Showing results 7 to 26 of 26
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Preview | Issue Date | Title | Author(s) |
| 2009 | DNA from Buccal Swabs Suitable for High-Throughput SNP Multiplex Analysis | McMichael, G.; Gibson, C.; O'Callaghan, M.; Goldwater, P.; Dekker, G.; Haan, E.; MacLennan, A. |
| 2011 | Epidemiologic associations with cerebral palsy | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Goldwater, P.; Dekker, G. |
| 2012 | Fetal and maternal candidate single nucleotide polymorphism associations with Cerebral Palsy: a case-control study | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Goldwater, P.; Painter, J.; Montgomery, G.; Dekker, G. |
| 2008 | Fetal exposure to herpesviruses may be associated with pregnancy-induced hypertensive disorders and preterm birth in a Caucasian population | Gibson, C.; Goldwater, P.; MacLennan, A.; Haan, E.; Priest, K.; Dekker, G. |
| 2011 | Fetal MBL2 haplotypes combined with viral exposure are associated with adverse pregnancy outcomes | Gibson, C.; MacLennan, A.; Haan, E.; Priest, K.; Dekker, G. |
| 2013 | Genetic and clinical contributions to cerebral palsy: A multi-variable analysis | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Baghurst, P.; Goldwater, P.; Dekker, G. |
| 2010 | Genetic and environmental risk factors that contribute to cerebral palsy | McMichael, 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) |
| 2009 | Genetic susceptibility to viral exposure may increase the risk of cerebral palsy | Djukic, 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. |
| 2008 | Mannose-binding lectin haplotypes may be associated with cerebral palsy only after perinatal viral exposure | Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G. |
| 2006 | Neurotropic viruses and cerebral palsy: population based case-control study | Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G. |
| 2000 | New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome | Cox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G. |
| 2013 | NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy | McMichael, G.; Haan, E.; Gardner, A.; Yap, T.; Thompson, S.; Ouvrier, R.; Dale, R.; Gecz, J.; MacLennan, A. |
| 2013 | Rare copy number variation in cerebral palsy | McMichael, 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. |
| 2013 | Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysis | O'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; Dekker, G. |
| 2006 | The association between inherited cytokine polymorphisms and cerebral palsy | Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; Hague, W.; Morton, M. |
| 2011 | The Australian cerebral palsy research study - Protocol for a national collaborative study investigating genomic and clinical associations with cerebral palsy | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Priest, K.; Goldwater, P.; Dekker, G. |
| 2009 | The genomic basis of cerebral palsy: A HuGE systematic literature review | O'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G. |
| 2005 | The Hunter-McAlpine syndrome results from duplication 5q35-qter | Hunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C. |
| 2005 | The prevalence of inherited thrombophilias in a Caucasian Australian population | Gibson, C.; MacLennan, A.; Rudzki, Z.; Hague, W.; Haan, E.; Sharpe, P.; Priest, K.; Chan, A.; Dekker, G.; Khong, T. |
| 2013 | ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity | Hirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J. |