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NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy.
McMichael G, Haan E, Gardner A, Yap TY, Thompson S, Ouvrier R, Dale RC, Gecz J, Maclennan AH. McMichael G, et al. Among authors: maclennan ah. Eur J Med Genet. 2013 Sep;56(9):506-9. doi: 10.1016/j.ejmg.2013.07.003. Epub 2013 Jul 30. Eur J Med Genet. 2013. PMID: 23911641
Rare copy number variation in cerebral palsy.
McMichael G, Girirajan S, Moreno-De-Luca A, Gecz J, Shard C, Nguyen LS, Nicholl J, Gibson C, Haan E, Eichler E, Martin CL, MacLennan A. McMichael G, et al. Eur J Hum Genet. 2014 Jan;22(1):40-5. doi: 10.1038/ejhg.2013.93. Epub 2013 May 22. Eur J Hum Genet. 2014. PMID: 23695280 Free PMC article.
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.
McMichael G, Bainbridge MN, Haan E, Corbett M, Gardner A, Thompson S, van Bon BW, van Eyk CL, Broadbent J, Reynolds C, O'Callaghan ME, Nguyen LS, Adelson DL, Russo R, Jhangiani S, Doddapaneni H, Muzny DM, Gibbs RA, Gecz J, MacLennan AH. McMichael G, et al. Among authors: maclennan ah. Mol Psychiatry. 2015 Feb;20(2):176-82. doi: 10.1038/mp.2014.189. Epub 2015 Feb 10. Mol Psychiatry. 2015. PMID: 25666757
Fetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study.
O'Callaghan ME, Maclennan AH, Gibson CS, McMichael GL, Haan EA, Broadbent JL, Goldwater PN, Painter JN, Montgomery GW, Dekker GA; Australian Collaborative Cerebral Palsy Research Group. O'Callaghan ME, et al. Among authors: maclennan ah. Pediatrics. 2012 Feb;129(2):e414-23. doi: 10.1542/peds.2011-0739. Epub 2012 Jan 30. Pediatrics. 2012. PMID: 22291124
Genetic and clinical contributions to cerebral palsy: a multi-variable analysis.
O'Callaghan ME, Maclennan AH, Gibson CS, McMichael GL, Haan EA, Broadbent JL, Baghurst PA, Goldwater PN, Dekker GA; Australian Collaborative Cerebral Palsy Research Group. O'Callaghan ME, et al. Among authors: maclennan ah. J Paediatr Child Health. 2013 Jul;49(7):575-81. doi: 10.1111/jpc.12279. Epub 2013 Jun 11. J Paediatr Child Health. 2013. PMID: 23773706
The genetic basis of cerebral palsy.
Fahey MC, Maclennan AH, Kretzschmar D, Gecz J, Kruer MC. Fahey MC, et al. Among authors: maclennan ah. Dev Med Child Neurol. 2017 May;59(5):462-469. doi: 10.1111/dmcn.13363. Epub 2017 Jan 1. Dev Med Child Neurol. 2017. PMID: 28042670 Free article. Review.
The association between inherited cytokine polymorphisms and cerebral palsy.
Gibson CS, MacLennan AH, Goldwater PN, Haan EA, Priest K, Dekker GA; South Australian Cerebral Palsy Research Group. Gibson CS, et al. Among authors: maclennan ah. Am J Obstet Gynecol. 2006 Mar;194(3):674.e1-11. doi: 10.1016/j.ajog.2006.01.093. Am J Obstet Gynecol. 2006. PMID: 16522396
199 results