Literature DB >> 20125193

Common genetic variation and performance on standardized cognitive tests.

Elizabeth T Cirulli1, Dalia Kasperaviciūte, Deborah K Attix, Anna C Need, Dongliang Ge, Greg Gibson, David B Goldstein.   

Abstract

One surprising feature of the recently completed waves of genome-wide association studies is the limited impact of common genetic variation in individually detectable polymorphisms on many human traits. This has been particularly pronounced for studies on psychiatric conditions, which have failed to produce clear, replicable associations for common variants. One popular explanation for these negative findings is that many of these traits may be genetically heterogeneous, leading to the idea that relevant endophenotypes may be more genetically tractable. Aspects of cognition may be the most important endophenotypes for psychiatric conditions such as schizophrenia, leading many researchers to pursue large-scale studies on the genetic contributors of cognitive performance in the normal population as a surrogate for aspects of liability to disease. Here, we perform a genome-wide association study with two tests of executive function, Digit Symbol and Stroop Color-Word, in 1086 healthy volunteers and with an expanded cognitive battery in 514 of these volunteers. We show that, consistent with published studies of the psychiatric conditions themselves, no single common variant has a large effect (explaining >4-8% of the population variation) on the performance of healthy individuals on standardized cognitive tests. Given that these are important endophenotypes, our work is consistent with the idea that identifying rare genetic causes of psychiatric conditions may be more important for future research than identifying genetically homogenous endophenotypes.

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Year:  2010        PMID: 20125193      PMCID: PMC2987367          DOI: 10.1038/ejhg.2010.2

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  46 in total

1.  PLINK: a tool set for whole-genome association and population-based linkage analyses.

Authors:  Shaun Purcell; Benjamin Neale; Kathe Todd-Brown; Lori Thomas; Manuel A R Ferreira; David Bender; Julian Maller; Pamela Sklar; Paul I W de Bakker; Mark J Daly; Pak C Sham
Journal:  Am J Hum Genet       Date:  2007-07-25       Impact factor: 11.025

Review 2.  Genome-wide association studies for complex traits: consensus, uncertainty and challenges.

Authors:  Mark I McCarthy; Gonçalo R Abecasis; Lon R Cardon; David B Goldstein; Julian Little; John P A Ioannidis; Joel N Hirschhorn
Journal:  Nat Rev Genet       Date:  2008-05       Impact factor: 53.242

3.  Failure to replicate effect of Kibra on human memory in two large cohorts of European origin.

Authors:  Anna C Need; Deborah K Attix; Jill M McEvoy; Elizabeth T Cirulli; Kristen N Linney; Ana Patricia Wagoner; Curtis E Gumbs; Ina Giegling; Hans-Jürgen Möller; Clyde Francks; Pierandrea Muglia; Allen Roses; Greg Gibson; Mike E Weale; Dan Rujescu; David B Goldstein
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-07-05       Impact factor: 3.568

4.  Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Authors:  Tom Walsh; Jon M McClellan; Shane E McCarthy; Anjené M Addington; Sarah B Pierce; Greg M Cooper; Alex S Nord; Mary Kusenda; Dheeraj Malhotra; Abhishek Bhandari; Sunday M Stray; Caitlin F Rippey; Patricia Roccanova; Vlad Makarov; B Lakshmi; Robert L Findling; Linmarie Sikich; Thomas Stromberg; Barry Merriman; Nitin Gogtay; Philip Butler; Kristen Eckstrand; Laila Noory; Peter Gochman; Robert Long; Zugen Chen; Sean Davis; Carl Baker; Evan E Eichler; Paul S Meltzer; Stanley F Nelson; Andrew B Singleton; Ming K Lee; Judith L Rapoport; Mary-Claire King; Jonathan Sebat
Journal:  Science       Date:  2008-03-27       Impact factor: 47.728

5.  Impact of the COMT Val108/158 Met and DAT genotypes on prefrontal function in healthy subjects.

Authors:  Xavier Caldú; Pere Vendrell; David Bartrés-Faz; Inmaculada Clemente; Núria Bargalló; María Angeles Jurado; Josep Maria Serra-Grabulosa; Carme Junqué
Journal:  Neuroimage       Date:  2007-07-04       Impact factor: 6.556

6.  Testing for neuropsychological endophenotypes in siblings discordant for attention-deficit/hyperactivity disorder.

Authors:  L Cinnamon Bidwell; Erik G Willcutt; John C Defries; Bruce F Pennington
Journal:  Biol Psychiatry       Date:  2007-06-22       Impact factor: 13.382

7.  Association between microdeletion and microduplication at 16p11.2 and autism.

Authors:  Lauren A Weiss; Yiping Shen; Joshua M Korn; Dan E Arking; David T Miller; Ragnheidur Fossdal; Evald Saemundsen; Hreinn Stefansson; Manuel A R Ferreira; Todd Green; Orah S Platt; Douglas M Ruderfer; Christopher A Walsh; David Altshuler; Aravinda Chakravarti; Rudolph E Tanzi; Kari Stefansson; Susan L Santangelo; James F Gusella; Pamela Sklar; Bai-Lin Wu; Mark J Daly
Journal:  N Engl J Med       Date:  2008-01-09       Impact factor: 91.245

8.  Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.

Authors:  L M Butcher; O S P Davis; I W Craig; R Plomin
Journal:  Genes Brain Behav       Date:  2008-01-22       Impact factor: 3.449

9.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
Journal:  Nature       Date:  2007-06-07       Impact factor: 49.962

10.  Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.

