Evidence map›Paper›PMID 20861579›Full record

ArticleJournal of genetics2010

Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of India.

Mainak Sengupta, Amrita Chakraborty, Indian Genome Variation Consortium, Kunal Ray

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of genetics, 2010. 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, top 86% of its field
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, 1 citations in OpenAlex.

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

4 authors at 1 institution in 1 country.

Mainak SenguptaIndian Institute of Chemical Biology, Kolkata, India.
Amrita Chakraborty
Indian Genome Variation Consortium
Kunal Ray
Indian Institute of Chemical Biology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AllelesGenetic LinkageGenetic VariationGenotypeHumansIndiaPolymorphism, Single NucleotidePrion DiseasesPrion ProteinsPrionsPrion ProteinsPrionsPRNP protein, human

Identifiers

PMID20861579
OpenAlexW2136679017

What OpenQuestion holds

Textmetadata
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.