Diana Chase

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

Gillian Rice, Gabriella Forte, Marcin Szynkiewicz et al. · The Lancet Neurology · 2013 · 438 citations

Life Sciences, Genetics, Molecular Genetics +16

A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability

Catherine S. Healey, Alison M. Dunning, M. Dawn Teare et al. · Nature Genetics · 2000 · 171 citations

Medicine, Genetics, Molecular Genetics +16

CNR1 Gene is Associated with High Neuroticism and Low Agreeableness and Interacts with Recent Negative Life Events to Predict Current Depressive Symptoms

Gabriella Juhász, Diana Chase, Emma Pegg et al. · Neuropsychopharmacology · 2009 · 169 citations · Full text

Social Sciences, Psychiatry, Psychology +11

The CREB1-BDNF-NTRK2 Pathway in Depression: Multiple Gene-Cognition-Environment Interactions

Gabriella Juhász, Jason S. Dunham, Shane McKie et al. · Biological Psychiatry · 2011 · 162 citations

Life Sciences, Neuroscience, Psychiatry +12