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Rare and de novo coding variants in chromodomain genes in Chiari I malformation
Brooke Sadler, Jackson Wilborn, Lilian Antunes, Timothy Kuensting, Andrew T. Hale, Stephen R. Gannon, Kevin McCall, Carlos Cruchaga, Matthew Harms, Norine Voisin, Alexandre Reymond, Gerarda Cappuccio, Nicola Burnetti-Pierri, Marco Tartaglia, Marcello Niceta, Chiara Leoni, Giuseppe Zampino, Allison Ashley-Koch, Aintzane Urbizu, Melanie E. Garrett
- Division of Hematology & Oncology
- Institute of Clinical and Translational Sciences (ICTS)
- Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- McDonnell Genome Institute (MGI)
- NeuroGenomics and Informatics Center
- COVID-19 Researchers
- Department of Neurosurgery
- Siteman Cancer Center
- Department of Genetics
- Department of Neurology
- Division of Pediatric Neurosurgery
- Division of Pediatric and Developmental Neurology
- Institute for Public Health
- Neurofibromatosis (NF) Center
- DBBS - Neurosciences
- DBBS - Human and Statistical Genetics
- DBBS - Biomedical Informatics and Data Science
- DBBS - Molecular Genetics and Genomics
- DBBS - Computational and Systems Biology
- Hope Center for Neurological Disorders
- Brain Tumor Center
- Intellectual and Developmental Disabilities Research Center (IDDRC)
- Division of Basic Science Research
Research output: Contribution to journal › Article › peer-review
19
Scopus
citations