Flax JF - Search Results

1

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. Bartlett CW, et al. Among authors: flax jf. Am J Psychiatry. 2014 Jan;171(1):72-81. doi: 10.1176/appi.ajp.2013.12081103. Am J Psychiatry. 2014. PMID: 24170272 Free PMC article.

2

Familial aggregation in specific language impairment.

Tallal P, Hirsch LS, Realpe-Bonilla T, Miller S, Brzustowicz LM, Bartlett C, Flax JF. Tallal P, et al. Among authors: flax jf. J Speech Lang Hear Res. 2001 Oct;44(5):1172-82. doi: 10.1044/1092-4388(2001/091). J Speech Lang Hear Res. 2001. PMID: 11708534

3

A major susceptibility locus for specific language impairment is located on 13q21.

Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM. Bartlett CW, et al. Among authors: flax jf. Am J Hum Genet. 2002 Jul;71(1):45-55. doi: 10.1086/341095. Epub 2002 Jun 4. Am J Hum Genet. 2002. PMID: 12048648 Free PMC article.

4

Specific language impairment in families: evidence for co-occurrence with reading impairments.

Flax JF, Realpe-Bonilla T, Hirsch LS, Brzustowicz LM, Bartlett CW, Tallal P. Flax JF, et al. J Speech Lang Hear Res. 2003 Jun;46(3):530-43. doi: 10.1044/1092-4388(2003/043). J Speech Lang Hear Res. 2003. PMID: 14696984

5

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.

Bartlett CW, Flax JF, Logue MW, Smith BJ, Vieland VJ, Tallal P, Brzustowicz LM. Bartlett CW, et al. Among authors: flax jf. Hum Hered. 2004;57(1):10-20. doi: 10.1159/000077385. Hum Hered. 2004. PMID: 15133308 Free PMC article.

6

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. Simmons TR, et al. Among authors: flax jf. Hum Hered. 2010;70(4):232-44. doi: 10.1159/000320367. Epub 2010 Oct 14. Hum Hered. 2010. PMID: 20948219 Free PMC article.

7

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.

Flax JF, Hare A, Azaro MA, Vieland VJ, Brzustowicz LM. Flax JF, et al. J Neurodev Disord. 2010 Dec;2(4):210-223. doi: 10.1007/s11689-010-9063-2. Epub 2010 Oct 12. J Neurodev Disord. 2010. PMID: 21125004 Free PMC article.

8

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. Logan J, et al. Behav Genet. 2011 Sep;41(5):651-9. doi: 10.1007/s10519-010-9435-0. Epub 2010 Dec 31. Behav Genet. 2011. PMID: 21193955 Free PMC article.

9

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. Bartlett CW, et al. Among authors: flax jf. Biol Psychiatry. 2012 Oct 15;72(8):692-9. doi: 10.1016/j.biopsych.2012.05.019. Epub 2012 Jun 15. Biol Psychiatry. 2012. PMID: 22704665 Free PMC article.

10

Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds.

Bruni M, Flax JF, Buyske S, Shindhelm AD, Witton C, Brzustowicz LM, Bartlett CW. Bruni M, et al. Among authors: flax jf. Behav Genet. 2017 Mar;47(2):193-201. doi: 10.1007/s10519-016-9821-3. Epub 2016 Nov 9. Behav Genet. 2017. PMID: 27826669 Free PMC article.

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