:
22365959
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Validation of a cost-efficient multi-purpose SNP panel for disease based research.

Hou L, Phillips C, Azaro M, Brzustowicz LM, Bartlett CW.

PLoS One. 2011;6(5):e19699. doi: 10.1371/journal.pone.0019699. Epub 2011 May 17.

PMID:
21611176
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment.

Logan J, Petrill SA, Flax J, Justice LM, Hou L, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW.

Behav Genet. 2011 Sep;41(5):651-9. doi: 10.1007/s10519-010-9435-0. Epub 2010 Dec 31.

PMID:
21193955
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.

Simmons TR, Flax JF, Azaro MA, Hayter JE, Justice LM, Petrill SA, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW.

Hum Hered. 2010;70(4):232-44. doi: 10.1159/000320367. Epub 2010 Oct 14.

PMID:
20948219
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Exploiting gene x gene interaction in linkage analysis.

Huang Y, Bartlett CW, Segre AM, O'Connell JR, Mangin L, Vieland VJ.

BMC Proc. 2007;1 Suppl 1:S64. Epub 2007 Dec 18.

PMID:
18466565
[PubMed]
Free PMC Article
14.

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci.

Cordell HJ, de Andrade M, Babron MC, Bartlett CW, Beyene J, Bickeböller H, Culverhouse R, Cupples LA, Daw EW, Dupuis J, Falk CT, Ghosh S, Goddard KA, Goode EL, Hauser ER, Martin LJ, Martinez M, North KE, Saccone NL, Schmidt S, Tapper W, Thomas D, Tritchler D, Vieland VJ, Wijsman EM, Wilcox MA, Witte JS, Yang Q, Ziegler A, Almasy L, Maccluer JW.

BMC Proc. 2007;1 Suppl 1:S1. Epub 2007 Dec 18. No abstract available.

PMID:
18466438
[PubMed]
Free PMC Article
15.

Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.

Wassink TH, Vieland VJ, Sheffield VC, Bartlett CW, Goedken R, Childress D, Piven J.

Psychiatr Genet. 2008 Apr;18(2):85-91. doi: 10.1097/YPG.0b013e3282f9b48e.

PMID:
18349700
[PubMed - indexed for MEDLINE]
16.

Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky.

Bartlett CW, Vieland VJ, Bartlett J, Bell JT, Bhattacharjee S, Clerget-Darpoux F, Bush WS, Edwards TL, Gao G, Halder I, Huang Y, Kotti S, Larkin EK, Li H, Motsinger AA, Mukhopadhyay N, Namkung J, Park T, Ritchie MD, Stein CM, Zhou JY.

Genet Epidemiol. 2007;31 Suppl 1:S61-7.

PMID:
18046759
[PubMed - indexed for MEDLINE]
17.

Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage.

Bartlett CW, Vieland VJ.

Genet Epidemiol. 2007 Feb;31(2):91-102.

PMID:
17123305
[PubMed - indexed for MEDLINE]
18.

Calculation of multipoint likelihoods using flanking marker data: a simulation study.

George AW, Mangin LA, Bartlett CW, Logue MW, Segre AM, Vieland VJ.

BMC Genet. 2005 Dec 30;6 Suppl 1:S44.

PMID:
16451655
[PubMed - indexed for MEDLINE]
Free PMC Article
19.
20.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Jenkins L, Frantz R, Bartlett CW, Goedken R, Childress D, Spence MA, Smith M, Sheffield VC.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):36-44.

PMID:
15892143
[PubMed - indexed for MEDLINE]

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