DSM-5 and Psychiatric Genetics - Round Hole, Meet Square Peg

被引:7
作者
Buxbaum, Joseph D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, Friedman Brain Inst, Dept Psychiat, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, Friedman Brain Inst, Dept Neurosci, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, Friedman Brain Inst, Dept Genet, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, Friedman Brain Inst, Dept Genom Sci, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Mindich Child Hlth & Dev Inst, New York, NY 10029 USA
关键词
AUTISM; MUTATIONS; GENES; RISK;
D O I
10.1016/j.biopsych.2015.02.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
引用
收藏
页码:766 / 768
页数:3
相关论文
共 10 条
[1]   The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders [J].
Buxbaum, Joseph D. ;
Daly, Mark J. ;
Devlin, Bernie ;
Lehner, Thomas ;
Roeder, Kathryn ;
State, Matthew W. .
NEURON, 2012, 76 (06) :1052-1056
[2]   A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? [J].
Chaste, Pauline ;
Klei, Lambertus ;
Sanders, Stephan J. ;
Hus, Vanessa ;
Murtha, Michael T. ;
Lowe, Jennifer K. ;
Willsey, A. Jeremy ;
Moreno-De-Luca, Daniel ;
Yu, Timothy W. ;
Fombonne, Eric ;
Geschwind, Daniel ;
Grice, Dorothy E. ;
Ledbetter, David H. ;
Mane, Shrikant M. ;
Martin, Donna M. ;
Morrow, Eric M. ;
Walsh, Christopher A. ;
Sutcliffe, James S. ;
Martin, Christa Lese ;
Beaudet, Arthur L. ;
Lord, Catherine ;
State, Matthew W. ;
Cook, Edwin H., Jr. ;
Devlin, Bernie .
BIOLOGICAL PSYCHIATRY, 2015, 77 (09) :775-784
[3]   Synaptic, transcriptional and chromatin genes disrupted in autism [J].
De Rubeis, Silvia ;
He, Xin ;
Goldberg, Arthur P. ;
Poultney, Christopher S. ;
Samocha, Kaitlin ;
Cicek, A. Ercument ;
Kou, Yan ;
Liu, Li ;
Fromer, Menachem ;
Walker, Susan ;
Singh, Tarjinder ;
Klei, Lambertus ;
Kosmicki, Jack ;
Fu, Shih-Chen ;
Aleksic, Branko ;
Biscaldi, Monica ;
Bolton, Patrick F. ;
Brownfeld, Jessica M. ;
Cai, Jinlu ;
Campbell, Nicholas G. ;
Carracedo, Angel ;
Chahrour, Maria H. ;
Chiocchetti, Andreas G. ;
Coon, Hilary ;
Crawford, Emily L. ;
Crooks, Lucy ;
Curran, Sarah R. ;
Dawson, Geraldine ;
Duketis, Eftichia ;
Fernandez, Bridget A. ;
Gallagher, Louise ;
Geller, Evan ;
Guter, Stephen J. ;
Hill, R. Sean ;
Ionita-Laza, Iuliana ;
Gonzalez, Patricia Jimenez ;
Kilpinen, Helena ;
Klauck, Sabine M. ;
Kolevzon, Alexander ;
Lee, Irene ;
Lei, Jing ;
Lehtimaeki, Terho ;
Lin, Chiao-Feng ;
Ma'ayan, Avi ;
Marshall, Christian R. ;
McInnes, Alison L. ;
Neale, Benjamin ;
Owen, Michael J. ;
Ozaki, Norio ;
Parellada, Mara .
NATURE, 2014, 515 (7526) :209-+
[4]   Most genetic risk for autism resides with common variation [J].
Gaugler, Trent ;
Klei, Lambertus ;
Sanders, Stephan J. ;
Bodea, Corneliu A. ;
Goldberg, Arthur P. ;
Lee, Ann B. ;
Mahajan, Milind ;
Manaa, Dina ;
Pawitan, Yudi ;
Reichert, Jennifer ;
Ripke, Stephan ;
Sandin, Sven ;
Sklar, Pamela ;
Svantesson, Oscar ;
Reichenberg, Abraham ;
Hultman, Christina M. ;
Devlin, Bernie ;
Roeder, Kathryn ;
Buxbaum, Joseph D. .
NATURE GENETICS, 2014, 46 (08) :881-885
[5]   The ESSENCE in child psychiatry: Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations [J].
Gillberg, Christopher .
RESEARCH IN DEVELOPMENTAL DISABILITIES, 2010, 31 (06) :1543-1551
[6]   The contribution of de novo coding mutations to autism spectrum disorder [J].
Iossifov, Ivan ;
O'Roak, Brian J. ;
Sanders, Stephan J. ;
Ronemus, Michael ;
Krumm, Niklas ;
Levy, Dan ;
Stessman, Holly A. ;
Witherspoon, Kali T. ;
Vives, Laura ;
Patterson, Karynne E. ;
Smith, Joshua D. ;
Paeper, Bryan ;
Nickerson, Deborah A. ;
Dea, Jeanselle ;
Dong, Shan ;
Gonzalez, Luis E. ;
Mandell, Jeffrey D. ;
Mane, Shrikant M. ;
Murtha, Michael T. ;
Sullivan, Catherine A. ;
Walker, Michael F. ;
Waqar, Zainulabedin ;
Wei, Liping ;
Willsey, A. Jeremy ;
Yamrom, Boris ;
Lee, Yoon-ha ;
Grabowska, Ewa ;
Dalkic, Ertugrul ;
Wang, Zihua ;
Marks, Steven ;
Andrews, Peter ;
Leotta, Anthony ;
Kendall, Jude ;
Hakker, Inessa ;
Rosenbaum, Julie ;
Ma, Beicong ;
Rodgers, Linda ;
Troge, Jennifer ;
Narzisi, Giuseppe ;
Yoon, Seungtai ;
Schatz, Michael C. ;
Ye, Kenny ;
McCombie, W. Richard ;
Shendure, Jay ;
Eichler, Evan E. ;
State, Matthew W. ;
Wigler, Michael .
