1. A Heterozygous ABCB4, RUNDC3B, and ABCB1 Deletion Associated With Severe Cholestatic Liver Disease in Adulthood. Issue 4 (26th June 2019) Authors: Terziroli Beretta‐Piccoli, Benedetta; Thompson, Richard; Foskett, Pierre; Cerny, Andreas; Merlo, Elisabetta; Vergani, Diego; Rougemont, Anne‐Laure; Moix, Isabelle; Mieli‐Vergani, Giorgina; Morris, Michael Journal: Hepatology Issue: Volume 70:Issue 4(2019) Page Start: 1484 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Assessment of quantitative polymerase chain reaction for BCR–ABL1 transcripts in chronic myeloid leukaemia: Are improved outcomes in patients with e14a2 transcripts an artefact of technology?. (8th January 2022) Authors: Dominy, Katherine M.; Claudiani, Simone; O'Hare, Matthew; Szydlo, Richard; Gerrard, Gareth; Foskett, Pierre; Foroni, Letizia; Milojkovic, Dragana; Apperley, Jane F.; Khorashad, Jamshid Journal: British journal of haematology Issue: Volume 197:Number 1(2022) Page Start: 52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. BRAF V600E mutation in biliary proliferations associated with α1‐antitrypsin deficiency. Issue 3 (15th November 2016) Authors: Angkathunyakul, Napat; Rosini, Francesca; Heaton, Nigel; Foskett, Pierre; Quaglia, Alberto Journal: Histopathology Issue: Volume 70:Issue 3(2017) Page Start: 485 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cholestasis Due to USP53 Deficiency. Issue 5 (May 2021) Authors: Bull, Laura N.; Ellmers, Rebecca; Foskett, Pierre; Strautnieks, Sandra; Sambrotta, Melissa; Czubkowski, Piotr; Jankowska, Irena; Wagner, Bart; Deheragoda, Maesha; Thompson, Richard J. Journal: Journal of pediatric gastroenterology and nutrition Issue: Volume 72:Issue 5(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical phenotype of adult‐onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1. Issue 10 (27th July 2022) Authors: Nayagam, Jeremy S.; Foskett, Pierre; Strautnieks, Sandra; Agarwal, Kosh; Miquel, Rosa; Joshi, Deepak; Thompson, Richard J. Journal: Hepatology communications Issue: Volume 6:Issue 10(2022) Page Start: 2654 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Donor transmitted mutation of the ABCB11 gene and ensuing intrahepatic cholestasis of pregnancy in a liver transplant recipient. Issue 9 (September 2017) Authors: Lim, Tiong Yeng; Coltart, Iona; Foskett, Pierre; Thompson, Richard; Strautnieks, Sandra; Penna, Leonie; Williamson, Catherine; Miquel, Rosa; Heneghan, Michael A. Journal: Liver transplantation Issue: Volume 23:Issue 9(2017:Sep.) Page Start: 1229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Hepatocellular carcinoma associated with tight‐junction protein 2 deficiency. Issue 6 (19th June 2015) Authors: Zhou, Shengmei; Hertel, Paula M.; Finegold, Milton J.; Wang, Larry; Kerkar, Nanda; Wang, Jing; Wong, Lee‐Jun C.; Plon, Sharon E.; Sambrotta, Melissa; Foskett, Pierre; Niu, Zhiyv; Thompson, Richard J.; Knisely, A.S. Journal: Hepatology Issue: Volume 62:Issue 6(2015:Dec.) Page Start: 1914 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1. Issue 3 (22nd October 2021) Authors: 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 Journal: Hepatology communications Issue: Volume 6:Issue 3(2022) Page Start: 473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mutations in Myosin 5B in Children With Early-onset Cholestasis. Issue 2 (August 2020) Authors: Cockar, Iram; Foskett, Pierre; Strautnieks, Sandra; Clinch, Yasmin; Fustok, Jana; Rahman, Obydur; Sutton, Harry; Mtegha, Marumbo; Fessatou, Smaragdi; Kontaki, Elena; Papaevangelou, Vassiliki; Deheragoda, Maesha; Thompson, Richard J.; Grammatikopoulos, Tassos Journal: Journal of pediatric gastroenterology and nutrition Issue: Volume 71:Issue 2(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Synonymous mutation in adenosine triphosphatase copper‐transporting beta causes enhanced exon skipping in Wilson disease. Issue 7 (10th March 2022) Authors: Panzer, Marlene; Viveiros, André; Schaefer, Benedikt; Baumgartner, Nadja; Seppi, Klaus; Djamshidian, Atbin; Todorov, Theodor; Griffiths, William J. H.; Schott, Eckart; Schuelke, Markus; Eurich, Dennis; Stättermayer, Albert Friedrich; Bomford, Adrian; Foskett, Pierre; Vodopiutz, Julia; Stauber, Ru... Journal: Hepatology communications Issue: Volume 6:Issue 7(2022) Page Start: 1611 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