Evidence map›Paper›PMID 27812259›Full record

ArticleIndian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion2016

Genotyping of Intron Inversions and Point Mutations in Exon 14 of the FVIII Gene in Iranian Azeri Turkish Families with Hemophilia A.

Mahmoud Shekari Khaniani, Abdollah Ebrahimi, Setareh Daraei, Sima Mansoori Derakhshan

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Mutational Profiles ofMediterranean journal of hematology and infectious diseases · 2018
    Article
  2. Molecular Genetic Diagnosis of the Inherited Bleeding Disorders: Are We Close to the Perfect Test?Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2016
    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

4 authors.

Mahmoud Shekari KhanianiHematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran ; Department of Medical Genetics, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Abdollah EbrahimiHematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran ; Department of Medical Genetics, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Setareh DaraeiEbnsina Medical Genetic Center, Outpatient Clinic of Tabriz University of Medical Sciences, Tabriz, Iran.
Sima Mansoori DerakhshanHematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran ; Department of Medical Genetics, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemophilia A (HA) is an inherited X-linked bleeding disorder caused by a variety of mutations that are distributed throughout the large

Indexed as

FVIII geneHemophilia AIntron 22 inversionIS-PCRLong-range PCR

Identifiers

PMID27812259
PMCPMC5074980

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.