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.
Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes
2002544 citationsJérôme Feldmann, Anne‐Marie Prieur et al.The American Journal of Human Geneticsprofile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
hero ref
Countries citing papers authored by D Teillac-Hamel
Since
Specialization
Citations
This map shows the geographic impact of D Teillac-Hamel'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 D Teillac-Hamel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D Teillac-Hamel more than expected).
This network shows the impact of papers produced by D Teillac-Hamel. 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 D Teillac-Hamel. The network helps show where D Teillac-Hamel may publish in the future.
Co-authorship network of co-authors of D Teillac-Hamel
This figure shows the co-authorship network connecting the top 25 collaborators of D Teillac-Hamel.
A scholar is included among the top collaborators of D Teillac-Hamel 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 D Teillac-Hamel. D Teillac-Hamel is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Feldmann, Jérôme, Anne‐Marie Prieur, Pierre Quartier, et al.. (2002). Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes. The American Journal of Human Genetics. 71(1). 198–203.544 indexed citations breakdown →
4.
Pinson, S., Alain Créange, S. Barbarot, et al.. (2002). [Recommendations for the treatment of neurofibromatosis type 1].. PubMed. 25(4). 423–33.7 indexed citations
Bennaceur, S, et al.. (1997). [Use of iterative expansion in the early surgical treatment of complex nevi of the head in children].. PubMed. 98(4). 235–9.1 indexed citations
11.
Teillac-Hamel, D, et al.. (1996). [Rothmund-Thomson syndrome with reduced DNA repair capacity].. PubMed. 123(6-7). 395–7.8 indexed citations
Fraitag, Sylvie, D Teillac-Hamel, Y. De Prost, & Nicole Brousse. (1993). [Dermatomyofibroma: a case in a child].. PubMed. 120(11). 818–20.9 indexed citations
19.
Bodemer, C., et al.. (1992). [Chronic leg ulcer in children with prolidase deficiency].. PubMed. 119(11). 818–21.
20.
Teillac-Hamel, D, et al.. (1992). [Kasabach-Merritt syndrome in children].. PubMed. 39(7). 435–41.10 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.