Campbell L - 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: campbell l. 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

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. Brain. 2006 May;129(Pt 5):1218-28. doi: 10.1093/brain/awl066. Epub 2006 Mar 28. Brain. 2006. PMID: 16569671

3

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. Neuropsychologia. 2009 Mar;47(4):1034-44. doi: 10.1016/j.neuropsychologia.2008.10.029. Epub 2008 Nov 13. Neuropsychologia. 2009. PMID: 19061904

4

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. 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

5

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. Aust N Z J Psychiatry. 2010 Apr;44(4):364-71. doi: 10.3109/00048670903489882. Aust N Z J Psychiatry. 2010. PMID: 20307169

6

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

Campbell LE, Stevens AF, McCabe K, Cruickshank L, Morris RG, Murphy DG, Murphy KC. Campbell LE, et al. J Neurodev Disord. 2011 Jun;3(2):152-61. doi: 10.1007/s11689-011-9082-7. Epub 2011 May 5. J Neurodev Disord. 2011. PMID: 21544568 Free PMC article.

7

Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study.

Azuma R, Daly EM, Campbell LE, Stevens AF, Deeley Q, Giampietro V, Brammer MJ, Glaser B, Ambery FZ, Morris RG, Williams SC, Owen MJ, Murphy DG, Murphy KC. Azuma R, et al. J Neurodev Disord. 2009 Mar;1(1):46-60. doi: 10.1007/s11689-009-9008-9. Epub 2009 Mar 5. J Neurodev Disord. 2009. PMID: 21547621 Free PMC article.

8

Practical guidelines for managing patients with 22q11.2 deletion syndrome.

Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium. Bassett AS, et al. J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. J Pediatr. 2011. PMID: 21570089 Free PMC article. No abstract available.

9

White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents.

Sundram F, Campbell LE, Azuma R, Daly E, Bloemen OJ, Barker GJ, Chitnis X, Jones DK, van Amelsvoort T, Murphy KC, Murphy DG. Sundram F, et al. J Neurodev Disord. 2010 Jun;2(2):77-92. doi: 10.1007/s11689-010-9043-6. Epub 2010 Mar 5. J Neurodev Disord. 2010. PMID: 22127856 Free PMC article.

10

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.

Sinderberry B, Brown S, Hammond P, Stevens AF, Schall U, Murphy DG, Murphy KC, Campbell LE. Sinderberry B, et al. Res Dev Disabil. 2013 Jan;34(1):116-25. doi: 10.1016/j.ridd.2012.07.025. Epub 2012 Aug 30. Res Dev Disabil. 2013. PMID: 22940165

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