S. Heuertz

2.0k total citations
40 papers, 883 citations indexed

About

S. Heuertz is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, S. Heuertz has authored 40 papers receiving a total of 883 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 21 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in S. Heuertz's work include Connective tissue disorders research (11 papers), Genetic and rare skin diseases. (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). S. Heuertz is often cited by papers focused on Connective tissue disorders research (11 papers), Genetic and rare skin diseases. (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). S. Heuertz collaborates with scholars based in France, Canada and Germany. S. Heuertz's co-authors include M. C. Hors‐Cayla, Martine Le Merrer, J Frézal, A. Sefiani, Jacky Bonaventure, Damian Labuda, Valérie Cormier‐Daire, Jelena Martinović, Daniel Sinnett and Laurent Abel and has published in prestigious journals such as Journal of Virology, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

S. Heuertz

40 papers receiving 842 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S. Heuertz France 18 676 494 93 67 65 40 883
M. C. Hors‐Cayla France 21 645 1.0× 603 1.2× 85 0.9× 56 0.8× 73 1.1× 43 1.1k
Karen Fitch United States 9 250 0.4× 366 0.7× 158 1.7× 78 1.2× 70 1.1× 11 668
Elizabeth A. Smith United States 10 356 0.5× 682 1.4× 244 2.6× 53 0.8× 135 2.1× 11 966
Judith A. Fantes United Kingdom 14 302 0.4× 611 1.2× 42 0.5× 51 0.8× 272 4.2× 28 843
Vesna Jurecic United States 14 656 1.0× 1.5k 3.0× 64 0.7× 42 0.6× 115 1.8× 19 1.7k
Leslie Boghosian-Sell United States 9 124 0.2× 320 0.6× 48 0.5× 105 1.6× 23 0.4× 10 536
Aaron Avivi Israel 7 276 0.4× 493 1.0× 104 1.1× 49 0.7× 8 0.1× 9 719
Dorothea Bornholdt Germany 13 543 0.8× 703 1.4× 249 2.7× 57 0.9× 16 0.2× 19 1.0k
Amber K. O’Connor United States 8 558 0.8× 686 1.4× 200 2.2× 44 0.7× 14 0.2× 15 877
Alexander N. Yatsenko United States 18 527 0.8× 787 1.6× 76 0.8× 35 0.5× 51 0.8× 35 1.4k

Countries citing papers authored by S. Heuertz

Since Specialization
Citations

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

Fields of papers citing papers by S. Heuertz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

20 of 20 papers shown
1.
Pannier, Stéphanie, Jelena Martinović, S. Heuertz, et al.. (2009). Thanatophoric dysplasia caused by double missense FGFR3 mutations. American Journal of Medical Genetics Part A. 149A(6). 1296–1301. 16 indexed citations
2.
Heuertz, S., Martine Le Merrer, Bernhard Zabel, et al.. (2006). Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia. European Journal of Human Genetics. 14(12). 1240–1247. 65 indexed citations
3.
Fiedler, Jörg, Martine Le Merrer, Geert Mortier, et al.. (2004). X-linked spondyloepiphyseal dysplasia tarda: Novel and recurrent mutations in 13 European families. Human Mutation. 24(1). 103–103. 19 indexed citations
4.
Colleaux, Laurence, S. Heuertz, Florence Molinari, & Marlène Rio. (2003). Fluorescence Genotyping for Screening Cryptic Telomeric Rearrangements. Molecular Cytogenetics. 204. 181–190. 5 indexed citations
5.
Rio, Marlène, Florence Molinari, S. Heuertz, et al.. (2002). Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. Journal of Medical Genetics. 39(4). 266–270. 54 indexed citations
6.
Colleaux, Laurence, Marlène Rio, S. Heuertz, et al.. (2001). A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation. European Journal of Human Genetics. 9(5). 319–327. 47 indexed citations
7.
Gedeon, Ági K., George E. Tiller, M. Le Merrer, et al.. (2001). The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda. The American Journal of Human Genetics. 68(6). 1386–1397. 70 indexed citations
8.
Aradhya, Swaroop, Richard A. Lewis, David L. Nelson, et al.. (2000). Filamin (FLN1),plexin (SEX), major palmitoylated proteinp55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2. American Journal of Medical Genetics. 94(1). 79–84. 3 indexed citations
9.
Heuertz, S., et al.. (1995). Fine deletion mapping of the p22 region of the human X chromosome using a radiation-induced hybrid panel. Cytogenetic and Genome Research. 69(1-2). 7–10. 1 indexed citations
10.
Heuertz, S., Asma Smahi, Andrew O.M. Wilkie, et al.. (1995). Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL). Human Genetics. 96(4). 407–410. 17 indexed citations
11.
Hors‐Cayla, M. C., S. Heuertz, & Asma Smahi. (1994). Refinement of the localization of the gene responsible for spondylo epiphyseal dysplasia in Xp22. The American Journal of Human Genetics. 55. 1 indexed citations
12.
Heuertz, S., Marcel Nelen, Andrew O.M. Wilkie, et al.. (1993). The Gene for Spondyloepiphyseal Dysplasia (SEDL) Maps to Xp22 between DXS16 and DXS92. Genomics. 18(1). 100–104. 20 indexed citations
13.
Sanak, Marek, Georges Deschênes, Jing Zhou, et al.. (1992). Alport syndrome: a genetic study of 31 families. Human Genetics. 90(4). 420–6. 12 indexed citations
14.
Kaplan, Jeffrey, Anna Pelet, M Guilloud-Bataille, et al.. (1990). [An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia].. PubMed. 37(1). 13–9. 2 indexed citations
15.
Sefiani, A., Laurent Abel, S. Heuertz, et al.. (1989). The gene for incontinentia pigmenti is assigned to Xq28. Genomics. 4(3). 427–429. 85 indexed citations
16.
Sefiani, A., M Guilloud-Bataille, S. Heuertz, et al.. (1988). Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome. Human Genetics. 81(1). 61–63. 29 indexed citations
17.
Sefiani, A., Daniel Sinnett, Laurent Abel, et al.. (1988). Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11. Human Genetics. 80(3). 282–286. 25 indexed citations
18.
Mitchell, G. H., et al.. (1985). Maple syrup urine disease: Two different forms within a single family. Human Genetics. 71(1). 89–91. 1 indexed citations
19.
Hors‐Cayla, M. C., et al.. (1981). Regional assignment of arylsulfatase A, mitochondrial aconitase and NADH-cytochrome b5 reductase by somatic cell hybridization. Human Genetics. 58(2). 140–143. 17 indexed citations
20.
Hors‐Cayla, M. C., et al.. (1972). Elvolution caryotypique de cellules hybrides homme x homme.. Annales de Génétique. 15(3). 1 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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