Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 18

1.

Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis.

Sidorov MS, Deck GM, Dolatshahi M, Thibert RL, Bird LM, Chu CJ, Philpot BD.

J Neurodev Disord. 2017 May 8;9:17. doi: 10.1186/s11689-017-9195-8. eCollection 2017.

2.

Dysfunctional mTORC1 Signaling: A Convergent Mechanism between Syndromic and Nonsyndromic Forms of Autism Spectrum Disorder?

Magdalon J, Sánchez-Sánchez SM, Griesi-Oliveira K, Sertié AL.

Int J Mol Sci. 2017 Mar 18;18(3). pii: E659. doi: 10.3390/ijms18030659. Review.

3.

Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.

Casanova EL, Sharp JL, Chakraborty H, Sumi NS, Casanova MF.

Mol Autism. 2016 Mar 15;7:18. doi: 10.1186/s13229-016-0082-z. eCollection 2016.

4.

The Effect of Menstrual Issues on Young Women with Angelman Syndrome.

Kaskowitz AP, Dendrinos M, Murray PJ, Quint EH, Ernst S.

J Pediatr Adolesc Gynecol. 2016 Aug;29(4):348-52. doi: 10.1016/j.jpag.2015.12.004. Epub 2015 Dec 21.

PMID:
26718530
5.

Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.

LaSalle JM, Reiter LT, Chamberlain SJ.

Epigenomics. 2015 Oct;7(7):1213-28. doi: 10.2217/epi.15.70. Epub 2015 Nov 20. Review.

7.

Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms.

Gamsiz ED, Sciarra LN, Maguire AM, Pescosolido MF, van Dyck LI, Morrow EM.

Neurotherapeutics. 2015 Jul;12(3):553-71. doi: 10.1007/s13311-015-0363-9. Review.

8.

Genetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disorders.

Kim YS, Leventhal BL.

Biol Psychiatry. 2015 Jan 1;77(1):66-74. doi: 10.1016/j.biopsych.2014.11.001. Epub 2014 Nov 5. Review.

10.

Angelman syndrome: review of clinical and molecular aspects.

Bird LM.

Appl Clin Genet. 2014 May 16;7:93-104. doi: 10.2147/TACG.S57386. eCollection 2014. Review.

11.

Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.

Yang L, Zhan GD, Ding JJ, Wang HJ, Ma D, Huang GY, Zhou WH.

PLoS One. 2013 Aug 14;8(8):e72640. doi: 10.1371/journal.pone.0072640. eCollection 2013.

13.

Aberrant expression of long noncoding RNAs in autistic brain.

Ziats MN, Rennert OM.

J Mol Neurosci. 2013 Mar;49(3):589-93. doi: 10.1007/s12031-012-9880-8. Epub 2012 Sep 5.

14.
15.

Pathology from evolutionary conflict, with a theory of X chromosome versus autosome conflict over sexually antagonistic traits.

Frank SA, Crespi BJ.

Proc Natl Acad Sci U S A. 2011 Jun 28;108 Suppl 2:10886-93. doi: 10.1073/pnas.1100921108. Epub 2011 Jun 20. Review.

16.

The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders.

Levitt P, Campbell DB.

J Clin Invest. 2009 Apr;119(4):747-54. doi: 10.1172/JCI37934. Epub 2009 Apr 1. Review.

17.

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.

Hogart A, Wu D, LaSalle JM, Schanen NC.

Neurobiol Dis. 2010 May;38(2):181-91. doi: 10.1016/j.nbd.2008.08.011. Epub 2008 Sep 18. Review.

18.

Behavior and neuropsychiatric manifestations in Angelman syndrome.

Pelc K, Cheron G, Dan B.

Neuropsychiatr Dis Treat. 2008 Jun;4(3):577-84.

Supplemental Content

Support Center