# Giulio Genovese

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/giulio-genovese/

## Facts

| Field | Value |
| --- | --- |
| Citations | 81,736 |
| Field | Genetic Associations and Epidemiology |
| h-index | 68 |
| i10-index | 119 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5008886933 |
| ORCID iD | https://orcid.org/0000-0003-3066-5575 |
| Works | 240 |

## Researcher papers

- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence](https://scholariq.org/papers/clonal-hematopoiesis-and-blood-cancer-risk-inferred-from-blood-dna-sequence/)
- [Mapping genomic loci implicates genes and synaptic biology in schizophrenia](https://scholariq.org/papers/mapping-genomic-loci-implicates-genes-and-synaptic-biology-in-schizophrenia/)
- [Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans](https://scholariq.org/papers/association-of-trypanolytic-apol1-variants-with-kidney-disease-in-african/)
- [Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores](https://scholariq.org/papers/modeling-linkage-disequilibrium-increases-accuracy-of-polygenic-risk-scores/)
- [Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects](https://scholariq.org/papers/contribution-of-copy-number-variants-to-schizophrenia-from-a-genome-wide-study/)
- [APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy](https://scholariq.org/papers/apol1-genetic-variants-in-focal-segmental-glomerulosclerosis-and-hiv-associated/)
- [Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases](https://scholariq.org/papers/partitioning-heritability-of-regulatory-and-cell-type-specific-variants-across/)
- [Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel](https://scholariq.org/papers/integrating-sequence-and-array-data-to-create-an-improved-1000-genomes-project/)
- [Genetic predisposition to mosaic Y chromosome loss in blood](https://scholariq.org/papers/genetic-predisposition-to-mosaic-y-chromosome-loss-in-blood/)
- [A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts](https://scholariq.org/papers/a-comparison-of-ten-polygenic-score-methods-for-psychiatric-disorders-applied/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Cancer Genomics and Diagnostics](https://scholariq.org/topics/cancer-genomics-and-diagnostics/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)

## Researcher university

- [Broad Institute](https://scholariq.org/institutions/broad-institute/)

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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.