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S H Juo

Researcher at Columbia University

Publications -  8
Citations -  1424

S H Juo is an academic researcher from Columbia University. The author has contributed to research in topics: Genetic linkage & Bipolar disorder. The author has an hindex of 6, co-authored 8 publications receiving 1415 citations. Previous affiliations of S H Juo include Kaohsiung Medical University & Icahn School of Medicine at Mount Sinai.

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Journal ArticleDOI

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

Ricardo Segurado, +79 more
TL;DR: The present results for the very narrow model are promising but suggest that more and larger data sets are needed to support linkage, as well as suggest that linkage might be detected in certain populations or subsets of pedigrees.
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Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q

Matthew B. McQueen, +56 more
TL;DR: It is demonstrated that combining original genome-scan data is a powerful approach for the elucidation of linkage regions underlying complex disease, and genomewide significant linkage to BP on chromosomes 6q and 8q is established.
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Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.

TL;DR: The results suggest that BP in conjunction with psychosis is a potentially useful phenotype that may expedite the detection of susceptibility loci for BP and cast light on the genetic relationship between BP and schizophrenia.
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Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder

TL;DR: The first large-scale linkage scan of bipolar disorder to analyze simultaneously bipolar disorder, psychosis, suicidal behavior, and panic disorder is conducted, suggesting that dissection of the disease phenotype can enrich the harvest of linkage signals and expedite the search for susceptibility genes.
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Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.

TL;DR: This systematic, large-scale study identified novel putative loci for BP (on 2p13–16, 8q13 and 14q21) and found support for previously proposed loci (on 4q31, 7q34, 9Q31, 10q21–24, 13q32 and 17q11–12).