A genome-wide association study identifies THBS2 as a candidate modifier of liver disease severity in Alagille syndrome | | | Conference Presentation | 2014 | | PROBE | | Contributing Study |
A molecular signature of biliary atresia highly distinct from other cholestatic diseases at diagnosis | | | Conference Presentation | 2011 | | PROBE | | Contributing Study |
A multi-center analysis of outcome at 24 months of age in children with biliary atresia in the United States | | | Conference Presentation | 2004 | | PROBE | | Contributing Study |
A multi-institutional study of interobserver agreement on the histologic diagnosis of biliary obstruction in liver biopsies of cholestatic infants less than six months of age | | | Conference Presentation | 2006 | | BARC, PROBE | | Contributing Study |
A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. | 16647406 | | Journal | 2006 | 10.1016/j.jpeds.2005.12.054 | PROBE, BARC | | Contributing Study |
A new defect in beta-oxidation presenting as sudden liver failure | | | Conference Presentation | 2005 | | PROBE | | Contributing Study |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency | | | Conference Presentation | 2005 | | PROBE | | Contributing Study |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency. | 17564966 | PMC1950923 | Journal | 2007 | 10.1086/519219 | PROBE | | Contributing Study |
A prospective multi-centered investigation of vitamin supplementation in infants with biliary atresia: interim analysis from the Biliary Atresia Research Consortium (BARC) | | | Conference Presentation | 2009 | | PROBE | | Contributing Study |
A toxin that induces biliary atresia causes disruption of microtubules and loss of primary cilia | | | Conference Presentation | 2012 | | PROBE | | Contributing Study |
Acyl-CoA dehydrogenases: Dynamic history of protein family evolution. | 19639238 | PMC4136416 | Journal | 2009 | 10.1007/s00239-009-9263-0 | PROBE | | Contributing Study |
Analysis of gene mutations in children with cholestasis of undefined etiology. | 20683201 | PMC4090691 | Journal | 2010 | 10.1097/MPG.0b013e3181dffe8f | PROBE | | Contributing Study |
Baseline Analysis of a Young α-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension. | 25651489 | PMC4692167 | Journal | 2015 | 10.1097/MPG.0000000000000753 | PROBE, LOGIC | | Contributing Study |
Baseline Ultrasound and Clinical Correlates in Children with Cystic Fibrosis. | 26254836 | PMC4586395 | Journal | 2015 | 10.1016/j.jpeds.2015.06.062 | PROBE | | Contributing Study |
Baseline analysis of the largest reported cohort of children and young adults with Alpha-1-Antitrypsin deficiency liver disease reveals a significant burden of portal hypertension without jaundice | | | Conference Presentation | 2012 | | PROBE | | Contributing Study |
Bile salt kinetics in children with genetic cholestasis and bile diversion therapy | | | Conference Presentation | 2012 | | PROBE | | Contributing Study |
Biliary Atresia Research Consortium (BARC). | 15057888 | | Journal | 2004 | 10.1002/hep.20185 | PROBE, BARC | | Contributing Study |
Biliary Atresia Research Consortium (BARC): NIH-funded network to advance knowledge and improve care and outcomes in biliary atresia | | | Conference Presentation | 2006 | | BARC, PROBE | | Contributing Study |
Biliary atresia screening: why, when, and how? | 19403487 | PMC3881183 | Journal | 2009 | 10.1542/peds.2008-3108 | PROBE | | Contributing Study |
Biliary atresia: will blocking inflammation tame the disease? | 21226614 | PMC4096311 | Journal | 2011 | 10.1146/annurev-med-042909-093734 | PROBE | | Contributing Study |
Childhood Liver Disease Research and Education Network (ChiLDREN) | | | Conference Presentation | 2010 | | PROBE | | Contributing Study |
Cholangiocyte cilia are abnormal in syndromic and non-syndromic biliary atresia. | 22301700 | PMC3341539 | Journal | 2012 | 10.1038/modpathol.2011.212 | PROBE | | Contributing Study |
Circulating microRNA is a biomarker of biliary atresia. | 22732895 | PMC3459263 | Journal | 2012 | 10.1097/MPG.0b013e318264e648 | PROBE | | Contributing Study |
Clinical and demographic features of three major biliary atresia phenotypes in the BARC study | | | Conference Presentation | 2008 | | BARC, PROBE | | Contributing Study |
Clinical research for rare disease: opportunities, challenges, and solutions. | 19013090 | PMC3134795 | Journal | 2009 | 10.1016/j.ymgme.2008.10.003 | PROBE | | Contributing Study |
