| scholarly article | Q13442814 |
| P50 | author | Ramakrishnan Rajagopalan | Q85622356 |
| Nancy B Spinner | Q88684077 | ||
| P2093 | author name string | Kathleen M Loomes | |
| Marcella Devoto | |||
| Ellen A Tsai | |||
| Susan M Kelly | |||
| Christopher M Grochowski | |||
| P2860 | cites work | Variation in genome-wide mutation rates within and between human families | Q22122055 |
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| Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. | Q33947872 | ||
| Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene. | Q34323617 | ||
| CFC1 gene involvement in biliary atresia with polysplenia syndrome | Q34731101 | ||
| Identification of HSP90 as potential biomarker of biliary atresia using two-dimensional electrophoresis and mass spectrometry | Q34849635 | ||
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| Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. | Q35770210 | ||
| The Role of ARF6 in Biliary Atresia. | Q35778598 | ||
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| Sox17 haploinsufficiency results in perinatal biliary atresia and hepatitis in C57BL/6 background mice | Q36580293 | ||
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| Extrahepatic anomalies in infants with biliary atresia: results of a large prospective North American multicenter study | Q37351226 | ||
| Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia | Q37512003 | ||
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| Glutathione antioxidant pathway activity and reserve determine toxicity and specificity of the biliary toxin biliatresone in zebrafish | Q40787130 | ||
| Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development | Q41935728 | ||
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| Recurrence of extrahepatic biliary atresia in two half sibs | Q43625081 | ||
| Association of X-prolyl aminopeptidase 1 rs17095355 polymorphism with biliary atresia in Thai children | Q44846325 | ||
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| Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3. | Q53332303 | ||
| A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 | Q57112027 | ||
| Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine | Q57250562 | ||
| Familial Extrahepatic Biliary Atresia | Q68294056 | ||
| CFCI gene mutation and biliary atresia with polysplenia syndrome | Q77977057 | ||
| The inv mouse as an experimental model of biliary atresia | Q81233807 | ||
| Biliary atresia in two sets of twins | Q93609860 | ||
| The mutational constraint spectrum quantified from variation in 141,456 humans | Q97664663 | ||
| P433 | issue | 1 | |
| P921 | main subject | biliary atresia | Q659033 |
| P304 | page(s) | 2709 | |
| P577 | publication date | 2020-02-17 | |
| P1433 | published in | Scientific Reports | Q2261792 |
| P1476 | title | Exome Sequencing in Individuals with Isolated Biliary Atresia | |
| P478 | volume | 10 |
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