Murphy KC - Search Results

1

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.

Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, Tran OT, Miller D, Lin JR, Zackai E, Johnston HR, Chow EWC, Vorstman JAS, Vingerhoets C, van Amelsvoort T, Gothelf D, Swillen A, Breckpot J, Vermeesch JR, Eliez S, Schneider M, van den Bree MBM, Owen MJ, Kates WR, Repetto GM, Shashi V, Schoch K, Bearden CE, Digilio MC, Unolt M, Putotto C, Marino B, Pontillo M, Armando M, Vicari S, Angkustsiri K, Campbell L, Busa T, Heine-Suñer D, Murphy KC, Murphy D, García-Miñaúr S, Fernández L; International 22q11.2 Brain and Behavior Consortium (IBBC); Zhang ZD, Goldmuntz E, Gur RE, Emanuel BS, Zheng D, Marshall CR, Bassett AS, Wang T, Morrow BE. Zhao Y, et al. Among authors: murphy kc. NPJ Genom Med. 2023 Jul 18;8(1):17. doi: 10.1038/s41525-023-00363-y. NPJ Genom Med. 2023. PMID: 37463940 Free PMC article.

2

Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome.

van Amelsvoort T, Henry J, Morris R, Owen M, Linszen D, Murphy K, Murphy D. van Amelsvoort T, et al. Schizophr Res. 2004 Oct 1;70(2-3):223-32. doi: 10.1016/j.schres.2003.10.004. Schizophr Res. 2004. PMID: 15329299

3

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

van Amelsvoort T, Daly E, Henry J, Robertson D, Ng V, Owen M, Murphy KC, Murphy DG. van Amelsvoort T, et al. Among authors: murphy kc, murphy dg. Arch Gen Psychiatry. 2004 Nov;61(11):1085-96. doi: 10.1001/archpsyc.61.11.1085. Arch Gen Psychiatry. 2004. PMID: 15520356

4

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

Campbell LE, Daly E, Toal F, Stevens A, Azuma R, Catani M, Ng V, van Amelsvoort T, Chitnis X, Cutter W, Murphy DG, Murphy KC. Campbell LE, et al. Among authors: murphy kc, murphy dg. Brain. 2006 May;129(Pt 5):1218-28. doi: 10.1093/brain/awl066. Epub 2006 Mar 28. Brain. 2006. PMID: 16569671

5

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Paylor R, Glaser B, Mupo A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi CH, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, Scambler PJ, Lindsay E. Paylor R, et al. Among authors: murphy kc. Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34. doi: 10.1073/pnas.0600206103. Epub 2006 May 9. Proc Natl Acad Sci U S A. 2006. PMID: 16684884 Free PMC article.

6

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.

Glaser B, Moskvina V, Kirov G, Murphy KC, Williams H, Williams N, Owen MJ, O'Donovan MC. Glaser B, et al. Among authors: murphy kc. Schizophr Res. 2006 Oct;87(1-3):21-7. doi: 10.1016/j.schres.2006.05.024. Epub 2006 Jul 21. Schizophr Res. 2006. PMID: 16860541

7

Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging.

van Amelsvoort T, Schmitz N, Daly E, Deeley Q, Critchley H, Henry J, Robertson D, Owen M, Murphy KC, Murphy DG. van Amelsvoort T, et al. Among authors: murphy kc, murphy dg. Br J Psychiatry. 2006 Dec;189:560-1. doi: 10.1192/bjp.bp.105.019876. Br J Psychiatry. 2006. PMID: 17139043

8

A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome.

Campbell LE, Stevens A, Daly E, Toal F, Azuma R, Karmiloff-Smith A, Murphy DG, Murphy KC. Campbell LE, et al. Among authors: murphy kc, murphy dg. Neuropsychologia. 2009 Mar;47(4):1034-44. doi: 10.1016/j.neuropsychologia.2008.10.029. Epub 2008 Nov 13. Neuropsychologia. 2009. PMID: 19061904

9

Brain structural differences associated with the behavioural phenotype in children with Williams syndrome.

Campbell LE, Daly E, Toal F, Stevens A, Azuma R, Karmiloff-Smith A, Murphy DG, Murphy KC. Campbell LE, et al. Among authors: murphy kc, murphy dg. Brain Res. 2009 Mar 3;1258:96-107. doi: 10.1016/j.brainres.2008.11.101. Epub 2008 Dec 11. Brain Res. 2009. PMID: 19118537

10

Executive functions and memory abilities in children with 22q11.2 deletion syndrome.

Campbell LE, Azuma R, Ambery F, Stevens A, Smith A, Morris RG, Murphy DG, Murphy KC. Campbell LE, et al. Among authors: murphy kc, murphy dg. Aust N Z J Psychiatry. 2010 Apr;44(4):364-71. doi: 10.3109/00048670903489882. Aust N Z J Psychiatry. 2010. PMID: 20307169

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