S. Picaud

11.8k total citations · 1 hit paper
56 papers, 5.0k citations indexed

About

S. Picaud is a scholar working on Molecular Biology, Hematology and Oncology. According to data from OpenAlex, S. Picaud has authored 56 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 21 papers in Hematology and 6 papers in Oncology. Recurrent topics in S. Picaud's work include Protein Degradation and Inhibitors (29 papers), Multiple Myeloma Research and Treatments (21 papers) and Ubiquitin and proteasome pathways (10 papers). S. Picaud is often cited by papers focused on Protein Degradation and Inhibitors (29 papers), Multiple Myeloma Research and Treatments (21 papers) and Ubiquitin and proteasome pathways (10 papers). S. Picaud collaborates with scholars based in United Kingdom, United States and Canada. S. Picaud's co-authors include P. Filippakopoulos, Stefan Knapp, Susanne Müller, I. Felletar, O. Fedorov, Anne‐Claude Gingras, Tracy Keates, Jean‐Philippe Lambert, C.H. Arrowsmith and Maria Mangos and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

S. Picaud

56 papers receiving 4.9k 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.

Histone Recognition and Large-Scale Structural Analysis of the Human Bromodomain Family

2012 1.2k citations P. Filippakopoulos, S. Picaud et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Picaud United Kingdom	34	4.4k	1.5k	569	317	292	56	5.0k
O. Fedorov United Kingdom	41	4.4k 1.0×	1.2k 0.8×	832 1.5×	67 0.2×	731 2.5×	56	5.4k
Joachim Gullbo Sweden	36	2.9k 0.7×	431 0.3×	1.1k 2.0×	576 1.8×	329 1.1×	100	4.0k
Monica Schenone United States	17	2.7k 0.6×	764 0.5×	604 1.1×	50 0.2×	254 0.9×	33	3.5k
Jean‐Philippe Lambert Canada	29	3.4k 0.8×	491 0.3×	395 0.7×	159 0.5×	87 0.3×	81	4.0k
Sandra W. Cowan‐Jacob Switzerland	30	1.9k 0.4×	2.2k 1.4×	801 1.4×	55 0.2×	863 3.0×	51	4.6k
Brian D. Marsden United Kingdom	30	2.7k 0.6×	318 0.2×	642 1.1×	75 0.2×	303 1.0×	65	3.9k
Helmut Mett Switzerland	28	1.7k 0.4×	870 0.6×	656 1.2×	84 0.3×	736 2.5×	59	3.3k
Jennifer L. Meagher United States	33	2.2k 0.5×	370 0.2×	708 1.2×	83 0.3×	453 1.6×	53	2.9k
Xiaoyun Lu China	34	2.1k 0.5×	315 0.2×	828 1.5×	120 0.4×	1.1k 3.7×	159	3.6k
Alessio Ciulli United Kingdom	49	8.2k 1.9×	1.8k 1.2×	2.9k 5.1×	77 0.2×	658 2.3×	133	8.8k

Countries citing papers authored by S. Picaud

Since Specialization

Citations

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

Fields of papers citing papers by S. Picaud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Picaud

This figure shows the co-authorship network connecting the top 25 collaborators of S. Picaud. A scholar is included among the top collaborators of S. Picaud 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 S. Picaud. S. Picaud 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

1.

Scaffidi, Salvatore, S. Picaud, T. Krojer, et al.. (2025). Water Networks as Hydrophobic Recognition Motifs in Proteins. Angewandte Chemie International Edition. 65(2). e21138–e21138. 1 indexed citations

2.

Lambert, Jean‐Philippe, Markéta Tomková, Arianna Baggiolini, et al.. (2024). DNA damage remodels the MITF interactome to increase melanoma genomic instability. Genes & Development. 38(1-2). 70–94. 4 indexed citations

3.

Louphrasitthiphol, Pakavarin, Alessia Loffreda, Vivian Pogenberg, et al.. (2023). Acetylation reprograms MITF target selectivity and residence time. Nature Communications. 14(1). 6051–6051. 10 indexed citations

4.

Cipriano, Alessandra, Ciro Milite, Alessandra Feoli, et al.. (2022). Discovery of Benzo[d]imidazole‐6‐sulfonamides as Bromodomain and Extra‐Terminal Domain (BET) Inhibitors with Selectivity for the First Bromodomain. ChemMedChem. 17(20). e202200343–e202200343. 9 indexed citations

5.

