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Paper Details

Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes.
J Hepatol
1
2023
AFAP1, BA, BA-associated genes, BA-associated variants, Biliary atresia, CPLANE, CPLANE genes, Human, SNPs, TUSC3, biliary atresia, biliary dysgenesis, birth defects, cancers, cells, children, genes, highly specialized genes, human, infections, intronic, liver transcripts, mouse, mouse tracheal cells, neighboring SNPs, planar polarity effector genes, portal vein anomalies, rs34599046, rs6446628, single nucleotide, unique genes, zebrafish
Author NameAffiliation
Joseph T GlessnerCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Mylarappa NingappaHillman Center for Pediatric Transplantation, UPMC-Children's Hospital of Pittsburgh, and Thomas E Starzl Transplant Institute, University of Pittsburgh
Kim A NgoUniversity of California
Maliha ZahidUniversity of Pittsburgh
Juhoon SoUniversity of Pittsburgh
Brandon W HiggsHillman Center for Pediatric Transplantation, UPMC-Children's Hospital of Pittsburgh, and Thomas E Starzl Transplant Institute, University of Pittsburgh
Brandon W HiggsHillman Center for Pediatric Transplantation, UPMC-Children's Hospital of Pittsburgh, and Thomas E Starzl Transplant Institute, University of Pittsburgh
Patrick M A SleimanCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Patrick M A SleimanCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Tejaswini NarayananUniversity of California
Sarangarajan RanganathanCincinnati Children's Hospital Medical Center
Michael E MarchCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Krishna PrasadanRangos Research Center Animal Imaging Core, UPMC Children's Hospital of Pittsburgh
Courtney VaccaroCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Miguel Reyes-MúgicaUPMC Children's Hospital of Pittsburgh
Jeremy J VelazquezPittsburgh Liver Research Center, McGowan Institute for Regenerative Medicine, University of Pittsburgh
Cláudia M SalgadoUPMC Children's Hospital of Pittsburgh
Mohammad R EbrahimkhaniPittsburgh Liver Research Center, McGowan Institute for Regenerative Medicine, University of Pittsburgh
Lori SchmittUPMC Children's Hospital of Pittsburgh
Dhivyaa RajasundaramChildren's Hospital of Pittsburgh
Morgan PaulHillman Center for Pediatric Transplantation, UPMC-Children's Hospital of Pittsburgh, and Thomas E Starzl Transplant Institute, University of Pittsburgh
Renata PellegrinoCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
George K GittesUPMC Children's Hospital of Pittsburgh
Dong LiCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Xiang WangCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Jonathan BillingsCenter for Applied Genomics (CAG), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Robert H SquiresUPMC Children's Hospital of Pittsburgh
Robert H SquiresUPMC Children's Hospital of Pittsburgh
Chethan AshokkumarHillman Center for Pediatric Transplantation, UPMC-Children's Hospital of Pittsburgh, and Thomas E Starzl Transplant Institute, University of Pittsburgh
Khalid SharifBirmingham Women's and Children's NHS Foundation Trust
Deirdre KellyBirmingham Women's and Children's NHS Foundation Trust
Anil DhawanNHS Foundation Trust, King's College Hospital
Simon HorslenUPMC Children's Hospital of Pittsburgh
Cecilia W LoUniversity of Pittsburgh
Cecilia W LoUniversity of Pittsburgh
Donghun ShinUniversity of Pittsburgh
Shankar SubramaniamUniversity of California
Shankar SubramaniamUniversity of California
Hakon HakonarsonChildren's Hospital of Philadelphia
Hakon HakonarsonChildren's Hospital of Philadelphia
Rakesh SindhiHillman Center for Pediatric Transplantation, UPMC-Children's Hospital of Pittsburgh, and Thomas E Starzl Transplant Institute, University of Pittsburgh
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Datasets

Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink