Common genetic variants and risk of brain injury after preterm birth.

Boardman, James P; Walley, Andrew; Ball, Gareth; Takousis, Petros; Krishnan, Michelle L; Hughes-Carre, Laurelle; Aljabar, Paul; Serag, Ahmed; King, Caroline; Merchant, Nazakat; Srinivasan, Latha; Froguel, Philippe; Hajnal, Jo; Rueckert, Daniel; Counsell, Serena; Edwards, A David

Boardman, James P; Walley, Andrew; Ball, Gareth; Takousis, Petros; Krishnan, Michelle L; Hughes-Carre, Laurelle; Aljabar, Paul; Serag, Ahmed; King, Caroline; Merchant, Nazakat; Srinivasan, Latha; Froguel, Philippe; Hajnal, Jo; Rueckert, Daniel; Counsell, Serena; Edwards, A David.

Afiliación

Boardman JP; Medical Research Council/University of Edinburgh Centre for Reproductive Health, Edinburgh, United Kingdom; james.boardman@ed.ac.uk.
Walley A; Departments of Genomics of Common Disease, School of Public Health,Molecular Genetics and Genomics, National Heart and Lung Institute.
Ball G; Centre for the Developing Brain, King's College London, London, England, United Kingdom;
Takousis P; Departments of Genomics of Common Disease, School of Public Health.
Krishnan ML; Centre for the Developing Brain, King's College London, London, England, United Kingdom;
Hughes-Carre L; Paediatrics, and.
Aljabar P; Centre for the Developing Brain, King's College London, London, England, United Kingdom;
Serag A; The Advanced Pediatric Brain Imaging Research Laboratory, Children's National Medical Center, Washington, District of Columbia; and.
King C; Paediatrics, and.
Merchant N; Centre for the Developing Brain, King's College London, London, England, United Kingdom;
Srinivasan L; Paediatrics, and.
Froguel P; Departments of Genomics of Common Disease, School of Public Health,Centre National de la Recherche Scientifique-CNRS 8199, Lille 2 University, Paris, France.
Hajnal J; Centre for the Developing Brain, King's College London, London, England, United Kingdom;
Rueckert D; Computing, Imperial College London, London, England, United Kingdom;
Counsell S; Centre for the Developing Brain, King's College London, London, England, United Kingdom;
Edwards AD; Centre for the Developing Brain, King's College London, London, England, United Kingdom;

Pediatrics ; 133(6): e1655-63, 2014 Jun.

Article en En | MEDLINE | ID: mdl-24819575

Asunto(s)

Daño Encefálico Crónico/diagnóstico; Daño Encefálico Crónico/genética; Estudios de Asociación Genética; Predisposición Genética a la Enfermedad/genética; Variación Genética/genética; Enfermedades del Prematuro/diagnóstico; Enfermedades del Prematuro/genética; Alelos; Proteínas del Dominio Armadillo/genética; Encéfalo/patología; Catecol O-Metiltransferasa/genética; Moléculas de Adhesión Celular/genética; Cromosomas Humanos Par 11/genética; Cromosomas Humanos Par 22/genética; Estudios de Cohortes; Imagen de Difusión por Resonancia Magnética; Endofenotipos; Ácido Graso Desaturasas/genética; Biblioteca de Genes; Tamización de Portadores Genéticos; Genotipo; Humanos; Interpretación de Imagen Asistida por Computador; Recién Nacido; Inteligencia/genética; Imagen por Resonancia Magnética; Fosfoproteínas/genética; Polimorfismo de Nucleótido Simple/genética; Esquizofrenia/genética

Palabras clave

genetics; magnetic resonance image; neonate; preterm

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Daño Encefálico Crónico / Predisposición Genética a la Enfermedad / Estudios de Asociación Genética / Enfermedades del Prematuro Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Newborn Idioma: En Revista: Pediatrics Año: 2014 Tipo del documento: Article

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