Picaud, S., Régis Millet, Gilles Gasser, et al.. (2021). Probing BRD Inhibition Substituent Effects in Bulky Analogues of (+)‐JQ1. Helvetica Chimica Acta. 104(3). 1 indexed citations

6.

Lukacik, Petra, David Owen, Gemma Harris, et al.. (2021). The structure of nontypeable Haemophilus influenzae SapA in a closed conformation reveals a constricted ligand-binding cavity and a novel RNA binding motif. PLoS ONE. 16(10). e0256070–e0256070. 7 indexed citations

7.

Song, Yan, Paul M.C. Park, Lei Wu, et al.. (2019). Development and preclinical validation of a novel covalent ubiquitin receptor Rpn13 degrader in multiple myeloma. Leukemia. 33(11). 2685–2694. 31 indexed citations

8.

Guillaume, Philippe, S. Picaud, Petra Baumgaertner, et al.. (2018). The C-terminal extension landscape of naturally presented HLA-I ligands. Proceedings of the National Academy of Sciences. 115(20). 5083–5088. 35 indexed citations

9.

Friedrichsen, Hans, S. Picaud, Laurent Volpon, et al.. (2018). A TFEB nuclear export signal integrates amino acid supply and glucose availability. Nature Communications. 9(1). 2685–2685. 95 indexed citations

10.

Mahajan, P., Oleg Fedorov, Francesco P. Marchese, et al.. (2017). Tryptophan-Mediated Interactions between Tristetraprolin and the CNOT9 Subunit Are Required for CCR4-NOT Deadenylase Complex Recruitment. Journal of Molecular Biology. 430(5). 722–736. 35 indexed citations

11.

Rooney, Timothy P. C., P. Filippakopoulos, O. Fedorov, et al.. (2014). A Series of Potent CREBBP Bromodomain Ligands Reveals an Induced‐Fit Pocket Stabilized by a Cation–π Interaction. Angewandte Chemie. 126(24). 6240–6244. 13 indexed citations

12.

Rooney, Timothy P. C., P. Filippakopoulos, O. Fedorov, et al.. (2014). A Series of Potent CREBBP Bromodomain Ligands Reveals an Induced‐Fit Pocket Stabilized by a Cation–π Interaction. Angewandte Chemie International Edition. 53(24). 6126–6130. 93 indexed citations

13.

Filippakopoulos, P., S. Picaud, Maria Mangos, et al.. (2012). Histone Recognition and Large-Scale Structural Analysis of the Human Bromodomain Family. Cell. 149(1). 214–231. 1230 indexed citations breakdown →

14.

Philpott, Martin, Jing Yang, O. Fedorov, et al.. (2011). Bromodomain-peptide displacement assays for interactome mapping and inhibitor discovery. Molecular BioSystems. 7(10). 2899–2908. 107 indexed citations

15.

Filippakopoulos, P., S. Picaud, O. Fedorov, et al.. (2011). Benzodiazepines and benzotriazepines as protein interaction inhibitors targeting bromodomains of the BET family. Bioorganic & Medicinal Chemistry. 20(6). 1878–1886. 97 indexed citations

16.

Picaud, S., J.R.C. Muniz, Ewa S. Pilka, et al.. (2009). Crystal structure of human carbonic anhydrase‐related protein VIII reveals the basis for catalytic silencing. Proteins Structure Function and Bioinformatics. 76(2). 507–511. 42 indexed citations

17.

Picaud, S., Mikael Emil Olsson, & Peter E. Brodelius. (2006). Improved conditions for production of recombinant plant sesquiterpene synthases in Escherichia coli. Protein Expression and Purification. 51(1). 71–79. 26 indexed citations

18.

Picaud, S., P. Mercke, Xiaofei He, et al.. (2005). Amorpha-4,11-diene synthase: Mechanism and stereochemistry of the enzymatic cyclization of farnesyl diphosphate. Archives of Biochemistry and Biophysics. 448(1-2). 150–155. 61 indexed citations

19.

Picaud, S., Linda Olofsson, Maria Brodelius, & Peter E. Brodelius. (2005). Expression, purification and characterization of amorpha-4,11-diene synthase from Artemisia annua L. Archives of Biochemistry and Biophysics. 215–226. 1 indexed citations

20.

Picaud, S., Maria Brodelius, & Peter E. Brodelius. (2005). Expression, purification and characterization of recombinant (E)-β-farnesene synthase from Artemisia annua. Phytochemistry. 66(9). 961–967. 107 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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