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A review of brain circuitries involved in stuttering.

Craig-McQuaide A, Akram H, Zrinzo L, Tripoliti E.

Front Hum Neurosci. 2014 Nov 17;8:884. doi: 10.3389/fnhum.2014.00884. eCollection 2014. Review.


A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.

Han TU, Park J, Domingues CF, Moretti-Ferreira D, Paris E, Sainz E, Gutierrez J, Drayna D.

Neurobiol Dis. 2014 Sep;69:23-31. doi: 10.1016/j.nbd.2014.04.019. Epub 2014 May 5.


Epidemiology of stuttering: 21st century advances.

Yairi E, Ambrose N.

J Fluency Disord. 2013 Jun;38(2):66-87. doi: 10.1016/j.jfludis.2012.11.002. Epub 2012 Nov 27. Review.


Neurogenomics of speech and language disorders: the road ahead.

Deriziotis P, Fisher SE.

Genome Biol. 2013 Apr 18;14(4):204. doi: 10.1186/gb-2013-14-4-204. Review.


Using brain imaging to unravel the mysteries of stuttering.

Chang SE.

Cerebrum. 2011 Jul;2011:12. Epub 2011 Aug 23.


Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance.

Raza MH, Gertz EM, Mundorff J, Lukong J, Kuster J, Schäffer AA, Drayna D.

Hum Genet. 2013 Apr;132(4):385-96. doi: 10.1007/s00439-012-1252-5. Epub 2012 Dec 13.


Stuttering: Genetic updates and a case report.

Nouri N, Nouri N, Abdali H, Shafie M, Karimi H.

Adv Biomed Res. 2012;1:14. doi: 10.4103/2277-9175.96070. Epub 2012 May 11.


A role for inherited metabolic deficits in persistent developmental stuttering.

Kang C, Drayna D.

Mol Genet Metab. 2012 Nov;107(3):276-80. doi: 10.1016/j.ymgme.2012.07.020. Epub 2012 Jul 28. Review.


Linking neurogenetics and individual differences in language learning: the dopamine hypothesis.

Wong PC, Morgan-Short K, Ettlinger M, Zheng J.

Cortex. 2012 Oct;48(9):1091-102. doi: 10.1016/j.cortex.2012.03.017. Epub 2012 Mar 30. Review.


Genetic bases of stuttering: the state of the art, 2011.

Kraft SJ, Yairi E.

Folia Phoniatr Logop. 2012;64(1):34-47. doi: 10.1159/000331073. Review.


Genetic approaches to understanding the causes of stuttering.

Drayna D, Kang C.

J Neurodev Disord. 2011 Dec;3(4):374-80. doi: 10.1007/s11689-011-9090-7. Epub 2011 Aug 18.


Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case.

Petrin AL, Giacheti CM, Maximino LP, Abramides DV, Zanchetta S, Rossi NF, Richieri-Costa A, Murray JC.

Am J Med Genet A. 2010 Dec;152A(12):3164-72. doi: 10.1002/ajmg.a.33749.


Speech-induced suppression of evoked auditory fields in children who stutter.

Beal DS, Quraan MA, Cheyne DO, Taylor MJ, Gracco VL, De Nil LF.

Neuroimage. 2011 Feb 14;54(4):2994-3003. doi: 10.1016/j.neuroimage.2010.11.026. Epub 2010 Nov 21.


Genetic advances in the study of speech and language disorders.

Newbury DF, Monaco AP.

Neuron. 2010 Oct 21;68(2):309-20. doi: 10.1016/j.neuron.2010.10.001. Review.


Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation.

Fedyna A, Drayna D, Kang C.

J Hum Genet. 2011 Jan;56(1):80-2. doi: 10.1038/jhg.2010.125. Epub 2010 Oct 14.


Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.

Raza MH, Riazuddin S, Drayna D.

Hum Genet. 2010 Oct;128(4):461-3. doi: 10.1007/s00439-010-0871-y. Epub 2010 Aug 13.


Mutations in the lysosomal enzyme-targeting pathway and persistent stuttering.

Kang C, Riazuddin S, Mundorff J, Krasnewich D, Friedman P, Mullikin JC, Drayna D.

N Engl J Med. 2010 Feb 25;362(8):677-85. doi: 10.1056/NEJMoa0902630. Epub 2010 Feb 10.


Speaking genes or genes for speaking? Deciphering the genetics of speech and language.

Grigorenko EL.

J Child Psychol Psychiatry. 2009 Jan;50(1-2):116-25. doi: 10.1111/j.1469-7610.2008.02006.x. Review.


Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan.

Miller EN, Fadl M, Mohamed HS, Elzein A, Jamieson SE, Cordell HJ, Peacock CS, Fakiola M, Raju M, Khalil EA, Elhassan A, Musa AM, Ibrahim ME, Blackwell JM.

PLoS Genet. 2007 May 11;3(5):e71. Epub 2007 Mar 19.


Genetic studies of stuttering in a founder population.

Wittke-Thompson JK, Ambrose N, Yairi E, Roe C, Cook EH, Ober C, Cox NJ.

J Fluency Disord. 2007;32(1):33-50. Epub 2006 Dec 30.

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