Evidence map›Paper›PMID 33268503›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2021

Effect of Sickle Cell Trait and

Alexander P Reiner, Laura M Raffield, Nora Franceschini, Paul L Auer, Ethan M Lange, Deborah A Nickerson, Neil A Zakai, Adolfo Correa, Nels Olson, National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine Consortium and 1 more

Open access · bronzeAbstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2021. 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
0.6field-weighted citation impact, top 32% 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, 5 citations in OpenAlex.

  1. 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

11 authors at 6 institutions in 1 country.

Alexander P ReinerDepartment of Epidemiology, University of Washington, Seattle, Washington apreiner@uw.edu.
Laura M RaffieldDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina.
Nora FranceschiniDepartment of Epidemiology, University of North Carolina, Chapel Hill, North Carolina.
Paul L AuerDepartment of Biostatistics, Joseph J. Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin.
Ethan M LangeDivision of Biomedical Informatics and Personalized Medicine, School of Medicine, University of Colorado, Anschutz Medical Campus, Aurora, Colorado.
Deborah A NickersonDepartment of Genome Sciences, University of Washington, Seattle, Washington.
Neil A ZakaiDepartment of Medicine, Larner College of Medicine at the University of Vermont, Burlington, Vermont.
Adolfo CorreaDepartment of Pediatrics and Medicine, University of Mississippi Medical Center, Jackson, Mississippi.ORCID 0000-0002-9501-600X
Nels OlsonDepartment of Pathology and Laboratory Medicine, Larner College of Medicine at the University of Vermont, Burlington, Vermont.
National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine Consortium
Natinal Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine Consortium
University of North Carolina at Chapel Hill · USUniversity of Vermont · USUniversity of Washington · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Mississippi Medical Center · USUniversity of Wisconsin–Milwaukee · US

Funding

North Carolina Translational and Clinical Science Institute (NC TraCS) KL2KL2TR002490 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEINBERGER, MORRIS · 2018 to 2022
$11.0M
Studies of Rare Genetic Variation in the Isolated Population of SardiniaR01HL117626 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2013 to 2016
$10.5M
Rare variants and NHLBI traits in deeply phenotyped cohortsR01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2014 to 2016
$8.9M
Center for Hemoglobin Research in Minorities (CHaRM)P50HL118006 · NHLBI · HOWARD UNIVERSITY · PI NEKHAI, SERGEI · 2013 to 2017
$7.0M
Rare variants and NHLBI traits in deeply phenotyped cohortsU01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2017 to 2018
$5.6M
The Genetic Epidemiology of Heart, Lung, and Blood TraitsTraining Grant (GenHLB)T32HL129982 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Christy Leigh Avery, KAREN L. MOHLKE · 2016 to 2026
$3.8M
Leveraging ancestry to map kidney lociR01MD012765 · NIMHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRANCESCHINI, NORA · 2017 to 2021
$3.6M
Thrombosis genetics in African AmericansR01HL132947 · NHLBI · UNIVERSITY OF WASHINGTON · PI LANGE, LESLIE A, REINER, ALEXANDER P · 2017 to 2020
$3.1M
Genetics of kidney disease in diverse populationsR01DK117445 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRANCESCHINI, NORA · 2018 to 2022
$2.7M
Immune Activation and Immunosenescence Biomarkers and Cardiovascular Disease RiskR00HL129045 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI OLSON, NELS C. · 2018 to 2020
$745k
DNA methylation markers of Multimorbidity in Aging Humans and MiceK01AG059898 · NIA · UNIVERSITY OF WASHINGTON · PI SALIMI, SHABNAM · 2019 to 2023
$613k
Phenome-wide association of protein function-altering variants in a family studyR21HL140385 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRANCESCHINI, NORA · 2017 to 2018
$229k
NCATS NIH HHS KL2 TR002490NHLBI NIH HHS HHSN268201100037CNHLBI NIH HHS HHSN268201800001CNHLBI NIH HHS HHSN268201800010INHLBI NIH HHS HHSN268201800011CNHLBI NIH HHS HHSN268201800011INHLBI NIH HHS HHSN268201800012CNHLBI NIH HHS HHSN268201800012INHLBI NIH HHS HHSN268201800014CNHLBI NIH HHS HHSN268201800014INHLBI NIH HHS HHSN268201800015INHLBI NIH HHS P50 HL118006NHLBI NIH HHS R00 HL129045NHLBI NIH HHS R01 HL117626NHLBI NIH HHS R01 HL120393NHLBI NIH HHS R01 HL132947NHLBI NIH HHS R21 HL140385NHLBI NIH HHS T32 HL129982NHLBI NIH HHS U01 HL120393NIA NIH HHS K01 AG059898NIDDK NIH HHS R01 DK117445NIMHD NIH HHS HHSN268201800013INIMHD NIH HHS R01 MD012765
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdultAgedAged, 80 and overAlbuminuriaApolipoprotein L1Black or African AmericanCreatinineFemaleGenotypeGlomerular Filtration RateHumansIncidenceKidneyLongitudinal StudiesMaleMiddle AgedAPOL1 protein, humanApolipoprotein L1CreatinineReceptors, Urokinase Plasminogen Activatorchronic kidney diseaseclinical epidemiologygenetic renal diseasesickle cell trait

Identifiers

PMID33268503
PMCPMC7863645
OpenAlexW3106662720

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.