Lauren Véronèse

1.0k total citations
30 papers, 369 citations indexed

About

Lauren Véronèse is a scholar working on Genetics, Genetics and Molecular Biology. According to data from OpenAlex, Lauren Véronèse has authored 30 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Lauren Véronèse's work include Chronic Lymphocytic Leukemia Research (9 papers), Prenatal Screening and Diagnostics (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Lauren Véronèse is often cited by papers focused on Chronic Lymphocytic Leukemia Research (9 papers), Prenatal Screening and Diagnostics (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Lauren Véronèse collaborates with scholars based in France, United States and Uruguay. Lauren Véronèse's co-authors include Andréï Tchirkov, Philippe Vago, Carole Goumy, Emmanuel Chautard, Pierre Verrelle, Laëtitia Gouas, Karima Mokhtari, T. Khalil, B. Irthum and Fabrice Kwiatkowski and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and British Journal of Cancer.

In The Last Decade

Lauren Véronèse

21 papers receiving 362 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lauren Véronèse France 12 155 97 79 72 71 30 369
Alexandra Friemel Germany 15 223 1.4× 113 1.2× 100 1.3× 63 0.9× 79 1.1× 24 519
Gunnhildur Ásta Traustadóttir Iceland 13 281 1.8× 132 1.4× 34 0.4× 79 1.1× 66 0.9× 23 446
Jo Lynne Rokita United States 11 193 1.2× 111 1.1× 27 0.3× 48 0.7× 108 1.5× 19 389
Crocifissa Lo Cunsolo Italy 10 227 1.5× 119 1.2× 31 0.4× 53 0.7× 103 1.5× 17 412
Oriana Romano Italy 12 349 2.3× 49 0.5× 151 1.9× 68 0.9× 46 0.6× 21 542
Dustin L. Gable United States 9 226 1.5× 57 0.6× 44 0.6× 77 1.1× 61 0.9× 12 530
Vasundhra Kashyap United States 6 532 3.4× 103 1.1× 52 0.7× 84 1.2× 117 1.6× 6 635
P. A. Bernabei Italy 8 162 1.0× 71 0.7× 104 1.3× 66 0.9× 41 0.6× 20 328
Barbara Dessars Belgium 9 159 1.0× 124 1.3× 47 0.6× 43 0.6× 89 1.3× 14 328
Mohammad Shahidul Makki United States 12 287 1.9× 62 0.6× 30 0.4× 42 0.6× 165 2.3× 21 487

Countries citing papers authored by Lauren Véronèse

Since Specialization
Citations

This map shows the geographic impact of Lauren Véronèse'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 Lauren Véronèse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lauren Véronèse more than expected).

Fields of papers citing papers by Lauren Véronèse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lauren Véronèse. 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 Lauren Véronèse. The network helps show where Lauren Véronèse may publish in the future.

