Research Topics
Species | Jennifer Gladys MulleSummaryAffiliation: Emory University Country: USA Publications
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Detail Information
Publications
Microdeletions of 3q29 confer high risk for schizophreniaJennifer Gladys Mulle
Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
Am J Hum Genet 87:229-36. 2010....- Cardiovascular disease, psychosocial factors, and genetics: the case of depressionJennifer Gladys Mulle
Department of Epidemiology, Rollins School of Public Health, Emory University Department of Human Genetics, School of Medicine, Emory University Electronic address
Prog Cardiovasc Dis 55:557-62. 2013..Even without knowledge of a specific mechanism, epidemiological observations offer new directions to explain the relationship between depression and CVD that have both research and clinical applications... - The gut microbiome: a new frontier in autism researchJENNIFER G MULLE
Department of Epidemiology, Emory University Rollins School of Public Health, Mailstop 1518 002 3BB, Atlanta, GA, 30322, USA
Curr Psychiatry Rep 15:337. 2013..The evidence reviewed here suggests that a deeper understanding of the gut microbiome could open up new avenues of research on ASD, including potential novel treatment strategies... 
Schizophrenia genetics: progress, at lastJennifer Gladys Mulle
Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, GA, United States
Curr Opin Genet Dev 22:238-44. 2012..It is likely that investigations of common variants have surrendered their full yield, but rare variant exploration is at the very beginning...- Empirical evaluation of oligonucleotide probe selection for DNA microarraysJENNIFER G MULLE
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America
PLoS ONE 5:e9921. 2010..These findings, when incorporated into future microarray probe selection algorithms, may improve microarray performance for a wide variety of applications... - Segmental duplications mediate novel, clinically relevant chromosome rearrangementsM Katharine Rudd
Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
Hum Mol Genet 18:2957-62. 2009..Here, we discuss the genetic factors that can modify the phenotypic expression of such gains and losses, which likely play a role in these and other recurrent genomic disorders... - Microarray-based mutation detection in the dystrophin geneMadhuri R Hegde
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA
Hum Mutat 29:1091-9. 2008..This assay can be readily adopted by clinical molecular testing laboratories and represents a rapid, cost-effective approach for screening a large gene, such as dystrophin... - Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca
Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
Am J Hum Genet 87:618-30. 2010..In addition, the phenotypic features of patients with this CNV are consistent with a contiguous gene syndrome that extends beyond RCAD, which is caused by HNF1B mutations only... 
The pathophysiology of fragile x syndromeOlga Penagarikano
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA
Annu Rev Genomics Hum Genet 8:109-29. 2007..An advancing understanding of the pathophysiology of this disorder has led to promising strategies for pharmacologic interventions...- Genomic structural variation and schizophreniaJennifer Gladys Mulle
Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30317, USA
Curr Psychiatry Rep 10:171-7. 2008..Although much optimism surrounds this burgeoning field, the technical challenges in reliably identifying structural variation mean recent literature should be approached with caution... - Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variantsMartin F Arlt
Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA
Am J Hum Genet 84:339-50. 2009..This is a previously unrecognized consequence of replication stress and suggests that replication fork stalling and subsequent error-prone repair are important mechanisms in the formation of CNVs and pathogenic CNCs in humans... - Replication stress induces tumor-like microdeletions in FHIT/FRA3BSandra G Durkin
Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109 5618, USA
Proc Natl Acad Sci U S A 105:246-51. 2008....