Works matching IS 15524841 AND DT 2017 AND VI 174 AND IP 4

Results: 16

Issue Information - TOC.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 333, doi. 10.1002/ajmg.b.32484
Publication type:: Article

Cover Image, Volume 174B, Number 4, June 2017.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. i, doi. 10.1002/ajmg.b.32557
Publication type:: Article

Can lncRNAs be indicators for the diagnosis of early onset or acute schizophrenia and distinguish major depressive disorder and generalized anxiety disorder?-A cross validation analysis.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 335, doi. 10.1002/ajmg.b.32521

By:

Cui, Xuelian;
Niu, Wei;
Kong, Lingming;
He, Mingjun;
Jiang, Kunhong;
Chen, Shengdong;
Zhong, Aifang;
Li, Wanshuai;
Lu, Jim;
Zhang, Liyi

Publication type:

Article

Visuoperceptual processing in children with neurofibromatosis type 1: True deficit or artefact?

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 342, doi. 10.1002/ajmg.b.32522

By:

Van Eylen, Lien;
Plasschaert, Ellen;
Wagemans, Johan;
Boets, Bart;
Legius, Eric;
Steyaert, Jean;
Noens, Ilse

Publication type:

Article

Delusional and psychotic disorders in juvenile myotonic dystrophy type-1.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 359, doi. 10.1002/ajmg.b.32524

By:

Jacobs, Delphine;
Willekens, Diane;
de Die‐Smulders, Christine;
Frijns, Jean‐Pierre;
Steyaert, Jean

Publication type:

Article

Developmental trajectories for young children with 16p11.2 copy number variation.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 367, doi. 10.1002/ajmg.b.32525

By:

Bernier, Raphael;
Hudac, Caitlin M.;
Chen, Qixuan;
Zeng, Chubing;
Wallace, Arianne Stevens;
Gerdts, Jennifer;
Earl, Rachel;
Peterson, Jessica;
Wolken, Anne;
Peters, Alana;
Hanson, Ellen;
Goin‐Kochel, Robin P.;
Kanne, Stephen;
Snyder, LeeAnne Green;
Chung, Wendy K.

Publication type:

Article

Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 381, doi. 10.1002/ajmg.b.32527

By:

Kim, Daniel Seung;
Burt, Amber A.;
Ranchalis, Jane E.;
Wilmot, Beth;
Smith, Joshua D.;
Patterson, Karynne E.;
Coe, Bradley P.;
Li, Yatong K.;
Bamshad, Michael J.;
Nikolas, Molly;
Eichler, Evan E.;
Swanson, James M.;
Nigg, Joel T.;
Nickerson, Deborah A.;
Jarvik, Gail P.

Publication type:

Article

Investigation of SHANK3 in schizophrenia.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 390, doi. 10.1002/ajmg.b.32528

By:

de Sena Cortabitarte, Ana;
Degenhardt, Franziska;
Strohmaier, Jana;
Lang, Maren;
Weiss, Birgit;
Roeth, Ralph;
Giegling, Ina;
Heilmann‐Heimbach, Stefanie;
Hofmann, Andrea;
Rujescu, Dan;
Fischer, Christine;
Rietschel, Marcella;
Nöthen, Markus M.;
Rappold, Gudrun A.;
Berkel, Simone

Publication type:

Article

FMR1 genotype interacts with parenting stress to shape health and functional abilities in older age.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 399, doi. 10.1002/ajmg.b.32529

By:

Mailick, Marsha;
Hong, Jinkuk;
Greenberg, Jan;
Dawalt, Leann Smith;
Baker, Mei Wang;
Rathouz, Paul J.

Publication type:

Article

Genetic risk variants for social anxiety.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 470, doi. 10.1002/ajmg.b.32541

By:

Stein, Murray B.;
Chen, Chia‐Yen;
Jain, Sonia;
Jensen, Kevin P.;
He, Feng;
Heeringa, Steven G.;
Kessler, Ronald C.;
Maihofer, Adam;
Nock, Matthew K.;
Ripke, Stephan;
Sun, Xiaoying;
Thomas, Michael L.;
Ursano, Robert J.;
Smoller, Jordan W.;
Gelernter, Joel

Publication type:

Article

Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 413, doi. 10.1002/ajmg.b.32530

By:

Jia, Peilin;
Zhao, Zhongming;
Hulgan, Todd;
Bush, William S.;
Samuels, David C.;
Bloss, Cinnamon S.;
Heaton, Robert K.;
Ellis, Ronald J.;
Schork, Nicholas;
Marra, Christina M.;
Collier, Ann C.;
Clifford, David B.;
Gelman, Benjamin B.;
Sacktor, Ned;
Morgello, Susan;
Simpson, David M.;
McCutchan, J. Allen;
Barnholtz‐Sloan, Jill S.;
Franklin, Donald R.;
Rosario, Debralee

Publication type:

Article

The genome-wide expression effects of escitalopram and its relationship to neurogenesis, hippocampal volume, and antidepressant response.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 427, doi. 10.1002/ajmg.b.32532

By:

Powell, Timothy R.;
Murphy, Tytus;
de Jong, Simone;
Lee, Sang Hyuck;
Tansey, Katherine E.;
Hodgson, Karen;
Uher, Rudolf;
Price, Jack;
Thuret, Sandrine;
Breen, Gerome

Publication type:

Article

Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 435, doi. 10.1002/ajmg.b.32533

By:

Peng, Qian;
Schork, Nicholas J.;
Wilhelmsen, Kirk C.;
Ehlers, Cindy L.

Publication type:

Article

Familial cases and male cases with MECP2 mutations.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 451, doi. 10.1002/ajmg.b.32534

By:

Zhang, Qingping;
Zhao, Ying;
Bao, Xinhua;
Luo, Jinjun;
Zhang, Xiaoying;
Li, Jiarui;
Wei, Liping;
Wu, Xiru

Publication type:

Article

Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 458, doi. 10.1002/ajmg.b.32535

By:

Bidwell, L. Cinnamon;
Gray, Joshua C.;
Weafer, Jessica;
Palmer, Abraham A.;
de Wit, Harriet;
MacKillop, James

Publication type:

Article

Anxiety genetics: Dispatches from the frontier.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 467, doi. 10.1002/ajmg.b.32539

By:

Smoller, Jordan W.

Publication type:

Article