# Alan E. Guttmacher

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/alan-e-guttmacher/

## Facts

| Field | Value |
| --- | --- |
| Citations | 24,001 |
| Field | Vascular Anomalies and Treatments |
| h-index | 40 |
| i10-index | 57 |
| OpenAlex ID | https://openalex.org/A5111622584 |
| Works | 86 |

## Researcher papers

- [Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1](https://scholariq.org/papers/endoglin-a-tgf-binding-protein-of-endothelial-cells-is-the-gene-for-hereditary/)
- [Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2](https://scholariq.org/papers/mutations-in-the-activin-receptor-like-kinase-1-gene-in-hereditary-haemorrhagic/)
- [International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia](https://scholariq.org/papers/international-guidelines-for-the-diagnosis-and-management-of-hereditary/)

## Researcher topics

- [Vascular Anomalies and Treatments](https://scholariq.org/topics/vascular-anomalies-and-treatments-2/)
- [BRCA gene mutations in cancer](https://scholariq.org/topics/brca-gene-mutations-in-cancer/)
- [Tracheal and airway disorders](https://scholariq.org/topics/tracheal-and-airway-disorders-2/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics, Bioinformatics, and Biomedical Research](https://scholariq.org/topics/genetics-bioinformatics-and-biomedical-research/)

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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.