| Zahm AM, Hand NJ, Boateng LA, Friedman JR. Circulating microRNA is a biomarker of biliary atresia. J Pediatr Gastroenterol Nutr 2012 Oct;55(4):366-9. |
| Zahm A, Hand NJ, Horner A, Friedman J. Serum microRNA is a novel biomarker of biliary atresia. Proceedings of American Association for the Study of Liver Diseases (AASLD) 62nd Annual Meeting; November 4-8, 2011; San Francisco, CA. 2011 Nov. |
| Ye W, Rosenthal P, Magee JC, Whitington PF, Childhood Liver Disease Research and Education Network. Factors Determining δ-Bilirubin Levels in Infants With Biliary Atresia. J Pediatr Gastroenterol Nutr 2015 May;60(5):659-63. |
| Wang KS, Section on Surgery, Committee on Fetus and Newborn, Childhood Liver Disease Research Network. Newborn Screening for Biliary Atresia. Pediatrics 2015 Dec;136(6):e1663-9. |
| Wang H, Malone JP, Gilmore PE, Davis AE, Magee JC, Townsend RR, Heuckeroth RO. Serum markers may distinguish biliary atresia from other forms of neonatal cholestasis. J Pediatr Gastroenterol Nutr 2010 Apr;50(4):411-6. |
| Venkat VL, Shneider BL, Magee JC, Turmelle Y, Arnon R, Bezerra JA, Hertel PM, Karpen SJ, Kerkar N, Loomes KM, Molleston J, Murray KF, Ng VL, Raghunathan T, Rosenthal P, Schwartz K, Sherker AH, Sokol RJ, Teckman J, Wang K, Whitington PF, Heubi JE, Childhood Liver Disease Research and Education Network. Total serum bilirubin predicts fat-soluble vitamin deficiency better than serum bile acids in infants with biliary atresia. J Pediatr Gastroenterol Nutr 2014 Dec;59(6):702-7. |
| Van Hove JL, Saenz MS, Thomas JA, Gallagher RC, Lovell MA, Fenton LZ, Shanske S, Myers SM, Wanders RJ, Ruiter J, Turkenburg M, Waterham HR. Succinyl-CoA ligase deficiency: a mitochondrial hepatoencephalomyopathy. Pediatr Res 2010 Aug;68(2):159-64. |
| Tsai EA, Grochowski CM, Loomes KM, Bessho K, Hakonarson H, Bezerra JA, Russo PA, Haber BA, Spinner NB, Devoto M. Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia. Hum Genet 2014 Feb;133(2):235-43. Epub 2013 Oct 9. |
| Tsai EA, Grochowski CM, Falsey AM, Rajagopalan R, Wendel D, Devoto M, Krantz ID, Loomes KM, Spinner NB. Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. Hum Mutat 2015 Jun;36(6):631-7. Epub 2015 Apr 21. |
| Teckman JH, Rosenthal P, Abel R, Bass LM, Michail S, Murray KF, Rudnick DA, Thomas DW, Spino C, Arnon R, Hertel PM, Heubi J, Kamath BM, Karnsakul W, Loomes KM, Magee JC, Molleston JP, Romero R, Shneider BL, Sherker AH, Sokol RJ, Childhood Liver Disease Research Network (ChiLDReN). Baseline Analysis of a Young α-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension. J Pediatr Gastroenterol Nutr 2015 Jul;61(1):94-101. |
| Teckman J, Spino C, Murray KF, Haber B, Rudnick DA, Abel R, Thomas DW, Rosenthal P. 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. Proceedings of Digestive Disease Week (DDW) Annual Meeting; May 19-22, 2012; San Diego, CA. 2012 May. |
| Swigonová Z, Mohsen AW, Vockley J. Acyl-CoA dehydrogenases: Dynamic history of protein family evolution. J Mol Evol 2009 Aug;69(2):176-93. Epub 2009 Jul 29. |
| Superina R, Magee JC, Brandt ML, Healey PJ, Tiao G, Ryckman F, Karrer FM, Iyer K, Fecteau A, West K, Burns RC, Flake A, Lee H, Lowell JA, Dillon P, Colombani P, Ricketts R, Li Y, Moore J, Wang KS, Childhood Liver Disease Research and Education Network. The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg 2011 Oct;254(4):577-85. |
