Evidence map›Paper›PMID 26354101›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2016

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.

Minoo Atakhorrami, Simin Rahimi-Aliabadi, Javad Jamshidi, Elham Moslemi, Abolfazl Movafagh, Mina Ohadi, Arash Mirabzadeh, Babak Emamalizadeh, Hamid Ghaedi, Fatemeh Gholipour and 10 more

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Article in Journal of neural transmission (Vienna, Austria : 1996), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

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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

20 authors at 6 institutions in 1 country.

Minoo AtakhorramiDepartment of Biology, Faculty of Basic Sciences, Islamic Azad University, East Tehran Branch (Ghiamdasht), Tehran, Iran.
Simin Rahimi-AliabadiDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Javad JamshidiNoncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Elham MoslemiDepartment of Biology, Faculty of Basic Sciences, Islamic Azad University, East Tehran Branch (Ghiamdasht), Tehran, Iran.
Abolfazl MovafaghDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mina OhadiGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Arash MirabzadehDepartment of Psychiatry, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Babak EmamalizadehDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Hamid GhaediDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Fatemeh GholipourDepartment of Psychiatry, Emam Hossien Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Atena FazeliDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Marzieh MotallebiDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Shaghayegh TaghaviDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Azadeh AhmadifardDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Saeed MohammadihosseinabadDepartment of Genetics, School of Medicine, Unit of Medical Sciences, Islamic Azad University, Tehran, Iran.
Amir Ehtesham Shafiei ZarnehDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neda ShahmohammadibeniCellular and Molecular Biology Research Center, Babol University of Medical Sciences, Babol, Iran.
Faranak MadadiDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Monavvar AndarvaDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Hossein DarvishDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. darvish_mg@sbmu.ac.ir.
Shahid Beheshti University of Medical Sciences · IRIslamic Azad University, Tehran · IRUniversity of Social Welfare and Rehabilitation Sciences · IRBabol University of Medical Sciences · IRFasa University of Medical Sciences · IRIslamic Azad University Medical Branch of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recent large-scale study have reported that rs1063843, a single nucleotide polymorphism located in the CAMKK2 gene is highly associated with schizophrenia in European and Han Chinese populations. Increasing evidences show that schizophrenia and bipolar disorder have some common genetic variance. Here, we evaluated the association of this variant with schizophrenia and bipolar disorder in Iranian population. Genomic DNA was extracted from peripheral blood of 500 schizophrenic patients, 500 bipolar patients and 500 normal controls and all were genotyped for the rs1063843 using a PCR-RFLP method. The allele frequency of rs1063843 was significantly different in both schizophrenia and bipolar patients comparing to control group. For the first time, we showed that rs1063843 is highly associated with bipolar disorder, although more replication studies are needed to confirm our findings. Our results also support the findings of previous studies suggesting a significant association between rs1063843 and schizophrenia.

Indexed as

AdultAsian PeopleBipolar DisorderCalcium-Calmodulin-Dependent Protein Kinase KinaseFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansIranMaleMiddle AgedPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideSchizophreniaCalcium-Calmodulin-Dependent Protein Kinase KinaseCAMKK2 protein, humanBipolarCAMKK2IranianPolymorphismSchizophrenia

Identifiers

PMID26354101
OpenAlexW2217874157

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.