Neurocognitive Phenotypes and Genetic Dissection of Disorders of Brain and Behavior

被引:14
|
作者
Congdon, Eliza [1 ,2 ]
Poldrack, Russell A. [3 ,4 ,5 ]
Freimer, Nelson B. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Ctr Neurobehav Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Psychiat, Los Angeles, CA 90095 USA
[3] Univ Texas Austin, Dept Psychol, Austin, TX 78712 USA
[4] Univ Texas Austin, Dept Neurobiol, Austin, TX 78712 USA
[5] Univ Texas Austin, Imaging Res Ctr, Austin, TX 78712 USA
关键词
GENOME-WIDE ASSOCIATION; NEUROIMAGING INITIATIVE ADNI; EXTENDED PEDIGREE; WORKING-MEMORY; NEUROPSYCHIATRIC DISEASE; PERSONALITY DIMENSIONS; CANDIDATE GENES; HERITABILITY; EXPRESSION; ALZHEIMERS;
D O I
10.1016/j.neuron.2010.10.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Elucidating the molecular mechanisms underlying quantitative neurocognitive phenotypes will further our understanding of the brain's structural and functional architecture and advance the diagnosis and treatment of the psychiatric disorders that these traits underlie. Although many neurocognitive traits are highly heritable, little progress has been made in identifying genetic variants unequivocally associated with these phenotypes. A major obstacle to such progress is the difficulty in identifying heritable neurocognitive measures that are precisely defined and systematically assessed and represent unambiguous mental constructs, yet are also amenable to the high-throughput phenotyping necessary to obtain adequate power for genetic association studies. In this perspective we compare the current status of genetic investigations of neurocognitive phenotypes to that of other categories of biomedically relevant traits and suggest strategies for genetically dissecting traits that may underlie disorders of brain and behavior.
引用
收藏
页码:218 / 230
页数:13
相关论文
共 50 条
  • [41] Training the developing brain: a neurocognitive perspective
    Jolles, Dietsje D.
    Crone, Eveline A.
    FRONTIERS IN HUMAN NEUROSCIENCE, 2012, 6
  • [42] Potential Serum Biomarkers for Postoperative Neurocognitive Disorders Based on Proteomic Analysis of Cognitive-Related Brain Regions
    Li, Yitong
    Chen, Lei
    Li, Zhengqian
    Song, Yanan
    Yuan, Yi
    Liu, Taotao
    Hong, Jingshu
    Wang, Qian
    Chang, Huixian
    Kuang, Zhongshen
    He, Jindan
    Li, Yue
    Mi, Xinning
    Han, Dengyang
    Yang, Ning
    Guo, Xiangyang
    FRONTIERS IN AGING NEUROSCIENCE, 2021, 13
  • [43] Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease
    Yan, Jingwen
    Kim, Sungeun
    Nho, Kwangsik
    Chen, Rui
    Risacher, Shannon L.
    Moore, Jason H.
    Saykin, Andrew J.
    Shen, Li
    FRONTIERS IN GENETICS, 2015, 6
  • [44] Dissection of genetic factors associated with amyotrophic lateral sclerosis
    Leblond, Claire S.
    Kaneb, Hannah M.
    Dion, Patrick A.
    Rouleau, Guy A.
    EXPERIMENTAL NEUROLOGY, 2014, 262 : 91 - 101
  • [45] The genetic architecture of human brainstem structures and their involvement in common brain disorders
    Elvsashagen, Torbjorn
    Bahrami, Shahram
    van der Meer, Dennis
    Agartz, Ingrid
    Alnaes, Dag
    Barch, Deanna M.
    Baur-Streubel, Ramona
    Bertolino, Alessandro
    Beyer, Mona K.
    Blasi, Giuseppe
    Borgwardt, Stefan
    Boye, Birgitte
    Buitelaar, Jan
    Boen, Erlend
    Celius, Elisabeth Gulowsen
    Cervenka, Simon
    Conzelmann, Annette
    Coynel, David
    Di Carlo, Pasquale
    Djurovic, Srdjan
    Eisenacher, Sarah
    Espeseth, Thomas
    Fatouros-Bergman, Helena
    Flyckt, Lena
    Franke, Barbara
    Frei, Oleksandr
    Gelao, Barbara
    Harbo, Hanne Flinstad
    Hartman, Catharina A.
    Haberg, Asta
    Heslenfeld, Dirk
    Hoekstra, Pieter J.
    Hogestol, Einar A.
    Jonassen, Rune
    Jonsson, Erik G.
    Kirsch, Peter
    Kloszewska, Iwona
    Lagerberg, Trine Vik
    Landro, Nils Inge
    Le Hellard, Stephanie
    Lesch, Klaus-Peter
    Maglanoc, Luigi A.
    Malt, Ulrik F.
    Mecocci, Patrizia
    Melle, Ingrid
    Meyer-Lindenberg, Andreas
    Moberget, Torgeir
    Nordvik, Jan Egil
    Nyberg, Lars
    O'Connell, Kevin S.
    NATURE COMMUNICATIONS, 2020, 11 (01)
  • [46] The genetic architecture of psychophysiological phenotypes
    Munafo, Marcus R.
    Flint, Jonathan
    PSYCHOPHYSIOLOGY, 2014, 51 (12) : 1331 - 1332
  • [47] Navigating the Gene Co-Expression Network and Drug Repurposing Opportunities for Brain Disorders Associated with Neurocognitive Impairment
    Manuel, Mathew Timothy Artuz
    Tayo, Lemmuel L.
    BRAIN SCIENCES, 2023, 13 (11)
  • [48] Genetic bases of hypertriglyceridemic phenotypes
    Johansen, Christopher T.
    Hegele, Robert A.
    CURRENT OPINION IN LIPIDOLOGY, 2011, 22 (04) : 247 - 253
  • [49] Neurocognitive vulnerability to youth suicidal behavior
    Ruch, Donna
    Sheftall, Arielle H.
    Heck, Kendra
    McBee-Strayer, Sandra M.
    Tissue, Jaclyn
    Reynolds, Brady
    Ackerman, John
    Brent, David A.
    Campo, John, V
    Bridge, Jeffrey A.
    JOURNAL OF PSYCHIATRIC RESEARCH, 2020, 131 : 119 - 126
  • [50] Migraine, Stroke, and Cervical Arterial Dissection Shared Genetics for a Triad of Brain Disorders With Vascular Involvement
    Daghals, Iyas
    Sargurupremraj, Muralidharan
    Danning, Rebecca
    Gormley, Padhraig
    Malik, Rainer
    Amouyel, Philippe
    Metso, Tiina
    Pezzini, Alessandro
    Kurth, Tobias
    Debette, Stephanie
    Chasman, Daniel
    NEUROLOGY-GENETICS, 2022, 8 (01)