Cerebral palsy and genomics: an international consortium

Developmental Medicine and Child Neurology

Volumn 60, Issue 2, 2018, Pages 209-210

  MacLennan, Alastair H ^a   Kruer, Michael C ^b   Baynam, Gareth ^c,d,e,f,g   Moreno De Luca, Andres ^h,i   Wilson, Yana A ^j,k   Zhu, Changlian ^l,m   Wintle, Richard F ⁿ   Gecz, Jozef ^a,o,p  

^a UNIVERSITY OF ADELAIDE   (Australia)

^b UNIVERSITY OF ARIZONA COLLEGE OF MEDICINE   (United States)

^c DEPARTMENT OF HEALTH   (Australia)

^d UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^e MURDOCH UNIVERSITY   (Australia)

^f UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^g CURTIN UNIVERSITY   (Australia)

^h GEISINGER HEALTH SYSTEM   (United States)

ⁱ HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

^j UNIVERSITY OF SYDNEY   (Australia)

^k GARVAN INSTITUTE OF MEDICAL RESEARCH   (Australia)

^l UNIVERSITY OF GOTHENBURG   (Sweden)

^m ZHENGZHOU UNIVERSITY   (China)

ⁿ HOSPITAL FOR SICK CHILDREN   (Canada)

^o UNIVERSITY OF ADELAIDE   (Australia)

^p SOUTH AUSTRALIAN HEALTH AND MEDICAL RESEARCH INSTITUTE   (Australia)

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Author keywords

[No Author keywords available]

Indexed keywords

BIOBANK; BIOLOGY; CEREBRAL PALSY; COMMON DATA ELEMENTS; FETUS GROWTH; GENETIC VARIATION; GENOMICS; GROSS MOTOR FUNCTION CLASSIFICATION SYSTEM; HUMAN; LETTER; MEDICAL PRACTICE; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; WORKFLOW; GENETICS; INTERNATIONAL COOPERATION; PROCEDURES;

CEREBRAL PALSY; GENOMICS; HUMANS; INTERNATIONAL COOPERATION;

EID: 85042136132     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/dmcn.13643     Document Type: Letter

References (5)

1. Nelson KB, Ellenberg JH. Antecedents of cerebral palsy. Multivariate analysis of risk. N Engl J Med 1986; 315: 81–6.
2. MacLennan AH, Thompson SC, Gecz J. Cerebral palsy: causes, pathways, and the role of genetic variants. Am J Obstet Gynecol 2015; 213: 779–88.
3. Fahey MC, Maclennan AH, Kretzschmar D, Gecz J, Kruer MC. The genetic basis of cerebral palsy. Dev Med Child Neurol 2017; 59: 462–9.
4. Boycott KM, Rath A, Chong JX, et al. International cooperation to enable the diagnosis of all rare genetic diseases. Am J Hum Genet 2017; 100: 695–705.
5. Robinson PN, Köhler S, Bauer S, Seelow D, Horn D, Mundlos S. The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. Am J Hum Genet 2008; 83: 610–5.