Jean‐Philippe Brandel

3.6k total citations · 1 hit paper
53 papers, 1.4k citations indexed

About

Jean‐Philippe Brandel is a scholar working on Molecular Biology, Neurology and Neurology. According to data from OpenAlex, Jean‐Philippe Brandel has authored 53 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 21 papers in Neurology and 9 papers in Neurology. Recurrent topics in Jean‐Philippe Brandel's work include Prion Diseases and Protein Misfolding (47 papers), Neurological diseases and metabolism (21 papers) and Alcoholism and Thiamine Deficiency (4 papers). Jean‐Philippe Brandel is often cited by papers focused on Prion Diseases and Protein Misfolding (47 papers), Neurological diseases and metabolism (21 papers) and Alcoholism and Thiamine Deficiency (4 papers). Jean‐Philippe Brandel collaborates with scholars based in France, United Kingdom and Morocco. Jean‐Philippe Brandel's co-authors include Stéphane Haı̈k, Takeshi Sato, Jean Laplanche, Paul Brown, Robert Will, Maurizio Pocchiari, Anna Ladogana, Katell Peoc’h, Jan Mackenzie and Jean‐Jacques Hauw and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Jean‐Philippe Brandel

49 papers receiving 1.4k citations

Hit Papers

align trajectories sort by overperformance

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.

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

2021 171 citations Péter Hermann, Brian S. Appleby et al. The Lancet Neurology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean‐Philippe Brandel France	21	1.2k	632	276	237	231	53	1.4k
Gianfranco Puoti Italy	16	915 0.8×	442 0.7×	254 0.9×	237 1.0×	202 0.9×	53	1.1k
E Mitrová Slovakia	16	839 0.7×	388 0.6×	241 0.9×	160 0.7×	158 0.7×	47	989
N. Delasnerie–Lauprêtre France	14	1.2k 1.0×	512 0.8×	296 1.1×	118 0.5×	179 0.8×	35	1.4k
K. Jendroska Germany	14	688 0.6×	545 0.9×	165 0.6×	325 1.4×	288 1.2×	22	1.2k
Monika Bodemer Germany	21	1.7k 1.4×	765 1.2×	497 1.8×	196 0.8×	254 1.1×	30	2.0k
Thomas Blättler Switzerland	10	902 0.7×	561 0.9×	79 0.3×	112 0.5×	376 1.6×	13	1.0k
Françoise Cathala France	16	967 0.8×	498 0.8×	222 0.8×	89 0.4×	238 1.0×	25	1.1k
Aissa Haman United States	8	457 0.4×	169 0.3×	362 1.3×	92 0.4×	42 0.2×	9	691
Ursula Unterberger Austria	13	505 0.4×	215 0.3×	67 0.2×	208 0.9×	126 0.5×	23	721
Xiaojing Gu China	17	336 0.3×	123 0.2×	381 1.4×	128 0.5×	14 0.1×	85	961

Countries citing papers authored by Jean‐Philippe Brandel

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Philippe Brandel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Philippe Brandel. 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 Jean‐Philippe Brandel. The network helps show where Jean‐Philippe Brandel may publish in the future.

Co-authorship network of co-authors of Jean‐Philippe Brandel

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Philippe Brandel. A scholar is included among the top collaborators of Jean‐Philippe Brandel 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 Jean‐Philippe Brandel. Jean‐Philippe Brandel 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

Delorme, Cécile, Antoine Pégat, Jean‐Philippe Brandel, et al.. (2025). Demyelinating neuropathy as the initial presentation of familial E200K Creutzfeldt–Jakob disease in two patients. Annals of Clinical and Translational Neurology. 12(3). 653–658.

Brandel, Jean‐Philippe, et al.. (2025). Switching from Levodopa/Carbidopa Intestinal Gel to Continuous Subcutaneous Foslevodopa/Carbidopa Infusion in Advanced Parkinson's Disease: A Case Series. Movement Disorders Clinical Practice. 13(2). 521–527.

