ArticleCirculation. Cardiovascular genetics2017
Modifying Mendel Redux: Unbiased Approaches Can Find Modifiers.
Kim L McBride, Stephanie M Ware
Abstract readEditorialComment
In one paragraphArticle in Circulation. Cardiovascular genetics, 2017. 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
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
5 · Who and what moneyAuthors and funding
2 authors.
Kim L McBrideFrom the Center for Cardiovascular Research (K.L.M.) and Department of Pediatrics, College of Medicine (K.L.M.), Nationwide Children's Hospital, Ohio State University, Columbus; and Departments of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis (S.M.W.). Kim.McBride@NationwideChildrens.org.
Stephanie M WareFrom the Center for Cardiovascular Research (K.L.M.) and Department of Pediatrics, College of Medicine (K.L.M.), Nationwide Children's Hospital, Ohio State University, Columbus; and Departments of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis (S.M.W.).
Funding
Transcriptional regulation of cardiac morphogenesisP01HL134599 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI Anthony B. Firulli · 2017 to 2026
$25.7MExome sequencing and functional studies in familial CHDR01HL109758 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI GARG, VIDU, MCBRIDE, KIM LEWIS · 2012 to 2015
$2.7MRole of the Embryonic Node in Cardiac Development and Congenital Heart DiseaseR01HL088639 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI WARE, STEPHANIE M · 2007 to 2011
$2.0MNHLBI NIH HHS P01 HL134599NHLBI NIH HHS R01 HL088639NHLBI NIH HHS R01 HL109758
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
ArachnodactylyDiGeorge SyndromeMarfan SyndromeTetralogy of FallotGenome-Wide Association StudyHumansReceptors, G-Protein-CoupledADGRV1 protein, humanReceptors, G-Protein-CoupledEditorialsgenome-wide association studygenomicsheart defects, congenitaltetralogy of Fallot
Identifiers
PMID29025762
PMCPMC5659730
What OpenQuestion holds
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