Authors:  Sudha Seshadri; Anita L DeStefano; Rhoda Au; Joseph M Massaro; Alexa S Beiser; Margaret Kelly-Hayes; Carlos S Kase; Ralph B D'Agostino; Charles Decarli; Larry D Atwood; Philip A Wolf
Journal:  BMC Med Genet       Date:  2007-09-19       Impact factor: 2.103

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  46 in total

Review 1.  Uncovering the roles of rare variants in common disease through whole-genome sequencing.

Authors:  Elizabeth T Cirulli; David B Goldstein
Journal:  Nat Rev Genet       Date:  2010-06       Impact factor: 53.242

2.  Heritability and genetic association analysis of cognition in the Diabetes Heart Study.

Authors:  Amanda J Cox; Christina E Hugenschmidt; Laura M Raffield; Carl D Langefeld; Barry I Freedman; Jeff D Williamson; Fang-Chi Hsu; Donald W Bowden
Journal:  Neurobiol Aging       Date:  2014-03-11       Impact factor: 4.673

3.  Genome-Wide Analyses of Working-Memory Ability: A Review.

Authors:  E E M Knowles; S R Mathias; D R McKay; E Sprooten; John Blangero; Laura Almasy; D C Glahn
Journal:  Curr Behav Neurosci Rep       Date:  2014-12

4.  A systematic eQTL study of cis-trans epistasis in 210 HapMap individuals.

Authors:  Jessica Becker; Jens R Wendland; Britta Haenisch; Markus M Nöthen; Johannes Schumacher
Journal:  Eur J Hum Genet       Date:  2011-08-17       Impact factor: 4.246

Review 5.  The BDNF Val66Met Polymorphism Promotes Changes in the Neuronal Integrity and Alters the Time Perception.

Authors:  Victor Marinho; Giovanny Rebouças Pinto; Rogério Figueiredo; Carla Ayres; Juliete Bandeira; Silmar Teixeira
Journal:  J Mol Neurosci       Date:  2018-11-17       Impact factor: 3.444

6.  Potassium channel gene associations with joint processing speed and white matter impairments in schizophrenia.

Authors:  H A Bruce; P Kochunov; S A Paciga; C L Hyde; X Chen; Z Xie; B Zhang; H S Xi; P O'Donnell; C Whelan; C R Schubert; A Bellon; S A Ament; D K Shukla; X Du; L M Rowland; H O'Neill; L E Hong
Journal:  Genes Brain Behav       Date:  2017-03-13       Impact factor: 3.449

7.  Multivariate analysis reveals genetic associations of the resting default mode network in psychotic bipolar disorder and schizophrenia.

Authors:  Shashwath A Meda; Gualberto Ruaño; Andreas Windemuth; Kasey O'Neil; Clifton Berwise; Sabra M Dunn; Leah E Boccaccio; Balaji Narayanan; Mohan Kocherla; Emma Sprooten; Matcheri S Keshavan; Carol A Tamminga; John A Sweeney; Brett A Clementz; Vince D Calhoun; Godfrey D Pearlson
Journal:  Proc Natl Acad Sci U S A       Date:  2014-04-28       Impact factor: 11.205

8.  Converging genetic and functional brain imaging evidence links neuronal excitability to working memory, psychiatric disease, and brain activity.

Authors:  Angela Heck; Matthias Fastenrath; Sandra Ackermann; Bianca Auschra; Horst Bickel; David Coynel; Leo Gschwind; Frank Jessen; Hanna Kaduszkiewicz; Wolfgang Maier; Annette Milnik; Michael Pentzek; Steffi G Riedel-Heller; Stephan Ripke; Klara Spalek; Patrick Sullivan; Christian Vogler; Michael Wagner; Siegfried Weyerer; Steffen Wolfsgruber; Dominique J-F de Quervain; Andreas Papassotiropoulos
Journal:  Neuron       Date:  2014-02-13       Impact factor: 17.173

9.  Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.

Authors:  Dalia Kasperaviciūte; Claudia B Catarino; Erin L Heinzen; Chantal Depondt; Gianpiero L Cavalleri; Luis O Caboclo; Sarah K Tate; Jenny Jamnadas-Khoda; Krishna Chinthapalli; Lisa M S Clayton; Kevin V Shianna; Rodney A Radtke; Mohamad A Mikati; William B Gallentine; Aatif M Husain; Saud Alhusaini; David Leppert; Lefkos T Middleton; Rachel A Gibson; Michael R Johnson; Paul M Matthews; David Hosford; Kjell Heuser; Leslie Amos; Marcos Ortega; Dominik Zumsteg; Heinz-Gregor Wieser; Bernhard J Steinhoff; Günter Krämer; Jörg Hansen; Thomas Dorn; Anne-Mari Kantanen; Leif Gjerstad; Terhi Peuralinna; Dena G Hernandez; Kai J Eriksson; Reetta K Kälviäinen; Colin P Doherty; Nicholas W Wood; Massimo Pandolfo; John S Duncan; Josemir W Sander; Norman Delanty; David B Goldstein; Sanjay M Sisodiya
Journal:  Brain       Date:  2010-06-03       Impact factor: 13.501

10.  Neurogenetic effects on cognition in aging brains: a window of opportunity for intervention?

Authors:  Ivar Reinvang; Ian J Deary; Anders M Fjell; Vidar M Steen; Thomas Espeseth; Raja Parasuraman
Journal:  Front Aging Neurosci       Date:  2010-11-02       Impact factor: 5.750

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