Erin L. Heinzen
Structural Genomics Consortium(CA)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Epilepsy research and treatment, Genetic Associations and Epidemiology
Most-Cited Works
- → Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance(2009)3,514 cited
- → Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes(2013)988 cited
- → HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans(2011)905 cited
- → Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies(2018)499 cited
- → Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations(2012)475 cited
- → A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia(2009)445 cited
- → De novo mutations in ATP1A3 cause alternating hemiplegia of childhood(2012)418 cited
- → Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals(2019)299 cited
- → Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits(2008)269 cited
- → Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes(2010)259 cited