# Martin B. Delatycki

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/martin-b-delatycki/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,391 |
| Field | Genetic Neurodegenerative Diseases |
| h-index | 70 |
| i10-index | 311 |
| Last Known Institution | Royal Children's Hospital |
| OpenAlex ID | https://openalex.org/A5022824964 |
| ORCID iD | https://orcid.org/0000-0002-8769-2569 |
| Works | 522 |

## Researcher papers

- [Iron-Overload–Related Disease in<i>HFE</i>Hereditary Hemochromatosis](https://scholariq.org/papers/iron-overload-related-disease-in-i-hfe-i-hereditary-hemochromatosis/)
- [C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy](https://scholariq.org/papers/c-terminal-truncations-in-human-3-5-dna-exonuclease-trex1-cause-autosomal/)
- [Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders](https://scholariq.org/papers/large-scale-targeted-sequencing-identifies-risk-genes-for-neurodevelopmental/)

## Researcher topics

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)

## Researcher university

- [Royal Children's Hospital](https://scholariq.org/institutions/royal-children-s-hospital/)

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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.