Evidence map›Paper›PMID 42074284›Full record

ArticleInternational journal of molecular sciences2026

Genetic and Clinical Characteristics of Russian Patients with Congenital Factor V Deficiency.

Olesya Pshenichnikova, Julia Poznyakova, Ekaterina Shchemeleva, Vadim Surin, Elena Yakovleva, Elena Likhacheva, Oksana Dimitrieva, Olga Yastrubinetskaya, Nikolay Andreev, Natalia Sats and 1 more

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Article in International journal of molecular sciences, 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

11 authors.

Olesya PshenichnikovaLaboratory of Genetic Engineering, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.ORCID 0000-0001-5752-8146
Julia PoznyakovaLaboratory of Genetic Engineering, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Ekaterina ShchemelevaLaboratory of Genetic Engineering, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Vadim SurinLaboratory of Genetic Engineering, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Elena YakovlevaClinical and Diagnostic Department of Hematology and Hemostasis Disorders, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Elena LikhachevaClinical and Diagnostic Department of Hematology and Hemostasis Disorders, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Oksana DimitrievaClinical and Diagnostic Department of Hematology and Hemostasis Disorders, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Olga YastrubinetskayaClinical and Diagnostic Department of Hematology and Hemostasis Disorders, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Nikolay AndreevClinical and Diagnostic Department of Hematology and Hemostasis Disorders, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Natalia SatsLaboratory of Hematopoiesis Physiology, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Nadezhda ZozulyaClinical and Diagnostic Department of Hematology and Hemostasis Disorders, National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital factor V (FV) deficiency is a rare autosomal recessive bleeding disorder caused by pathogenic variants in

Indexed as

Factor VFactor V DeficiencyChildChild, PreschoolFemaleGenetic Association StudiesHumansMaleMutationPedigreeRussiaFactor Vaberrant splicingF5 genefactor V deficiencyintronic variantsmutation spectrum

Identifiers

PMID42074284
PMCPMC13116891

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Registered trials

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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.