Evidence map›Paper›PMID 21738478›Full record

ArticlePLoS genetics2011

Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.

Yukinori Okada, Tomomitsu Hirota, Yoichiro Kamatani, Atsushi Takahashi, Hiroko Ohmiya, Natsuhiko Kumasaka, Koichiro Higasa, Yumi Yamaguchi-Kabata, Naoya Hosono, Michael A Nalls and 21 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 10 pooled it
6.4field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 10 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  17. Factors associated with genetic markers for rotator cuff disease in patients with atraumatic rotator cuff tears.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2024
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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

31 authors at 14 institutions in 6 countries.

Yukinori OkadaLaboratory for Statistical Analysis, Center for Genomic Medicine, Institute of Physical and Chemical Research, Yokohama, Japan. yokada@src.riken.jp
Tomomitsu Hirota
Yoichiro Kamatani
Atsushi Takahashi
Hiroko Ohmiya
Natsuhiko Kumasaka
Koichiro Higasa
Yumi Yamaguchi-Kabata
Naoya Hosono
Michael A Nalls
Ming Huei Chen
Frank J A van Rooij
Albert V Smith
Toshiko Tanaka
David J Couper
Neil A Zakai
Luigi Ferrucci
Dan L Longo
Dena G Hernandez
Jacqueline C M Witteman
Tamara B Harris
Christopher J O'Donnell
Santhi K Ganesh
Koichi Matsuda
Tatsuhiko Tsunoda
Toshihiro Tanaka
Michiaki Kubo
Yusuke Nakamura
Mayumi Tamari
Kazuhiko Yamamoto
Naoyuki Kamatani
RIKEN Center for Integrative Medical Sciences · JPNational Institutes of Health · USNational Institute on Aging · USRIKEN · JPThe University of Tokyo · JPBoston University · USErasmus University Rotterdam · NLFondation Jean Dausset-CEPH · FRIcelandic Heart Association · ISMichigan Medicine · USNational Heart Lung and Blood Institute · USNetherlands Consortium for Healthy Ageing · NLUniversity of North Carolina at Chapel Hill · USUniversity of Vermont · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

White blood cells (WBCs) mediate immune systems and consist of various subtypes with distinct roles. Elucidation of the mechanism that regulates the counts of the WBC subtypes would provide useful insights into both the etiology of the immune system and disease pathogenesis. In this study, we report results of genome-wide association studies (GWAS) and a replication study for the counts of the 5 main WBC subtypes (neutrophils, lymphocytes, monocytes, basophils, and eosinophils) using 14,792 Japanese subjects enrolled in the BioBank Japan Project. We identified 12 significantly associated loci that satisfied the genome-wide significance threshold of P<5.0×10(-8), of which 9 loci were novel (the CDK6 locus for the neutrophil count; the ITGA4, MLZE, STXBP6 loci, and the MHC region for the monocyte count; the SLC45A3-NUCKS1, GATA2, NAALAD2, ERG loci for the basophil count). We further evaluated associations in the identified loci using 15,600 subjects from Caucasian populations. These WBC subtype-related loci demonstrated a variety of patterns of pleiotropic associations within the WBC subtypes, or with total WBC count, platelet count, or red blood cell-related traits (n = 30,454), which suggests unique and common functional roles of these loci in the processes of hematopoiesis. This study should contribute to the understanding of the genetic backgrounds of the WBC subtypes and hematological traits.

Indexed as

Asian PeopleGene Expression ProfilingGene Expression RegulationGenetic LociGenome-Wide Association StudyHumansLeukocytesPolymorphism, Single NucleotideWhite People

Identifiers

PMID21738478
PMCPMC3128095
OpenAlexW2123706805

What OpenQuestion holds

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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.