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Items: 1 to 20 of 25

1.

Strong association of de novo copy number mutations with sporadic schizophrenia.

Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M.

Nat Genet. 2008 Jul;40(7):880-5. doi: 10.1038/ng.162. Epub 2008 May 30.

PMID:
18511947
2.

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
3.

De novo mutations in human genetic disease.

Veltman JA, Brunner HG.

Nat Rev Genet. 2012 Jul 18;13(8):565-75. doi: 10.1038/nrg3241. Review.

PMID:
22805709
4.

From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease.

Ku CS, Tan EK, Cooper DN.

J Med Genet. 2013 Apr;50(4):203-11. doi: 10.1136/jmedgenet-2013-101519. Epub 2013 Feb 9. Review.

PMID:
23396985
5.

Genetics of schizophrenia: I. Familial patterns and mode of inheritance.

Baron M.

Biol Psychiatry. 1986 Sep;21(11):1051-66. Review.

PMID:
3527282
6.

Schizophrenia genetics: putting all the pieces together.

Girard SL, Dion PA, Rouleau GA.

Curr Neurol Neurosci Rep. 2012 Jun;12(3):261-6. doi: 10.1007/s11910-012-0266-7. Review.

PMID:
22456906
7.

[Genetic risk factors in schizophrenia].

Fabisch H, Kroisel PM, Fabisch K.

Fortschr Neurol Psychiatr. 2005 Nov;73 Suppl 1:S44-50. Review. German.

PMID:
16270244
8.

Genomic rearrangements and sporadic disease.

Lupski JR.

Nat Genet. 2007 Jul;39(7 Suppl):S43-7. Review.

PMID:
17597781
9.

Schizophrenia genetics: advancing on two fronts.

Owen MJ, Williams HJ, O'Donovan MC.

Curr Opin Genet Dev. 2009 Jun;19(3):266-70. doi: 10.1016/j.gde.2009.02.008. Epub 2009 Apr 1. Review.

PMID:
19345090
10.

A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease.

Ku CS, Polychronakos C, Tan EK, Naidoo N, Pawitan Y, Roukos DH, Mort M, Cooper DN.

Mol Psychiatry. 2013 Feb;18(2):141-53. doi: 10.1038/mp.2012.58. Epub 2012 May 29. Review.

PMID:
22641181
11.

Linkage and associated studies of schizophrenia.

Riley BP, McGuffin P.

Am J Med Genet. 2000 Spring;97(1):23-44. Review.

PMID:
10813802
12.

Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future.

Alaerts M, Del-Favero J.

Hum Mutat. 2009 Aug;30(8):1139-52. doi: 10.1002/humu.21042. Review.

PMID:
19626716
13.

Extending genome-wide association studies to copy-number variation.

McCarroll SA.

Hum Mol Genet. 2008 Oct 15;17(R2):R135-42. doi: 10.1093/hmg/ddn282. Review.

14.

Genetic studies of schizophrenia: an update.

Chen J, Cao F, Liu L, Wang L, Chen X.

Neurosci Bull. 2015 Feb;31(1):87-98. doi: 10.1007/s12264-014-1494-4. Epub 2015 Feb 6. Review.

PMID:
25652814
15.

Chromosome copy number variation and breast cancer risk.

Tchatchou S, Burwinkel B.

Cytogenet Genome Res. 2008;123(1-4):183-7. doi: 10.1159/000184707. Epub 2009 Mar 11. Review.

PMID:
19287154
16.

The genetic architecture of schizophrenia: new mutations and emerging paradigms.

Rodriguez-Murillo L, Gogos JA, Karayiorgou M.

Annu Rev Med. 2012;63:63-80. doi: 10.1146/annurev-med-072010-091100. Epub 2011 Oct 27. Review.

PMID:
22034867
17.

Review of the 6th symposium for the search for the causes of schizophrenia, Sao Paulo, Brazil, 3-6 February 2009.

Kirkbride JB, Scoriels L.

Eur Arch Psychiatry Clin Neurosci. 2009 Dec;259(8):505-9. doi: 10.1007/s00406-009-0025-1. Epub 2009 Jun 16. Review.

PMID:
19533045
18.
19.

Growth and schizophrenia: aetiology, epidemiology and epigenetics.

Malaspina D, Perrin M, Kleinhaus KR, Opler M, Harlap S.

Novartis Found Symp. 2008;289:196-203; discussion 203-7, 238-40. Review.

PMID:
18497104
20.

New methods for assessing male germ line mutations in humans and genetic risks in their offspring.

Verhofstad N, Linschooten JO, van Benthem J, Dubrova YE, van Steeg H, van Schooten FJ, Godschalk RW.

Mutagenesis. 2008 Jul;23(4):241-7. doi: 10.1093/mutage/gen022. Epub 2008 May 20. Review.

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