Co-authorship network of co-authors of Lauren Véronèse

This figure shows the co-authorship network connecting the top 25 collaborators of Lauren Véronèse. A scholar is included among the top collaborators of Lauren Véronèse 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 Lauren Véronèse. Lauren Véronèse is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Antonio, Marie De, Victoria Cacheux, Lauren Véronèse, et al.. (2024). Faster clinical decisions in B‐cell acute lymphoblastic leukaemia: A single flow cytometric 12‐colour tube improves diagnosis and minimal residual disease follow‐up. British Journal of Haematology. 204(5). 1872–1881.
2.
Chapiro, Élise, Agnès Daudignon, Nathalie Nadal, et al.. (2023). Cytogenetics in the management of mature T-cell and NK-cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH). Current Research in Translational Medicine. 71(4). 103428–103428.
3.
Soler, Gwendoline, et al.. (2023). Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute Leukemia. Cancers. 15(7). 2131–2131. 13 indexed citations
4.
Lefebvre, Christine, Lauren Véronèse, Nathalie Nadal, et al.. (2023). Cytogenetics in the management of mature B-cell non-Hodgkin lymphomas: Guidelines from the Groupe Francophone de Cytogénétique Hematologique (GFCH). Current Research in Translational Medicine. 71(4). 103425–103425.
5.
Goumy, Carole, Gwendoline Soler, Éléonore Eymard-Pierre, et al.. (2023). Optical genome mapping for prenatal diagnosis: A prospective study. Clinica Chimica Acta. 551. 117594–117594. 12 indexed citations
6.
Nguyen‐Khac, Florence, Audrey Bidet, Agnès Daudignon, et al.. (2022). The complex karyotype in hematological malignancies: a comprehensive overview by the Francophone Group of Hematological Cytogenetics (GFCH). Leukemia. 36(6). 1451–1466. 17 indexed citations
7.
Goumy, Carole, Lauren Véronèse, Denis Gallot, et al.. (2022). Reduced telomere length in amniocytes: an early biomarker of abnormal fetal development?. Human Molecular Genetics. 31(16). 2669–2677. 5 indexed citations
8.
Véronèse, Lauren, Patricia Combes, Éléonore Eymard-Pierre, et al.. (2017). TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancer. Oncotarget. 8(44). 77540–77551. 37 indexed citations
9.
Pebrel‐Richard, Céline, Laëtitia Gouas, Lauren Véronèse, et al.. (2013). Prenatal ultrasound diagnosis of a 48,XXYY syndrome. Morphologie. 97(317). 65–67.
10.
Véronèse, Lauren, Olivier Tournilhac, Patricia Combes, et al.. (2013). Contribution of MLPA to routine diagnostic testing of recurrent genomic aberrations in chronic lymphocytic leukemia. Cancer Genetics. 206(1-2). 19–25. 14 indexed citations
11.
Lemal, Richard, et al.. (2011). Translocations récurrentes en onco-hématologie : physiopathologie, intérêt clinique et thérapeutique. Bulletin du Cancer. 98(12). 1403–1418.
12.
Goumy, Carole, Laëtitia Gouas, Céline Pebrel‐Richard, et al.. (2010). Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities. Genetics in Medicine. 12(6). 376–380. 6 indexed citations
13.
Debost‐Legrand, Anne, Yline Capri, Laëtitia Gouas, et al.. (2010). De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features. Pathologie Biologie. 59(6). 309–313.
14.
Goumy, Carole, Laëtitia Gouas, Geoffroy Marceau, et al.. (2010). Retinoid Pathway and Congenital Diaphragmatic Hernia: Hypothesis from the Analysis of Chromosomal Abnormalities. Fetal Diagnosis and Therapy. 28(3). 129–139. 34 indexed citations
15.
Tchirkov, Andréï, Vincent Sapin, Geoffroy Marceau, et al.. (2010). Increased expression of the oncogenic KLF6-SV1 transcript in human glioblastoma. Clinical Chemistry and Laboratory Medicine (CCLM). 48(8). 1167–1170. 14 indexed citations
16.
Véronèse, Lauren, Olivier Tournilhac, Pierre Verrelle, et al.. (2009). Strong correlation between VEGF and MCL-1 mRNA expression levels in B-cell chronic lymphocytic leukemia. Leukemia Research. 33(12). 1623–1626. 17 indexed citations
17.
Goumy, Carole, Laëtitia Gouas, Andréï Tchirkov, et al.. (2008). Familial deletion 11q14.3–q22.1 without apparent phenotypic consequences: A haplosufficient 8.5 Mb region. American Journal of Medical Genetics Part A. 146A(20). 2668–2672. 10 indexed citations
18.
Gouas, Laëtitia, Carole Goumy, Lauren Véronèse, Andréï Tchirkov, & Philippe Vago. (2008). Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities. Pathologie Biologie. 56(6). 345–353. 23 indexed citations
19.
Goumy, Carole, Andréï Tchirkov, Laëtitia Gouas, et al.. (2008). Larsen‐like phenotype associated with partial trisomy 3p and monosomy 5p. Prenatal Diagnosis. 28(2). 131–134. 1 indexed citations
20.
Tchirkov, Andréï, T. Khalil, Emmanuel Chautard, et al.. (2007). Interleukin-6 gene amplification and shortened survival in glioblastoma patients. British Journal of Cancer. 96(3). 474–476. 108 indexed citations

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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