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Items: 1 to 20 of 84

1.

Allelic diversity in human developmental neurogenetics: insights into biology and disease.

Walsh CA, Engle EC.

Neuron. 2010 Oct 21;68(2):245-53. doi: 10.1016/j.neuron.2010.09.042. Review.

2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
3.

The developmental transcriptome of the human brain: implications for neurodevelopmental disorders.

Tebbenkamp AT, Willsey AJ, State MW, Sestan N.

Curr Opin Neurol. 2014 Apr;27(2):149-56. doi: 10.1097/WCO.0000000000000069. Review.

4.

Inherited neuronal ion channelopathies: new windows on complex neurological diseases.

Catterall WA, Dib-Hajj S, Meisler MH, Pietrobon D.

J Neurosci. 2008 Nov 12;28(46):11768-77. doi: 10.1523/JNEUROSCI.3901-08.2008. Review.

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7.

Genomic and epigenomic insights into nutrition and brain disorders.

Dauncey MJ.

Nutrients. 2013 Mar 15;5(3):887-914. doi: 10.3390/nu5030887.

8.

Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders.

Duong L, Klitten LL, Møller RS, Ingason A, Jakobsen KD, Skjødt C, Didriksen M, Hjalgrim H, Werge T, Tommerup N.

Am J Med Genet B Neuropsychiatr Genet. 2012 Apr;159B(3):354-8. doi: 10.1002/ajmg.b.32036. Epub 2012 Feb 15.

PMID:
22337556
9.

DISC1: a key lead in studying cortical development and associated brain disorders.

Narayan S, Nakajima K, Sawa A.

Neuroscientist. 2013 Oct;19(5):451-64. doi: 10.1177/1073858412470168. Epub 2013 Jan 8. Review.

10.

Progress in the genetics of polygenic brain disorders: significant new challenges for neurobiology.

McCarroll SA, Hyman SE.

Neuron. 2013 Oct 30;80(3):578-87. doi: 10.1016/j.neuron.2013.10.046. Review.

11.

Neurocognitive phenotypes and genetic dissection of disorders of brain and behavior.

Congdon E, Poldrack RA, Freimer NB.

Neuron. 2010 Oct 21;68(2):218-30. doi: 10.1016/j.neuron.2010.10.007. Review.

12.

Somatic mutation, genomic variation, and neurological disease.

Poduri A, Evrony GD, Cai X, Walsh CA.

Science. 2013 Jul 5;341(6141):1237758. doi: 10.1126/science.1237758. Review.

13.

Analysis of microarray studies performed in the neurosciences.

Aarnio V, Paananen J, Wong G.

J Mol Neurosci. 2005;27(3):261-8.

PMID:
16280595
14.

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.

Moreno-De-Luca A, Myers SM, Challman TD, Moreno-De-Luca D, Evans DW, Ledbetter DH.

Lancet Neurol. 2013 Apr;12(4):406-14. doi: 10.1016/S1474-4422(13)70011-5. Epub 2013 Mar 18. Review. Erratum in: Lancet Neurol. 2013 May;12(5):423.

15.

A strategy to identify de novo mutations in common disorders such as autism and schizophrenia.

Julie G, Hamdan FF, Rouleau GA.

J Vis Exp. 2011 Jun 15;(52). pii: 2534. doi: 10.3791/2534.

16.

Neurogenetics: advancing the "next-generation" of brain research.

Zoghbi HY, Warren ST.

Neuron. 2010 Oct 21;68(2):165-73. doi: 10.1016/j.neuron.2010.10.015.

17.

Somatic cell genomics of brain disorders: a new opportunity to clarify genetic-environmental interactions.

Iourov IY, Vorsanova SG, Yurov YB.

Cytogenet Genome Res. 2013;139(3):181-8. doi: 10.1159/000347053. Epub 2013 Feb 20.

PMID:
23428498
18.

On the allelic spectrum of human disease.

Reich DE, Lander ES.

Trends Genet. 2001 Sep;17(9):502-10.

PMID:
11525833
19.

The sudden infant death syndrome gene: does it exist?

Opdal SH, Rognum TO.

Pediatrics. 2004 Oct;114(4):e506-12.

PMID:
15466077
20.

TCF4, schizophrenia, and Pitt-Hopkins Syndrome.

Blake DJ, Forrest M, Chapman RM, Tinsley CL, O'Donovan MC, Owen MJ.

Schizophr Bull. 2010 May;36(3):443-7. doi: 10.1093/schbul/sbq035. Epub 2010 Apr 26.

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