Ingrid Stec

733 total citations
9 papers, 527 citations indexed

About

Ingrid Stec is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Ingrid Stec has authored 9 papers receiving a total of 527 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 4 papers in Genetics. Recurrent topics in Ingrid Stec's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Chromatin Dynamics (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Ingrid Stec is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Chromatin Dynamics (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Ingrid Stec collaborates with scholars based in Netherlands, Germany and United Kingdom. Ingrid Stec's co-authors include Johan T. den Dunnen, Sylvia Nagl, Gert‐Jan B. van Ommen, Arie van Haeringen, Antoon F.M. Moorman, Tracy J. Wright, Michael R. Altherr, C. R. Müller, Gabriele Senger and Suzanne M. Leal and has published in prestigious journals such as FEBS Letters, Human Molecular Genetics and Genomics.

In The Last Decade

Ingrid Stec

9 papers receiving 518 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ingrid Stec Netherlands 7 422 142 60 55 48 9 527
Marianna Trakala Spain 11 346 0.8× 57 0.4× 52 0.9× 12 0.2× 17 0.4× 16 545
K. Burkhart-Schultz United States 11 439 1.0× 149 1.0× 121 2.0× 27 0.5× 30 0.6× 14 571
Sunmi Han South Korea 6 419 1.0× 39 0.3× 33 0.6× 24 0.4× 35 0.7× 15 617
Julian Pan United States 8 296 0.7× 69 0.5× 20 0.3× 42 0.8× 7 0.1× 10 442
N G Copeland United States 7 215 0.5× 91 0.6× 20 0.3× 3 0.1× 34 0.7× 8 350
Ido Tamir Austria 7 557 1.3× 90 0.6× 54 0.9× 20 0.4× 13 0.3× 7 800
N B Spinner United States 7 220 0.5× 186 1.3× 73 1.2× 74 1.3× 15 0.3× 9 332
Richard A. Voit United States 11 542 1.3× 200 1.4× 42 0.7× 96 1.7× 3 0.1× 17 783
Rosine Onclercq France 11 327 0.8× 131 0.9× 46 0.8× 7 0.1× 7 0.1× 12 436
NP Anagnou United States 14 464 1.1× 125 0.9× 16 0.3× 57 1.0× 10 0.2× 21 657

Countries citing papers authored by Ingrid Stec

Since Specialization
Citations

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

Fields of papers citing papers by Ingrid Stec

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Stec

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

All Works

9 of 9 papers shown
1.
Stec, Ingrid, et al.. (2001). WHSC1L1, on Human Chromosome 8p11.2, Closely Resembles WHSC1 and Maps to a Duplicated Region Shared with 4p16.3. Genomics. 76(1-3). 5–8. 49 indexed citations
2.
Stec, Ingrid, M. van Vliet, Ronald van Eijk, et al.. (2001). A partial BRCA1 sequence homology mapping to 4q28. Cytogenetic and Genome Research. 94(1-2). 26–29. 2 indexed citations
3.
Stec, Ingrid, Sylvia Nagl, Gert‐Jan B. van Ommen, & Johan T. den Dunnen. (2000). The PWWP domain: a potential protein–protein interaction domain in nuclear proteins influencing differentiation?. FEBS Letters. 473(1). 1–5. 178 indexed citations
4.
5.
Peters, Ulrike, Gabriele Senger, Ingrid Stec, et al.. (1997). Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13.. PubMed. 5(1). 9–14. 10 indexed citations
6.
Peters, Annette, Gabriele Senger, Ingrid Stec, et al.. (1997). Nephropathie Cystinosis (CTNS-LSB): Construction of a YAC Contig Comprising the Refined Critical Region on Chromosome 17p13. European Journal of Human Genetics. 5(1). 9–14. 8 indexed citations
7.
Kant, Sarina G., Arie van Haeringen, Ingrid Stec, et al.. (1997). Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.. Journal of Medical Genetics. 34(7). 569–572. 12 indexed citations
8.
Stec, Ingrid, Ulrike Peters, Erik Harms, et al.. (1996). Yeast artificial chromosome mapping of the cystinosis locus on chromosome 17p by fluorescence in situ hybridization. Human Genetics. 98(3). 321–322. 4 indexed citations
9.

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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