Smail Hadj-Rabia
Smail Hadj-Rabia is an expert in Dermatology at Hôpital Necker-Enfants Malades (France). As of October 2026, ScienceLeadR ranks Smail Hadj-Rabia in the top 1% of experts worldwide for Skin Abnormalities, Pigmentation Disorders and Congenital Abnormalities. Smail Hadj-Rabia has authored 424 publications, the most recent in 2026, and is an investigator in 3 clinical trials, 1 of them ongoing. SLR score: 1,139 (community average: 125). How the SLR is computed.
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Dermatology
Subspecialties: Genetics - Pediatrics - Biochemistry
Main Topics
Publications and Clinical Studies
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Organizations
Career arc: 1999 - 2026
Number : 424
Citations
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Latest Publications
5 most recent indexed articles
Source: Pubmed
| Title | Journal | Year | Citations |
|---|---|---|---|
| Clinical findings of women with X-linked hypohidrotic ectodermal dysplasia. PMID 42803177 — sexually transmitted diseases, skin diseases, breast feeding, ectodermal dysplasia 1, anhidrotic, ectodermal dysplasia, genes, x-linked | J Eur Acad Dermatol Venereol | 2026 | 0 |
| Epidermal Necrolysis in Children: Clinical Characteristics and Prognosis: An International Retrospective Multicenter Study (ChildTEN Study). PMID 42791607 — syphilis, dermatology, prognosis, child | Br J Dermatol | 2026 | 0 |
| An isogenic hiPSC-derived keratinocyte model reveals CXCL10/CXCL11 inflammatory dysregulation in epidermolysis bullosa simplex. PMID 42698624 — cells, epidermolysis bullosa simplex, phenotype, epidermolysis bullosa, induced pluripotent stem cells, keratinocytes, therapeutics, keratins | Front Cell Dev Biol | 2026 | 0 |
| How much sweating is enough? Predicting thermoregulatory capacity in patients with ectodermal dysplasia based on a minimal pilocarpine-induced sweat volume. PMID 42683232 — sweating, pilocarpine, iontophoresis, body temperature regulation, signs and symptoms, ectodermal dysplasia 1, anhidrotic, mutation, temperature, ectodermal dysplasia | Front Pediatr | 2026 | 0 |
| Deep Phenotyping and Molecular Elucidation of a New Syndrome: Ectodermal Dysplasia Caused by IRF6 Variants. PMID 42487474 — skin, natal teeth, genes, tooth, skin diseases, hearing, diagnosis, hearing loss, ectoderm, ectodermal dysplasia | Exp Dermatol | 2026 | 1 |
Clinical Studies 3
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Cohort/Consortium Investigators 2
Ongoing Clinical Trials
Ongoing trial started since 2021, where this expert is an investigator
Source: ClinicalTrials
| Study | Phase | Status | Start |
|---|---|---|---|
| Peripheral Serotonin and Albinism NCT06138509 — hemoglobins, laboratories, hematology, blood, serum, reticulocytes, anemia, transferrin, c-reactive protein, albinism, central nervous system, albinism, oculocutaneous, serotonin, ferritins, work, erythropoietin, nervous system, blood platelets, child, iron deficiencies | N/A | Recruiting | 2024 |
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