Evidence map›Paper›PMID 41881807›Full record

ArticleBritish journal of haematology2026

Co-inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction.

Perla Bandini, Nina Borràs, Laura Martin-Fernandez, Nuria Fernández-Mosteirín, Maria Reyes Aguinaco, Olga Benítez, Natàlia Comes, Lorena Ramírez, Noemí González, Carina Lera and 3 more

Abstract read
In one paragraph

Article in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Perla BandiniLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.ORCID https://orcid.org/0000-0002-6002-7454
Nina BorràsLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.ORCID https://orcid.org/0000-0001-7909-9995
Laura Martin-FernandezLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.
Nuria Fernández-MosteirínServicio de Hematología y Hemoterapia, Hospital Universitario Miguel Servet, Zaragoza, Spain.
Maria Reyes AguinacoServicio de Hematología, Hospital Universitario Joan XXIII, Institut Català d'Oncologia (ICO), Tarragona, Spain.
Olga BenítezUnidad de Hemofilia, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Natàlia ComesLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.
Lorena RamírezLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.
Noemí GonzálezLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.
Carina LeraLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.
Carme Altisent *Medicina Transfusional, Vall d'Hebron Institut de Recerca, Universitat Autònoma de Barcelona (VHIR-UAB), Barcelona, Spain.
Francisco VidalLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.ORCID https://orcid.org/0000-0001-8089-4945
Irene CorralesLaboratori de Coagulopaties Congènites, Banc de Sang i Teixits, Barcelona, Spain.ORCID https://orcid.org/0000-0002-0647-0340

Funding

Centro de Investigación Biomédica en Red Enfermedades CardiovascularesFundació Privada Catalana de l'HemofíliaMinisterio de Economía y Competitividad PI18/01492Ministerio de Economía y Competitividad PI23/01672Real Fundación Victoria Eugenia
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

family segregationinherited platelet disordersITGA2Bplatelet‐type 16 bleeding disorderRNA sequencingTUBB1

Identifiers

PMID41881807
PMCPMC13267432

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.