Thierry Soussi
Visiting professor at Department of Immunology, Genetics and Pathology; Research programme: Cancer Precision Medicine; Research group Panagiotis Baliakas
- E-mail:
- thierry.soussi@igp.uu.se
- Visiting address:
- Dag Hammarskjölds väg 20
751 85 Uppsala - Postal address:
- Rudbecklaboratoriet
751 85 UPPSALA
Publications
Recent publications
Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations
Part of Nature Genetics, p. 140-153, 2025
- DOI for Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations
- Download full text (pdf) of Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations
Part of Scientific Reports, 2024
- DOI for Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
- Download full text (pdf) of Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update
Part of Leukemia, p. 1455-1468, 2024
- DOI for ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update
- Download full text (pdf) of ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update
The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots
Part of Human Mutation, 2023
Part of Human Molecular Genetics, p. 2121-2123, 2023
All publications
Articles in journal
Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations
Part of Nature Genetics, p. 140-153, 2025
- DOI for Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations
- Download full text (pdf) of Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations
Part of Scientific Reports, 2024
- DOI for Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
- Download full text (pdf) of Cancer associated variant enrichment CAVE, a gene agnostic approach to identify low burden variants in chronic lymphocytic leukemia
The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots
Part of Human Mutation, 2023
Part of Human Molecular Genetics, p. 2121-2123, 2023
Part of Cell Death and Disease, 2022
- DOI for Evolutionary history of the p53 family DNA-binding domain: insights from an Alvinella pompejana homolog
- Download full text (pdf) of Evolutionary history of the p53 family DNA-binding domain: insights from an Alvinella pompejana homolog
Colorectal Cancer Is Associated with the Presence of Cancer Driver Mutations in Normal Colon
Part of Cancer Research, p. 1492-1502, 2022
Part of American Journal of Hematology, 2022
Part of Cell Death and Differentiation, p. 1477-1492, 2021
- DOI for Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene
- Download full text (pdf) of Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene
Part of British Journal of Haematology, 2020
Articles, review/survey
ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update
Part of Leukemia, p. 1455-1468, 2024
- DOI for ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update
- Download full text (pdf) of ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update
Landscape of TP53 Alterations in Chronic Lymphocytic Leukemia via Data Mining Mutation Databases
Part of Frontiers in Oncology, 2022
- DOI for Landscape of TP53 Alterations in Chronic Lymphocytic Leukemia via Data Mining Mutation Databases
- Download full text (pdf) of Landscape of TP53 Alterations in Chronic Lymphocytic Leukemia via Data Mining Mutation Databases
Benign SNPs in the Coding Region of TP53: Finding the Needles in a Haystack of Pathogenic Variants
Part of Cancer Research, p. 3420-3431, 2022