# Polina Stepensky

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/polina-stepensky/

## Facts

| Field | Value |
| --- | --- |
| Citations | 7,557 |
| Field | Immunodeficiency and Autoimmune Disorders |
| h-index | 46 |
| i10-index | 136 |
| Last Known Institution | Hebrew University of Jerusalem |
| OpenAlex ID | https://openalex.org/A5019096874 |
| ORCID iD | 0000-0002-4923-3660 |
| Works | 262 |

## Researcher papers

- [Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study](https://scholariq.org/papers/reduced-intensity-conditioning-and-hla-matched-haemopoietic-stem-cell/)
- [The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency](https://scholariq.org/papers/the-extended-phenotype-of-lps-responsive-beige-like-anchor-protein-lrba/)
- [Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency](https://scholariq.org/papers/update-on-the-safety-and-efficacy-of-retroviral-gene-therapy-for/)
- [Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies](https://scholariq.org/papers/monogenic-mutations-differentially-affect-the-quantity-and-quality-of-t/)
- [The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis](https://scholariq.org/papers/the-syndrome-of-hemophagocytic-lymphohistiocytosis-in-primary-immunodeficiencies/)
- [Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects](https://scholariq.org/papers/deficiency-of-caspase-recruitment-domain-family-member-11-card11-causes-profound/)
- [Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults](https://scholariq.org/papers/hematopoietic-cell-transplantation-in-chronic-granulomatous-disease-a-study-of/)
- [Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score](https://scholariq.org/papers/long-term-outcome-of-lrba-deficiency-in-76-patients-after-various-treatment/)
- [Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia](https://scholariq.org/papers/germline-etv6-mutations-confer-susceptibility-to-acute-lymphoblastic-leukemia/)
- [The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency](https://scholariq.org/papers/the-card11-bcl10-malt1-cbm-signalosome-complex-stepping-into-the-limelight-of/)
- [Clinical presentation and analysis of genotype-phenotype correlations in patients with malignant infantile osteopetrosis](https://scholariq.org/papers/clinical-presentation-and-analysis-of-genotype-phenotype-correlations-in/)

## Researcher topics

- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Hematopoietic Stem Cell Transplantation](https://scholariq.org/topics/hematopoietic-stem-cell-transplantation/)
- [Immune Cell Function and Interaction](https://scholariq.org/topics/immune-cell-function-and-interaction/)
- [CAR-T cell therapy research](https://scholariq.org/topics/car-t-cell-therapy-research/)
- [Blood disorders and treatments](https://scholariq.org/topics/blood-disorders-and-treatments/)

## Researcher university

- [Hebrew University of Jerusalem](https://scholariq.org/institutions/hebrew-university-of-jerusalem/)

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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.