Psychotic disorders (incl schizophrenia)

Citations 1-10 of 22 total displayed.

Original articles
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders

S Ben-Shachar, B Lanpher, J R German, M Qasaymeh, L Potocki, S C Sreenath Nagamani, L M Franco, A Malphrus, G W Bottenfield, J E Spence, S Amato, J A Rousseau, B Moghaddam, C Skinner, S A Skinner, S Bernes, N Armstrong, M Shinawi, P Stankiewicz, A Patel, S-W Cheung, J R Lupski, A L Beaudet, T Sahoo
J. Med. Genet. 2009 46: 382 -388; published online before print as 10.1136/jmg.2008.064378 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Premature death in adults with 22q11.2 deletion syndrome

A S Bassett, E W C Chow, J Husted, K A Hodgkinson, E Oechslin, L Harris, C Silversides
J. Med. Genet. 2009 46: 324 -330; published online before print as 10.1136/jmg.2008.063800 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Association of haplotypes spanning PDZ-GEF2, LOC728637 and ACSL6 with schizophrenia in Han Chinese

X-j Luo, H-b Diao, J-k Wang, H Zhang, Z-m Zhao, B Su
J. Med. Genet. 2008 45: 818 -826; published online before print as 10.1136/jmg.2008.060657 [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendix ]  

Letters to JMG
Connexin 50 gene on human chromosome 1q21 is associated with schizophrenia in matched case–control and family-based studies

Xingqun Ni, Jose Valente, Maria H Azevedo, Michelle T Pato, Carlos N Pato, James L Kennedy
J. Med. Genet. 2007 44: 532 -536; published online before print as 10.1136/jmg.2006.047944 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

J L Seal, M C Gornick, N Gogtay, P Shaw, D K Greenstein, M Coffey, P A Gochman, T Stromberg, Z Chen, B Merriman, S F Nelson, J Brooks, S Arepalli, F Wavrant-De Vrièze, J Hardy, J L Rapoport, A M Addington
J. Med. Genet. 2006 43: 887 -892; published online before print as 10.1136/jmg.2006.043380 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

M L Hamshere, N M Williams, N Norton, H Williams, A G Cardno, S Zammit, L A Jones, K C Murphy, R D Sanders, G McCarthy, M Y Gray, G Jones, P Holmans, M C O’Donovan, M J Owen, N Craddock
J. Med. Genet. 2006 43: 563 -567; published online before print as 10.1136/jmg.2005.035345 [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy

J Vijai, A Kapoor, H M Ravishankar, P J Cherian, G Kuruttukulam, B Rajendran, R Sridharan, G Rangan, A S Girija, S Jayalakshmi, S Mohandas, K S Mani, K Radhakrishnan, A Anand
J. Med. Genet. 2005; 42: 439-442. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
The ser9gly SNP in the dopamine D₃ receptor causes a shift from cAMP related to PGE₂ related signal transduction mechanisms in transfected CHO cells

M Hellstrand, E A Danielsen, V M Steen, A Ekman, E Eriksson, C L Nilsson
J. Med. Genet. 2004; 41: 867-871. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Evidence for association between single nucleotide polymorphisms in T complex protein 1 gene and schizophrenia in the Chinese Han population

M S Yang, L Yu, T W Guo, S M Zhu, H J Liu, Y Y Shi, N-F Gu, G Y Feng, L He
J. Med. Genet. 2004; 41: e63. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
Genotype and psychological phenotype in tuberous sclerosis

J C Lewis, H V Thomas, K C Murphy, J R Sampson
J. Med. Genet. 2004; 41: 203-207. [Extract] [Full text] [PDF] [Request Permissions]