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Browsing "Cerebral Palsy Research Group publications" by Author McMichael, G.

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Showing results 7 to 15 of 15 < previous 
PreviewIssue DateTitleAuthor(s)
2012Fetal and maternal candidate single nucleotide polymorphism associations with Cerebral Palsy: a case-control studyO'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Goldwater, P.; Painter, J.; Montgomery, G.; Dekker, G.
2013Genetic and clinical contributions to cerebral palsy: A multi-variable analysisO'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Baghurst, P.; Goldwater, P.; Dekker, G.
2010Genetic and environmental risk factors that contribute to cerebral palsyMcMichael, G.; Gibson, C.; Goldwater, P.; Haan, E.; Priest, K.; O’Callaghan, M.; MacLennan, A.; Biennial Conference of the Australasian Academy of Cerebral Palsy & Developmental Medicine (5th : 2010 : Christchurch, New Zealand)
2009Genetic susceptibility to viral exposure may increase the risk of cerebral palsyDjukic, M.; Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; McMichael, G.; Priest, K.; Dekker, G.; Hague, W.; Chan, A.; Rudzki, Z.; van Essen, P.; Khong, T.; Morton, M.; Ranieri, E.; Scott, H.; Tapp, H.; Casey, G.
2013NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyMcMichael, G.; Haan, E.; Gardner, A.; Yap, T.; Thompson, S.; Ouvrier, R.; Dale, R.; Gecz, J.; MacLennan, A.
2013Rare copy number variation in cerebral palsyMcMichael, G.; Girirajan, S.; Moreno-De-Luca, A.; Gecz, J.; Shard, C.; Nguyen, L.; Nicholl, J.; Gibson, C.; Haan, E.; Eichler, E.; Martin, C.; MacLennan, A.
2013Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysisO'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; Dekker, G.
2011The Australian cerebral palsy research study - Protocol for a national collaborative study investigating genomic and clinical associations with cerebral palsyO'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Priest, K.; Goldwater, P.; Dekker, G.
2013ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
Showing results 7 to 15 of 15 < previous