Danielle Gleason
Hartford Hospital(US)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Hereditary Neurological Disorders, Neurological diseases and metabolism, Autism Spectrum Disorder Research, DNA Repair Mechanisms
Most-Cited Works
- → Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry(2008)744 cited
- → Mutations in PNKP cause microcephaly, seizures and defects in DNA repair(2010)290 cited
- → A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly(2009)142 cited
- → A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts(2010)104 cited
- → CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development(2012)104 cited
- → CC2D1A Regulates Human Intellectual and Social Function as well as NF-κB Signaling Homeostasis(2014)78 cited
- → Ethnically diverse causes of Walker-Warburg syndrome (WWS):FCMDmutations are a more common cause of WWS outside of the Middle East(2008)71 cited
- → Developmental and degenerative features in a complicated spastic paraplegia(2009)36 cited
- → Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort(2010)23 cited
- → Opioid Avoidance in Liver Transplant Recipients: Reduction in Postoperative Opioid Use Through a Multidisciplinary Multimodal Approach(2020)19 cited