Pierre Marijon

2.4k total citations
8 papers, 67 citations indexed

About

Pierre Marijon is a scholar working on Molecular Biology, Artificial Intelligence and Genetics. According to data from OpenAlex, Pierre Marijon has authored 8 papers receiving a total of 67 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Artificial Intelligence and 2 papers in Genetics. Recurrent topics in Pierre Marijon's work include Genomics and Phylogenetic Studies (4 papers), Renal and related cancers (3 papers) and Genetic and Kidney Cyst Diseases (2 papers). Pierre Marijon is often cited by papers focused on Genomics and Phylogenetic Studies (4 papers), Renal and related cancers (3 papers) and Genetic and Kidney Cyst Diseases (2 papers). Pierre Marijon collaborates with scholars based in France, Germany and Poland. Pierre Marijon's co-authors include Rayan Chikhi, Jean‐Stéphane Varré, Yoann Dufresne, Tristan Montier, Marek Kokot, Paul Medvedev, Pierre Peterlongo, Sebastian Deorowicz, Zahra Assouline and Olivier Gribouval and has published in prestigious journals such as Bioinformatics, Kidney International and European Journal of Human Genetics.

In The Last Decade

Pierre Marijon

8 papers receiving 66 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pierre Marijon France	3	39	16	13	9	6	8	67
Riccardo Vicedomini France	5	110 2.8×	25 1.6×	47 3.6×	15 1.7×	4 0.7×	9	139
Hamid Mirebrahim United States	3	57 1.5×	24 1.5×	29 2.2×	15 1.7×	1 0.2×	4	81
Semar Petrus United States	4	63 1.6×	16 1.0×	31 2.4×	11 1.2×	6 1.0×	6	108
Michael Stratton United States	2	32 0.8×	12 0.8×	5 0.4×	18 2.0×	2 0.3×	5	57
Sandra Dérozier France	6	56 1.4×	22 1.4×	21 1.6×	17 1.9×	2 0.3×	9	82
Yanbing Xu China	2	56 1.4×	8 0.5×	23 1.8×	7 0.8×	3 0.5×	2	70
Kim Philipp Jablonski Switzerland	6	65 1.7×	12 0.8×	20 1.5×	18 2.0×	3 0.5×	10	99
Matthew Alpert United States	2	26 0.7×	8 0.5×	13 1.0×	6 0.7×	2 0.3×	3	42
Denisa Duma United States	2	26 0.7×	8 0.5×	13 1.0×	6 0.7×	2 0.3×	3	42

Countries citing papers authored by Pierre Marijon

Since Specialization

Citations

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

Fields of papers citing papers by Pierre Marijon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pierre Marijon

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

All Works

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8 of 8 papers shown

1.

Arrondel, Christelle, Giulia Barcia, Zahra Assouline, et al.. (2025). Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism. Pediatric Nephrology. 40(9). 2823–2828. 1 indexed citations

2.

Boutaud, Lucile, Chloé Quēlin, Philippe Roth, et al.. (2025). Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliogenesis. European Journal of Human Genetics. 33(3). 387–392. 2 indexed citations

3.

Marijon, Pierre, et al.. (2024). Back to sequences: Find the origin of k-mers. The Journal of Open Source Software. 9(101). 7066–7066. 1 indexed citations

4.

Dorval, Guillaume, Gérald Le Gac, Vincent Morinière, et al.. (2024). Targeted RNAseq from patients’ urinary cells to validate pathogenic noncoding variants in autosomal dominant polycystic kidney disease genes: a proof of concept. Kidney International. 106(3). 532–535. 1 indexed citations

5.

Dufresne, Yoann, Pierre Marijon, Pierre Peterlongo, et al.. (2022). The K-mer File Format: a standardized and compact disk representation of sets ofk-mers. Bioinformatics. 38(18). 4423–4425. 5 indexed citations

6.

Marijon, Pierre, et al.. (2021). Cutevariant: a standalone GUI-based desktop application to explore genetic variations from an annotated VCF file. Bioinformatics Advances. 2(1). vbab028–vbab028. 3 indexed citations

7.

Marijon, Pierre, Rayan Chikhi, & Jean‐Stéphane Varré. (2020). yacrd and fpa: upstream tools for long-read genome assembly. Bioinformatics. 36(12). 3894–3896. 52 indexed citations

8.

Marijon, Pierre, Rayan Chikhi, & Jean‐Stéphane Varré. (2019). Graph analysis of fragmented long-read bacterial genome assemblies. Bioinformatics. 35(21). 4239–4246. 2 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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