Literature DB >> 21397722

Autism candidate genes via mouse phenomics.

Terrence F Meehan1, Christopher J Carr2, Jeremy J Jay3, Carol J Bult4, Elissa J Chesler5, Judith A Blake6.   

Abstract

Autism spectrum disorders (ASD) represent a group of developmental disabilities with a strong genetic basis. The laboratory mouse is increasingly used as a model organism for ASD, and MGI, the Mouse Genome Informatics resource, is the primary model organism database for the laboratory mouse. MGI uses the Mammalian Phenotype (MP) ontology to describe mouse models of human diseases. Using bioinformatics tools including Phenologs, MouseNET, and the Ontological Discovery Environment, we tested data associated with MP terms to characterize new gene-phenotype associations related to ASD. Our integrative analysis using these tools identified numerous mouse genotypes that are likely to have previously uncharacterized autistic-like phenotypes. The genes implicated in these mouse models had considerable overlap with a set of over 300 genes recently associated with ASD due to small, rare copy number variation (Pinto et al., 2010). Prediction and characterization of autistic mutant mouse alleles assists researchers in studying the complex nature of ASD and provides a generalizable approach to candidate gene prioritization.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21397722      PMCID: PMC3263820          DOI: 10.1016/j.jbi.2011.03.003

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  25 in total

1.  GO::TermFinder--open source software for accessing Gene Ontology information and finding significantly enriched Gene Ontology terms associated with a list of genes.

Authors:  Elizabeth I Boyle; Shuai Weng; Jeremy Gollub; Heng Jin; David Botstein; J Michael Cherry; Gavin Sherlock
Journal:  Bioinformatics       Date:  2004-08-05       Impact factor: 6.937

2.  Overlapping probabilities of top ranking gene lists, hypergeometric distribution, and stringency of gene selection criterion.

Authors:  Wen Fury; Franak Batliwalla; Peter K Gregersen; Wentian Li
Journal:  Conf Proc IEEE Eng Med Biol Soc       Date:  2006

3.  The future of genetic studies of complex human diseases.

Authors:  N Risch; K Merikangas
Journal:  Science       Date:  1996-09-13       Impact factor: 47.728

Review 4.  Behavioral phenotyping of mouse models of neurodevelopmental disorders: relevant social behavior patterns across the life span.

Authors:  Laura Ricceri; Anna Moles; Jacqueline Crawley
Journal:  Behav Brain Res       Date:  2006-09-22       Impact factor: 3.332

Review 5.  The mammalian phenotype ontology: enabling robust annotation and comparative analysis.

Authors:  Cynthia L Smith; Janan T Eppig
Journal:  Wiley Interdiscip Rev Syst Biol Med       Date:  2009 Nov-Dec

6.  Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Authors:  Maricela Alarcón; Brett S Abrahams; Jennifer L Stone; Jacqueline A Duvall; Julia V Perederiy; Jamee M Bomar; Jonathan Sebat; Michael Wigler; Christa L Martin; David H Ledbetter; Stanley F Nelson; Rita M Cantor; Daniel H Geschwind
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

7.  A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Authors:  Dan E Arking; David J Cutler; Camille W Brune; Tanya M Teslovich; Kristen West; Morna Ikeda; Alexis Rea; Moltu Guy; Shin Lin; Edwin H Cook; Aravinda Chakravarti
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

Review 8.  The genetics of autism.

Authors:  Rebecca Muhle; Stephanie V Trentacoste; Isabelle Rapin
Journal:  Pediatrics       Date:  2004-05       Impact factor: 7.124

Review 9.  Advances in behavioral genetics: mouse models of autism.

