Literature DB >> 18395317

Neural phenotypes of common and rare genetic variants.

Carrie E Bearden1, David C Glahn, Agatha D Lee, Ming-Chang Chiang, Theo G M van Erp, Tyrone D Cannon, Allan L Reiss, Arthur W Toga, Paul M Thompson.   

Abstract

Neuroimaging methods offer a powerful way to bridge the gaps between genes, neurobiology and behavior. Such investigations may be further empowered by complementary strategies involving chromosomal abnormalities associated with particular neurobehavioral phenotypes, which can help to localize causative genes and better understand the genetics of complex traits in the general population. Here we review the evidence from studies using these convergent approaches to investigate genetic influences on brain structure: (1) studies of common genetic variations associated with particular neuroanatomic phenotypes, and (2) studies of possible 'genetic subtypes' of neuropsychiatric disorders with very high penetrance, with a focus on neuroimaging studies using novel computational brain mapping algorithms. Finally, we discuss the contribution of behavioral neurogenetics research to our understanding of the genetic basis of neuropsychiatric disorders in the broader population.

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Year:  2008        PMID: 18395317      PMCID: PMC2535822          DOI: 10.1016/j.biopsycho.2008.02.005

Source DB:  PubMed          Journal:  Biol Psychol        ISSN: 0301-0511            Impact factor:   3.251


  207 in total

1.  Genetic influences on brain structure.

Authors:  P M Thompson; T D Cannon; K L Narr; T van Erp; V P Poutanen; M Huttunen; J Lönnqvist; C G Standertskjöld-Nordenstam; J Kaprio; M Khaledy; R Dail; C I Zoumalan; A W Toga
Journal:  Nat Neurosci       Date:  2001-12       Impact factor: 24.884

2.  Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

Authors:  R Paylor; K L McIlwain; R McAninch; A Nellis; L A Yuva-Paylor; A Baldini; E A Lindsay
Journal:  Hum Mol Genet       Date:  2001-11-01       Impact factor: 6.150

3.  Enlarged cerebellar vermis in Williams syndrome.

Authors:  J E Schmitt; S Eliez; I S Warsofsky; U Bellugi; A L Reiss
Journal:  J Psychiatr Res       Date:  2001 Jul-Aug       Impact factor: 4.791

4.  The brain in infantile autism: posterior fossa structures are abnormal.

Authors:  E Courchesne; J Townsend; O Saitoh
Journal:  Neurology       Date:  1994-02       Impact factor: 9.910

5.  Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

Authors:  A K Ewart; C A Morris; D Atkinson; W Jin; K Sternes; P Spallone; A D Stock; M Leppert; M T Keating
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

Review 6.  Frontal-subcortical circuits and human behavior.

Authors:  J L Cummings
Journal:  Arch Neurol       Date:  1993-08

Review 7.  Magnetic resonance imaging. Its role in the neuroradiologic evaluation of neurofibromatosis, tuberous sclerosis, and Sturge-Weber syndrome.

Authors:  A P Truhan; P A Filipek
Journal:  Arch Dermatol       Date:  1993-02

8.  Behavioral and psychiatric disorders in adult male carriers of fragile X.

Authors:  M B Dorn; M M Mazzocco; R J Hagerman
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1994-02       Impact factor: 8.829

9.  Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.

Authors:  K H Gustavson; H K Blomquist; G Holmgren
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

10.  Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene.

Authors:  A K Ewart; W Jin; D Atkinson; C A Morris; M T Keating
Journal:  J Clin Invest       Date:  1994-03       Impact factor: 14.808

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  5 in total

Review 1.  Genetic architecture of declarative memory: implications for complex illnesses.

Authors:  Carrie E Bearden; Katherine H Karlsgodt; Peter Bachman; Theo G M van Erp; Anderson M Winkler; David C Glahn
Journal:  Neuroscientist       Date:  2011-08-10       Impact factor: 7.519

Review 2.  Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome.

Authors:  E Walter; P K Mazaika; A L Reiss
Journal:  Neuroscience       Date:  2009-04-17       Impact factor: 3.590

3.  Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients.

Authors:  Carolina Bonilla; Jérémie H Lefèvre; Bruce Winney; Elaine Johnstone; Susan Tonks; Chrystelle Colas; Tammy Day; Katarzyna Hutnik; Abdelhamid Boumertit; Rachel Midgley; David Kerr; Yann Parc; Walter F Bodmer
Journal:  J Hum Genet       Date:  2010-11-25       Impact factor: 3.172

4.  Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis?

Authors:  Maria Jalbrzikowski; Chelsea Carter; Damla Senturk; Carolyn Chow; Jessica M Hopkins; Michael F Green; Adriana Galván; Tyrone D Cannon; Carrie E Bearden
Journal:  Schizophr Res       Date:  2012-10-31       Impact factor: 4.939

Review 5.  The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA.

Authors:  Robert Plomin; Oliver S P Davis
Journal:  J Child Psychol Psychiatry       Date:  2009-01       Impact factor: 8.982

  5 in total

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