Neither single-marker nor haplotype analyses support an association between genetic variation near NOTCH4 and bipolar disorder

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 131 B, Issue 1, 2004, Pages 10-15

  Prathikanti, Sridhar ^a   Schulze, Thomas G ^a,d   Chen, Yu Sheng ^a   Harr, Bettina ^a   Akula, Nirmala ^a   Hennessy, Kathy ^a   Potluri, Suneeta ^a   Lyons, Jennifer ^b   Nguyen, Tu ^a   McMahon, Francis J ^a,c  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^c NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^d CENTRAL INSTITUTE OF MENTAL HEALTH   (Germany)

Author keywords

Association studies; Bipolar disorder; Chromosome 6p21.3; NOTCH4

Indexed keywords

NOTCH RECEPTOR; NOTCH4 RECEPTOR; UNCLASSIFIED DRUG;

ARTICLE; BIPOLAR DISORDER; CAUCASIAN; CHROMOSOME 6P; DNA FLANKING REGION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PARENT; PRIORITY JOURNAL; SCHIZOPHRENIA; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; BIPOLAR DISORDER; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC MARKERS; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; TRINUCLEOTIDE REPEATS; VARIATION (GENETICS);

EID: 7644240343     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.20123     Document Type: Article

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