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Association of the manganese superoxide dismutase gene Ala-9Val polymorphism with age of smoking initiation in male schizophrenia smokers.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 243, doi. 10.1002/ajmg.b.32398
By:
- Zhang, Xiang Yang;
- Rao, Wen‐Wang;
- Yu, Qiong;
- Yu, Yaqin;
- Kou, Changgui;
- Tan, Yun‐Long;
- Chen, Da‐Chun;
- Zuo, Lingjun;
- Luo, Xiangguang;
- Soares, Jair C.
Publication type:
Article
Influence of family history of dementia in the development and progression of late-onset Alzheimer's disease.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 250, doi. 10.1002/ajmg.b.32399
By:
- Scarabino, Daniela;
- Gambina, Giuseppe;
- Broggio, Elisabetta;
- Pelliccia, Franca;
- Corbo, Rosa Maria
Publication type:
Article
Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 175, doi. 10.1002/ajmg.b.32390
By:
- Cervera‐Carles, Laura;
- Pagonabarraga, Javier;
- Pascual‐Sedano, Berta;
- Pastor, Pau;
- Campolongo, Antonia;
- Fortea, Juan;
- Blesa, Rafael;
- Alcolea, Daniel;
- Morenas‐Rodríguez, Estrella;
- Sala, Isabel;
- Lleó, Alberto;
- Kulisevsky, Jaime;
- Clarimón, Jordi
Publication type:
Article
Issue Information - TOC.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 143, doi. 10.1002/ajmg.b.32367
Publication type:
Article
Common variants in QPCT gene confer risk of schizophrenia in the Han Chinese population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 237, doi. 10.1002/ajmg.b.32397
By:
- Khan, Raja Amjad Waheed;
- Chen, Jianhua;
- Shen, Jiawei;
- Li, Zhiqiang;
- Wang, Meng;
- Wen, Zujia;
- Song, Zhijian;
- Li, Wenjin;
- Xu, Yifeng;
- Shi, Yongyong;
- Yi, Qizhong;
- Ji, Weidong
Publication type:
Article
Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 181, doi. 10.1002/ajmg.b.32391
By:
- Butler, Merlin G.;
- McGuire, Austen B.;
- Masoud, Humaira;
- Manzardo, Ann M.
Publication type:
Article
Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 203, doi. 10.1002/ajmg.b.32392
By:
- Kong, Rui;
- Shao, Shanshan;
- Wang, Jia;
- Zhang, Xiaohui;
- Guo, Shengnan;
- Zou, Li;
- Zhong, Rong;
- Lou, Jiao;
- Zhou, Jie;
- Zhang, Jiajia;
- Song, Ranran
Publication type:
Article
A role for HLA-DRB1*1101 and DRB1*0801 in cognitive ability and its decline with age.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 209, doi. 10.1002/ajmg.b.32393
By:
- Payton, Antony;
- Dawes, Piers;
- Platt, Hazel;
- Morton, Cynthia C.;
- Moore, David R.;
- Massey, Jonathan;
- Horan, Michael;
- Ollier, William;
- Munro, Kevin J.;
- Pendleton, Neil
Publication type:
Article
Does refining the phenotype improve replication rates? A review and replication of candidate gene studies on Major Depressive Disorder and Chronic Major Depressive Disorder.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 215, doi. 10.1002/ajmg.b.32396
By:
- Luo, Xiaochen;
- Stavrakakis, Nikolaos;
- Penninx, Brenda W.;
- Bosker, Fokko J.;
- Nolen, Willem A.;
- Boomsma, Dorret I.;
- de Geus, Eco J.;
- Smit, Johan H.;
- Snieder, Harold;
- Nolte, Ilja M.;
- Hartman, Catharina A.
Publication type:
Article
TPH2 gene polymorphisms and bipolar disorder: A meta-analysis.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 145, doi. 10.1002/ajmg.b.32381
By:
- Gao, Jin;
- Jia, Mingrui;
- Qiao, Dongdong;
- Qiu, Huimin;
- Sokolove, Jeremy;
- Zhang, Jingxuan;
- Pan, Zhenglun
Publication type:
Article
The association between childhood autistic traits and adolescent psychotic experiences is explained by general neuropsychiatric problems.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 153, doi. 10.1002/ajmg.b.32386
By:
- Cederlöf, Martin;
- Pettersson, Erik;
- Sariaslan, Amir;
- Larsson, Henrik;
- Östberg, Per;
- Kelleher, Ian;
- Långström, Niklas;
- Gumpert, Clara Hellner;
- Lundström, Sebastian;
- Lichtenstein, Paul
Publication type:
Article
Telomere longitudinal shortening as a biomarker for dementia status of adults with Down syndrome.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 169, doi. 10.1002/ajmg.b.32389
By:
- Jenkins, Edmund C.;
- Ye, Lingling;
- Krinsky‐McHale, Sharon J.;
- Zigman, Warren B.;
- Schupf, Nicole;
- Silverman, Wayne P.
Publication type:
Article
