Evidence map›Paper›PMID 33192543›Full record

ArticleFrontiers in physiology2020

Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality.

Juhoon So, Mylarappa Ningappa, Joseph Glessner, Jun Min, Chethan Ashokkumar, Sarangarajan Ranganathan, Brandon W Higgs, Dong Li, Qing Sun, Lori Schmitt and 24 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Biliary atresia-related liver fibrosis.Frontiers in cell and developmental biology · 2026
    Review
  6. Review
  7. Genetic background and biliary atresia.World journal of pediatric surgery · 2025
    Review
  8. Organoids in biliary atresia.World journal of pediatric surgery · 2025
    Review
  9. Biliary atresia.Nature reviews. Disease primers · 2024
    Review
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  11. Article
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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 9 institutions in 2 countries.

Juhoon SoDepartment of Developmental Biology, McGowan Institute of Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Mylarappa NingappaHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Joseph GlessnerCenter for Applied Genomics of the Children's Hospital of Philadelphia, Philadelphia, PA, United States.
Jun MinDepartments of Bioengineering, Cellular and Molecular Medicine, and Computer Science and Engineering, University of California San Diego, La Jolla, CA, United States.
Chethan AshokkumarHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Sarangarajan RanganathanDivision of Pediatric Pathology, Department of Pathology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Brandon W HiggsHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Dong LiCenter for Applied Genomics of the Children's Hospital of Philadelphia, Philadelphia, PA, United States.
Qing SunHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Lori SchmittHistology Core Laboratory, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Amy C BieryDivision of Pediatric Pathology, Department of Pathology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Steven DobrowolskiDivision of Pediatric Pathology, Department of Pathology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Christine TrautzHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Leah FuhrmanHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Molly Christine SchwartzDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, PA, United States.
Nikolai Thomas KlenaDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, PA, United States.
Joseph FuscoPediatric General and Thoracic Surgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Krishna PrasadanPediatric General and Thoracic Surgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Morayooluwa AdenugaHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Nada MohamedPediatric General and Thoracic Surgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Qi YanDepartments of Human Genetics and Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Wei ChenDepartments of Human Genetics and Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
William HorneRichard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Anil DhawanPaediatric Liver, GI, and Nutrition, King's College Hospital, London, United Kingdom.
Khalid SharifChildren's Hospital of Birmingham, Birmingham, United Kingdom.
Deirdre KellyChildren's Hospital of Birmingham, Birmingham, United Kingdom.
Robert H SquiresPediatric Gastroenterology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
George K GittesPediatric General and Thoracic Surgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Hakon HakonarsonCenter for Applied Genomics of the Children's Hospital of Philadelphia, Philadelphia, PA, United States.
Victor MorellDivision of Cardiac Surgery, Department of Cardiothoracic Surgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, United States.
Cecilia LoDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, PA, United States.
Shankar SubramaniamDepartments of Bioengineering, Cellular and Molecular Medicine, and Computer Science and Engineering, University of California San Diego, La Jolla, CA, United States.
Donghun ShinDepartment of Developmental Biology, McGowan Institute of Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Rakesh SindhiHillman Center for Pediatric Transplantation of the Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA, United States.
Children's Hospital of Pittsburgh · USUniversity of Pittsburgh · USChildren's Hospital of Philadelphia · USUniversity of Pittsburgh Medical Center · USBirmingham Children's Hospital · GBUniversity of California, San Diego · USKing's College Hospital · GBMcGowan Institute for Regenerative Medicine · USRichard King Mellon Foundation · US

Funding

Elucidating the role of the FXR-PTEN-PI3K-AKT-mTOR axis in liver progenitor cell-driven liver regenerationR01DK101426 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHIN, DONGHUN · 2014 to 2023
$3.8M
Mapping Disease Pathways for Biliary AtresiaR01DK109365 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHIN, DONGHUN, SINDHI, RAKESH K. · 2017 to 2020
$2.4M
NIDDK NIH HHS R01 DK101426NIDDK NIH HHS R01 DK109365
6 · The paper itself

Abstract

BACKGROUND/

aimsInfectious and genetic factors are invoked, respectively in isolated biliary atresia (BA), or syndromic BA, with major extrahepatic anomalies. However, isolated BA is also associated with minor extrahepatic gut and cardiovascular anomalies and multiple susceptibility genes, suggesting common origins.

methodsWe investigated novel susceptibility genes with genome-wide association, targeted sequencing and tissue staining in BA requiring liver transplantation, independent of BA subtype. Candidate gene effects on morphogenesis, developmental pathways, and ciliogenesis, which regulates left-right patterning were investigated with zebrafish knockdown and mouse knockout models, mouse airway cell cultures, and liver transcriptome analysis.

resultsSingle nucleotide polymorphisms in Mannosidase-1-α-2 (

conclusionBA requiring transplantation associates with sequence variants in

Indexed as

biliary atresiabiliary morphogenesiscilialateralityliver transplantation

Identifiers

PMID33192543
PMCPMC7662016
OpenAlexW3094657941

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.