Penton AL, Leonard LD, Spinner NB. Notch signaling in human development and disease. Semin Cell Dev Biol 2012 Jun;23(4):450-7. Epub 2012 Jan 28. |
Pawlikowska L, Strautnieks S, Jankowska I, Czubkowski P, Emerick K, Antoniou A, Wanty C, Fischler B, Jacquemin E, Wali S, Blanchard S, Nielsen IM, Bourke B, McQuaid S, Lacaille F, Byrne JA, van Eerde AM, Kolho KL, Klomp L, Houwen R, Bacchetti P, Lobritto S, Hupertz V, McClean P, Mieli-Vergani G, Shneider B, Nemeth A, Sokal E, Freimer NB, Knisely AS, Rosenthal P, Whitington PF, Pawlowska J, Thompson RJ, Bull LN. Differences in presentation and progression between severe FIC1 and BSEP deficiencies. J Hepatol 2010 Jul;53(1):170-8. Epub 2010 Apr 13. |
Ogawa M, Ogawa S, Bear CE, Ahmadi S, Chin S, Li B, Grompe M, Keller G, Kamath BM, Ghanekar A. Directed differentiation of cholangiocytes from human pluripotent stem cells. Nat Biotechnol 2015 Aug;33(8):853-61. Epub 2015 Jul 13. |
Ng VL, Haber BH, Magee JC, Miethke A, Murray KF, Michail S, Karpen SJ, Kerkar N, Molleston JP, Romero R, Rosenthal P, Schwarz KB, Shneider BL, Turmelle YP, Alonso EM, Sherker AH, Sokol RJ, Childhood Liver Disease Research and Education Network (CHiLDREN). Medical status of 219 children with biliary atresia surviving long-term with their native livers: results from a North American multicenter consortium. J Pediatr 2014 Sep;165(3):539-546.e2. Epub 2014 Jul 9. |
Ng VL, Haber B, Magee J, Karpen S, Miethke A, Schwarz K, Shneider B, Whitington P, Turmelle Y, Kerkar N, Rosenthal P, Molleston J, Wang K, Romero R, Murray K, Abel R, Sokol R, Childhood Liver Disease Research and Education Network. Medical status of 192 children with biliary atresia surviving >5 years after Kasai portoenterostomy with their native liver. Proceedings of American Association for the Study of Liver Diseases (AASLD) 62nd Annual Meeting; November 4-8, 2011; San Francisco, CA. 2011 Nov. |
Ng V, Sorensen L, Alonso E, Fredericks E, Ye W, Karpen S, Shneider B, Bezerra J, Molleston J, Murray K, Rosenthal P, Wang K, Loomes K, Hertel P, Kerkar N, Schwarz K, Turmelle Y, Haber B, Sherker A, Magee J, Sokol R, ChiLDReN Network. Neurodevelopmental Outcomes in Patients with Biliary Atresia and Native Liver at Ages 1 and 2 Years: Results from ChiLDReN. Proceedings of American Association for the Study of Liver Diseases (AASLD) 66th Annual Meeting; November 13-17, 2015; San Francisco, CA. 2015 Nov. p. 78A. |
Narkewicz MR, Leung DH, Molleston JP, Weymann A, Ling S, Pranjape S, Schwarzenberg SJ, Palermo J, Romero R, Siegel M, Ye W, Magee JC, CFLD Network Group. High frequency of unsuspected cirrhosis in children with Cystic Fibrosis (CF). Proceedings of American Association for the Study of Liver Diseases (AASLD) 63rd Annual Meeting; November 9-13, 2012; Boston, MA. 2012 Nov. |
Narkewicz MR, Leung D, Molleston JP, Weymann A, Pranjape S, Romero R, Schwarzenberg SJ, Palermo J, Siegel M, Krishnamurthy R, Karmazyn B, Harned R, Ye W, Magee JC, CFLD Network Group. Later diagnosis and CF related diabetes are associated with abnormal UltraSound (US) in children with CF in the CF Liver Disease Network Study. Proceedings of 27th Annual North American Cystic Fibrosis Conference (NACFC); October 17-19, 2013; Salt Lake City, UT. 2013 Oct. |
Moyer KD, Kaimal V, Pacheco MC, Mourya R, Xu H, Shivakumar P, Bove KE, Chakraborty R, Rao M, Magee J, Jegga AG, Bezerra JA. Novel molecular subtypes of biliary atresia with relevance to clinical outcome. Proceedings of American Association for the Study of Liver Diseases (AASLD) 59th Annual Meeting; October 31-November 4, 2008; San Francisco, CA. 2008 Oct. |
Moyer K, Kaimal V, Pacheco C, Mourya R, Xu H, Shivakumar P, Chakraborty R, Rao M, Magee JC, Bove K, Aronow BJ, Jegga AG, Bezerra JA. Staging of biliary atresia at diagnosis by molecular profiling of the liver. Genome Med 2010 May 13;2(5):33. |
Molleston JP, Sokol RJ, Karnsakul W, Miethke A, Horslen S, Magee JC, Romero R, Squires RH, Van Hove JL, Childhood Liver Disease Research Education Network (ChiLDREN). Evaluation of the child with suspected mitochondrial liver disease. J Pediatr Gastroenterol Nutr 2013 Sep;57(3):269-76. |
