Identification of genetic variants influencing the human plasma proteome

Proceedings of the National Academy of Sciences of the United States of America

Volumn 110, Issue 12, 2013, Pages 4673-4678

  Johansson, Åsa ^a,b   Enroth, Stefan ^a   Palmblad, Magnus ^c   Deelder, André M ^c   Bergquist, Jonas ^d   Gyllensten, Ulf ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b UPPSALA UNIVERSITY   (Sweden)

^c LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^d UPPSALA UNIVERSITY   (Sweden)

Author keywords

Population proteomics; Protein quantitative trait loci

Indexed keywords

APOLIPOPROTEIN E; PLASMA PROTEIN; PROTEOME;

ALLELE; ALZHEIMER DISEASE; AMINO ACID SEQUENCE; ARTICLE; GENE LINKAGE DISEQUILIBRIUM; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEOMICS; QUANTITATIVE TRAIT LOCUS; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; ALLELES; BIOLOGICAL MARKERS; BLOOD PROTEINS; COHORT STUDIES; FEMALE; GENETIC MARKERS; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEOME;

EID: 84875238998     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1217238110     Document Type: Article

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