Article detail · 2017
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
YÖKSİS
OpenAlex
Open access · green
SJR Q1
JCR Q1
Citations 283
Top 1%
Percentile 99.2%
FWCI 13.01
- Year
- 2017
- Type
- article
Data source split
- YÖKSİS YÖKSİS article record
- YÖKSİS venue Journal of Allergy and Clinical Immunology
- Catalog match (ISSN) Journal of Allergy and Clinical Immunology
- OpenAlex OpenAlex enrichment (abstract, citations, topics)
Abstract
Abstract not compiled yet; it will appear after the DergiPark / OpenAlex queue runs.
Topics
Citations
OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.
283 citations
OpenAlex cited_by_count (cache / database)
24 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
- Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants 2023
- Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome 2022
- Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency 2017
- Consensus Middle East and North Africa Registry on Inborn Errors of Immunity 2021
- Consensus Middle East and North Africa Registry on Inborn Errors of Immunity 2021
- Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience 2021
- Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community 2020
- Approach to genetic diagnosis of inborn errors of immunity through next-generation sequencing 2021
- Infliximab therapy for inflammatory colitis in an infant with NEMO deficiency 2019
- Infliximab therapy for inflammatory colitis in an infant with NEMO deficiency 2019