No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 160, doi. 10.1002/ajmg.b.32387
By:
- Li, Ming;
- Huang, Liang;
- Wang, Jinkai;
- Su, Bing;
- Luo, Xiong‐Jian
Publication type:
Article
Genome-wide association study with the risk of schizophrenia in a Korean population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 257, doi. 10.1002/ajmg.b.32400
By:
- Kim, Lyoung Hyo;
- Park, Byung Lae;
- Cheong, Hyun Sub;
- Namgoong, Suhg;
- Kim, Ji On;
- Kim, Jeong‐Hyun;
- Shin, Joong‐Gon;
- Park, Chul Soo;
- Kim, Bong‐Jo;
- Kim, Jae Won;
- Choi, Ihn‐Geun;
- Hwang, Jaeuk;
- Shin, Hyoung Doo;
- Woo, Sung‐Il
Publication type:
Article
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 276, doi. 10.1002/ajmg.b.32402
By:
- Bigdeli, Tim B.;
- Ripke, Stephan;
- Bacanu, Silviu‐Alin;
- Lee, Sang Hong;
- Wray, Naomi R.;
- Gejman, Pablo V.;
- Rietschel, Marcella;
- Cichon, Sven;
- St Clair, David;
- Corvin, Aiden;
- Kirov, George;
- McQuillin, Andrew;
- Gurling, Hugh;
- Rujescu, Dan;
- Andreassen, Ole A.;
- Werge, Thomas;
- Blackwood, Douglas H. R.;
- Pato, Carlos N.;
- Pato, Michele T.;
- Malhotra, Anil K.
Publication type:
Article
Transcranial direct current stimulation reduces food-craving and measures of hyperphagia behavior in participants with Prader-Willi syndrome.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 266, doi. 10.1002/ajmg.b.32401
By:
- Bravo, Gabriela L.;
- Poje, Albert B.;
- Perissinotti, Iago;
- Marcondes, Bianca F.;
- Villamar, Mauricio F.;
- Manzardo, Ann M.;
- Luque, Laura;
- LePage, Jean F.;
- Stafford, Diane;
- Fregni, Felipe;
- Butler, Merlin G.
Publication type:
Article
What are the benefits of phenotype analyses to special education?
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 301, doi. 10.1002/ajmg.b.32405
By:
- Lee, Brason
Publication type:
Article
A need for precision medicine to enable tailored special education.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 300, doi. 10.1002/ajmg.b.32404
By:
- Polyak, Andrew;
- Girirajan, Santhosh
Publication type:
Article
A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 290, doi. 10.1002/ajmg.b.32406
By:
- Biamino, Elisa;
- Di Gregorio, Eleonora;
- Belligni, Elga Fabia;
- Keller, Roberto;
- Riberi, Evelise;
- Gandione, Marina;
- Calcia, Alessandro;
- Mancini, Cecilia;
- Giorgio, Elisa;
- Cavalieri, Simona;
- Pappi, Patrizia;
- Talarico, Flavia;
- Fea, Antonio M.;
- De Rubeis, Silvia;
- Cirillo Silengo, Margherita;
- Ferrero, Giovanni Battista;
- Brusco, Alfredo
Publication type:
Article

Found: 19

Association of the manganese superoxide dismutase gene Ala-9Val polymorphism with age of smoking initiation in male schizophrenia smokers.

Influence of family history of dementia in the development and progression of late-onset Alzheimer's disease.

Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases.

Issue Information - TOC.

Common variants in QPCT gene confer risk of schizophrenia in the Han Chinese population.

Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation.

Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population.

A role for HLA-DRB11101 and DRB10801 in cognitive ability and its decline with age.

Does refining the phenotype improve replication rates? A review and replication of candidate gene studies on Major Depressive Disorder and Chronic Major Depressive Disorder.

TPH2 gene polymorphisms and bipolar disorder: A meta-analysis.

The association between childhood autistic traits and adolescent psychotic experiences is explained by general neuropsychiatric problems.

Telomere longitudinal shortening as a biomarker for dementia status of adults with Down syndrome.

No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects.

Genome-wide association study with the risk of schizophrenia in a Korean population.

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.

Transcranial direct current stimulation reduces food-craving and measures of hyperphagia behavior in participants with Prader-Willi syndrome.

What are the benefits of phenotype analyses to special education?

A need for precision medicine to enable tailored special education.

A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity.