Richard Thompson

King’s College London

United Kingdom

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Articles (17)

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2025

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2025

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2025

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2022

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2021

Collaborators (8)

Wayel Jassem

King’s College London

UNITED KINGDOM

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Marianne Hørby Jørgensen

Copenhagen University Hospital

DENMARK

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Douglas Mogul

Johns Hopkins University

UNITED STATES

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Sabina Wiecek

Medical University of Silesia

POLAND

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Tassos Grammatikopoulos

Honorary Clinical Senior Lecturer

King’s College London

UNITED KINGDOM

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Henkjan J. Verkade

NETHERLANDS

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Emmanuel GONZALES

Full Professor of Pediatrics

Université Paris-Saclay

FRANCE

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Ronald Sokol

Distinguished Professor

University of Denver

UNITED STATES

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Richard Thompson

Research Interests

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Articles (17)

Transposable elements as novel therapeutic targets for PARPi-induced synthetic lethality in PcG-mutated blood cancer

High Frequency of CTNNB1 Variants Associated with Benign and Malignant Liver Tumors in Patients with Congenital Porto-Systemic Shunts.

Phenotypic Divergence of JAG1- and NOTCH2-Associated Alagille Syndrome & Disease-Specific NOTCH2 Variant Classification Guidelines

Comment on opinion paper on the diagnosis and treatment of progressive familial intrahepatic cholestasis

Genetic cholestasis in children and adults

Event-free survival of maralixibat-treated patients with Alagille syndrome compared to a real-world cohort from GALA.

Genetic aetiologies of acute liver failure

Maralixibat in progressive familial intrahepatic cholestasis (MARCH-PFIC)

Clinical outcomes of ABCB4 heterozygosity in infants and children with cholestatic liver disease

Choluresis?

Interim results from an ongoing, open-label, single-arm trial of odevixibat in progressive familial intrahepatic cholestasis

ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function Variants

Predictors of 6-year event-free survival in Alagille syndrome patients treated with maralixibat, an ileal bile acid transporter inhibitor

Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

Clinical phenotype of adult‐onset liver disease in patients with variants in ABCB4 , ABCB11 , and ATP8B1

Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial

The Influence of Donor and Recipient Complement C3 Polymorphisms on Liver Transplant Outcome

Collaborators (8)

Wayel Jassem

Marianne Hørby Jørgensen

Douglas Mogul

Sabina Wiecek

Tassos Grammatikopoulos

Henkjan J. Verkade

Emmanuel GONZALES

Ronald Sokol

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