Research Topics
| Neilson C MartinSummaryAffiliation: Curtin University of Technology Country: Australia Publications
| Collaborators
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Detail Information
Publications
Relationship between endophenotype and phenotype in ADHDNanda Nj Rommelse
Department of Clinical Neuropsychology, VU University Amsterdam, Van der Boechorststraat 1, 1081 BT Amsterdam, The Netherlands
Behav Brain Funct 4:4. 2008..abstract:..
An examination of the relationship between movement problems and four common developmental disordersNeilson C Martin
Curtin Health Innovation Research Institute, Curtin University of Technology, GPO Box U1987, Perth 6845, Western Australia, Australia
Hum Mov Sci 29:799-808. 2010..Despite the close link previously identified with ODD and CD, this finding suggests a different aetiology for CD...
What are the key directions in the genetics of attention deficit hyperactivity disorder?Neilson Martin
School of Psychology, Curtin University of Technology, Perth, Western Australia
Curr Opin Psychiatry 21:356-61. 2008..Such interactions are studied to explain what happens when individuals with a susceptible genotype are exposed to a particular environment...
DCD and ADHD: a genetic study of their shared aetiologyNeilson C Martin
School of Psychology, Curtin University of Technology, Perth, Western Australia
Hum Mov Sci 25:110-24. 2006..On the SWAN scale the results were similar but the general coordination scale was also very strongly linked. Implications for the use of different assessment tools are discussed...
The ADHD resource: creation of an online tool for attention deficit hyperactivity disorder information and researchN C Martin
School of Psychology, Curtin University of Technology, Perth, Western Australia, Australia
Am J Med Genet B Neuropsychiatr Genet 147:112-3. 2008..The ADHD Resource was created to be this tool. It has been designed to act as the first point of reference for researchers in the field. It has also been created to facilitate the collaborative effects amongst the research groups...
An investigation into etiological pathways of DCD and ADHD using a monozygotic twin designJillian G Pearsall-Jones
School of Psychology, Curtin University of Technology, Australia The Centre for Cerebral Palsy, Perth, Australia
Twin Res Hum Genet 12:381-91. 2009..All twins positive for ADHD were male. This adds support to our hypothesis that ADHD symptoms found in some participants may reflect secondary ADHD associated with environmental factors, rather than developmental ADHD...
Motor disorder and anxious and depressive symptomatology: a monozygotic co-twin control approachJillian G Pearsall-Jones
School of Psychology and Speech Pathology, Curtin Health Innovation Research Institute, Curtin University, Perth, Western Australia 6845, Australia
Res Dev Disabil 32:1245-52. 2011....
Depressive symptomatology in child and adolescent twins with attention-deficit hyperactivity disorder and/or developmental coordination disorderJan P Piek
School of Psychology, Curtin University of Technology, Perth, Western Australia, Australia
Twin Res Hum Genet 10:587-96. 2007..The implications of these findings are discussed with emphasis on understanding and recognizing the relationship between ADHD, DCD, and depression in the assessment and intervention for children and adolescents with these disorders...
Attention deficit hyperactivity disorder: a Rasch analysis of the SWAN Rating ScaleDeidra J Young
School of Psychology, Curtin University of Technology, WA, Australia
Child Psychiatry Hum Dev 40:543-59. 2009..Further, the combined subtype appeared to be an entirely different type, with unique features unlike the other two subtypes. Further work is needed to distinguish the diagnostic features of each subtype of ADHD...
The Australian Twin ADHD Project: current status and future directionsKellie S Bennett
School of Psychology, Curtin University of Technology, Perth, Western Australia 6945, Australia
Twin Res Hum Genet 9:718-26. 2006..Recruitment, assessment and retention of twin families require a major commitment but create a significant resource for collaboration in areas outside the original aim...
PKDB: Polycystic Kidney Disease Mutation Database--a gene variant database for autosomal dominant polycystic kidney diseaseAlexander M Gout
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
Hum Mutat 28:654-9. 2007..Through a series of user-friendly advanced search facilities, users are able to query the database as required. The PKDB server is accessible at http://pkdb.mayo.edu...
