Your browser doesn't support javascript.
loading
Dominant Genetic Variation and Missing Heritability for Human Complex Traits: Insights from Twin versus Genome-wide Common SNP Models.
Chen, Xu; Kuja-Halkola, Ralf; Rahman, Iffat; Arpegård, Johannes; Viktorin, Alexander; Karlsson, Robert; Hägg, Sara; Svensson, Per; Pedersen, Nancy L; Magnusson, Patrik K E.
Afiliação
  • Chen X; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden.
  • Kuja-Halkola R; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden.
  • Rahman I; Institute of Environmental Medicine, Karolinska Institutet, Stockholm 17177, Sweden.
  • Arpegård J; Department of Medicine-Solna, Karolinska Institutet, Stockholm 17177, Sweden; Department of Emergency Medicine, Karolinska University Hospital, Stockholm 17177, Sweden.
  • Viktorin A; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden.
  • Karlsson R; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden.
  • Hägg S; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden.
  • Svensson P; Department of Medicine-Solna, Karolinska Institutet, Stockholm 17177, Sweden; Department of Emergency Medicine, Karolinska University Hospital, Stockholm 17177, Sweden.
  • Pedersen NL; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden.
  • Magnusson PK; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm 17177, Sweden. Electronic address: patrik.magnusson@ki.se.
Am J Hum Genet ; 97(5): 708-14, 2015 Nov 05.
Article em En | MEDLINE | ID: mdl-26544805
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gêmeos / Genoma Humano / Característica Quantitativa Herdável / Polimorfismo de Nucleotídeo Único / Modelos Genéticos Idioma: En Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gêmeos / Genoma Humano / Característica Quantitativa Herdável / Polimorfismo de Nucleotídeo Único / Modelos Genéticos Idioma: En Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia