Evidence map›Paper›PMID 35650273›Full record

ArticleCommunications biology2022

Genetic architecture of band neutrophil fraction in Iceland.

Gudjon R Oskarsson, Magnus K Magnusson, Asmundur Oddsson, Brynjar O Jensson, Run Fridriksdottir, Gudny A Arnadottir, Hildigunnur Katrinardottir, Solvi Rognvaldsson, Gisli H Halldorsson, Gardar Sveinbjornsson and 24 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Novel loci for Alzheimer's disease identified by a genome-wide association study in Ashkenazi Jews.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    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

34 authors at 4 institutions in 2 countries.

Gudjon R OskarssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0002-1842-8799
Magnus K MagnussondeCODE genetics/Amgen Inc., Reykjavik, Iceland. magnus.magnusson@decode.is.ORCID 0000-0001-8593-4934
Asmundur OddssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0002-4606-5163
Brynjar O JenssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0002-2252-4134
Run FridriksdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Gudny A ArnadottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0001-6571-423X
Hildigunnur KatrinardottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Solvi RognvaldssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Gisli H HalldorssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0001-7067-9862
Gardar SveinbjornssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Erna V IvarsdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0002-2069-0681
Lilja StefansdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Egil FerkingstaddeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0001-8090-7988
Kristjan NorlanddeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Vinicius TragantedeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Jona SaemundsdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Aslaug JonasdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Adalbjorg JonasdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Svanhvit SigurjonsdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Karen O PetursdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Olafur B DavidssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Thorunn RafnardeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0003-0491-7046
Hilma HolmdeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0002-9517-6636
Isleifur OlafssonDepartment of Clinical Biochemistry, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland.
Pall T OnundarsonFaculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.
Brynjar VidarssonDepartment of Laboratory Hematology, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland.
Olof SigurdardottirDepartment of Clinical Biochemistry, Akureyri Hospital, Akureyri, Iceland.
Gisli MassondeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Daniel F GudbjartssondeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0002-5222-9857
Ingileif JonsdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0001-8339-150X
Gudmundur L NorddahldeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Unnur ThorsteinsdottirdeCODE genetics/Amgen Inc., Reykjavik, Iceland.
Patrick SulemdeCODE genetics/Amgen Inc., Reykjavik, Iceland.ORCID 0000-0001-7123-6123
Kari StefanssondeCODE genetics/Amgen Inc., Reykjavik, Iceland. kstefans@decode.is.ORCID 0000-0003-1676-864X
deCODE Genetics (Iceland) · ISNational University Hospital of Iceland · ISAkureyri Hospital · ISUniversity of Iceland · IS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The characteristic lobulated nuclear morphology of granulocytes is partially determined by composition of nuclear envelope proteins. Abnormal nuclear morphology is primarily observed as an increased number of hypolobulated immature neutrophils, called band cells, during infection or in rare envelopathies like Pelger-Huët anomaly. To search for sequence variants affecting nuclear morphology of granulocytes, we performed a genome-wide association study using band neutrophil fraction from 88,101 Icelanders. We describe 13 sequence variants affecting band neutrophil fraction at nine loci. Five of the variants are at the Lamin B receptor (LBR) locus, encoding an inner nuclear membrane protein. Mutations in LBR are linked to Pelger-Huët anomaly. In addition, we identify cosegregation of a rare stop-gain sequence variant in LBR and Pelger Huët anomaly in an Icelandic eight generation pedigree, initially reported in 1963. Two of the other loci include genes which, like LBR, play a role in the nuclear membrane function and integrity. These GWAS results highlight the role proteins of the inner nuclear membrane have as important for neutrophil nuclear morphology.

Indexed as

Pelger-Huet AnomalyGenome-Wide Association StudyGranulocytesHumansIcelandNeutrophils

Identifiers

PMID35650273
PMCPMC9160026
OpenAlexW4281665365

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.