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Page 1
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Bassett AS, Lowther C, Merico D, Costain G, Chow EWC, van Amelsvoort T, McDonald-McGinn D, Gur RE, Swillen A, Van den Bree M, Murphy K, Gothelf D, Bearden CE, Eliez S, Kates W, Philip N, Sashi V, Campbell L, Vorstman J, Cubells J, Repetto GM, Simon T, Boot E, Heung T, Evers R, Vingerhoets C, van Duin E, Zackai E, Vergaelen E, Devriendt K, Vermeesch JR, Owen M, Murphy C, Michaelovosky E, Kushan L, Schneider M, Fremont W, Busa T, Hooper S, McCabe K, Duijff S, Isaev K, Pellecchia G, Wei J, Gazzellone MJ, Scherer SW, Emanuel BS, Guo T, Morrow BE, Marshall CR; International 22q11.2DS Brain and Behavior Consortium. Bassett AS, et al. Among authors: gur re. Am J Psychiatry. 2017 Nov 1;174(11):1054-1063. doi: 10.1176/appi.ajp.2017.16121417. Epub 2017 Jul 28. Am J Psychiatry. 2017. PMID: 28750581 Free PMC article.
An fMRI study of facial emotion processing in patients with schizophrenia.
Gur RE, McGrath C, Chan RM, Schroeder L, Turner T, Turetsky BI, Kohler C, Alsop D, Maldjian J, Ragland JD, Gur RC. Gur RE, et al. Among authors: gur rc. Am J Psychiatry. 2002 Dec;159(12):1992-9. doi: 10.1176/appi.ajp.159.12.1992. Am J Psychiatry. 2002. PMID: 12450947
Strong synaptic transmission impact by copy number variations in schizophrenia.
Glessner JT, Reilly MP, Kim CE, Takahashi N, Albano A, Hou C, Bradfield JP, Zhang H, Sleiman PM, Flory JH, Imielinski M, Frackelton EC, Chiavacci R, Thomas KA, Garris M, Otieno FG, Davidson M, Weiser M, Reichenberg A, Davis KL, Friedman JI, Cappola TP, Margulies KB, Rader DJ, Grant SF, Buxbaum JD, Gur RE, Hakonarson H. Glessner JT, et al. Among authors: gur re. Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10584-9. doi: 10.1073/pnas.1000274107. Epub 2010 May 20. Proc Natl Acad Sci U S A. 2010. PMID: 20489179 Free PMC article.
Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis.
Goldenberg PC, Calkins ME, Richard J, McDonald-McGinn D, Zackai E, Mitra N, Emanuel B, Devoto M, Borgmann-Winter K, Kohler C, Conroy CG, Gur RC, Gur RE. Goldenberg PC, et al. Among authors: gur rc, gur re. Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):87-93. doi: 10.1002/ajmg.b.32005. Epub 2011 Dec 13. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22170773 Free PMC article.
Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia.
Greenwood TA, Swerdlow NR, Gur RE, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RC, Lazzeroni LC, Nuechterlein KH, Olincy A, Radant AD, Ray A, Schork NJ, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Tsuang DW, Tsuang MT, Turetsky BI, Light GA, Braff DL. Greenwood TA, et al. Among authors: gur rc, gur re. Am J Psychiatry. 2013 May;170(5):521-32. doi: 10.1176/appi.ajp.2012.12020186. Am J Psychiatry. 2013. PMID: 23511790 Free PMC article.
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome.
Yi JJ, Tang SX, McDonald-McGinn DM, Calkins ME, Whinna DA, Souders MC, Zackai EH, Goldmuntz E, Gaynor JW, Gur RC, Emanuel BS, Gur RE. Yi JJ, et al. Among authors: gur rc, gur re. Am J Med Genet B Neuropsychiatr Genet. 2014 Mar;165B(2):137-47. doi: 10.1002/ajmg.b.32215. Epub 2013 Nov 22. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24265253 Free PMC article.
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, Vorstman J, Duijff SN, Klaassen PW, Swillen A, Gothelf D, Green T, Weizman A, Van Amelsvoort T, Evers L, Boot E, Shashi V, Hooper SR, Bearden CE, Jalbrzikowski M, Armando M, Vicari S, Murphy DG, Ousley O, Campbell LE, Simon TJ, Eliez S; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. Schneider M, et al. Among authors: gur re. Am J Psychiatry. 2014 Jun;171(6):627-39. doi: 10.1176/appi.ajp.2013.13070864. Am J Psychiatry. 2014. PMID: 24577245 Free PMC article. Review.
Subthreshold psychotic symptoms in 22q11.2 deletion syndrome.
Tang SX, Yi JJ, Moore TM, Calkins ME, Kohler CG, Whinna DA, Souders MC, Zackai EH, McDonald-McGinn DM, Emanuel BS, Bilker WB, Gur RC, Gur RE. Tang SX, et al. Among authors: gur rc, gur re. J Am Acad Child Adolesc Psychiatry. 2014 Sep;53(9):991-1000.e2. doi: 10.1016/j.jaac.2014.05.009. Epub 2014 Jun 19. J Am Acad Child Adolesc Psychiatry. 2014. PMID: 25151422 Free PMC article.
Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome.
Schmitt JE, Vandekar S, Yi J, Calkins ME, Ruparel K, Roalf DR, Whinna D, Souders MC, Satterwaite TD, Prabhakaran K, McDonald-McGinn DM, Zackai EH, Gur RC, Emanuel BS, Gur RE. Schmitt JE, et al. Among authors: gur rc, gur re. Biol Psychiatry. 2015 Jul 15;78(2):135-43. doi: 10.1016/j.biopsych.2014.10.025. Epub 2014 Nov 21. Biol Psychiatry. 2015. PMID: 25555483 Free PMC article.
770 results