# Ekaterina Rogaeva

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/ekaterina-rogaeva/

## Facts

| Field | Value |
| --- | --- |
| Citations | 58,780 |
| Field | Alzheimer's disease research and treatments |
| h-index | 94 |
| i10-index | 318 |
| Last Known Institution | University of Toronto |
| OpenAlex ID | https://openalex.org/A5012586710 |
| ORCID iD | https://orcid.org/0000-0002-2852-0329 |
| Works | 466 |

## Researcher papers

Showing 12 of 13.

- [Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease](https://scholariq.org/papers/meta-analysis-of-74-046-individuals-identifies-11-new-susceptibility-loci-for/)
- [A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD](https://scholariq.org/papers/a-hexanucleotide-repeat-expansion-in-c9orf72-is-the-cause-of-chromosome-9p21/)
- [Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease](https://scholariq.org/papers/cloning-of-a-gene-bearing-missense-mutations-in-early-onset-familial-alzheimer-s/)
- [Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease](https://scholariq.org/papers/multicenter-analysis-of-glucocerebrosidase-mutations-in-parkinson-s-disease/)
- [Analysis of shared heritability in common disorders of the brain](https://scholariq.org/papers/analysis-of-shared-heritability-in-common-disorders-of-the-brain/)
- [Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease](https://scholariq.org/papers/common-variants-at-ms4a4-ms4a6e-cd2ap-cd33-and-epha1-are-associated-with-late/)
- [Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease](https://scholariq.org/papers/gene-wide-analysis-detects-two-new-susceptibility-genes-for-alzheimer-s-disease/)
- [Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference](https://scholariq.org/papers/uncovering-the-heterogeneity-and-temporal-complexity-of-neurodegenerative/)
- [Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-matrin-3-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [Frontotemporal dementia and its subtypes: a genome-wide association study](https://scholariq.org/papers/frontotemporal-dementia-and-its-subtypes-a-genome-wide-association-study/)
- [<i>SQSTM1</i> mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis](https://scholariq.org/papers/i-sqstm1-i-mutations-in-frontotemporal-lobar-degeneration-and-amyotrophic/)
- [The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter](https://scholariq.org/papers/the-c9orf72-repeat-size-correlates-with-onset-age-of-disease-dna-methylation-and/)

## Researcher topics

- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Dementia and Cognitive Impairment Research](https://scholariq.org/topics/dementia-and-cognitive-impairment-research/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)

## Researcher university

- [University of Toronto](https://scholariq.org/institutions/university-of-toronto/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.