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Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants

The American Journal of Surgery(2021)10.1016/j.amjsurg.2021.07.016Source: DataRank Database

Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants is a research paper published in The American Journal of Surgery (2021). On theSindex it has a DataRank of 0. It has been cited 10 times.

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10 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 1.62)OA: closedTopics (43)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (0/2)

Interoperable (0/2)

Reusable (0/3)

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Authors (8)

Shan Dong ORCID,Billie R. Lianoglou ORCID,Alessandra F. Aguilar Lucero ORCID,Grace Schwartz ORCID,Mary E. Norton ORCID

Live enrichment

PubMed:34315577 OpenAlex:https://openalex.org/W3185132117

National Institutes of Health

Grant: T32AI125222

University of California, San Francisco

National Institute of Health

FWCI

1.62

Citation Percentile

0.8%

Citation Trend

2021

2022

2023

2024

2025

closedLicense: http://www.elsevier.com/open-access/userlicense/1.0/

publisherhttps://api.elsevier.com/content/article/PII:S0002961021003962?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0002961021003962?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.amjsurg.2021.07.016

repositoryhttps://pubmed.ncbi.nlm.nih.gov/34315577

Fields of Study

Congenital Diaphragmatic Hernia StudiesRNA modifications and cancerNeurogenetic and Muscular Disorders ResearchCOUP Transcription Factor IIExomeFemaleFetusGenetic TestingHernias, Diaphragmatic, CongenitalHumansMalePregnancyProtein Tyrosine Phosphatase, Non-Receptor Type 11Ultrasonography, PrenatalWT1 Proteins

MeSH Terms

FemaleFetusGenetic TestingHumansMalePregnancyUltrasonography, PrenatalWT1 ProteinsCOUP Transcription Factor IIProtein Tyrosine Phosphatase, Non-Receptor Type 11ExomeHernias, Diaphragmatic, Congenital

Keywords

Exome sequencingCongenital diaphragmatic herniaMedicinePTPN11ExomeBioinformaticsGeneticsFetusBiologyPregnancyGeneKRASMutationWT1Hdac6Nr2f2

Sustainable Development Goals

SDG 0: Good health and well-being