Denouel, Angéline, Jean‐Philippe Brandel, Danielle Seilhean, et al.. (2023). The role of environmental factors on sporadic Creutzfeldt-Jakob disease mortality: evidence from an age-period-cohort analysis. European Journal of Epidemiology. 38(7). 757–764. 4 indexed citations

Watson, Neil, Jean‐Philippe Brandel, Alison Green, et al.. (2021). The importance of ongoing international surveillance for Creutzfeldt–Jakob disease. Nature Reviews Neurology. 17(6). 362–379. 76 indexed citations

Hermann, Péter, Brian S. Appleby, Jean‐Philippe Brandel, et al.. (2021). Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease. The Lancet Neurology. 20(3). 235–246. 171 indexed citations breakdown →

Frontzek, Karl, Marco Losa, Georg Meisl, et al.. (2020). Autoantibodies against the prion protein in individuals with PRNP mutations. Neurology. 95(14). e2028–e2037. 10 indexed citations

Brandel, Jean‐Philippe, et al.. (2019). Genetic Testing in Prion Disease: Psychological Consequences of the Decisions to Know or Not to Know. Frontiers in Genetics. 10. 895–895. 9 indexed citations

Xiao, Xiangzhu, Jue Yuan, Ignazio Calì, et al.. (2013). Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease. PLoS ONE. 8(10). 17 indexed citations

Hannaoui, Samia, Nicolas Privat, Etienne Levavasseur, et al.. (2013). Cycline Efficacy on the Propagation of Human Prions in Primary Cultured Neurons is Strain-Specific. The Journal of Infectious Diseases. 209(7). 1144–1148. 26 indexed citations

10.

Peoc’h, Katell, Etienne Levavasseur, Émilien Delmont, et al.. (2012). Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. Human Molecular Genetics. 21(26). 5417–5428. 23 indexed citations

11.

Brandel, Jean‐Philippe, Craig A. Heath, Mark Head, et al.. (2009). Variant Creutzfeldt–Jakob disease in France and the United Kingdom: Evidence for the same agent strain. Annals of Neurology. 65(3). 249–256. 43 indexed citations

12.

Levavasseur, Etienne, Baptiste Faucheux, Nicolas Privat, et al.. (2008). Regulating Factors of PrPres Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains. PLoS ONE. 3(7). e2786–e2786. 28 indexed citations

13.

Levavasseur, Etienne, Baptiste Faucheux, Nicolas Privat, et al.. (2008). Correction: Regulating Factors of PrPres Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains. PLoS ONE. 3(9). 1 indexed citations

14.

Haı̈k, Stéphane, Damien Galanaud, Marius George Linguraru, et al.. (2008). In Vivo Detection of Thalamic Gliosis. Archives of Neurology. 65(4). 545–545. 22 indexed citations

15.

Brandel, Jean‐Philippe, et al.. (2008). [Creutzfeldt-Jakob disease in patients before and after 80 years of age].. PubMed. 6(3). 219–24. 2 indexed citations

16.

Brandel, Jean‐Philippe. (2007). [Creutzfeldt-Jakob disease: what's new?].. PubMed. 57(16). 1745–7.

17.

Chasseigneaux, Stéphanie, Stéphane Haı̈k, Olivier Marco, et al.. (2006). V180I mutation of the prion protein gene associated with atypical PrPSc glycosylation. Neuroscience Letters. 408(3). 165–169. 37 indexed citations

18.

Linguraru, Marius George, Miguel Á. González Ballester, Éric Bardinet, et al.. (2004). Automated Analysis of Basal Ganglia Intensity Distribution in Multisequence MRI of the Brain - Application to Creutzfeldt-Jakob Disease. HAL (Le Centre pour la Communication Scientifique Directe). 55. 3 indexed citations

19.

d’Aignaux, Jérôme Huillard, Simon Cousens, N. Delasnerie–Lauprêtre, et al.. (2002). Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998. International Journal of Epidemiology. 31(2). 490–495. 12 indexed citations

20.

Brandel, Jean‐Philippe, Katell Peoc’h, Patrice Beaudry, et al.. (2001). 14-3-3 Protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients. Annals of Neurology. 49(2). 257–260. 21 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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