Jennifer Gladys Mulle

Summary

Affiliation: Emory University
Country: USA

Publications

  1. pmc Microdeletions of 3q29 confer high risk for schizophrenia
    Jennifer Gladys Mulle
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
    Am J Hum Genet 87:229-36. 2010
  2. doi request reprint Reciprocal duplication of the williams-beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia
    Jennifer Gladys Mulle
    Department of Epidemiology, Rollins School of Public Health, Emory University Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia Electronic address
    Biol Psychiatry 75:371-7. 2014
  3. pmc Cardiovascular disease, psychosocial factors, and genetics: the case of depression
    Jennifer Gladys Mulle
    Department of Epidemiology, Rollins School of Public Health, Emory University, GA 30322, USA
    Prog Cardiovasc Dis 55:557-62. 2013
  4. pmc The gut microbiome: a new frontier in autism research
    JENNIFER 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
  5. doi request reprint Schizophrenia genetics: progress, at last
    Jennifer Gladys Mulle
    Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, GA, United States
    Curr Opin Genet Dev 22:238-44. 2012
  6. pmc Empirical evaluation of oligonucleotide probe selection for DNA microarrays
    JENNIFER G MULLE
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America
    PLoS ONE 5:e9921. 2010
  7. pmc Segmental duplications mediate novel, clinically relevant chromosome rearrangements
    M Katharine Rudd
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
    Hum Mol Genet 18:2957-62. 2009
  8. pmc Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
    Daniel Moreno-De-Luca
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
    Am J Hum Genet 87:618-30. 2010
  9. pmc Microarray-based mutation detection in the dystrophin gene
    Madhuri R Hegde
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA
    Hum Mutat 29:1091-9. 2008
  10. ncbi request reprint The pathophysiology of fragile x syndrome
    Olga Penagarikano
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA
    Annu Rev Genomics Hum Genet 8:109-29. 2007

Collaborators

Detail Information

Publications13

  1. pmc Microdeletions of 3q29 confer high risk for schizophrenia
    Jennifer Gladys Mulle
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
    Am J Hum Genet 87:229-36. 2010
    ....
  2. doi request reprint Reciprocal duplication of the williams-beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia
    Jennifer Gladys Mulle
    Department of Epidemiology, Rollins School of Public Health, Emory University Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia Electronic address
    Biol Psychiatry 75:371-7. 2014
    ..Recently, de novo duplications of a region on chromosome 7q11.23 were associated with autism spectrum disorders. The reciprocal deletion of this region causes Williams-Beuren syndrome...
  3. pmc Cardiovascular disease, psychosocial factors, and genetics: the case of depression
    Jennifer Gladys Mulle
    Department of Epidemiology, Rollins School of Public Health, Emory University, GA 30322, USA
    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...
  4. pmc The gut microbiome: a new frontier in autism research
    JENNIFER 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...
  5. doi request reprint Schizophrenia genetics: progress, at last
    Jennifer 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...
  6. pmc Empirical evaluation of oligonucleotide probe selection for DNA microarrays
    JENNIFER 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...
  7. pmc Segmental duplications mediate novel, clinically relevant chromosome rearrangements
    M 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...
  8. pmc Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
    Daniel 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...
  9. pmc Microarray-based mutation detection in the dystrophin gene
    Madhuri 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...
  10. ncbi request reprint The pathophysiology of fragile x syndrome
    Olga 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...
  11. ncbi request reprint Genomic structural variation and schizophrenia
    Jennifer 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...
  12. pmc Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants
    Martin 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...
  13. pmc Replication stress induces tumor-like microdeletions in FHIT/FRA3B
    Sandra 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
    ....