Publications by authors named "Pauline Robbe"

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Enabling whole genome sequencing analysis from FFPE specimens in clinical oncology.
Dylan Domenico, Gunes Gundem, Max F Levine, Juan Esteban Arango-Ossa, Pauline Robbe

Nat Commun· November 2025

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Protocol for direct cDNA cap analysis of gene expression for paired-end patterned flow cell sequencing.
Diane Delobel, Hiromi Nishiyori-Sueki, Ilaria Nisoli, Hideya Kawaji, Pauline Robbe

STAR Protoc· March 2025

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Large-scale analysis of whole genome sequencing data from formalin-fixed paraffin-embedded cancer specimens demonstrates preservation of clinical utility.
Shadi Basyuni, Laura Heskin, Andrea Degasperi, Daniella Black, Gene C C Koh, Pauline Robbe

Nat Commun· September 2024

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Genomic Stratification of Hematological Malignancies.
Pauline Robbe, Anna Schuh

Hemasphere· June 2023

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Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.
Pauline Robbe, Kate E Ridout, Dimitrios V Vavoulis, Helene Dréau, Ben Kinnersley

Nat Genet· November 2022

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Long-term follow-up of 415 patients with chronic lymphocytic leukemia treated with fludarabine and cyclophosphamide-based chemoimmunotherapy in the frontline ADMIRE and ARCTIC trials: A comprehensive assessment of prognostic factors.
David John Allsup, Zoe Craig, David Cairns, Dena Howard, Anna Hockaday, Pauline Robbe

Am J Hematol· May 2022

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Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia.
Jenny Klintman, Niamh Appleby, Basile Stamatopoulos, Katie Ridout, Toby A Eyre, Pauline Robbe

Blood· May 2021

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Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia.
Wei-Yu Lin, Sarah E Fordham, Nicola Sunter, Claire Elstob, Thahira Rahman, Pauline Robbe

Nat Commun· January 2021

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Clinical significance of TP53, BIRC3, ATM and MAPK-ERK genes in chronic lymphocytic leukaemia: data from the randomised UK LRF CLL4 trial.
Stuart J Blakemore, Ruth Clifford, Helen Parker, Pavlos Antoniou, Ewa Stec-Dziedzic, Pauline Robbe

Leukemia· July 2020

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Comparative analysis of somatic variant calling on matched FF and FFPE WGS samples.
Louise de Schaetzen van Brienen, Maarten Larmuseau, Kim Van der Eecken, Frederic De Ryck, Pauline Robbe

BMC Med Genomics· July 2020

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Clinical significance of DNA methylation in chronic lymphocytic leukemia patients: results from 3 UK clinical trials.
Tomasz K Wojdacz, Harindra E Amarasinghe, Latha Kadalayil, Alice Beattie, Jade Forster, Pauline Robbe

Blood Adv· August 2019

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Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project.
Pauline Robbe, Niko Popitsch, Samantha J L Knight, Pavlos Antoniou, Jennifer Becq

Genet Med· October 2018

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The Light Chain IgLV3-21 Defines a New Poor Prognostic Subgroup in Chronic Lymphocytic Leukemia: Results of a Multicenter Study.
Basile Stamatopoulos, Thomas Smith, Emerence Crompot, Karlien Pieters, Ruth Clifford, Pauline Robbe

Clin Cancer Res· October 2018

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Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL.
Jenny Klintman, Katerina Barmpouti, Samantha J L Knight, Pauline Robbe, Hélène Dreau

Br J Haematol· August 2018

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Using Genomic Information to Guide Ibrutinib Treatment Decisions in Chronic Lymphocytic Leukaemia: A Cost-Effectiveness Analysis.
James Buchanan, Sarah Wordsworth, Ruth Clifford, Pauline Robbe, Jenny C Taylor

Pharmacoeconomics· August 2017

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Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL.
Romain Guièze, Pauline Robbe, Ruth Clifford, Sophie de Guibert, Bruno Pereira

Blood· October 2015

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SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage.
Ruth Clifford, Tania Louis, Pauline Robbe, Sam Ackroyd, Adam Burns

Blood· February 2014

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