Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder

Genome

Volumn 56, Issue 10, 2013, Pages 634-640

  Cruceanu, Cristiana ^a,b   Ambalavanan, Amirthagowri ^a,c   Spiegelman, Dan ^c   Gauthier, Julie ^c   Lafrenière, Ronald G ^c   Dion, Patrick A ^c   Alda, Martin ^d   Turecki, Gustavo ^a,b   Rouleau, Guy A ^a,c,e  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

^c UNIVERSITY OF MONTREAL   (Canada)

^d DALHOUSIE UNIVERSITY   (Canada)

^e MCGILL UNIVERSITY   (Canada)

Author keywords

Bipolar disorder; Exome sequencing; Lithium

Indexed keywords

LITHIUM DERIVATIVE;

BIPOLAR DISORDER; DNA MICROARRAY; EXOME; FEMALE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN; MALE; PEDIGREE; PHENOTYPE; REVIEW;

BIPOLAR DISORDER; EXOME; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; LITHIUM COMPOUNDS; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PEDIGREE; PHENOTYPE;

EID: 84889864585     PISSN: 08312796     EISSN: None     Source Type: Journal    
DOI: 10.1139/gen-2013-0081     Document Type: Review

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