Lise Larcher

754 total citations
10 papers, 61 citations indexed

About

Lise Larcher is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Lise Larcher has authored 10 papers receiving a total of 61 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Hematology. Recurrent topics in Lise Larcher's work include Acute Myeloid Leukemia Research (2 papers), DNA Repair Mechanisms (2 papers) and BRCA gene mutations in cancer (2 papers). Lise Larcher is often cited by papers focused on Acute Myeloid Leukemia Research (2 papers), DNA Repair Mechanisms (2 papers) and BRCA gene mutations in cancer (2 papers). Lise Larcher collaborates with scholars based in France, United Kingdom and United States. Lise Larcher's co-authors include Boris Keren, Julien Buratti, V. Descamps, F. Bouscarat, Joy Norris, Cyril Mignot, Charles E. Schwartz, Cathérine Garel, Bao Phung and Yazdan Yazdanpanah and has published in prestigious journals such as Nucleic Acids Research, Blood and Human Molecular Genetics.

In The Last Decade

Lise Larcher

10 papers receiving 60 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lise Larcher France	5	33	16	12	8	7	10	61
Silvia Tiberti Italy	3	9 0.3×	9 0.6×	7 0.6×	4 0.5×	9 1.3×	4	70
Jerry Lee United States	4	38 1.2×	12 0.8×	3 0.3×	3 0.4×		5	65
Tiarlan Sirait France	4	10 0.3×	6 0.4×	2 0.2×	2 0.3×	8 1.1×	6	43
Volha Skrahina Germany	6	26 0.8×	23 1.4×		7 0.9×	5 0.7×	13	87
Sally Connolly United Kingdom	3	18 0.5×	26 1.6×		7 0.9×	3 0.4×	4	51
Ardeshir Bahmanimehr Iran	6	25 0.8×	72 4.5×		6 0.8×	4 0.6×	11	108
Ronaldo da Silva Francisco Brazil	5	25 0.8×	20 1.3×	4 0.3×	1 0.1×	1 0.1×	10	51
Lamu Gusang China	4	11 0.3×	21 1.3×		6 0.8×	4 0.6×	4	35
Mathilde Pacault France	6	23 0.7×	28 1.8×		2 0.3×	4 0.6×	9	82
Per Hoffman Germany	2	16 0.5×	6 0.4×	2 0.2×		8 1.1×	2	39

Countries citing papers authored by Lise Larcher

Since Specialization

Citations

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

Fields of papers citing papers by Lise Larcher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lise Larcher

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

All Works

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10 of 10 papers shown

Zhao, Lin‐Pierre, Vincent Jachiet, Olivier Kosmider, et al.. (2025). Very long-term remission with azacitidine in VEXAS syndrome. Haematologica. 110(6). 1432–1435. 1 indexed citations

Larcher, Lise, Nadia Vasquez, Mélanie Da Costa, et al.. (2023). A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cells. Nucleic Acids Research. 51(15). 7988–8004. 3 indexed citations

Prata, Pedro Henrique, Jacques‐Emmanuel Galimard, Flore Sicre de Fontbrune, et al.. (2023). Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuria. Blood. 141(15). 1812–1816. 7 indexed citations

Schündeln, Michael M., Lisa Müller, Johannes Ptok, et al.. (2023). A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutations. Human Molecular Genetics. 32(11). 1836–1849. 7 indexed citations

Larcher, Lise, Nadia Vasquez, Mélanie Da Costa, et al.. (2022). Characteristics of Germline CHEK2 Mutated Patients in a Large Cohort of 2322 Myeloid Malignancies. Blood. 140(Supplement 1). 4082–4083. 1 indexed citations

Vulliamy, Tom, Inderjeet Dokal, Jean Soulier, et al.. (2021). Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease. Blood. 138(Supplement 1). 864–864. 1 indexed citations

Larcher, Lise, Julien Buratti, Brigitte Benzacken, et al.. (2019). New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability. Clinical Genetics. 97(4). 639–643. 7 indexed citations

Larcher, Lise, Joy Norris, Julien Buratti, et al.. (2019). The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndrome. European Journal of Medical Genetics. 63(4). 103777–103777. 21 indexed citations

Mammeri, Hedi, Lise Larcher, V. Descamps, et al.. (2018). Orogenital Transmission of Neisseria meningitidis Causing Acute Urethritis in Men Who Have Sex with Men. Emerging infectious diseases. 25(1). 175–176. 12 indexed citations

10.

Larcher, Lise, Guillaume Lefèvre, S. Bailleul, Michel Daudon, & Vincent Frochot. (2017). Importance of pre-analytical for urinalysis with urinary crystals. Annales de biologie clinique. 75(5). 525–530. 1 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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