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Items: 1 to 20 of 22

1.

Decoding the molecular evolution of human cognition using comparative genomics.

Usui N, Co M, Konopka G.

Brain Behav Evol. 2014;84(2):103-16. doi: 10.1159/000365182. Epub 2014 Sep 20.

2.

Heterogeneity within Autism Spectrum Disorders: What have We Learned from Neuroimaging Studies?

Lenroot RK, Yeung PK.

Front Hum Neurosci. 2013 Oct 30;7:733. doi: 10.3389/fnhum.2013.00733. Review.

3.

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.

4.

The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders.

Bacon C, Rappold GA.

Hum Genet. 2012 Nov;131(11):1687-98. doi: 10.1007/s00439-012-1193-z. Epub 2012 Jun 27. Review.

5.

New frontiers in animal research of psychiatric illness.

Kaffman A, Krystal JH.

Methods Mol Biol. 2012;829:3-30. doi: 10.1007/978-1-61779-458-2_1. Review. Erratum in: Methods Mol Biol. 2012;829:E1. Krystal, Uohn J [corrected to Krystal, John H].

6.

Genetics in non-genetic model systems.

Lois C, Groves JO.

Curr Opin Neurobiol. 2012 Feb;22(1):79-85. doi: 10.1016/j.conb.2011.11.002. Epub 2011 Nov 24. Review.

7.

An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning.

French CA, Jin X, Campbell TG, Gerfen E, Groszer M, Fisher SE, Costa RM.

Mol Psychiatry. 2012 Nov;17(11):1077-85. doi: 10.1038/mp.2011.105. Epub 2011 Aug 30.

9.

Human brain evolution: harnessing the genomics (r)evolution to link genes, cognition, and behavior.

Konopka G, Geschwind DH.

Neuron. 2010 Oct 21;68(2):231-44. doi: 10.1016/j.neuron.2010.10.012.

10.

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.

Hamdan FF, Daoud H, Rochefort D, Piton A, Gauthier J, Langlois M, Foomani G, Dobrzeniecka S, Krebs MO, Joober R, Lafrenière RG, Lacaille JC, Mottron L, Drapeau P, Beauchamp MH, Phillips MS, Fombonne E, Rouleau GA, Michaud JL.

Am J Hum Genet. 2010 Nov 12;87(5):671-8. doi: 10.1016/j.ajhg.2010.09.017. Epub 2010 Oct 14.

11.

Cerebellum, language, and cognition in autism and specific language impairment.

Hodge SM, Makris N, Kennedy DN, Caviness VS Jr, Howard J, McGrath L, Steele S, Frazier JA, Tager-Flusberg H, Harris GJ.

J Autism Dev Disord. 2010 Mar;40(3):300-16. doi: 10.1007/s10803-009-0872-7.

12.

At the height of fashion: what genetics can teach us about neurodevelopmental disabilities.

Grigorenko EL.

Curr Opin Neurol. 2009 Apr;22(2):126-30. doi: 10.1097/WCO.0b013e3283292414.

13.

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.

Vernes SC, MacDermot KD, Monaco AP, Fisher SE.

Eur J Hum Genet. 2009 Oct;17(10):1354-8. doi: 10.1038/ejhg.2009.43. Epub 2009 Apr 8.

14.

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.

15.

A functional genetic link between distinct developmental language disorders.

Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE.

N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5.

16.

Auditory hallucinations in schizophrenia: the role of cognitive, brain structural and genetic disturbances in the left temporal lobe.

Hugdahl K, Løberg EM, Specht K, Steen VM, van Wageningen H, Jørgensen HA.

Front Hum Neurosci. 2008 Mar 28;1:6. doi: 10.3389/neuro.09.006.2007. eCollection 2007.

17.

Association of common variants in the Joubert syndrome gene (AHI1) with autism.

Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA, Geschwind DH.

Hum Mol Genet. 2008 Dec 15;17(24):3887-96. doi: 10.1093/hmg/ddn291. Epub 2008 Sep 9.

18.

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.

Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE.

Am J Hum Genet. 2007 Dec;81(6):1232-50. Epub 2007 Oct 31.

19.
20.

Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language.

White SA, Fisher SE, Geschwind DH, Scharff C, Holy TE.

J Neurosci. 2006 Oct 11;26(41):10376-9. Review.

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