Evidence map›Paper›PMID 39107201›Full record

SynthesisBlood reviews2024

Longitudinal clinical manifestations of Fanconi anemia: A systematized review.

Alex Hoover, Lucie M Turcotte, Rachel Phelan, Crystal Barbus, Arpana Rayannavar, Bradley S Miller, Erin E Reardon, Nicole Theis-Mahon, Margaret L MacMillan

Abstract readSystematic Review
In one paragraph

Synthesis in Blood reviews, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. DNA Damage in Pulmonary Arterial Hypertension and Veno-Occlusive Disease-FANCL as Dual Rescue?American journal of respiratory and critical care medicine · 2025
    Article
  8. Review
  9. Differential expression of a disease-associatedbioRxiv : the preprint server for biology · 2025
    Article
  10. Another Fanconi anemia gene joins the club.The Journal of clinical investigation · 2025
    Article
  11. Article
  12. [Advancements in CRISPR-Cas9 for Fanconi anemia].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2025
    Review
  13. Review
  14. Article
  15. Genes · 2024
    Article
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

9 authors.

Alex HooverDivision of Blood and Marrow Transplantation & Cellular Therapy, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: hoove231@umn.edu.
Lucie M TurcotteDivision of Hematology and Oncology, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Rachel PhelanDivision of Hematology, Oncology, and Blood and Marrow Transplant, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, USA.
Crystal BarbusDivision of Endocrinology, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Arpana RayannavarDivision of Endocrinology, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Bradley S MillerDivision of Endocrinology, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Erin E ReardonWoodruff Health Sciences Center Library, Emory University, Atlanta, GA, USA.
Nicole Theis-MahonHealth Sciences Library, University of Minnesota, Minneapolis, MN, USA.
Margaret L MacMillanDivision of Blood and Marrow Transplantation & Cellular Therapy, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.

Funding

Translational Pediatric Cancer Epidemiology Research Training GrantT32CA099936 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Logan G. Spector · 2004 to 2026
$5.1M
NCI NIH HHS T32 CA099936
6 · The paper itself

Abstract

Fanconi anemia (FA) is a rare and complex inherited genetic disorder characterized by impaired DNA repair mechanisms leading to genomic instability. Individuals with FA have increased susceptibility to congenital anomalies, progressive bone marrow failure, leukemia and malignant tumors, endocrinopathies and other medical issues. In recent decades, steadily improved approaches to hematopoietic cell transplantation (HCT), the only proven curative therapy for the hematologic manifestations of FA, have significantly increased the life expectancy of affected individuals, illuminating the need to understand the long-term consequences and multi-organ ramifications. Utilizing a systematized review approach with narrative synthesis of each primary issue and organ system, we shed light on the challenges and opportunities for optimizing the care and quality of life for individuals with FA and identify knowledge gaps informing future research directions.

Indexed as

Fanconi AnemiaDisease ManagementDisease ProgressionHematopoietic Stem Cell TransplantationHumansQuality of LifeFanconi anemiaLate effectsLong-termOutcomes

Identifiers

PMID39107201
PMCPMC11568946

What OpenQuestion holds

Textmetadata
LicenceTDM
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.