Divergence-Preserving MHD Solutions Using a Noniterative Hyperbolic Conservation Law Scheme von Thompson, Richard J., Moeller, Trevor

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Human Leukocyte Antigen Profile Predicts Severity of Autoimmune Liver Disease in Children of European Ancestry von Ma, Yun, Su, Haibin, Yuksel, Muhammed, Longhi, Maria Serena, McPhail, Mark J., Wang, Pengyun, Bansal, Sanjay, Wong, Guan‐Wee, Graham, Jonathon, Yang, Li, Thompson, Richard, Doherty, Derek G., Hadzic, Nedim, Zen, Yoh, Quaglia, Alberto, Heneghan, Michael A., Samyn, Marianne, Vergani, Diego, Mieli‐Vergani, Giorgina

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Mutations in TJP2 cause progressive cholestatic liver disease von Sambrotta, Melissa, Strautnieks, Sandra, Papouli, Efterpi, Rushton, Peter, Clark, Barnaby E, Parry, David A, Logan, Clare V, Newbury, Lucy J, Kamath, Binita M, Ling, Simon, Grammatikopoulos, Tassos, Wagner, Bart E, Magee, John C, Sokol, Ronald J, Mieli-Vergani, Giorgina, Smith, Joshua D, Johnson, Colin A, McClean, Patricia, Simpson, Michael A, Knisely, A S, Bull, Laura N, Thompson, Richard J

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Use of a Comprehensive 66‐Gene Cholestasis Sequencing Panel in 2171 Cholestatic Infants, Children, and Young Adults von Karpen, Saul J., Kamath, Binita M., Alexander, John J., Ichetovkin, Ilia, Rosenthal, Philip, Sokol, Ronald J., Dunn, Shelley, Thompson, Richard J., Heubi, James E.

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Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis von Grammatikopoulos, Tassos, Sambrotta, Melissa, Strautnieks, Sandra, Foskett, Pierre, Knisely, A.S, Wagner, Bart, Deheragoda, Maesha, Starling, Chris, Mieli-Vergani, Giorgina, Smith, Joshua, Bull, Laura, Thompson, Richard J

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Emerging therapeutic options for the management of hepatitis C infection von Thompson, J Richard

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Choluresis? von Thompson, Richard J

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Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre‐messenger RNA splicing von Byrne, Jane A., Strautnieks, Sandra S., Ihrke, Gudrun, Pagani, Franco, Knisely, A.S., Linton, Kenneth J., Mieli‐Vergani, Giorgina, Thompson, Richard J.

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Clinical phenotype of adult‐onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1 von Nayagam, Jeremy S., Foskett, Pierre, Strautnieks, Sandra, Agarwal, Kosh, Miquel, Rosa, Joshi, Deepak, Thompson, Richard J.

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Maralixibat for the treatment of PFIC: Long‐term, IBAT inhibition in an open‐label, Phase 2 study von Loomes, Kathleen M., Squires, Robert H., Kelly, Deirdre, Rajwal, Sanjay, Soufi, Nisreen, Lachaux, Alain, Jankowska, Irena, Mack, Cara, Setchell, Kenneth D. R., Karthikeyan, Palaniswamy, Kennedy, Ciara, Dorenbaum, Alejandro, Desai, Nirav K., Garner, Will, Jaecklin, Thomas, Vig, Pamela, Miethke, Alexander, Thompson, Richard J.

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Approximate Solutions of Combinatorial Problems via Quantum Relaxations von Fuller, Bryce, Hadfield, Charles, Glick, Jennifer R., Imamichi, Takashi, Itoko, Toshinari, Richard Thompson, J., Jiao, Yang, Marna Kagele, M., Adriana, W. Blom-Schieber, Raymond, Rudy, Mezzacapo, Antonio

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Genetic aetiologies of acute liver failure von Hegarty, Robert, Thompson, Richard J.

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The human bile salt export pump: Characterization of substrate specificity and identification of inhibitors von Byrne, Jane A., Strautnieks, Sandra S., Mieli–Vergani, Giorgina, Higgins, Christopher F., Linton, Kenneth J., Thompson, Richard J.

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Review article: liver disease in adults with variants in the cholestasis‐related genes ABCB11, ABCB4 and ATP8B1 von Nayagam, Jeremy S., Williamson, Catherine, Joshi, Deepak, Thompson, Richard J.

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Quantum computation of reactions on surfaces using local embedding von Gujarati, Tanvi P., Motta, Mario, Friedhoff, Triet Nguyen, Rice, Julia E., Nguyen, Nam, Barkoutsos, Panagiotis Kl, Thompson, Richard J., Smith, Tyler, Kagele, Marna, Brei, Mark, Jones, Barbara A., Williams, Kristen

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Genetic cholestasis in children and adults von Nayagam, Jeremy S., Miquel, Rosa, Thompson, Richard J., Joshi, Deepak

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Genetics of liver disease: From pathophysiology to clinical practice von Karlsen, Tom H, Lammert, Frank, Thompson, Richard J

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Impact of long‐term administration of maralixibat on children with cholestasis secondary to Alagille syndrome von Shneider, Benjamin L., Spino, Catherine A., Kamath, Binita M., Magee, John C., Ignacio, Rosalinda V., Huang, Suiyuan, Horslen, Simon P., Molleston, Jean P., Miethke, Alexander G., Kohli, Rohit, Leung, Daniel H., Jensen, M. Kyle, Loomes, Kathleen M., Karpen, Saul J., Mack, Cara, Rosenthal, Philip, Squires, Robert H., Baker, Alastair, Rajwal, Sanjay, Kelly, Deirdre, Sokol, Ronald J., Thompson, Richard J.

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Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1 von Grammatikopoulos, Tassos, Hadzic, Nedim, Foskett, Pierre, Strautnieks, Sandra, Samyn, Marianne, Vara, Roshni, Dhawan, Anil, Hertecant, Jozef, Al Jasmi, Fatma, Rahman, Obydur, Deheragoda, Maesha, Bull, Laura N., Thompson, Richard J

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Sequencing of transporter genes in cholestasis: We are still learning von Thompson, Richard J.

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