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Items: 15

1.

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.

Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, Gilbert DL, Heiman GA, Tischfield JA, Hoekstra PJ, Devlin B, Hakonarson H, Mane SM, Günel M, State MW.

Biol Psychiatry. 2012 Mar 1;71(5):392-402. doi: 10.1016/j.biopsych.2011.09.034. Epub 2011 Dec 14.

2.

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

Guilmatre A, Dubourg C, Mosca AL, Legallic S, Goldenberg A, Drouin-Garraud V, Layet V, Rosier A, Briault S, Bonnet-Brilhault F, Laumonnier F, Odent S, Le Vacon G, Joly-Helas G, David V, Bendavid C, Pinoit JM, Henry C, Impallomeni C, Germano E, Tortorella G, Di Rosa G, Barthelemy C, Andres C, Faivre L, Frébourg T, Saugier Veber P, Campion D.

Arch Gen Psychiatry. 2009 Sep;66(9):947-56. doi: 10.1001/archgenpsychiatry.2009.80. Review.

3.

Genomic copy number variation in disorders of cognitive development.

Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2010 Nov;49(11):1091-104. doi: 10.1016/j.jaac.2010.08.009. Review.

4.

Detection and characterization of copy number variation in autism spectrum disorder.

Marshall CR, Scherer SW.

Methods Mol Biol. 2012;838:115-35. doi: 10.1007/978-1-61779-507-7_5. Review.

PMID:
22228009
5.

Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2013 Apr;52(4):414-430.e14. doi: 10.1016/j.jaac.2013.01.003. Review.

6.

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Hiroi N, Takahashi T, Hishimoto A, Izumi T, Boku S, Hiramoto T.

Mol Psychiatry. 2013 Nov;18(11):1153-65. doi: 10.1038/mp.2013.92. Epub 2013 Aug 6. Review.

7.

CNVs: harbingers of a rare variant revolution in psychiatric genetics.

Malhotra D, Sebat J.

Cell. 2012 Mar 16;148(6):1223-41. doi: 10.1016/j.cell.2012.02.039. Review.

8.

Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.

Hochstenbach R, Buizer-Voskamp JE, Vorstman JA, Ophoff RA.

Cytogenet Genome Res. 2011;135(3-4):174-202. doi: 10.1159/000332928. Epub 2011 Nov 2. Review.

PMID:
22056632
9.

Copy-number variants in neurodevelopmental disorders: promises and challenges.

Merikangas AK, Corvin AP, Gallagher L.

Trends Genet. 2009 Dec;25(12):536-44. doi: 10.1016/j.tig.2009.10.006. Epub 2009 Nov 10. Review.

PMID:
19910074
10.

Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?

Hosak L, Silhan P, Hosakova J.

Neuro Endocrinol Lett. 2012;33(2):183-90. Review.

PMID:
22592199
11.

The genetic variability and commonality of neurodevelopmental disease.

Coe BP, Girirajan S, Eichler EE.

Am J Med Genet C Semin Med Genet. 2012 May 15;160C(2):118-29. doi: 10.1002/ajmg.c.31327. Epub 2012 Apr 12. Review.

12.

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA.

Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Review.

PMID:
19895225
13.

The role of DNA copy number variation in schizophrenia.

Tam GW, Redon R, Carter NP, Grant SG.

Biol Psychiatry. 2009 Dec 1;66(11):1005-12. doi: 10.1016/j.biopsych.2009.07.027. Epub 2009 Sep 12. Review.

PMID:
19748074
14.

Immune dysfunction in Tourette syndrome.

Elamin I, Edwards MJ, Martino D.

Behav Neurol. 2013;27(1):23-32. doi: 10.3233/BEN-120295. Review.

15.

Epistasis in Neuropsychiatric Disorders.

Webber C.

Trends Genet. 2017 Apr;33(4):256-265. doi: 10.1016/j.tig.2017.01.009. Epub 2017 Mar 6. Review.

PMID:
28268034

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