Evidence map›Paper›PMID 40765903›Full record

ArticleBlood vessels, thrombosis & hemostasis2025

Human and mouse platelet transcriptomes and proteomes for phenotyping 3474 genes with hemostatic and platelet traits.

Jingnan Huang, Federico Marini, Fiorella A Solari, Frauke Swieringa, Bas de Laat, Ilaria De Simone, Luigi Grassi, Xiang Gui, Kunpeng Li, Elizabeth A Middleton and 10 more

Abstract read
In one paragraph

Article in Blood vessels, thrombosis & hemostasis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

20 authors.

Jingnan HuangDepartment of Biochemistry, Maastricht University, Maastricht, The Netherlands.
Federico MariniInstitute of Medical Biostatistics, Epidemiology and Informatics, Mainz, Germany.
Fiorella A SolariLeibniz-Institut für Analytische Wissenschaften-ISAS-e.V., Dortmund, Germany.
Frauke SwieringaSynapse Research Institute Maastricht, Maastricht, The Netherlands.
Bas de LaatSynapse Research Institute Maastricht, Maastricht, The Netherlands.
Ilaria De SimoneSynapse Research Institute Maastricht, Maastricht, The Netherlands.
Luigi GrassiDepartment of Haematology, University of Cambridge, National Health Service Blood and Transplant, Cambridge, United Kingdom.
Xiang GuiSynapse Research Institute Maastricht, Maastricht, The Netherlands.
Kunpeng LiDepartment of Nephrology, The First Affiliated Hospital, Southern University of Science and Technology, Shenzhen, China.
Elizabeth A MiddletonMolecular Medicine Program, The University of Utah, Salt Lake City, UT.
Neil V MorganInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.
Isabella ProvenzaleDepartment of Biochemistry, Maastricht University, Maastricht, The Netherlands.
Carina SantosCenter for Thrombosis and Hemostasis, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Saskia ScholsDepartment of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
Sarah WestburyBristol Medical School, Faculty of Health and Life Sciences, University of Bristol, Bristol, United Kingdom.
Albert SickmannLeibniz-Institut für Analytische Wissenschaften-ISAS-e.V., Dortmund, Germany.
Matthew T RondinaDivision of Pulmonary and Critical Care Medicine, University of Utah School of Medicine, Salt Lake City, UT.
Wolfram RufCenter for Thrombosis and Hemostasis, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Mattia FrontiniDepartment of Haematology, University of Cambridge, National Health Service Blood and Transplant, Cambridge, United Kingdom.
Johan W M HeemskerkDepartment of Biochemistry, Maastricht University, Maastricht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hemostatic process relies on platelet and coagulation activation, with additional roles of red blood cells and the vessel wall. By systematic screening of databases for gene-linked information on hemostasis, we collected phenotypic profiles of 3474 orthologous human and mouse genes regarding bleeding, arterial thrombosis, thrombophilia, platelet traits, coagulation, and erythrocytes. Comparisons showed that defects in 252 mouse genes led to increased bleeding combined with platelet dysfunction or thrombocytopenia, in addition to 150 human orthologs that are registered for familial bleeding disorders, based on panel sequencing. Additionally, 139 mouse genes contributed to arterial thrombosis without bleeding phenotype. To further investigate the role of platelets in hemostasis, we integrated multiple genome-wide RNA-sequencing transcriptomes and proteomes from healthy subjects and C57BL/6 mice. This provided reference levels for 54 790 (54 247) transcripts and 6379 (4563) proteins in human (mouse) platelets. Orthologous transcripts in human and mouse platelets correlated with

Identifiers

PMID40765903
PMCPMC12320467

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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.