Schizophrenia genetics : uncovering positional candidate genesKARAYIORGOU, Maria; GOGOS, Joseph A.European journal of human genetics. 2006, Vol 14, Num 5, pp 512-519, issn 1018-4813, 8 p.Article

Lower prepulse inhibition in children with the 22q11 deletion syndromeSOBIN, Christina; KILEY-BRABECK, Karen; KARAYIORGOU, Maria et al.The American journal of psychiatry. 2005, Vol 162, Num 6, pp 1090-1099, issn 0002-953X, 10 p.Article

The molecular genetics of the 22q11-associated schizophreniaKARAYIORGOU, Maria; GOGOS, Joseph A.Molecular brain research. 2004, Vol 132, Num 2, pp 95-104, issn 0169-328X, 10 p.Conference Paper

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophreniaKARAYIORGOU, Maria; SIMON, Tony J; GOGOS, Joseph A et al.Nature reviews. Neuroscience (Print). 2010, Vol 11, Num 6, pp 402-416, issn 1471-003X, 15 p.Article

Resistance to salt-induced hypertension in catechol-O-methyltransferase-gene-disrupted miceHELKAMAA, Teemu; MÄNNISTÖ, Pekka T; RAUHALA, Pekka et al.Journal of hypertension. 2003, Vol 21, Num 12, pp 2365-2374, issn 0263-6352, 10 p.Article

Convergent evidence for impaired AKT1-GSK3β signaling in schizophreniaEMAMIAN, Effat S; HALL, Diana; BIRNBAUM, Morris J et al.Nature genetics. 2004, Vol 36, Num 2, pp 131-137, issn 1061-4036, 7 p.Article

Networks of attention in children with the 22q11 deletion syndromeSOBIN, Christina; KILEY-BRABECK, Karen; DANIELS, Sarah et al.Developmental neuropsychology. 2004, Vol 26, Num 2, pp 611-626, issn 8756-5641, 16 p.Article

De novo gene mutations highlight patterns of genetic and neural complexity in schizophreniaBIN XU; IONITA-LAZA, Iuliana; LOUW ROOS, J et al.Nature genetics. 2012, Vol 44, Num 12, pp 1365-1369, issn 1061-4036, 5 p.Article

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22qll-deletion mouse modelSTARK, Kimberly L; BIN XU; GOGOS, Joseph A et al.Nature genetics. 2008, Vol 40, Num 6, pp 751-760, issn 1061-4036, 10 p.Article

Stress-Induced Analgesia and Morphine Responses Are Changed in Catechol-O-methyltransferase-Deficient Male MiceKAMBUR, Oleg; MÄNNISTÖ, Pekka T; VILJAKKA, Kaarin et al.Basic & clinical pharmacology & toxicology (Print). 2008, Vol 103, Num 4, pp 367-373, issn 1742-7835, 7 p.Article

Strong association of de novo copy number mutations with sporadic schizophreniaBIN XU; LOUW ROOS, J; LEVY, Shawn et al.Nature genetics. 2008, Vol 40, Num 7, pp 880-885, issn 1061-4036, 6 p.Article

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studiesSERVICE, Susan; DEYOUNG, Joseph; HEUTINK, Peter et al.Nature genetics. 2006, Vol 38, Num 5, pp 556-560, issn 1061-4036, 5 p.Article

Increase in Free Choice Oral Ethanol Self-Administration in Catechol-O-Methyltransferase Gene-Disrupted Male MiceTAMMIMAKI, Anne; FORSBERG, Markus M; KARAYIORGOU, Maria et al.Basic & clinical pharmacology & toxicology (Print). 2008, Vol 103, Num 4, pp 297-304, issn 1742-7835, 8 p.Article

Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophreniaSIGURDSSON, Torfi; STARK, Kimberly L; KARAYIORGOU, Maria et al.Nature (London). 2010, Vol 464, Num 7289, pp 763-767, issn 0028-0836, 5 p.Article

Sex differences in the behavior of children with the 22q11 deletion syndromeSOBIN, Christina; KILEY-BRABECK, Karen; HADLEY MONK, Samantha et al.Psychiatry research (Print). 2009, Vol 166, Num 1, pp 24-34, issn 0165-1781, 11 p.Article

Neuromotor deficits in children with the 22q11 deletion syndromeSOBIN, Christina; MONK, Samantha H; KILEY-BRABECK, Karen et al.Movement disorders. 2006, Vol 21, Num 12, pp 2082-2089, issn 0885-3185, 8 p.Article

Targeting schizophrenia in miceGOGOS, Joseph A; KARAYIORGOU, Maria.American journal of medical genetics. 2001, Vol 105, Num 1, pp 50-52, issn 0148-7299Conference Paper

A Transient Inhibition and Permanent Lack of Catechol-O-Methyl-transferase have Minor Effects on Feeding Pattern of Female RodentsSCHENDZIELORZ, Nadia; MÄNNISTÖ, Pekka T; KARAYIORGOU, Maria et al.Basic & clinical pharmacology & toxicology (Print). 2012, Vol 110, Num 4, pp 307-313, issn 1742-7835, 7 p.Article

MicroRNAs in psychiatric and neurodevelopmental disordersBIN XU; KARAYIORGOU, Maria; GOGOS, Joseph A et al.Brain research. 2010, Vol 1338, pp 78-88, issn 0006-8993, 11 p.Article

d-Amphetamine responses in catechol-O-methyltransferase (COMT) disrupted miceHUOTARI, Marko; GARCIA-HORSMAN, J. Arturo; KARAYIORGOU, Maria et al.Psychopharmacologia. 2004, Vol 172, Num 1, pp 1-10, issn 0033-3158, 10 p.Article

Sequence variants of the brain-derived neurotrophic factor (BDNF) gene are strongly associated with obsessive-compulsive disorderHALL, Diana; DHILLA, Alefiya; CHARALAMBOUS, Anna et al.American journal of human genetics. 2003, Vol 73, Num 2, pp 370-376, issn 0002-9297, 7 p.Article

Fine Mapping on Chromosome 13q32-34 and Brain Expression Analysis Implicates MYO16 in SchizophreniaRODRIGUEZ-MURILLO, Laura; BIN XU; ROOS, J. Louw et al.Neuropsychopharmacology (New York, NY). 2014, Vol 39, Num 4, pp 934-943, issn 0893-133X, 10 p.Article

Exome sequencing supports a de novo mutational paradigm for schizophreniaBIN XU; LOUW ROOS, J; DEXHEIMER, Phillip et al.Nature genetics. 2011, Vol 43, Num 9, pp 864-868, issn 1061-4036, 5 p.Article

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophreniaVACIC, Vladimir; MCCARTHY, Shane; IAKOUCHEVA, Lilia M et al.Nature (London). 2011, Vol 471, Num 7339, pp 499-503, issn 0028-0836, 5 p.Article

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1ABECASIS, Goncalo R; BURT, Rachel A; HALL, Diana et al.American journal of human genetics. 2004, Vol 74, Num 3, pp 403-417, issn 0002-9297, 15 p.Article