Re-sequencing for Rare and Uncommon Genetic Variants that may Influence Behavioral Dyscontrol and Impulsivity

被引:0
|
作者
Bevilacqua, Laura [1 ]
Zhou, Zhifeng [1 ]
Yuan, Qiaoping [1 ]
Yamini, Goli [1 ]
Moore, Elisa [1 ]
Virkkunen, Matti [2 ]
Goldman, David [1 ]
机构
[1] NIAAA, Neurogenet Lab, NIH, Rockville, MD 20852 USA
[2] Univ Helsinki, Dept Psychiat, SF-00180 Helsinki, Finland
关键词
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
188
引用
收藏
页码:57S / 57S
页数:1
相关论文
共 50 条
  • [1] RE-SEQUENCING FOR RARE AND UNCOMMON GENETIC VARIANTS THAT MAY INFLUENCE IMPULSIVE BEHAVIOR IN ALCOHOLICS
    Bevilacqua, L.
    Zhou, Z.
    Yuan, Q.
    Yamini, G.
    Moore, E.
    Virkkunen, M.
    Goldman, D.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2009, 33 (06) : 13A - 13A
  • [2] Carrier re-sequencing reveals rare but benign variants in recessive deafness genes
    He, Longxia
    Pang, Xiuhong
    Chen, Penghui
    Wang, Xiaowen
    Yang, Tao
    Wu, Hao
    SCIENTIFIC REPORTS, 2017, 7
  • [3] Carrier re-sequencing reveals rare but benign variants in recessive deafness genes
    Longxia He
    Xiuhong Pang
    Penghui Chen
    Xiaowen Wang
    Tao Yang
    Hao Wu
    Scientific Reports, 7
  • [4] Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms
    Pensato, Viviana
    Magri, Stefania
    Dalla Bella, Eleonora
    Tannorella, Pierpaola
    Bersano, Enrica
    Soraru, Gianni
    Gatti, Marta
    Ticozzi, Nicola
    Taroni, Franco
    Lauria, Giuseppe
    Mariotti, Caterina
    Gellera, Cinzia
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (02)
  • [5] The genetic panorama in titin gene by re-sequencing projects
    Savarese, M.
    Evila, A.
    Torella, A.
    Arumilli, M.
    Nigro, V.
    Hackman, P.
    Udd, B.
    NEUROMUSCULAR DISORDERS, 2016, 26 : S113 - S113
  • [6] Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study
    Chen, Christina T. L.
    McDavid, Andrew N.
    Kahsai, Orsalem J.
    Zebari, Ahmad S.
    Carlson, Christopher S.
    NUCLEIC ACIDS RESEARCH, 2013, 41 (07)
  • [7] Deep Re-Sequencing to Identify Functional Variants at the CRP Gene
    Chen, Christina T. L.
    Stednick, Zach
    McDavid, Andrew N.
    Kahsai, Orsalem J.
    Zebari, Ahmad S.
    O'Shea, Dylan
    Carlson, Christopher S.
    GENETIC EPIDEMIOLOGY, 2010, 34 (08) : 924 - 924
  • [8] Unmasking of rare pathogenic variants by inherited deletions detected with multiplexed capture array-based re-sequencing
    Hochstenbach, Ron
    Nijman, Les
    Poot, Martin
    Kloosterman, Wigard
    Renkens, Ivo
    Duran, Karin
    van Binsbergen, Ellen
    van der Zwaag, Bert
    Guryev, Victor
    Koval, Slavik
    van Amstel, Hans Kristian Ploos
    Cuppen, Edwin
    CHROMOSOME RESEARCH, 2011, 19 : S58 - S59
  • [9] Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology
    Alexander, John
    Potamianou, Hera
    Xing, Jinchuan
    Deng, Li
    Karagiannidis, Iordanis
    Tsetsos, Fotis
    Drineas, Petros
    Tarnok, Zsanett
    Rizzo, Renata
    Wolanczyk, Tomasz
    Farkas, Luca
    Nagy, Peter
    Szymanska, Urszula
    Androutsos, Christos
    Tsironi, Vaia
    Koumoulas, Anastasia
    Barta, Csaba
    Sandor, Paul
    Barr, Cathy L.
    Tischfield, Jay
    Paschou, Peristera
    Heiman, Gary A.
    Georgitsi, Marianthi
    FRONTIERS IN NEUROSCIENCE, 2016, 10
  • [10] Genetic characteristics of Jiaji Duck by whole genome re-sequencing
    Gu, Lihong
    Wang, Feng
    Lin, Zhemin
    Xu, Tieshan
    Lin, Dajie
    Xing, Manping
    Yang, Shaoxiong
    Chao, Zhe
    Ye, Baoguo
    Lin, Peng
    Hui, Chunhui
    Lu, Lizhi
    Hou, Shuisheng
    PLOS ONE, 2020, 15 (02):