Bertrand Boisson

20.5k total citations · 1 hit paper
57 papers, 3.2k citations indexed

About

Bertrand Boisson is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Bertrand Boisson has authored 57 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Immunology, 20 papers in Genetics and 19 papers in Molecular Biology. Recurrent topics in Bertrand Boisson's work include Immunodeficiency and Autoimmune Disorders (22 papers), Blood disorders and treatments (11 papers) and Genomics and Rare Diseases (9 papers). Bertrand Boisson is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (22 papers), Blood disorders and treatments (11 papers) and Genomics and Rare Diseases (9 papers). Bertrand Boisson collaborates with scholars based in France, United States and United Kingdom. Bertrand Boisson's co-authors include Jean‐Laurent Casanova, Laurent Abel, Yuval Itan, Aziz Belkadi, Thierry Meinnel, Lei Shang, Carmela Giglione, Capucine Pïcard, Alexandre Bolze and Aurélie Cobat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Bertrand Boisson

52 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants

2015 384 citations Aziz Belkadi, Alexandre Bolze et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bertrand Boisson France	27	1.3k	1.2k	796	489	345	57	3.2k
Laurence Abrami Switzerland	37	3.6k 2.8×	1.6k 1.3×	707 0.9×	347 0.7×	426 1.2×	63	5.2k
Timothy Cardozo United States	33	2.9k 2.2×	714 0.6×	460 0.6×	267 0.5×	365 1.1×	96	4.6k
Angelina M. Bilate United States	27	1.7k 1.3×	1.5k 1.2×	419 0.5×	353 0.7×	624 1.8×	44	3.7k
Marília Cascalho United States	33	1.5k 1.2×	2.2k 1.9×	1.5k 1.9×	191 0.4×	283 0.8×	117	5.3k
Karl S. Matlin United States	31	2.7k 2.1×	606 0.5×	656 0.8×	269 0.6×	884 2.6×	63	5.0k
Jonathan L. Schmid‐Burgk Germany	26	4.5k 3.5×	2.5k 2.1×	524 0.7×	324 0.7×	567 1.6×	35	5.9k
Jay R. Hesselberth United States	31	2.5k 2.0×	669 0.6×	208 0.3×	263 0.5×	234 0.7×	69	3.7k
James E. Casanova United States	48	4.4k 3.4×	758 0.6×	459 0.6×	190 0.4×	389 1.1×	100	6.9k
Leonor Kremer Spain	33	1.5k 1.2×	1.0k 0.9×	248 0.3×	155 0.3×	224 0.6×	75	3.4k
Yair Benita United States	15	2.3k 1.8×	1.1k 0.9×	561 0.7×	231 0.5×	895 2.6×	21	4.4k

Countries citing papers authored by Bertrand Boisson

Since Specialization

Citations

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

Fields of papers citing papers by Bertrand Boisson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bertrand Boisson

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

All Works

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20 of 20 papers shown

Abolhassani, Hassan, Andrés Caballero-Oteyza, Mingyu Yang, et al.. (2025). Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency. PubMed. 1(4).

Stein, David, Matthew Mort, Peter D. Stenson, et al.. (2025). Expanding the utility of variant effect predictions with phenotype-specific models. Nature Communications. 16(1). 11113–11113.

Chbihi, Marwa, Frédéric Rieux‐Laucat, Jérémie Rosain, et al.. (2025). Two New Kindreds with Complete Factor D Deficiency. European Journal of Immunology. 55(3). e202451536–e202451536. 1 indexed citations

Tsumura, Miyuki, Masato Yashiro, Zenichiro Kato, et al.. (2024). Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency. Journal of Clinical Immunology. 44(7). 167–167.

Zhang, Peng, Masato Ogishi, Darawan Rinchai, et al.. (2023). Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites. Proceedings of the National Academy of Sciences. 120(46). e2314225120–e2314225120. 6 indexed citations

Zhang, Peng, Quentin Philippot, Weicheng Ren, et al.. (2022). Genome-wide detection of human variants that disrupt intronic branchpoints. Proceedings of the National Academy of Sciences. 119(44). e2211194119–e2211194119. 23 indexed citations

Borsani, Oscar, Takaki Asano, Bertrand Boisson, et al.. (2022). Isolated congenital asplenia: An overlooked cause of thrombocytosis. American Journal of Hematology. 97(8). 1110–1115. 3 indexed citations

Rapaport, Franck, Bertrand Boisson, Anne Gregor, et al.. (2021). Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance. Proceedings of the National Academy of Sciences. 118(3). 18 indexed citations

Bigio, Benedetta, Yoann Seeleuthner, Gaspard Kerner, et al.. (2021). Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing. NAR Genomics and Bioinformatics. 3(2). lqab037–lqab037. 5 indexed citations

10.

Yamashita, Motoi, Hye Sun Kuehn, Kazuki Okuyama, et al.. (2021). A variant in human AIOLOS impairs adaptive immunity by interfering with IKAROS. Nature Immunology. 22(7). 893–903. 40 indexed citations

11.

Abolhassani, Hassan, Ahmad Vosughimotlagh, Takaki Asano, et al.. (2021). X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia. Journal of Clinical Immunology. 42(1). 1–9. 28 indexed citations

12.

Ogishi, Masato, Rui Yang, Conor Gruber, et al.. (2020). Multibatch Cytometry Data Integration for Optimal Immunophenotyping. The Journal of Immunology. 206(1). 206–213. 15 indexed citations

13.

Zhang, Peng, Bertrand Boisson, Peter D. Stenson, et al.. (2019). SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing data. Nucleic Acids Research. 47(W1). W623–W631. 11 indexed citations

14.

Zhang, Peng, Benedetta Bigio, Franck Rapaport, et al.. (2018). PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations. Bioinformatics. 34(24). 4307–4309. 35 indexed citations

15.

Maffucci, Patrick, Jose Chavez, Patrick O’Brien, et al.. (2018). Biallelic mutations in DNA ligase 1 underlie a spectrum of immune deficiencies. Journal of Clinical Investigation. 128(12). 5489–5504. 29 indexed citations

16.

Bal, Élodie, Emmanuel Laplantine, Yamina Hamel, et al.. (2017). Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti. Journal of Allergy and Clinical Immunology. 140(6). 1671–1682.e2. 13 indexed citations

17.

Belkadi, Aziz, Alexandre Bolze, Yuval Itan, et al.. (2015). Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants. Proceedings of the National Academy of Sciences. 112(17). 5473–5478. 384 indexed citations breakdown →

18.

Amino, Rogério, Donatella Giovannini, Sabine Thiberge, et al.. (2008). Host Cell Traversal Is Important for Progression of the Malaria Parasite through the Dermis to the Liver. Cell Host & Microbe. 3(2). 88–96. 192 indexed citations

19.

Boisson, Bertrand, Carmela Giglione, & Thierry Meinnel. (2003). Unexpected Protein Families Including Cell Defense Components Feature in the N-Myristoylome of a Higher Eukaryote. Journal of Biological Chemistry. 278(44). 43418–43429. 128 indexed citations

20.

Benhamron, Sandrine, Johan Memelink, Nathalie Giglioli‐Guivarc’h, et al.. (2001). Catharanthus roseus G-box binding factors 1 and 2 act as repressors of strictosidine synthase gene expression in cell cultures. Plant Molecular Biology. 45(4). 477–488. 102 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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