Pauline Robbe

1.2k total citations
14 papers, 137 citations indexed

About

Pauline Robbe is a scholar working on Genetics, Pathology and Forensic Medicine and Immunology. According to data from OpenAlex, Pauline Robbe has authored 14 papers receiving a total of 137 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Pathology and Forensic Medicine and 6 papers in Immunology. Recurrent topics in Pauline Robbe's work include Chronic Lymphocytic Leukemia Research (11 papers), Lymphoma Diagnosis and Treatment (6 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). Pauline Robbe is often cited by papers focused on Chronic Lymphocytic Leukemia Research (11 papers), Lymphoma Diagnosis and Treatment (6 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). Pauline Robbe collaborates with scholars based in United Kingdom, Belgium and Japan. Pauline Robbe's co-authors include Anna Schuh, Hélène Dreau, Basile Stamatopoulos, Samantha J.L. Knight, Jenny C. Taylor, Ruth Clifford, Pavlos Antoniou, Jenny Klintman, Adele Timbs and Adam Burns and has published in prestigious journals such as Blood, British Journal of Haematology and Leukemia.

In The Last Decade

Pauline Robbe

10 papers receiving 135 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Pauline Robbe United Kingdom 5 91 88 42 34 32 14 137
Annalisa D’Avola United Kingdom 8 91 1.0× 67 0.8× 69 1.6× 65 1.9× 23 0.7× 13 159
Cecelia Miller United States 8 86 0.9× 63 0.7× 47 1.1× 101 3.0× 77 2.4× 28 201
Karol Pál Czechia 9 63 0.7× 67 0.8× 34 0.8× 27 0.8× 28 0.9× 19 152
Tatjana Pandzic Sweden 8 65 0.7× 64 0.7× 26 0.6× 94 2.8× 31 1.0× 14 203
David Martin‐García Spain 5 60 0.7× 82 0.9× 38 0.9× 90 2.6× 21 0.7× 5 187
Veronika Navrkalová Czechia 8 121 1.3× 97 1.1× 61 1.5× 85 2.5× 38 1.2× 18 217
Emma Flordal Thelander Sweden 4 49 0.5× 68 0.8× 25 0.6× 32 0.9× 21 0.7× 4 110
Moez Dawood United States 6 58 0.6× 88 1.0× 56 1.3× 64 1.9× 31 1.0× 11 185
Reina Improgo United States 4 107 1.2× 91 1.0× 51 1.2× 100 2.9× 71 2.2× 7 231
A Marossy United Kingdom 5 97 1.1× 116 1.3× 37 0.9× 86 2.5× 21 0.7× 5 199

Countries citing papers authored by Pauline Robbe

Since Specialization
Citations

This map shows the geographic impact of Pauline Robbe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Pauline Robbe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pauline Robbe more than expected).

Fields of papers citing papers by Pauline Robbe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pauline Robbe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Pauline Robbe. The network helps show where Pauline Robbe may publish in the future.

Co-authorship network of co-authors of Pauline Robbe

This figure shows the co-authorship network connecting the top 25 collaborators of Pauline Robbe. A scholar is included among the top collaborators of Pauline Robbe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Pauline Robbe. Pauline Robbe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
Nishiyori-Sueki, Hiromi, Ilaria Nisoli, Hideya Kawaji, et al.. (2025). Protocol for direct cDNA cap analysis of gene expression for paired-end patterned flow cell sequencing. STAR Protocols. 6(1). 103594–103594.
2.
Klintman, Jenny, Niamh Appleby, Basile Stamatopoulos, et al.. (2020). Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia. Blood. 137(20). 2800–2816. 59 indexed citations
3.
Eecken, Kim Van der, Frédéric De Ryck, Pauline Robbe, et al.. (2020). Comparative analysis of somatic variant calling on matched FF and FFPE WGS samples. BMC Medical Genomics. 13(1). 94–94. 14 indexed citations
4.
Ridout, Kate, Pauline Robbe, Dimitris Vavoulis, et al.. (2018). The Genomic Landscape of Chronic Lymphocytic Leukaemia: Clinical Implications. Clinical Lymphoma Myeloma & Leukemia. 18. S112–S115. 1 indexed citations
5.
Burns, Adam, David Bruce, Pauline Robbe, et al.. (2018). Detection of Clinically Relevant Molecular Alterations in Chronic Lymphocytic Leukemia (CLL) By Nanopore Sequencing. Blood. 132(Supplement 1). 1847–1847. 1 indexed citations
6.
Klintman, Jenny, Samantha J.L. Knight, Pauline Robbe, et al.. (2018). Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL. British Journal of Haematology. 182(3). 412–417. 11 indexed citations
7.
Buchanan, James, Sarah Wordsworth, Ruth Clifford, et al.. (2017). Using Genomic Information to Guide Ibrutinib Treatment Decisions in Chronic Lymphocytic Leukaemia: A Cost-Effectiveness Analysis. PharmacoEconomics. 35(8). 845–858. 10 indexed citations
8.
Blakemore, Stuart J., Ruth Clifford, Pavlos Antoniou, et al.. (2017). The contribution of gene mutations to long-term clinical outcomes: data from the randomised UK LRF CLL4 trial. ePrints Soton (University of Southampton). 2 indexed citations
9.
Stamatopoulos, Basile, Adele Timbs, Tom Smith, et al.. (2016). Targeted deep sequencing reveals clinically relevant subclonal IgHV rearrangements in chronic lymphocytic leukemia. Leukemia. 31(4). 837–845. 37 indexed citations
10.
Robbe, Pauline, Kate Ridout, Jennifer Becq, et al.. (2016). Identifying High-Risk CLL to Predict Early Relapse after FCR Based Treatment Using Whole Genome Sequencing: First Results from the Genomics England CLL Pilot. Blood. 128(22). 2022–2022. 1 indexed citations
11.
12.
Hamblin, Angela, Adam Burns, Ruth Clifford, et al.. (2014). Development and Evaluation of the Clinical Utility of a Next Generation Sequencing (NGS) Tool for Myeloid Disorders. Blood. 124(21). 2373–2373. 1 indexed citations
13.
14.
Robbe, Pauline, Adele Timbs, Adam Burns, et al.. (2013). COMPREHENSIVE GENOME-WIDE ANALYSIS OF CLL SAMPLES FROM UK 1ST LINE AND RELAPSED/REFRACTORY CLINICAL TRIALS. Haematologica. 98. 241–241.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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