ZDHHC8 Single Nucleotide Polymorphism rs175174 is not associated with psychiatric features of the 22q11 Deletion Syndrome or Schizophrenia [1]

Psychiatric Genetics

Volumn 17, Issue 5, 2007, Pages 311-312

  Demily, Caroline ^a,b   Legallic, Solenn ^b   Bou, Jacqueline ^b   Houy Durand, Emmanuelle ^b   Van Amelsvoort, Thérèse ^c   Zinkstok, Janneke ^c   Manouvrier Hanue, Sylvie ^d   Vogels, Annick ^e   Drouin Garraud, Valérie ^b   Philip, Nicole ^f   Philippe, Anne ^g   Héron, Delphine ^h   Sarda, Pierre ⁱ   Petit, Michel ^b   Thibaut, Florence ^b   Frébourg, Thierry ^b   Campion, Dominique ^b  

^a INSTITUT DES SCIENCES COGNITIVES   (France)

^b ROUEN UNIVERSITY HOSPITAL   (France)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d LILLE UNIVERSITY HOSPITAL   (France)

^e UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^f CHRU Nord   (France)

^g HÔPITAL NECKER ENFANTS MALADES   (France)

^h PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

ⁱ MONTPELLIER UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

22Q11 DELETION SYNDROME; ALLELE; CASE CONTROL STUDY; CAUCASIAN; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; FEMALE; GENE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INTERVIEW; LETTER; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PSYCHOSIS; RISK ASSESSMENT; SCHIZOPHRENIA; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; SYNDROME; VELOCARDIOFACIAL SYNDROME; ZDHHC8 GENE;

EID: 34548354956     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/YPG.0b013e328133f369     Document Type: Letter

References (4)

1. Chen WY, Shi YY, Zheng YL, Zhao XZ, Zhang GJ, Chen SQ, et al. (2004). Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Hum Mol Genet 13:2991-2995.
2. Glaser B, Schumacher J, Williams HJ, Jamra RA, Ianakiev N, Milev R, et al. (2005). No association between the putative functional ZDHHC8 single nucleotide polymorphism and schizophrenia in large European sample. Biol Psychiatry 58:78-80.
3. Mukaï J, Liu H, Burt RA, Swor DE, Lai WS, Karayiorgou M, Gogos J (2004). Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. Nat Genet 36:725-731.
4. Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, et al. (2007). Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Hum Mol Genet 16:83-91.