Authors:  S S Moy; J J Nadler
Journal:  Mol Psychiatry       Date:  2007-09-11       Impact factor: 15.992

10.  A genomewide functional network for the laboratory mouse.

Authors:  Yuanfang Guan; Chad L Myers; Rong Lu; Ihor R Lemischka; Carol J Bult; Olga G Troyanskaya
Journal:  PLoS Comput Biol       Date:  2008-09-26       Impact factor: 4.475

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  10 in total

1.  ANKS1B Gene Product AIDA-1 Controls Hippocampal Synaptic Transmission by Regulating GluN2B Subunit Localization.

Authors:  Jaafar O Tindi; Andrés E Chávez; Svetlana Cvejic; Erika Calvo-Ochoa; Pablo E Castillo; Bryen A Jordan
Journal:  J Neurosci       Date:  2015-06-17       Impact factor: 6.167

2.  MouseFinder: Candidate disease genes from mouse phenotype data.

Authors:  Chao-Kung Chen; Christopher J Mungall; Georgios V Gkoutos; Sandra C Doelken; Sebastian Köhler; Barbara J Ruef; Cynthia Smith; Monte Westerfield; Peter N Robinson; Suzanna E Lewis; Paul N Schofield; Damian Smedley
Journal:  Hum Mutat       Date:  2012-03-16       Impact factor: 4.878

3.  GeneWeaver: a web-based system for integrative functional genomics.

Authors:  Erich J Baker; Jeremy J Jay; Jason A Bubier; Michael A Langston; Elissa J Chesler
Journal:  Nucleic Acids Res       Date:  2011-11-12       Impact factor: 16.971

Review 4.  Accelerating discovery for complex neurological and behavioral disorders through systems genetics and integrative genomics in the laboratory mouse.

Authors:  Jason A Bubier; Elissa J Chesler
Journal:  Neurotherapeutics       Date:  2012-04       Impact factor: 7.620

5.  Cerebellar associative sensory learning defects in five mouse autism models.

Authors:  Alexander D Kloth; Aleksandra Badura; Amy Li; Adriana Cherskov; Sara G Connolly; Andrea Giovannucci; M Ali Bangash; Giorgio Grasselli; Olga Peñagarikano; Claire Piochon; Peter T Tsai; Daniel H Geschwind; Christian Hansel; Mustafa Sahin; Toru Takumi; Paul F Worley; Samuel S-H Wang
Journal:  Elife       Date:  2015-07-09       Impact factor: 8.140

6.  GeneWeaver: finding consilience in heterogeneous cross-species functional genomics data.

Authors:  Jason A Bubier; Charles A Phillips; Michael A Langston; Erich J Baker; Elissa J Chesler
Journal:  Mamm Genome       Date:  2015-06-20       Impact factor: 2.957

7.  Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants.

Authors:  Ron Nudel; Vivek Appadurai; Alfonso Buil; Merete Nordentoft; Thomas Werge
Journal:  J Neurodev Disord       Date:  2021-11-13       Impact factor: 4.025

8.  The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data.

Authors:  Cynthia L Smith; Janan T Eppig
Journal:  Mamm Genome       Date:  2012-09-09       Impact factor: 2.957

9.  Dovetailing biology and chemistry: integrating the Gene Ontology with the ChEBI chemical ontology.

Authors:  David P Hill; Nico Adams; Mike Bada; Colin Batchelor; Tanya Z Berardini; Heiko Dietze; Harold J Drabkin; Marcus Ennis; Rebecca E Foulger; Midori A Harris; Janna Hastings; Namrata S Kale; Paula de Matos; Christopher J Mungall; Gareth Owen; Paola Roncaglia; Christoph Steinbeck; Steve Turner; Jane Lomax
Journal:  BMC Genomics       Date:  2013-07-29       Impact factor: 3.969

10.  Haploinsufficiency in the ANKS1B gene encoding AIDA-1 leads to a neurodevelopmental syndrome.

Authors:  Abigail U Carbonell; Chang Hoon Cho; Jaafar O Tindi; Pamela A Counts; Juliana C Bates; Hediye Erdjument-Bromage; Svetlana Cvejic; Alana Iaboni; Ifat Kvint; Jenny Rosensaft; Ehud Banne; Evdokia Anagnostou; Thomas A Neubert; Stephen W Scherer; Sophie Molholm; Bryen A Jordan
Journal:  Nat Commun       Date:  2019-08-06       Impact factor: 17.694

  10 in total

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