Pierre Walrafen

406 total citations
5 papers, 248 citations indexed

About

Pierre Walrafen is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Pierre Walrafen has authored 5 papers receiving a total of 248 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 2 papers in Genetics. Recurrent topics in Pierre Walrafen's work include Cardiomyopathy and Myosin Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Muscle Physiology and Disorders (2 papers). Pierre Walrafen is often cited by papers focused on Cardiomyopathy and Myosin Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Muscle Physiology and Disorders (2 papers). Pierre Walrafen collaborates with scholars based in France, United States and Netherlands. Pierre Walrafen's co-authors include Alain Aurias, Jean Soulier, Jean‐Michel Cayuela, Anna Kalota, Bertrand Nadel, Antoine Crinquette, Willem A. Dik, Anton W. Langerak, Hervé Dombret and Thierry Leblanc and has published in prestigious journals such as Blood, Neurology and Annals of Neurology.

In The Last Decade

Pierre Walrafen

5 papers receiving 245 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pierre Walrafen France 4 140 95 71 38 37 5 248
Yuichiro Semba Japan 12 203 1.4× 60 0.6× 41 0.6× 33 0.9× 30 0.8× 35 305
Jessica Tatarek United States 2 208 1.5× 96 1.0× 86 1.2× 20 0.5× 55 1.5× 2 298
Sonali Narang United States 6 255 1.8× 134 1.4× 31 0.4× 27 0.7× 40 1.1× 9 326
Gue Su Chang United States 8 196 1.4× 120 1.3× 20 0.3× 41 1.1× 41 1.1× 13 288
Marta Tapia United Kingdom 10 310 2.2× 121 1.3× 41 0.6× 19 0.5× 27 0.7× 13 366
Cécile K. Lopez France 9 148 1.1× 64 0.7× 22 0.3× 24 0.6× 23 0.6× 13 227
Sewa Rijal Australia 5 150 1.1× 105 1.1× 42 0.6× 37 1.0× 46 1.2× 8 247
Bernhard Heilmeier Germany 10 250 1.8× 121 1.3× 48 0.7× 27 0.7× 44 1.2× 15 355
Panxiang Cao China 10 132 0.9× 160 1.7× 51 0.7× 53 1.4× 21 0.6× 32 255
Alain Zasadzinski France 3 125 0.9× 35 0.4× 21 0.3× 19 0.5× 23 0.6× 4 231

Countries citing papers authored by Pierre Walrafen

Since Specialization
Citations

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

Fields of papers citing papers by Pierre Walrafen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pierre Walrafen

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

All Works

5 of 5 papers shown
1.
Strom, Charles M., Vladimira Sulcova, David Tsao, et al.. (2013). DNA Combing Assay for Detection of Contraction-Dependent Facioscapulohumeral Muscular Dystrophy (FSHD1) (PD3.005). Neurology. 80(7_supplement). 1 indexed citations
2.
Cheeseman, Kevin, Étienne Rouleau, Anne Vannier, et al.. (2012). A diagnostic genetic test for the physical mapping of germline rearrangements in the susceptibility breast cancer genes BRCA1 and BRCA2. Human Mutation. 33(6). 998–1009. 15 indexed citations
3.
Nguyen, Karine, Pierre Walrafen, Rafaëlle Bernard, et al.. (2011). Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy. Annals of Neurology. 70(4). 627–633. 36 indexed citations
4.
Bénéteau, Claire, Emilie Landais, C. Philippe, et al.. (2011). Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability. Journal of Medical Genetics. 48(9). 635–639. 9 indexed citations
5.

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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2026