Erin L. Heinzen

机构：University of North Carolina at Chapel Hill · ORCID：0000-0002-7268-8559

发表论文 166 篇 · 总被引 16700 次 · h-index 54

代表论文

• GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture (2023 · Nature Genetics · 被引 226)
• Somatic variants in diverse genes leads to a spectrum of focal cortical malformations (2022 · Brain · 被引 84)
• Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy (2023 · JAMA Neurology · 被引 82)
• Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes (2024 · Nature Neuroscience · 被引 64)
• Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals (2023 · Nature Communications · 被引 59)
• Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery (2022 · EBioMedicine · 被引 43)