Evidence map›Paper›PMID 30903456›Full record

ArticleJournal of clinical immunology2019

A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.

Sinem Firtina, Funda Cipe, Yuk Yin Ng, Ayca Kiykim, Ozden Hatirnaz Ng, Tugce Sudutan, Cigdem Aydogmus, Safa Baris, Gulyuz Ozturk, Elif Aydiner and 2 more

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Journal of clinical immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Informed clinical decisions by outfoxing human FOXN1 variants.The Journal of allergy and clinical immunology · 2025
    Review
  2. Article
  3. Utilization of next-generation sequencing to define the role of heterozygousThe journal of allergy and clinical immunology. Global · 2024
    Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 9 institutions in 2 countries.

Sinem FirtinaDepartment of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
Funda CipeDepartment of Pediatric Allergy and Infection, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Yuk Yin NgDepartment of Genetics and Bioengineering, Istanbul Bilgi University, Istanbul, Turkey.
Ayca KiykimDepartment of Pediatric Allergy and Infection, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Ozden Hatirnaz NgDepartment of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
Tugce SudutanDepartment of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
Cigdem AydogmusDepartment of Pediatric Allergy and Infection, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Safa BarisDepartment of Pediatric Allergy and Immunology, Marmara University, Istanbul, Turkey.
Gulyuz OzturkPediatric Bone Marrow Transplantation Unit, Acibadem Atakent Hospital, Istanbul, Turkey.
Elif AydinerDepartment of Pediatric Allergy and Immunology, Marmara University, Istanbul, Turkey.
Ahmet OzenDepartment of Pediatric Allergy and Immunology, Marmara University, Istanbul, Turkey.
Muge SayitogluDepartment of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey. mugeay@istanbul.edu.tr.ORCID 0000-0002-8648-213X
Marmara University · TRİstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi · TRAcıbadem University Atakent Hospital · TRHUN-REN Institute of Experimental Medicine · HUIstanbul Bilgi University · TRIstanbul University · TRIstanbul University-Cerrahpaşa · TRIstinye University · TRKent Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ConsanguinityFemaleForkhead Transcription FactorsHumansInfantMaleSevere Combined ImmunodeficiencySiblingsTurkeyForkhead Transcription FactorsWhn protein

Identifiers

PMID30903456
OpenAlexW2929206389

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.