RNA-binding activity of TRIM25 is mediated by its PRY/SPRY domain and is required for ubiquitination.

BMC Biol     Nila Roy Choudhury , Gregory Heikel , Maryia Trubitsyna , Peter Kubik , Jakub Stanislaw Nowak , Shaun Webb , Sander Granneman , Christos Spanos , Juri Rappsilber , Alfredo Castello , Gracjan Michlewski

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes.

Mol. Psychiatry     M A Carless , D C Glahn , M P Johnson , J E Curran , K Bozaoglu , T D Dyer , A M Winkler , S A Cole , L Almasy , J W MacCluer , R Duggirala , E K Moses , H H H Göring , J Blangero

Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.

Haematologica     Rachel Wade , Maria Chiara Di Bernardo , Sue Richards , Davide Rossi , Dalemari Crowther-Swanepoel , Gianluca Gaidano , David G Oscier , Daniel Catovsky , Richard S Houlston

Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies.

Mol Psychiatry     A Schosser , D Gaysina , S Cohen-Woods , P C Chow , L Martucci , N Craddock , A Farmer , A Korszun , C Gunasinghe , J Gray , L Jones , F Tozzi , J Perry , P Muglia , M J Owen , I W Craig , P McGuffin

Expression of conjoined genes: another mechanism for gene regulation in eukaryotes.

PLoS ONE     Tulika Prakash , Vineet K Sharma , Naoki Adati , Ritsuko Ozawa , Naveen Kumar , Yuichiro Nishida , Takayoshi Fujikake , Tadayuki Takeda , Todd D Taylor

DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms.

Proc Natl Acad Sci U S A     Kenji Nakata , Barbara K Lipska , Thomas M Hyde , Tianzhang Ye , Erin N Newburn , Yukitaka Morita , Radhakrishna Vakkalanka , Maxim Barenboim , Yoshitatsu Sei , Daniel R Weinberger , Joel E Kleinman

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.

Proc Natl Acad Sci U S A     John E Landers , Judith Melki , Vincent Meininger , Jonathan D Glass , Leonard H van den Berg , Michael A van Es , Peter C Sapp , Paul W J van Vught , Diane M McKenna-Yasek , Hylke M Blauw , Ting-Jan Cho , Meraida Polak , Lijia Shi , Anne-Marie Wills , Wendy J Broom , Nicola Ticozzi , Vincenzo Silani , Aslihan Ozoguz , Ildefonso Rodriguez-Leyva , Jan H Veldink , Adrian J Ivinson , Christiaan G J Saris , Betsy A Hosler , Alayna Barnes-Nessa , Nicole Couture , John H J Wokke , Thomas J Kwiatkowski , Roel A Ophoff , Simon Cronin , Orla Hardiman , Frank P Diekstra , P Nigel Leigh , Christopher E Shaw , Claire L Simpson , Valerie K Hansen , John F Powell , Philippe Corcia , François Salachas , Simon Heath , Pilar Galan , Franck Georges , H Robert Horvitz , Mark Lathrop , Shaun Purcell , Ammar Al-Chalabi , Robert H Brown

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.

Am. J. Hum. Genet.     Gary W Beecham , Eden R Martin , Yi-Ju Li , Michael A Slifer , John R Gilbert , Jonathan L Haines , Margaret A Pericak-Vance

Chromosomal location and genomic structure of the human translin-associated factor X gene (TRAX; TSNAX) revealed by intergenic splicing to DISC1, a gene disrupted by a translocation segregating with schizophrenia.

Genomics     J K Millar , S Christie , C A Semple , D J Porteous