ISSN 0955-8829 (Print); ISSN 1473-5873 (Online)
Publisher: Wolters Kluwer
A systematic review and meta-analysis of the association between the apolipoprotein E genotype and delirium pp. 53-59(7) Authors: Adamis, Dimitrios; Meagher, David; Williams, John; Mulligan, Owen; McCarthy, Geraldine
Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation pp. 60-65(6) Authors: Carroll, Liam S.; Woolf, Rebecca; Ibrahim, Yousef; Williams, Hywel J.; Dwyer, Sarah; Walters, James; Kirov, George; O’Donovan, Michael C.; Owen, Michael J.
Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability pp. 66-73(8) Authors: Vasli, Nasim; Ahmed, Iltaf; Mittal, Kirti; Ohadi, Mehrnaz; Mikhailov, Anna; Rafiq, Muhammad A.; Bhatti, Attya; Carter, Melissa T.; Andrade, Danielle M.; Ayub, Muhammad; Vincent, John B.; John, Peter
Parents’ attitudes toward genetic research in autism spectrum disorder pp. 74-80(7) Authors: Johannessen, Jarle; Nærland, Terje; Bloss, Cinnamon; Rietschel, Marcella; Strohmaier, Jana; Gjevik, Elen; Heiberg, Arvid; Djurovic, Srdjan; Andreassen, Ole A.
Lack of association of SNPs from the FADS1-FADS2 gene cluster with major depression or suicidal behavior pp. 81-86(6) Authors: Sublette, M. Elizabeth; Vaquero, Concepcion; Baca-Garcia, Enrique; Pachano, Gabriela; Huang, Yung-yu; Oquendo, Maria A.; Mann, J. John
Meta-analysis of the association between a serotonin transporter 5-HTTLPR polymorphism and smoking cessation pp. 87-91(5) Authors: Choi, Hye D.; Shin, Wan G.
The C9ORF72 expansion sizes in patients with psychosis: a population-based study on the Northern Finland Birth Cohort 1966 pp. 92-94(3) Authors: Solje, Eino; Miettunen, Jouko; Marttila, Riikka; Helisalmi, Seppo; Laitinen, Marjo; Koivumaa-Honkanen, Heli; Isohanni, Matti; Hiltunen, Mikko; Jääskeläinen, Erika; Remes, Anne M.
Complex genomic variants contribute toward the genetic architecture of autism spectrum disorder pp. 95-96(2) Authors: Chen, Chia-Hsiang; Liao, Hsiao-Mei; Chen, Hsin-I; Fang, Jye-Siung; Chen, Yan-Jang; Lee, Kuei-Fang; Gau, Susan Shur-Fen
No association of GRIA1 polymorphisms with schizophrenia in the Chinese Han population pp. 97-98(2) Authors: Niu, Weibo; Huang, Xiaoye; Yu, Tao; Chen, Shiqing; Li, Xingwang; Wu, Xi; Cao, Yanfei; Zhang, Rui; Bi, Yan; Yang, Fengping; Wang, Lu; Li, Weidong; Xu, Yifeng; He, Lin; He, Guang
Genetic variant analysis of the putative regulatory regions of the LRRC7 gene in bipolar disorder pp. 99-100(2) Authors: Fiorentino, Alessia; Sharp, Sally I.; Kandaswamy, Radhika; Gurling, Hugh M.D.; Bass, Nicholas J.; McQuillin, Andrew