Molleston J, Sokol RJ, Karsakul WW, Miethke AG, Magee JC, Squires RH, VanHove JL, Childhood Liver Disease Research and Education Network. Evaluation guidelines for suspected mitochondrial hepatopathies. Proceedings of World Congress of Pediatric Gastroenterology, Hepatology and Nutrition 4th Annual Meeting; November 14-18, 2012; Taipei, Taiwan. 2012 Nov. |
Molleston J, Sokol RJ, Karsakul WW, Miethke AG, Magee JC, Squires RH, VanHove JL, Childhood Liver Disease Research and Education Network. Evaluation guidelines for suspected mitochondrial hepatopathies. Proceedings of North American Society of Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) 26th Annual Meeting; October 18-20, 2012; Salt Lake City, UT. 2012 Oct. |
Miethke A, Matte U, Liu C, Mourya R, Ryckman F, Balistreri W, Bove K, Bezerra J. Gene mutations and clinical outcome after biliary diversion surgery for intractable pruritus in children with intrahepatic cholestasis. Proceedings of Clinical Research for Rare Diseases: Opportunities, challenges and solutions; September 5, 2007; Bethesda, MD. 2007 Sep. |
Miethke A, Matte U, Liu C, Balistreri W, Ryckman F, Bezerra J. Gene mutations and clinical outcome after biliary diversion surgery for intractable pruritus in children with intrahepatic cholestasis. Proceedings of North American Society for Pediatric Gastroenterology, Hepatology And Nutrition (NASPHAN) Annual Meeting; October 25-27, 2007; Salt Lake City, UT. 2007 Oct. |
Mealer M, Kittelson J, Thompson BT, Wheeler AP, Magee JC, Sokol RJ, Moss M, Kahn MG. Remote source document verification in two national clinical trials networks: a pilot study. PLoS One 2013 Dec 5;8(12):e81890. doi: 10.1371/journal.pone.0081890. eCollection 2013. |
Matte U, Mourya R, Miethke A, Liu C, Kauffmann G, Moyer K, Zhang K, Bezerra JA. Analysis of gene mutations in children with cholestasis of undefined etiology. J Pediatr Gastroenterol Nutr 2010 Oct;51(4):488-493. |
Matte U, Liu C, Miethke A, Mourya R, Kauffmann G, Moyer K, Bull L, Spinner N, Thompson R, Bezerra J. High throughput sequence analysis identifies individual and combined genetic defects in children with syndromes of intrahepatic cholestasis. Proceedings of American Association for the Study of Liver Diseases (AASLD) 58th Annual Meeting; November 2-6, 2007; Boston, MA. 2007 Nov. |
Mack CL, Feldman AG, Sokol RJ. Clues to the etiology of bile duct injury in biliary atresia. Semin Liver Dis 2012 Nov;32(4):307-16. Epub 2013 Feb 8. |
Mack CL, Falta MT, Sullivan AK, Karrer F, Sokol RJ, Freed BM, Fontenot AP. Oligoclonal expansions of CD4+ and CD8+ T-cells in the target organ of patients with biliary atresia. Gastroenterology 2007 Jul;133(1):278-87. Epub 2007 Apr 20. |
Mack CL, Anderson KM, Aubrey MT, Rosenthal P, Sokol RJ, Freed BM. Lack of HLA predominance and HLA shared epitopes in biliary Atresia. Springerplus 2013 Dec;2(1):42. Epub 2013 Feb 8. |
Lorent K, Gong W, Koo KA, Waisbourd-Zinman O, Karjoo S, Zhao X, Sealy I, Kettleborough RN, Stemple DL, Windsor PA, Whittaker SJ, Porter JR, Wells RG, Pack M. Identification of a plant isoflavonoid that causes biliary atresia. Sci Transl Med 2015 May 6;7(286):286ra67. |
Loomes KM, Tsai EA, Underkoffler LA, Grochowski C, Falsey A, Kamath BM, Lin H, Hankenson KD, Devoto M, Spinner NB. A genome-wide association study identifies THBS2 as a candidate modifier of liver disease severity in Alagille syndrome. Proceedings of American Association for the Study of Liver Diseases (AASLD) 65th Annual Meeting; November 10, 2014; Boston, MA. 2014 Nov. p. 252A. |
Loomes K, Spino C, Goodrich N, Hangartner T, Marker A, Heubi J, Kamath B, Shneider B, Rosenthal P, Hertel P, Karpen S, Kerkar N, Molleston J, Murray K, Schwarz K, Teckman J, Turmelle Y, Whitington P, Sherker A, Magee J, Sokol R, Childhood Liver Disease Research Network (ChiLDReN). DXA Bone Density in Alagille Syndrome Correlates with Fracture History and Degree of Cholestasis. Proceedings of American Association for the Study of Liver Diseases (AASLD) 66th Annual Meeting; November 13-17, 2015; San Francisco, CA. 2015 Nov. |
Liu C, Aronow BJ, Jegga AG, Wang N, Miethke A, Mourya R, Bezerra JA. Novel resequencing chip customized to diagnose mutations in patients with inherited syndromes of intrahepatic cholestasis. Gastroenterology 2007 Jan;132(1):119-26. Epub 2006 Oct 21. |