Works matching IS 15524841 AND DT 2013 AND VI 162B AND IP 8

Results: 13

The XY gene hypothesis of psychosis: Origins and current status.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 800, doi. 10.1002/ajmg.b.32202
By:
- Crow, Timothy J.
Publication type:
Article
Genetic predictors of risk and resilience in psychiatric disorders: A cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 779, doi. 10.1002/ajmg.b.32190
By:
- McGrath, Lauren M.;
- Cornelis, Marilyn C.;
- Lee, Phil H.;
- Robinson, Elise B.;
- Duncan, Laramie E.;
- Barnett, Jennifer H.;
- Huang, Jie;
- Gerber, Gloria;
- Sklar, Pamela;
- Sullivan, Patrick;
- Perlis, Roy H.;
- Smoller, Jordan W.
Publication type:
Article
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 832, doi. 10.1002/ajmg.b.32187
By:
- An, Yu;
- Amr, Sami S.;
- Torres, Alcy;
- Weissman, Laura;
- Raffalli, Peter;
- Cox, Gerald;
- Sheng, Xiaoming;
- Lip, Va;
- Bi, Weimin;
- Patel, Ankita;
- Stankiewicz, Pawel;
- Wu, Bai‐Lin;
- Shen, Yiping
Publication type:
Article
Epigenetic studies in Alzheimer's disease: Current findings, caveats, and considerations for future studies.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 789, doi. 10.1002/ajmg.b.32201
By:
- Lunnon, Katie;
- Mill, Jonathan
Publication type:
Article
High frequency of intermediate alleles on huntington disease-associated haplotypes in British Columbia's general population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 864, doi. 10.1002/ajmg.b.32193
By:
- Semaka, Alicia;
- Kay, Chris;
- Doty, Crystal N.;
- Collins, Jennifer A.;
- Tam, Natalie;
- Hayden, Michael R.
Publication type:
Article
Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 825, doi. 10.1002/ajmg.b.32186
By:
- Melchior, Linea;
- Bertelsen, Birgitte;
- Debes, Nanette Mol;
- Groth, Camilla;
- Skov, Liselotte;
- Mikkelsen, Jens D;
- Brøndum‐Nielsen, Karen;
- Tümer, Zeynep
Publication type:
Article
Mood disorders in individuals with distal 18q deletions.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 879, doi. 10.1002/ajmg.b.32197
By:
- Daviss, William B.;
- O'Donnell, Louise;
- Soileau, Bridgette T.;
- Heard, Patricia;
- Carter, Erika;
- Pliszka, Steven R.;
- Gelfond, Jonathan A. L.;
- Hale, Daniel E.;
- Cody, Jannine D.
Publication type:
Article
Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence-based prioritization algorithm.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 898, doi. 10.1002/ajmg.b.32200
By:
- Bigdeli, T. Bernard;
- Maher, Brion S.;
- Zhao, Zhongming;
- Sun, Jingchun;
- Medeiros, Helena;
- Akula, Nirmala;
- McMahon, Francis J.;
- Carvalho, Celia;
- Ferreira, Susana R.;
- Azevedo, Maria H.;
- Knowles, James A.;
- Pato, Michele T.;
- Pato, Carlos N.;
- Fanous, Ayman H.
Publication type:
Article
Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated german multi-generation families.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 855, doi. 10.1002/ajmg.b.32192
By:
- Lin, Michelle K.;
- Freitag, Christine M.;
- Schote, Andrea B.;
- Pálmason, Haukur;
- Seitz, Christiane;
- Renner, Tobias J.;
- Romanos, Marcel;
- Walitza, Susanne;
- Jacob, Christian P.;
- Reif, Andreas;
- Warnke, Andreas;
- Cantor, Rita M.;
- Lesch, Klaus‐Peter;
- Meyer, Jobst
Publication type:
Article
High rates of comorbid depressive and anxiety disorders among women with premutation of the FMR1 gene.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 872, doi. 10.1002/ajmg.b.32196
By:
- Kenna, Heather A.;
- Tartter, Molly;
- Hall, Scott S.;
- Lightbody, Amy A.;
- Nguyen, Quynh;
- de los Angeles, C. Paula;
- Reiss, Allan L.;
- Rasgon, Natalie L.
Publication type:
Article
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 847, doi. 10.1002/ajmg.b.32189
By:
- Derks, Eske M.;
- Ayub, Muhammad;
- Chambert, Kimberly;
- Del Favero, Jurgen;
- Johnstone, Mandy;
- MacGregor, Stuart;
- Maclean, Alan;
- McKechanie, Andrew G.;
- McRae, Allan F.;
- Moran, Jennifer L.;
- Pickard, Benjamin S.;
- Purcell, Shaun;
- Sklar, Pamela;
- StCLair, David M.;
- Wray, Naomi R.;
- Visscher, Peter M.;
- Blackwood, Douglas H. R.
Publication type:
Article
Reaffirmation of GAK, but not HLA-DRA, as a Parkinson's disease susceptibility gene in a Taiwanese population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 841, doi. 10.1002/ajmg.b.32188
By:
- Lin, Chin‐Hsien;
- Chen, Meng‐Ling;
- Tai, Yi‐Cheng;
- Yu, Chin‐Yi;
- Wu, Ruey‐Meei
Publication type:
Article
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 889, doi. 10.1002/ajmg.b.32199
By:
- Veerappa, Avinash M.;
- Saldanha, Marita;
- Padakannaya, Prakash;
- Ramachandra, Nallur B.
Publication type:
Article