# Eli Sprecher

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/eli-sprecher/

## Facts

| Field | Value |
| --- | --- |
| Citations | 16,178 |
| Field | Skin and Cellular Biology Research |
| h-index | 62 |
| i10-index | 268 |
| Last Known Institution | Boston Children's Hospital |
| OpenAlex ID | https://openalex.org/A5050718731 |
| ORCID iD | 0000-0002-4093-1032 |
| Works | 538 |

## Researcher papers

- [Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009](https://scholariq.org/papers/revised-nomenclature-and-classification-of-inherited-ichthyoses-results-of-the/)
- [Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility](https://scholariq.org/papers/consensus-reclassification-of-inherited-epidermolysis-bullosa-and-other/)
- [Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis](https://scholariq.org/papers/mutations-in-galnt3-encoding-a-protein-involved-in-o-linked-glycosylation-cause/)
- [Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis](https://scholariq.org/papers/mutations-in-abca12-underlie-the-severe-congenital-skin-disease-harlequin/)
- [Updated S2K guidelines on the management of pemphigus vulgaris and foliaceus initiated by the european academy of dermatology and venereology (EADV)](https://scholariq.org/papers/updated-s2k-guidelines-on-the-management-of-pemphigus-vulgaris-and-foliaceus/)
- [Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting](https://scholariq.org/papers/desmoglein-1-deficiency-results-in-severe-dermatitis-multiple-allergies-and/)
- [SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4](https://scholariq.org/papers/serkal-syndrome-an-autosomal-recessive-disorder-caused-by-a-loss-of-function/)
- [Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14](https://scholariq.org/papers/familial-pityriasis-rubra-pilaris-is-caused-by-mutations-in-card14/)
- [Updated<scp>S2</scp>K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (<scp>EADV</scp>)](https://scholariq.org/papers/updated-scp-s2-scp-k-guidelines-for-the-management-of-bullous-pemphigoid/)
- [Association Between Vaccination With BNT162b2 and Incidence of Symptomatic and Asymptomatic SARS-CoV-2 Infections Among Health Care Workers](https://scholariq.org/papers/association-between-vaccination-with-bnt162b2-and-incidence-of-symptomatic-and/)
- [Ensuring Timely Connection to Early Intervention for Young Children With Developmental Delays](https://scholariq.org/papers/ensuring-timely-connection-to-early-intervention-for-young-children-with/)

## Researcher topics

- [Skin and Cellular Biology Research](https://scholariq.org/topics/skin-and-cellular-biology-research/)
- [Autoimmune Bullous Skin Diseases](https://scholariq.org/topics/autoimmune-bullous-skin-diseases/)
- [Wnt/β-catenin signaling in development and cancer](https://scholariq.org/topics/wnt-catenin-signaling-in-development-and-cancer/)
- [Hair Growth and Disorders](https://scholariq.org/topics/hair-growth-and-disorders/)
- [Genetic and rare skin diseases.](https://scholariq.org/topics/genetic-and-rare-skin-diseases/)

## Researcher university

- [Boston Children's Hospital](https://scholariq.org/institutions/boston-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.