NATURE, 2014, 515 (7526) :216-U136
[7]  
Moreno-De-Luca A, 2013, LANCET NEUROL, V12, P406, DOI 10.1016/S1474-4422(13)70011-5
[8]   Mapping autism risk loci using genetic linkage and chromosomal rearrangements [J].
Szatmari, Peter ;
Paterson, Andrew D. ;
Zwaigenbaum, Lonnie ;
Roberts, Wendy ;
Brian, Jessica ;
Liu, Xiao-Qing ;
Vincent, John B. ;
Skaug, Jennifer L. ;
Thompson, Ann P. ;
Senman, Lili ;
Feuk, Lars ;
Qian, Cheng ;
Bryson, Susan E. ;
Jones, Marshall B. ;
Marshall, Christian R. ;
Scherer, Stephen W. ;
Vieland, Veronica J. ;
Bartlett, Christopher ;
Mangin, La Vonne ;
Goedken, Rhinda ;
Segre, Alberto ;
Pericak-Vance, Margaret A. ;
Cuccaro, Michael L. ;
Gilbert, John R. ;
Wright, Harry H. ;
Abramson, Ruth K. ;
Betancur, Catalina ;
Bourgeron, Thomas ;
Gillberg, Christopher ;
Leboyer, Marion ;
Buxbaum, Joseph D. ;
Davis, Kenneth L. ;
Hollander, Eric ;
Silverman, Jeremy M. ;
Hallmayer, Joachim ;
Lotspeich, Linda ;
Sutcliffe, James S. ;
Haines, Jonathan L. ;
Folstein, Susan E. ;
Piven, Joseph ;
Wassink, Thomas H. ;
Sheffield, Val ;
Geschwind, Daniel H. ;
Bucan, Maja ;
Brown, W. Ted ;
Cantor, Rita M. ;
Constantino, John N. ;
Gilliam, T. Conrad ;
Herbert, Martha ;
LaJonchere, Clara .
NATURE GENETICS, 2007, 39 (03) :319-328
[9]   Whole-genome sequencing of quartet families with autism spectrum disorder [J].
Yuen, Ryan K. C. ;
Thiruvahindrapuram, Bhooma ;
Merico, Daniele ;
Walker, Susan ;
Tammimies, Kristiina ;
Hoang, Ny ;
Chrysler, Christina ;
Nalpathamkalam, Thomas ;
Pellecchia, Giovanna ;
Liu, Yi ;
Gazzellone, Matthew J. ;
D'Abate, Lia ;
Deneault, Eric ;
Howe, Jennifer L. ;
Liu, Richard S. C. ;
Thompson, Ann ;
Zarrei, Mehdi ;
Uddin, Mohammed ;
Marshall, Christian R. ;
Ring, Robert H. ;
Zwaigenbaum, Lonnie ;
Ray, Peter N. ;
Weksberg, Rosanna ;
Carter, Melissa T. ;
Fernandez, Bridget A. ;
Roberts, Wendy ;
Szatmari, Peter ;
Scherer, Stephen W. .
NATURE MEDICINE, 2015, 21 (02) :185-191
[10]   De novo mutations in histone-modifying genes in congenital heart disease [J].
Zaidi, Samir ;
Choi, Murim ;
Wakimoto, Hiroko ;
Ma, Lijiang ;
Jiang, Jianming ;
Overton, John D. ;
Romano-Adesman, Angela ;
Bjornson, Robert D. ;
Breitbart, Roger E. ;
Brown, Kerry K. ;
Carriero, Nicholas J. ;
Cheung, Yee Him ;
Deanfield, John ;
DePalma, Steve ;
Fakhro, Khalid A. ;
Glessner, Joseph ;
Hakonarson, Hakon ;
Italia, Michael J. ;
Kaltman, Jonathan R. ;
Kaski, Juan ;
Kim, Richard ;
Kline, Jennie K. ;
Lee, Teresa ;
Leipzig, Jeremy ;
Lopez, Alexander ;
Mane, Shrikant M. ;
Mitchell, Laura E. ;
Newburger, Jane W. ;
Parfenov, Michael ;
Pe'er, Itsik ;
Porter, George ;
Roberts, Amy E. ;
Sachidanandam, Ravi ;
Sanders, Stephan J. ;
Seiden, Howard S. ;
State, Mathew W. ;
Subramanian, Sailakshmi ;
Tikhonova, Irina R. ;
Wang, Wei ;
Warburton, Dorothy ;
White, Peter S. ;
Williams, Ismee A. ;
Zhao, Hongyu ;
Seidman, Jonathan G. ;
Brueckner, Martina ;
Chung, Wendy K. ;
Gelb, Bruce D. ;
Goldmuntz, Elizabeth ;
Seidman, Christine E. ;
Lifton, Richard P. .
NATURE, 2013, 498 (7453) :220-+