Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Behavioural phenotyping assays for mouse models of autismNature reviews. Neuroscience, 2010-07, Vol.11 (7), p.490-502 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2010 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2010 ;2010 Macmillan Publishers Limited. All rights reserved 2010 ;ISSN: 1471-003X ;EISSN: 1471-0048 ;DOI: 10.1038/nrn2851 ;PMID: 20559336Full text available |
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2 |
Material Type: Article
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Molecular mechanisms of memory reconsolidationNature reviews. Neuroscience, 2007-04, Vol.8 (4), p.262-275 [Peer Reviewed Journal]2007 INIST-CNRS ;COPYRIGHT 2007 Nature Publishing Group ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1471-003X ;ISSN: 1471-0048 ;EISSN: 1471-0048 ;DOI: 10.1038/nrn2090 ;PMID: 17342174Full text available |
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3 |
Material Type: Article
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The honeybee as a model for understanding the basis of cognitionNature reviews. Neuroscience, 2012-11, Vol.13 (11), p.758-768 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2012 ;ISSN: 1471-003X ;EISSN: 1471-0048 ;DOI: 10.1038/nrn3357 ;PMID: 23080415Full text available |
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4 |
Material Type: Article
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Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2Nature reviews. Neuroscience, 2012-12, Vol.13 (12), p.819-831 [Peer Reviewed Journal]2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Dec 2012 ;ISSN: 1471-003X ;EISSN: 1471-0048 ;DOI: 10.1038/nrn3386 ;PMID: 23165259Full text available |
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5 |
Material Type: Article
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Prenatal screening for Down syndrome: a survey of willingness in women and family physicians to engage in shared decision-makingPrenatal diagnosis, 2011-04, Vol.31 (4), p.319-326 [Peer Reviewed Journal]Copyright © 2011 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2624 ;PMID: 21268046 ;CODEN: PRDIDMFull text available |
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6 |
Material Type: Article
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A pilot open label, single dose trial of fenobam in adults with fragile X syndromeJournal of medical genetics, 2009-04, Vol.46 (4), p.266-271 [Peer Reviewed Journal]Berry-Kravis et al 2009 ;2009 INIST-CNRS ;Copyright: 2009 (c) Berry-Kravis et al 2009 ;Berry-Kravis et al 2009 2009 ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.2008.063701 ;PMID: 19126569 ;CODEN: JMDGAEFull text available |
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7 |
Material Type: Article
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High fat diet increases hippocampal oxidative stress and cognitive impairment in aged mice: implications for decreased Nrf2 signalingJournal of neurochemistry, 2010-09, Vol.114 (6), p.1581-1589 [Peer Reviewed Journal]2010 The Authors. Journal Compilation © 2010 International Society for Neurochemistry ;2015 INIST-CNRS ;2010 The Authors. Journal Compilation © 2010 International Society for Neurochemistry. ;Journal compilation © 2010 International Society for Neurochemistry ;ISSN: 0022-3042 ;EISSN: 1471-4159 ;DOI: 10.1111/j.1471-4159.2010.06865.x ;PMID: 20557430 ;CODEN: JONRA9Full text available |
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8 |
Material Type: Article
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Individual common variants exert weak effects on the risk for autism spectrum disorderspiHuman molecular genetics, 2012-11, Vol.21 (21), p.4781-4792 [Peer Reviewed Journal]2015 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/dds301Full text available |
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9 |
Material Type: Article
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Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiencesEuropean journal of human genetics : EJHG, 2011-06, Vol.19 (6), p.640-646 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright Nature Publishing Group Jun 2011 ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2011 Macmillan Publishers Limited 2011 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2010.258 ;PMID: 21326287Full text available |
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10 |
Material Type: Article
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Structural Variation of Chromosomes in Autism Spectrum DisorderAmerican journal of human genetics, 2008-02, Vol.82 (2), p.477-488 [Peer Reviewed Journal]2008 The American Society of Human Genetics ;2008 INIST-CNRS ;2008 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved.. 2008 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2007.12.009 ;PMID: 18252227 ;CODEN: AJHGAGFull text available |
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11 |
Material Type: Article
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The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutationEuropean journal of human genetics : EJHG, 2007-04, Vol.15 (4), p.453-462 [Peer Reviewed Journal]2007 INIST-CNRS ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201774 ;PMID: 17245406Full text available |
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12 |
Material Type: Article
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Sorting of the Alzheimer's Disease Amyloid Precursor Protein Mediated by the AP-4 ComplexDevelopmental cell, 2010-03, Vol.18 (3), p.425-436 [Peer Reviewed Journal]2010 Elsevier Inc. ;2015 INIST-CNRS ;Copyright 2010 Elsevier Inc. All rights reserved. ;ISSN: 1534-5807 ;EISSN: 1878-1551 ;DOI: 10.1016/j.devcel.2010.01.015 ;PMID: 20230749Full text available |
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13 |
Material Type: Article
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A prospective study on parental coping 4 months after termination of pregnancy for fetal anomaliesPrenatal diagnosis, 2007-08, Vol.27 (8), p.709-716 [Peer Reviewed Journal]Copyright © 2007 John Wiley & Sons, Ltd. ;2007 INIST-CNRS ;Copyright (c) 2007 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1763 ;PMID: 17533631 ;CODEN: PRDIDMFull text available |
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14 |
Material Type: Article
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Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorderHuman molecular genetics, 2011-12, Vol.20 (24), p.4786-4796 [Peer Reviewed Journal]The Author 2011. Published by Oxford University Press 2011 ;2015 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddr416 ;PMID: 21908516Full text available |
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15 |
Material Type: Article
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Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traitsHuman molecular genetics, 2012-07, Vol.21 (14), p.3083-3096 [Peer Reviewed Journal]2015 INIST-CNRS ;The Author 2012. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2012 ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/dds124 ;PMID: 22492990Full text available |
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16 |
Material Type: Article
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The genetics of panic disorderJournal of Medical Genetics, 2011-06, Vol.48 (6), p.361-368 [Peer Reviewed Journal]2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;2015 INIST-CNRS ;Copyright: 2011 (c) 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.2010.086876 ;PMID: 21493958 ;CODEN: JMDGAEFull text available |
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17 |
Material Type: Article
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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual DisabilityAmerican journal of human genetics, 2012-05, Vol.90 (5), p.847-855 [Peer Reviewed Journal]2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press May 4, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.03.021 ;PMID: 22541559 ;CODEN: AJHGAGFull text available |
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18 |
Material Type: Article
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Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective studyClinical genetics, 2007-01, Vol.71 (1), p.35-42 [Peer Reviewed Journal]2007 Blackwell Munksgaard ;2007 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2007.00731.x ;PMID: 17204044 ;CODEN: CLGNAYFull text available |
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19 |
Material Type: Article
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Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual DisabilityAmerican journal of human genetics, 2012-07, Vol.91 (1), p.73-82 [Peer Reviewed Journal]2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Jul 13, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.05.003 ;PMID: 22726846 ;CODEN: AJHGAGFull text available |
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20 |
Material Type: Article
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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorderNature genetics, 2008-09, Vol.40 (9), p.1056-1058 [Peer Reviewed Journal]2008 INIST-CNRS ;COPYRIGHT 2008 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2008 ;2008 Nature Publishing Group 2008 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.209 ;PMID: 18711365 ;CODEN: NGENECFull text available |