Diane Kissell
Cincinnati Children's Hospital Medical Center(US)
Publications by Year
Research Areas
Immune Cell Function and Interaction, Autoimmune and Inflammatory Disorders Research, Parvovirus B19 Infection Studies, Parkinson's Disease Mechanisms and Treatments, Hearing, Cochlea, Tinnitus, Genetics
Most-Cited Works
- → Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy(2015)670 cited
- → Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH(2011)418 cited
- → Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza(2015)169 cited
- → Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis(2014)144 cited
- → Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations(2009)73 cited
- → Genotype-Directed Dosing Leads to Optimized Voriconazole Levels in Pediatric Patients Receiving Hematopoietic Stem Cell Transplantation(2015)48 cited
- → Variation in GIGYF2 is not associated with Parkinson disease(2009)44 cited
- → A comprehensive next‐generation sequencing assay for the diagnosis of epidermolysis bullosa(2018)43 cited
- → Performance Evaluation of the Next‐Generation Sequencing Approach for Molecular Diagnosis of Hereditary Hearing Loss(2013)40 cited
- → The 253‐kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3(2014)36 cited