Clues to the etiology of bile duct injury in biliary atresia. | 23397531 | PMC3827890 | Journal | 2012 | 10.1055/s-0032-1329899 | PROBE | | Contributing Study |
Cross sectional assessment of Quality of Life in biliary atresia patients ages 2-25 years | | | Conference Presentation | 2009 | | BARC, PROBE | | Contributing Study |
Cross-sectional multi-center analysis of portal hypertension in 163 children with biliary atresia | | | Conference Presentation | 2010 | | PROBE | | Contributing Study |
Cytomegalovirus-specific T-cell reactivity in biliary atresia at the time of diagnosis is associated with deficits in regulatory T cells. | 22105891 | PMC3319336 | Journal | 2012 | 10.1002/hep.24807 | PROBE | | Contributing Study |
DXA Bone Density in Alagille Syndrome Correlates with Fracture History and Degree of Cholestasis | | | Conference Presentation | 2015 | | PROBE | | Contributing Study |
Defects in bile acid biosynthesis--diagnosis and treatment. | 16819396 | | Journal | 2006 | 10.1097/01.mpg.0000226386.79483.7b | PROBE | | Contributing Study |
Dendritic cells regulate natural killer cell activation and epithelial injury in experimental biliary atresia. | 21957172 | PMC4006997 | Journal | 2011 | 10.1126/scitranslmed.3002069 | PROBE | | Contributing Study |
Design and validation of the biliary atresia research consortium histologic assessment system for cholestasis in infancy. | 21238606 | PMC3400532 | Journal | 2011 | 10.1016/j.cgh.2011.01.003 | PROBE, BARC | | Contributing Study |
Development of the Pictorial Preschool Cystic Fibrosis Questionnaire-Revised: Child and Parent Report | | | Conference Presentation | 2014 | | PROBE | | Contributing Study |
Diagnostic imaging in neonatal cholestasis: a multi-center prospective analysis | | | Conference Presentation | 2006 | | BARC, PROBE | | Contributing Study |
Differences in presentation and progression between severe FIC1 and BSEP deficiencies. | 20447715 | PMC3042805 | Journal | 2010 | 10.1016/j.jhep.2010.01.034 | PROBE | | Contributing Study |
Directed differentiation of cholangiocytes from human pluripotent stem cells. | 26167630 | | Journal | 2015 | 10.1038/nbt.3294 | PROBE | | Contributing Study |
Discriminating features of biliary atresia - a prospective multi-centered analysis | | | Conference Presentation | 2007 | | PROBE | | Contributing Study |
Early growth failure after portoenterostomy is associated with liver transplantaion or death in infants with biliary atresia | | | Conference Presentation | 2005 | | PROBE, BARC | | Contributing Study |
Efficacy of fat-soluble vitamin supplementation in infants with biliary atresia. | 22891232 | PMC3428752 | Journal | 2012 | 10.1542/peds.2011-1423 | START, PROBE | | Contributing Study |
Evaluation guidelines for suspected mitochondrial hepatopathies | | | Conference Presentation | 2012 | | PROBE | | Contributing Study |
Evaluation guidelines for suspected mitochondrial hepatopathies | | | Conference Presentation | 2012 | | PROBE | | Contributing Study |
Evaluation of the child with suspected mitochondrial liver disease. | 23783016 | PMC3810178 | Journal | 2013 | 10.1097/MPG.0b013e31829ef67a | PROBE | | Contributing Study |
Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene. | 23336978 | PMC3736559 | Journal | 2013 | 10.1053/j.gastro.2013.01.022 | PROBE | | Contributing Study |
Extrahepatic anomalies in infants with biliary atresia: results of a large prospective North American multicenter study. | 23703680 | PMC3844083 | Journal | 2013 | 10.1002/hep.26512 | PROBE | | Contributing Study |
Extrahepatic cholangiocyte cilia are abnormal in biliary atresia. | 23609896 | PMC3696479 | Journal | 2013 | 10.1097/MPG.0b013e318296e525 | PROBE | | Contributing Study |
FXR response in cholestatic liver disease | | | Conference Presentation | 2008 | | PROBE | | Contributing Study |
Factors Determining δ-Bilirubin Levels in Infants With Biliary Atresia. | 25564820 | PMC4409472 | Journal | 2015 | 10.1097/MPG.0000000000000690 | PROBE | | Contributing Study |
Foxl1-Cre-marked adult hepatic progenitors have clonogenic and bilineage differentiation potential. | 21632825 | PMC3110956 | Journal | 2011 | 10.1101/gad.2027811 | PROBE | | Contributing Study |
Gene expression signature for biliary atresia and a role for interleukin-8 in pathogenesis of experimental disease. | 24493287 | PMC4077977 | Journal | 2014 | 10.1002/hep.27045 | PROBE | | Contributing Study |