314 related articles for article (PubMed ID: 24367288)
21. Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.
Sivagnanasundaram S; Fletcher D; Hubank M; Illingworth E; Skuse D; Scambler P
Brain Res; 2007 Mar; 1139():48-59. PubMed ID: 17292336
[TBL] [Abstract][Full Text] [Related]
22. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
Bassett AS; Marshall CR; Lionel AC; Chow EW; Scherer SW
Hum Mol Genet; 2008 Dec; 17(24):4045-53. PubMed ID: 18806272
[TBL] [Abstract][Full Text] [Related]
23. Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.
Butcher NJ; Kiehl TR; Hazrati LN; Chow EW; Rogaeva E; Lang AE; Bassett AS
JAMA Neurol; 2013 Nov; 70(11):1359-66. PubMed ID: 24018986
[TBL] [Abstract][Full Text] [Related]
24. Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
Guna A; Butcher NJ; Bassett AS
J Neurodev Disord; 2015; 7(1):18. PubMed ID: 26137170
[TBL] [Abstract][Full Text] [Related]
25. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.
Stark KL; Xu B; Bagchi A; Lai WS; Liu H; Hsu R; Wan X; Pavlidis P; Mills AA; Karayiorgou M; Gogos JA
Nat Genet; 2008 Jun; 40(6):751-60. PubMed ID: 18469815
[TBL] [Abstract][Full Text] [Related]
26. Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome.
Tabata H; Mori D; Matsuki T; Yoshizaki K; Asai M; Nakayama A; Ozaki N; Nagata KI
Biomolecules; 2023 Apr; 13(5):. PubMed ID: 37238632
[TBL] [Abstract][Full Text] [Related]
27. Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex.
Fénelon K; Mukai J; Xu B; Hsu PK; Drew LJ; Karayiorgou M; Fischbach GD; Macdermott AB; Gogos JA
Proc Natl Acad Sci U S A; 2011 Mar; 108(11):4447-52. PubMed ID: 21368174
[TBL] [Abstract][Full Text] [Related]
28. Visual processing deficits in 22q11.2 Deletion Syndrome.
Biria M; Tomescu MI; Custo A; Cantonas LM; Song KW; Schneider M; Murray MM; Eliez S; Michel CM; Rihs TA
Neuroimage Clin; 2018; 17():976-986. PubMed ID: 29527499
[TBL] [Abstract][Full Text] [Related]
29. [22q11.2DS Syndrome as a Genetic Subtype of Schizophrenia].
Huertas-Rodríguez CK; Payán-Gómez C; Forero-Castro RM
Rev Colomb Psiquiatr; 2015; 44(1):50-60. PubMed ID: 26578219
[TBL] [Abstract][Full Text] [Related]
30. Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11 deletion syndrome mouse model.
Toritsuka M; Kimoto S; Muraki K; Landek-Salgado MA; Yoshida A; Yamamoto N; Horiuchi Y; Hiyama H; Tajinda K; Keni N; Illingworth E; Iwamoto T; Kishimoto T; Sawa A; Tanigaki K
Proc Natl Acad Sci U S A; 2013 Oct; 110(43):17552-7. PubMed ID: 24101523
[TBL] [Abstract][Full Text] [Related]
31. Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndrome.
Dantas AG; Santoro ML; Nunes N; de Mello CB; Pimenta LSE; Meloni VA; Soares DCQ; Belangero SN; Carvalheira G; Kim CA; Melaragno MI
Hum Genet; 2019 Jan; 138(1):93-103. PubMed ID: 30627818
[TBL] [Abstract][Full Text] [Related]
32. [Formula: see text] Long-term verbal memory deficit and associated hippocampal alterations in 22q11.2 deletion syndrome.
Maeder J; Sandini C; Zöller D; Schneider M; Bostelmann M; Pouillard V; Caroni P; Kliegel M; Eliez S
Child Neuropsychol; 2020 Apr; 26(3):289-311. PubMed ID: 31460828
[TBL] [Abstract][Full Text] [Related]
33. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].
Demily C; Rossi M; Schneider M; Edery P; Leleu A; d'Amato T; Franck N; Eliez S
Encephale; 2015 Jun; 41(3):266-73. PubMed ID: 25523123
[TBL] [Abstract][Full Text] [Related]
34. Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.
Prasad S; Katina S; Hennessy RJ; Murphy KC; Bowman AW; Waddington JL
Am J Med Genet A; 2015 Mar; 167A(3):529-36. PubMed ID: 25691406
[TBL] [Abstract][Full Text] [Related]
35. MicroRNAs in the Onset of Schizophrenia.
Thomas KT; Zakharenko SS
Cells; 2021 Oct; 10(10):. PubMed ID: 34685659
[TBL] [Abstract][Full Text] [Related]
36. Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics.
Forsyth JK; Mennigen E; Lin A; Sun D; Vajdi A; Kushan-Wells L; Ching CRK; Villalon-Reina JE; Thompson PM; ; Bearden CE
Cereb Cortex; 2021 Jun; 31(7):3285-3298. PubMed ID: 33638978
[TBL] [Abstract][Full Text] [Related]
37. Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.
Carmel M; Zarchi O; Michaelovsky E; Frisch A; Patya M; Green T; Gothelf D; Weizman A
J Psychiatr Res; 2014 Sep; 56():28-35. PubMed ID: 24853458
[TBL] [Abstract][Full Text] [Related]
38. Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
Gothelf D; Law AJ; Frisch A; Chen J; Zarchi O; Michaelovsky E; Ren-Patterson R; Lipska BK; Carmel M; Kolachana B; Weizman A; Weinberger DR
Biol Psychiatry; 2014 Mar; 75(5):406-13. PubMed ID: 23992923
[TBL] [Abstract][Full Text] [Related]
39. TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.
Gao S; Moreno M; Eliason S; Cao H; Li X; Yu W; Bidlack FB; Margolis HC; Baldini A; Amendt BA
Hum Mol Genet; 2015 Apr; 24(8):2330-48. PubMed ID: 25556186
[TBL] [Abstract][Full Text] [Related]
40. Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.
Zarchi O; Carmel M; Avni C; Attias J; Frisch A; Michaelovsky E; Patya M; Green T; Weinberger R; Weizman A; Gothelf D
J Psychiatr Res; 2013 Nov; 47(11):1623-9. PubMed ID: 23910792
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]