Evidence map›Paper›PMID 39606185›Full record

ArticleFrontiers in cardiovascular medicine2024

Case Report: Allelic and biallelic variants in

Chen Liang, Jie-Yuan Jin, Hai-Hong Shi, Hao-Xian Li, Lin-Lin Chen, Yang-Hui Zhang, Qin Wang, Qiu-Li Li, Rui-Man Li

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in cardiovascular medicine, 2024. 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

9 authors.

Chen LiangDepartment of Clinical Research, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Jie-Yuan JinSchool of Life Sciences, Central South University, Changsha, China.
Hai-Hong ShiCenter for Medical Genetics, Jiangmen Maternal & Child Health Care Hospital, Jiangmen, China.
Hao-Xian LiCenter for Medical Genetics, Jiangmen Maternal & Child Health Care Hospital, Jiangmen, China.
Lin-Lin ChenDepartment of Pediatrics, Jiangmen Maternal & Child Health Care Hospital, Jiangmen, China.
Yang-Hui ZhangCenter of Reproductive Medicine, Jiangmen Maternal & Child Health Care Hospital, Jiangmen, China.
Qin WangDepartment of Nephrology, Xiangya Hospital, Central South University, Changsha, China.
Qiu-Li LiCenter for Medical Genetics, Jiangmen Maternal & Child Health Care Hospital, Jiangmen, China.
Rui-Man LiDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Jinan University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Factor XI deficiency is a rare inherited coagulation disorder with an estimated prevalence of affecting 1 in 1 million. It is characterized by mild and variable bleeding phenotypes, including bruises, nosebleeds, hematuria, and postpartum hemorrhage. It can be caused by either allelic or biallelic variants in

Indexed as

coagulation factor XIFactor XI deficiencyhemophiliamissense variantvariant characteristic

Identifiers

PMID39606185
PMCPMC11599221

What OpenQuestion holds

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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.