Works matching IS 15524841 AND DT 2018 AND VI 177 AND IP 1

Results: 13

Cover Image, Volume 177B, Number 1, January 2018.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. i, doi. 10.1002/ajmg.b.32617

By:

Farhan, Sali M. K.;
Gendron, Tania F.;
Petrucelli, Leonard;
Hegele, Robert A.;
Strong, Michael J.

Publication type:

Article

A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 21, doi. 10.1002/ajmg.b.32581

By:

Ranlund, Siri;
Calafato, Stella;
Thygesen, Johan H.;
Lin, Kuang;
Cahn, Wiepke;
Crespo‐Facorro, Benedicto;
de Zwarte, Sonja M. C.;
Díez, Álvaro;
Di Forti, Marta;
GROUP;
Iyegbe, Conrad;
Jablensky, Assen;
Jones, Rebecca;
Hall, Mei‐Hua;
Kahn, Rene;
Kalaydjieva, Luba;
Kravariti, Eugenia;
McDonald, Colm;
McIntosh, Andrew M.;
McQuillin, Andrew

Publication type:

Article

Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 10, doi. 10.1002/ajmg.b.32574

By:

Zhao, Jin J.;
Halvardson, Jonatan;
Zander, Cecilia S.;
Zaghlool, Ammar;
Georgii‐Hemming, Patrik;
Månsson, Else;
Brandberg, Göran;
Sävmarker, Helena E.;
Frykholm, Carina;
Kuchinskaya, Ekaterina;
Thuresson, Ann‐Charlotte;
Feuk, Lars

Publication type:

Article

Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 40, doi. 10.1002/ajmg.b.32593

By:

Van der Auwera, Sandra;
Peyrot, Wouter J.;
Milaneschi, Yuri;
Hertel, Johannes;
Baune, Bernhard;
Breen, Gerome;
Byrne, Enda;
Dunn, Erin C.;
Fisher, Helen;
Homuth, Georg;
Levinson, Douglas;
Lewis, Cathryn;
Mills, Natalie;
Mullins, Niamh;
Nauck, Matthias;
Pistis, Giorgio;
Preisig, Martin;
Rietschel, Marcella;
Ripke, Stephan;
Sullivan, Patrick

Publication type:

Article

Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 101, doi. 10.1002/ajmg.b.32610

By:

Balci, Tugce B.;
Davila, Jorge;
Lewis, Denice;
Boafo, Addo;
Sell, Erick;
Richer, Julie;
Nikkel, Sarah M.;
Armour, Christine M.;
Tomiak, Eva;
Lines, Matthew A.;
Sawyer, Sarah L.

Publication type:

Article

Association study of NDST3 gene for schizophrenia, bipolar disorder, major depressive disorder in the Han Chinese population.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 3, doi. 10.1002/ajmg.b.32573

By:

Wang, Lin;
Chen, Jianhua;
Li, Zhiqiang;
Sun, Weiming;
Chen, Boyu;
Li, Sining;
Li, Weidong;
Lu, Dajiang;
Wang, Yonggang;
Shi, Yongyong

Publication type:

Article

Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 35, doi. 10.1002/ajmg.b.32582

By:

Quarrell, Oliver W.;
Clarke, Angus J.;
Compton, Cecilia;
de Die‐Smulders, Christine E. M.;
Fryer, Alan;
Jenkins, Sian;
Lahiri, Nayana;
MacLeod, Rhona;
Miedzybrodzka, Zosia;
Morrison, Patrick J.;
Musgrave, Hannah;
O'Driscoll, Mary;
Strong, Mark;
van Belzen, Martine J.;
Vermeer, Sascha;
Verschuuren‐Bemelmans, Corien C.;
Bijlsma, Emilia K.

Publication type:

Article

Issue Information - TOC.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 1, doi. 10.1002/ajmg.b.32584
Publication type:: Article

Contribution of genes in the GABAergic pathway to bipolar disorder and its executive function deficit in the Chinese Han population.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 50, doi. 10.1002/ajmg.b.32601

By:

Ren, Hongyan;
Guan, Lijie;
Zhao, Liansheng;
Lin, Yin;
Wang, Yincheng;
Yang, Zhenxing;
Li, Xuan;
Ma, Xiaohong;
Cheng, Xiongchao;
Deng, Wenhao;
Aitchison, Katherine J.;
Cao, Liping;
Li, Tao

Publication type:

Article

Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 68, doi. 10.1002/ajmg.b.32605

By:

Nicolas, Gaël;
Charbonnier, Camille;
Campion, Dominique;
Veltman, Joris A.

Publication type:

Article

OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 75, doi. 10.1002/ajmg.b.32606

By:

Farhan, Sali M. K.;
Gendron, Tania F.;
Petrucelli, Leonard;
Hegele, Robert A.;
Strong, Michael J.

Publication type:

Article

Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 86, doi. 10.1002/ajmg.b.32607

By:

Gui, Hongsheng;
Li, Miaoxin;
Sham, Pak C.;
Baum, Larry;
International League Against Epilepsy Consortium on Complex Epilepsies;
Kwan, Patrick;
Cherny, Stacey S.

Publication type:

Article

Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 1, p. 93, doi. 10.1002/ajmg.b.32608

By:

Zhang, Yanqing;
Liu, Yi;
Zarrei, Mehdi;
Tong, Winnie;
Dong, Rui;
Wang, Ying;
Zhang, Haiyan;
Yang, Xiaomeng;
MacDonald, Jeffrey R.;
Uddin, Mohammed;
Scherer, Stephen W.;
Gai, Zhongtao

Publication type:

Article