Brzustowicz LM - Search Results

1

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: brzustowicz lm. 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.

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: brzustowicz lm. 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: brzustowicz lm. 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. Among authors: brzustowicz lm. 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: brzustowicz lm. Hum Hered. 2004;57(1):10-20. doi: 10.1159/000077385. Hum Hered. 2004. PMID: 15133308 Free PMC article.

6

The search for autism disease genes.

Wassink TH, Brzustowicz LM, Bartlett CW, Szatmari P. Wassink TH, et al. Among authors: brzustowicz lm. Ment Retard Dev Disabil Res Rev. 2004;10(4):272-83. doi: 10.1002/mrdd.20041. Ment Retard Dev Disabil Res Rev. 2004. PMID: 15666342 Review.

7

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.

Bartlett CW, Gharani N, Millonig JH, Brzustowicz LM. Bartlett CW, et al. Among authors: brzustowicz lm. Int J Dev Neurosci. 2005 Apr-May;23(2-3):221-34. doi: 10.1016/j.ijdevneu.2004.10.004. Int J Dev Neurosci. 2005. PMID: 15749247 Review.

8

Increased expression in dorsolateral prefrontal cortex of CAPON in schizophrenia and bipolar disorder.

Xu B, Wratten N, Charych EI, Buyske S, Firestein BL, Brzustowicz LM. Xu B, et al. Among authors: brzustowicz lm. PLoS Med. 2005 Oct;2(10):e263. doi: 10.1371/journal.pmed.0020263. Epub 2005 Sep 13. PLoS Med. 2005. PMID: 16146415 Free PMC article.

9

Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM. Wratten NS, et al. Among authors: brzustowicz lm. Am J Psychiatry. 2009 Apr;166(4):434-41. doi: 10.1176/appi.ajp.2008.08081266. Epub 2009 Mar 2. Am J Psychiatry. 2009. PMID: 19255043 Free PMC article.

10

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: brzustowicz lm. Hum Hered. 2010;70(4):232-44. doi: 10.1159/000320367. Epub 2010 Oct 14. Hum Hered. 2010. PMID: 20948219 Free PMC article.

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