| Superina R, Magee J, Healey P, Tiao G, Ryckman F, Karrer F, Li Y, Brandt M, Wang KS. The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Proceedings of American Surgical Association (ASA) 131st Annual Meeting; April 14-16, 2011; Boca Raton, FL. 2011 Apr. |
| Sundaram SS, Fredericks EM, Kamath BM, Haber B, Raghunathan T, Magee JC, Bezerra JA, Karpen SJ, Kerkar N, Rosethal P, Schwarz KB, Shepherd RW, Schneider BL, Whitington PF, Robuck PR, Sokol RJ, BARC. Cross sectional assessment of Quality of Life in biliary atresia patients ages 2-25 years. Proceedings of American Association for the Study of Liver Diseases (AASLD) 60th Annual Meeting, Boston; October 30-November 3, 2009; Boston, MA. 2009 Oct. |
| Sundaram SS, Bove KE, Lovell MA, Sokol RJ. Mechanisms of disease: Inborn errors of bile acid synthesis. Nat Clin Pract Gastroenterol Hepatol 2008 Aug;5(8):456-68. Epub 2008 Jun 24. |
| Sundaram SS, Alonso EM, Haber B, Magee JC, Fredericks E, Kamath B, Kerkar N, Rosenthal P, Shepherd R, Limbers C, Varni JW, Robuck P, Sokol RJ, Childhood Liver Disease Research and Education Network (ChiLDREN). Health related quality of life in patients with biliary atresia surviving with their native liver. J Pediatr 2013 Oct;163(4):1052-7.e2. Epub 2013 Jun 6. |
| Strautnieks SS, Byrne JA, Pawlikowska L, Cebecauerová D, Rayner A, Dutton L, Meier Y, Antoniou A, Stieger B, Arnell H, Ozçay F, Al-Hussaini HF, Bassas AF, Verkade HJ, Fischler B, Németh A, Kotalová R, Shneider BL, Cielecka-Kuszyk J, McClean P, Whitington PF, Sokal E, Jirsa M, Wali SH, Jankowska I, Pawłowska J, Mieli-Vergani G, Knisely AS, Bull LN, Thompson RJ. Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families. Gastroenterology 2008 Apr;134(4):1203-14. Epub 2008 Jan 18. |
| Sokol RJ. Reloading against rare liver diseases. J Pediatr Gastroenterol Nutr 2010 Jan;50(1):9-10. |
| Sokol RJ. New North American research network focuses on biliary atresia and neonatal liver disease. J Pediatr Gastroenterol Nutr 2003 Jan;36(1):1. |
| Sokol RJ. Biliary atresia screening: why, when, and how? Pediatrics 2009 May;123(5):e951-2. |
| Sokol RJ, Shepherd RW, Superina R, Bezerra JA, Robuck P, Hoofnagle JH. Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop. Hepatology 2007 Aug;46(2):566-81. |
| Sokol RJ, Magee JC, Hahn CL and Robuck PR, Childhood Liver Disease Research and Education Network. The new Childhood Liver Disease Research and Education Network (ChiLDREN): a new cooperative effort between NIDDK, academic centers and Patient Advocacy Groups. Proceedings of North American Society for Pediatric Gastroenterology, Hepatology And Nutrition (NASPGHAN) Annual Meeting; November 12-14, 2009; National Harbor, MD. 2009 Nov. |
| Sokol RJ, Hines J, CLiC. The Cholestatic Liver Disease Consortium (CLiC): a multi-institutional collaboration to better understand and treat liver disease in children. Proceedings of National Institutes of Health (NIH) Conference “Advancing Rare Diseases Research through Networks and Collaboration”; July 16, 2009; Bethesda, MD. 2009 Jul. |
| Sokol RJ, Childhood Liver Disease Research and Education Network. Childhood Liver Disease Research and Education Network (ChiLDREN). Proceedings of American Association for the Study of Liver Diseases (AASLD) 61th Annual Meeting; October 29-November 2, 2010; Boston, MA. 2010 Oct. |
