Evidence map›Paper›PMID 39534727›Full record

ArticleGeneral psychiatry2024

Genetic insights into male autism spectrum disorder in a small cohort of Indian simplex families: findings from whole exome sequencing.

Srividhya Durbagula, Snijesh Valiya Parambath, Ashitha Siddappa Niranjana Murthy, Meghana Rameshraju K, Chetan Ghati Kasturirangan, Gautham Arunachal Udupi, Nallur B Ramachandra, Aparna Huligerepura Sosalegowda, Vijaya Raman, Aruna Korlimarla and 1 more

Abstract read
In one paragraph

Article in General psychiatry, 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

11 authors.

Srividhya DurbagulaDepartment of Studies in Biotechnology, University of Mysore, Mysore, Karnataka, India.
Snijesh Valiya ParambathCAREADD, St John's Research Institute, Bangalore, Karnataka, India.
Ashitha Siddappa Niranjana MurthySt John's National Academy of Health Sciences, Bangalore, Karnataka, India.
Meghana Rameshraju KDepartment of Studies in Genetics and Genomics, University of Mysore, Mysore, Karnataka, India.
Chetan Ghati KasturiranganDepartment of Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
Gautham Arunachal UdupiDepartment of Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
Nallur B RamachandraDepartment of Studies in Genetics and Genomics, University of Mysore, Mysore, Karnataka, India.
Aparna Huligerepura SosalegowdaDepartment of Studies in Biotechnology, University of Mysore, Mysore, Karnataka, India.
Vijaya RamanSt John's National Academy of Health Sciences, Bangalore, Karnataka, India.
Aruna KorlimarlaCAREADD, St John's Research Institute, Bangalore, Karnataka, India.
Naveen Kumar Chandappa GowdaCAREADD, St John's Research Institute, Bangalore, Karnataka, India.ORCID 0000-0003-2944-6965

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

autism spectrum disorderchild psychiatrygenetics, behavioral

Identifiers

PMID39534727
PMCPMC11551974

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.