Skip to Main Content (Press Enter)

Logo UNILINK
  • ×
  • Home
  • Corsi
  • Insegnamenti
  • Professioni
  • Persone
  • Pubblicazioni
  • Strutture

UNI-FIND
Logo UNILINK

|

UNI-FIND

unilink.it
  • ×
  • Home
  • Corsi
  • Insegnamenti
  • Professioni
  • Persone
  • Pubblicazioni
  • Strutture
  1. Pubblicazioni

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Articolo
Data di Pubblicazione:
2011
Abstract:
Common sequence variants have recently joined rare structural polymorphisms as genetic factors with strong evidence for association with schizophrenia. Here we extend our previous genome-wide association study and meta-analysis (totalling 7 946 cases and 19 036 controls) by examining an expanded set of variants using an enlarged follow-up sample (up to 10 260 cases and 23 500 controls). In addition to previously reported alleles in the major histocompatibility complex region, near neurogranin (NRGN) and in an intron of transcription factor 4 (TCF4), we find two novel variants showing genome-wide significant association: rs2312147[C], upstream of vaccinia-related kinase 2 (VRK2) [odds ratio (OR) = 1.09, P = 1.9 × 10(-9)] and rs4309482[A], between coiled-coiled domain containing 68 (CCDC68) and TCF4, about 400 kb from the previously described risk allele, but not accounted for by its association (OR = 1.09, P = 7.8 × 10(-9)).
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Schizophrenia; Genotype; Risk; Alleles; Polymorphism; Single Nucleotide; Transcription Factors; Humans; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Genetic Predisposition to Disease; Protein-Serine-Threonine Kinases; Genome-Wide Association Study
Elenco autori:
Steinberg, S; De Jong, S; Andreassen, O; Werge, T; Børglum, A; Mors, O; Mortensen, P; Gustafsson, O; Costas, J; Pietiläinen, O; Demontis, D; Papiol, S; Huttenlocher, J; Mattheisen, M; Breuer, R; Vassos, E; Giegling, I; Fraser, G; Walker, N; Tuulio Henriksson, A; Suvisaari, J; Lönnqvist, J; Paunio, T; Agartz, I; Melle, I; Djurovic, S; Strengman, E; Jürgens, G; Glenthøj, B; Terenius, L; Hougaard, D; Ørntoft, T; Wiuf, C; Didriksen, M; Hollegaard, M; Nordentoft, M; Van Winkel, R; Kenis, G; Abramova, L; Kaleda, V; Arrojo, M; Sanjuán, J; Arango, C; Sperling, S; Rossner, M; Ribolsi, M; Magni, V; Siracusano, Alberto; Christiansen, C; Kiemeney, L; Veldink, J; Van Den Berg, L; Ingason, A; Muglia, P; Murray, R; Nöthen, M; Sigurdsson, E; Petursson, H; Thorsteinsdottir, U; Kong, A; Rubino, Ivo; De Hert, M; Réthelyi, J; Bitter, I; Jönsson, E; Golimbet, V; Carracedo, A; Ehrenreich, H; Craddock, N; Owen, M; O'Donovan, M; Ruggeri, M; Tosato, S; Peltonen, L; Ophoff, R; Collier, D; St Clair, D; Rietschel, M; Cichon, S; Stefansson, H; Rujescu, D; Stefansson, K.
Autori di Ateneo:
RIBOLSI MICHELE
Link alla scheda completa:
https://iris.unilink.it/handle/20.500.14085/60101
Pubblicato in:
HUMAN MOLECULAR GENETICS
Journal
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.6.0.0