A genome-wide study reveals copy number variants exclusive to childhood obesity cases

American Journal of Human Genetics

Volumn 87, Issue 5, 2010, Pages 661-666

  Glessner, Joseph T ^a   Bradfield, Jonathan P ^a   Wang, Kai ^a   Takahashi, Nagahide ^b   Zhang, Haitao ^a   Sleiman, Patrick M ^a   Mentch, Frank D ^a   Kim, Cecilia E ^a   Hou, Cuiping ^a   Thomas, Kelly A ^a   Garris, Maria L ^a   Deliard, Sandra ^a   Frackelton, Edward C ^a   Otieno, F George ^a   Zhao, Jianhua ^a   Chiavacci, Rosetta M ^a   Li, Mingyao ^c   Buxbaum, Joseph D ^b   Berkowitz, Robert I ^a,d   Hakonarson, Hakon ^a,b,d   Grant, Struan F A ^a,b,d   more..

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AFRICAN AMERICAN; ARTICLE; CHILD; CHILDHOOD DISEASE; COHORT ANALYSIS; CONTROLLED STUDY; COPY NUMBER VARIATION; GENE DELETION; GENE DUPLICATION; GENE LOCUS; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOME; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; OBESITY; PRIORITY JOURNAL; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

AFRICAN CONTINENTAL ANCESTRY GROUP; CHILD; DNA COPY NUMBER VARIATIONS; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; OBESITY;

EID: 78249239776     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajhg.2010.09.014     Document Type: Article

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