Evidence map›Paper›PMID 37230770›Full record

ArticleCold Spring Harbor molecular case studies2023

Perinatal-lethal nonimmune fetal hydrops attributed to

Camille A Dash, Jill A Madden, Christy Cummings, Melissa Rose, Sheria D Wilson, Mari Mori, Pankaj B Agrawal, Bimal P Chaudhari, Monica H Wojcik

Open access · diamondAbstract read
In one paragraph

Article in Cold Spring Harbor molecular case studies, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

9 authors at 2 institutions in 1 country.

Camille A DashDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Jill A MaddenDivision of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Christy CummingsDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.ORCID 0000-0003-1579-2947
Melissa RoseDivision of Hematology, Oncology, and Bone Marrow Transplant, Department of Pediatrics, Nationwide Children's Hospital and the Ohio State University College of Medicine, Columbus, Ohio 43205, USA.
Sheria D WilsonDivision of Neonatology, Department of Pediatrics, Nationwide Children's Hospital and the Ohio State University College of Medicine, Columbus, Ohio 43205, USA.
Mari MoriDivision of Genetics and Genomic Medicine, Department of Pediatrics, Nationwide Children's Hospital and the Ohio State University College of Medicine, Columbus, Ohio 43205, USA.ORCID 0000-0001-6425-7137
Pankaj B AgrawalThe Manton Center for Orphan Disease Research, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Bimal P ChaudhariDivision of Neonatology, Department of Pediatrics, Nationwide Children's Hospital and the Ohio State University College of Medicine, Columbus, Ohio 43205, USA.ORCID 0000-0002-0115-949X
Monica H WojcikDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA; monica.wojcik@childrens.harvard.edu.ORCID 0000-0002-8162-5031
Boston Children's Hospital · USNationwide Children's Hospital · US

Funding

Joint Center for Mendelian GenomicsUM1HG008900 · NHGRI · BROAD INSTITUTE, INC. · PI O'DONNELL-LURIA, ANNE, REHM, HEIDI L · 2016 to 2020
$16.5M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
A powerful web-based discovery platform for rare disease geneticsR01HG009141 · NHGRI · BROAD INSTITUTE, INC. · PI QUINLAN, AARON R, REHM, HEIDI L · 2017 to 2020
$2.9M
Optimizing Family Counseling for Anticipated Extremely Preterm Delivery R01HD094794 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI CUMMINGS, CHRISTY LYNN · 2019 to 2023
$1.9M
The Burden of Genetic Disorders in Infant MortalityK23HD102589 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI WOJCIK, MONICA HSIUNG · 2020 to 2024
$840k
NHGRI NIH HHS R01 HG009141NHGRI NIH HHS UM1 HG008900NICHD NIH HHS K23 HD102589NICHD NIH HHS R01 HD094794NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

Pathogenic variants in

Indexed as

AnemiaHydrops FetalisAdultBone Marrow Failure DisordersFemaleHumansInfantInfant, NewbornMDS1 and EVI1 Complex Locus ProteinPregnancyRadiusSynostosisTranscription FactorsUlnaMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanTranscription Factorsamegakaryocytic thrombocytopeniacongenital hypoplastic anemialeukopenianonimmune hydrops fetalis

Identifiers

PMID37230770
PMCPMC10393185
OpenAlexW4378194020

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.