Agnès Bourillon

590 total citations
13 papers, 357 citations indexed

About

Agnès Bourillon is a scholar working on Molecular Biology, Cell Biology and Dermatology. According to data from OpenAlex, Agnès Bourillon has authored 13 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Cell Biology and 3 papers in Dermatology. Recurrent topics in Agnès Bourillon's work include melanin and skin pigmentation (5 papers), Mast cells and histamine (3 papers) and DNA Repair Mechanisms (3 papers). Agnès Bourillon is often cited by papers focused on melanin and skin pigmentation (5 papers), Mast cells and histamine (3 papers) and DNA Repair Mechanisms (3 papers). Agnès Bourillon collaborates with scholars based in France, United States and Belgium. Agnès Bourillon's co-authors include Bernard Grandchamp, Érick Denamur, Philippe Saïag, V. Descamps, Nicole Basset‐Séguin, Nadem Soufir, Nadem Soufir, Walter E. Stamm, David M. Rothstein and Robert J. Suchland and has published in prestigious journals such as JNCI Journal of the National Cancer Institute, Annals of Neurology and Kidney International.

In The Last Decade

Agnès Bourillon

13 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Agnès Bourillon France 11 222 82 75 64 57 13 357
Olga P. Ryabinina United States 9 242 1.1× 41 0.5× 23 0.3× 47 0.7× 35 0.6× 12 396
Maria Giovanna Maturo Italy 10 206 0.9× 44 0.5× 35 0.5× 100 1.6× 24 0.4× 10 396
Cécile Chemin France 8 261 1.2× 141 1.7× 27 0.4× 21 0.3× 62 1.1× 9 349
Claire Hamilton United States 11 393 1.8× 64 0.8× 79 1.1× 13 0.2× 38 0.7× 15 544
Salma Taboubi France 6 154 0.7× 37 0.5× 77 1.0× 47 0.7× 33 0.6× 7 350
Michèle Lieb France 8 232 1.0× 67 0.8× 33 0.4× 55 0.9× 18 0.3× 14 437
Jüri Habicht Germany 10 207 0.9× 47 0.6× 32 0.4× 39 0.6× 24 0.4× 18 515
Špela Konjar Portugal 11 149 0.7× 22 0.3× 46 0.6× 71 1.1× 76 1.3× 14 469
Geneviève Morin Canada 12 347 1.6× 43 0.5× 33 0.4× 134 2.1× 57 1.0× 30 560
Anshu Sharma India 9 96 0.4× 19 0.2× 34 0.5× 60 0.9× 15 0.3× 25 346

Countries citing papers authored by Agnès Bourillon

Since Specialization
Citations

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

Fields of papers citing papers by Agnès Bourillon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Agnès Bourillon

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

All Works

13 of 13 papers shown
1.
Dewulf, Joseph P., Elsa Wiame, Imen Dorboz, et al.. (2019). SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation. Annals of Neurology. 85(3). 385–395. 19 indexed citations
2.
Bourillon, Agnès, Samia Pichard, Jean‐François Benoist, et al.. (2017). Mitochondrial acetoacetyl‐CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis. Journal of Inherited Metabolic Disease. 40(3). 415–422. 11 indexed citations
3.
Dorboz, Imen, Samia Pichard, Agnès Bourillon, et al.. (2016). Transient neonatal renal failure and massive polyuria in MEGDEL syndrome. Molecular Genetics and Metabolism Reports. 7. 8–10. 4 indexed citations
4.
Benfodda, M., Nicolas Dumaz, Steven Gazal, et al.. (2014). A Large French Case-Control Study Emphasizes the Role of RareMc1RVariants in Melanoma Risk. BioMed Research International. 2014. 1–10. 15 indexed citations
5.
Bourillon, Agnès, Wei Yang, Caroline Pouvelle, et al.. (2013). Correlation of Phenotype/Genotype in a Cohort of 23 Xeroderma Pigmentosum-Variant Patients Reveals 12 New Disease-CausingPOLHMutations. Human Mutation. 35(1). 117–128. 28 indexed citations
6.
Bourillon, Agnès, Gilles Hetet, J Lacapère, et al.. (2012). Genetic variation at KIT locus may predispose to melanoma. Pigment Cell & Melanoma Research. 26(1). 88–96. 5 indexed citations
7.
Guedj, Mickaël, V. Descamps, Thomas Jouary, et al.. (2011). Assessment of tyrosinase variants and skin cancer risk in a large cohort of French subjects. Journal of Dermatological Science. 64(2). 127–133. 21 indexed citations
8.
Soufir, Nadem, Cécile Ged, Agnès Bourillon, et al.. (2010). A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa. Journal of Investigative Dermatology. 130(6). 1537–1542. 69 indexed citations
9.
Denamur, Érick, Anne‐Lise Delezoide, Corinne Alberti, et al.. (2009). Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease. Kidney International. 77(4). 350–358. 55 indexed citations
10.
Guedj, Mickaël, J Lacapère, Maria Concetta Fargnoli, et al.. (2009). Variants of the xeroderma pigmentosum variant gene (POLH) are associated with melanoma risk. European Journal of Cancer. 45(18). 3228–3236. 36 indexed citations
11.
Guedj, Mickaël, Agnès Bourillon, Christophe Combadière, et al.. (2008). Variants of theMATP/SLC45A2gene are protective for melanoma in the French population. Human Mutation. 29(9). 1154–1160. 43 indexed citations
12.
Soufir, Nadem, J Lacapère, Guylène Bertrand, et al.. (2005). Association Between Endothelin Receptor B Nonsynonymous Variants and Melanoma Risk. JNCI Journal of the National Cancer Institute. 97(17). 1297–1301. 17 indexed citations
13.
Suchland, Robert J., Agnès Bourillon, Érick Denamur, Walter E. Stamm, & David M. Rothstein. (2005). Rifampin-Resistant RNA Polymerase Mutants of Chlamydia trachomatis Remain Susceptible to the Ansamycin Rifalazil. Antimicrobial Agents and Chemotherapy. 49(3). 1120–1126. 34 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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