# Pauline L. Lee

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/pauline-l-lee/

## Facts

| Field | Value |
| --- | --- |
| Citations | 2,090 |
| Field | Iron Metabolism and Disorders |
| h-index | 18 |
| i10-index | 26 |
| Last Known Institution | Scripps Research Institute |
| OpenAlex ID | https://openalex.org/A5036955609 |
| Works | 39 |

## Researcher papers

- [Purification and Complementary DNA Cloning of a Receptor for Basic Fibroblast Growth Factor](https://scholariq.org/papers/purification-and-complementary-dna-cloning-of-a-receptor-for-basic-fibroblast/)
- [The Human Nramp2 Gene: Characterization of the Gene Structure, Alternative Splicing, Promoter Region and Polymorphisms](https://scholariq.org/papers/the-human-nramp2-gene-characterization-of-the-gene-structure-alternative/)
- [Regulation of Hepcidin and Iron-Overload Disease](https://scholariq.org/papers/regulation-of-hepcidin-and-iron-overload-disease/)
- [Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin](https://scholariq.org/papers/genetic-abnormalities-and-juvenile-hemochromatosis-mutations-of-the-hjv-gene/)
- [Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans](https://scholariq.org/papers/ferroportin-1-scl40a1-variant-associated-with-iron-overload-in-african-americans/)
- [Diverse Forms of a Receptor for Acidic and Basic Fibroblast Growth Factors](https://scholariq.org/papers/diverse-forms-of-a-receptor-for-acidic-and-basic-fibroblast-growth-factors/)
- [Mutation Analysis of the Transferrin Receptor-2 Gene in Patients with Iron Overload](https://scholariq.org/papers/mutation-analysis-of-the-transferrin-receptor-2-gene-in-patients-with-iron/)
- [Hemojuvelin (<i>HJV</i>) mutations in persons of European, African‐American and Asian ancestry with adult onset haemochromatosis](https://scholariq.org/papers/hemojuvelin-i-hjv-i-mutations-in-persons-of-european-african-american-and-asian/)
- [Human transferrin G277S mutation: a risk factor for iron deficiency anaemia](https://scholariq.org/papers/human-transferrin-g277s-mutation-a-risk-factor-for-iron-deficiency-anaemia/)
- [Iron overload and prolonged ingestion of iron supplements: Clinical features and mutation analysis of hemochromatosis‐associated genes in four cases](https://scholariq.org/papers/iron-overload-and-prolonged-ingestion-of-iron-supplements-clinical-features-and/)
- [Intravenous Bevacizumab Therapy in a Patient with Hereditary Hemorrhagic Telangiectasia, ENG E137K, Alcoholic Cirrhosis, and Portal Hypertension](https://scholariq.org/papers/intravenous-bevacizumab-therapy-in-a-patient-with-hereditary-hemorrhagic/)

## Researcher topics

- [Iron Metabolism and Disorders](https://scholariq.org/topics/iron-metabolism-and-disorders/)
- [Hemoglobinopathies and Related Disorders](https://scholariq.org/topics/hemoglobinopathies-and-related-disorders/)
- [Folate and B Vitamins Research](https://scholariq.org/topics/folate-and-b-vitamins-research/)
- [Trace Elements in Health](https://scholariq.org/topics/trace-elements-in-health/)
- [Porphyrin Metabolism and Disorders](https://scholariq.org/topics/porphyrin-metabolism-and-disorders/)

## Researcher university

- [Scripps Research Institute](https://scholariq.org/institutions/scripps-research-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.