Sandra H. E. Sprenger

668 total citations
13 papers, 538 citations indexed

About

Sandra H. E. Sprenger is a scholar working on Cancer Research, Genetics and Molecular Biology. According to data from OpenAlex, Sandra H. E. Sprenger has authored 13 papers receiving a total of 538 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cancer Research, 7 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Sandra H. E. Sprenger's work include Glioma Diagnosis and Treatment (7 papers), Cancer, Hypoxia, and Metabolism (4 papers) and Cancer Genomics and Diagnostics (4 papers). Sandra H. E. Sprenger is often cited by papers focused on Glioma Diagnosis and Treatment (7 papers), Cancer, Hypoxia, and Metabolism (4 papers) and Cancer Genomics and Diagnostics (4 papers). Sandra H. E. Sprenger collaborates with scholars based in Netherlands, Belgium and Germany. Sandra H. E. Sprenger's co-authors include Judith W. M. Jeuken, Pieter Wesseling, Rudolf H. Boerman, Hans L. J. M. Teepen, Jacobus J. van Overbeeke, Andreas von Deimling, Merryn Macville, Florence Lefranc, Anneke Geurts‐Moespot and Isabelle Salmon and has published in prestigious journals such as Cancer, Journal of neurosurgery and The Journal of Pathology.

In The Last Decade

Sandra H. E. Sprenger

13 papers receiving 531 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra H. E. Sprenger Netherlands	12	257	239	205	126	93	13	538
Candice A. Romany United States	5	357 1.4×	259 1.1×	150 0.7×	55 0.4×	123 1.3×	8	661
Carl Henrik Heldin Sweden	5	275 1.1×	87 0.4×	93 0.5×	69 0.5×	99 1.1×	6	447
V A Levin United States	6	232 0.9×	183 0.8×	80 0.4×	61 0.5×	129 1.4×	7	466
Stewart P. Johnson United States	13	394 1.5×	228 1.0×	154 0.8×	51 0.4×	168 1.8×	19	564
Douglas D. Kolstoe United States	11	572 2.2×	345 1.4×	179 0.9×	60 0.5×	141 1.5×	11	739
Angela A. van Tilborg Netherlands	5	296 1.2×	163 0.7×	136 0.7×	83 0.7×	70 0.8×	5	485
Alfred Yung United States	16	279 1.1×	370 1.5×	150 0.7×	179 1.4×	167 1.8×	29	672
MB Kastan United States	11	390 1.5×	95 0.4×	155 0.8×	32 0.3×	303 3.3×	18	757
Juliet Williams United States	6	484 1.9×	50 0.2×	127 0.6×	110 0.9×	260 2.8×	14	707
Juan M. Funes United Kingdom	10	447 1.7×	87 0.4×	196 1.0×	109 0.9×	198 2.1×	15	686

Countries citing papers authored by Sandra H. E. Sprenger

Since Specialization

Citations

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

Fields of papers citing papers by Sandra H. E. Sprenger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra H. E. Sprenger. 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 Sandra H. E. Sprenger. The network helps show where Sandra H. E. Sprenger may publish in the future.

Co-authorship network of co-authors of Sandra H. E. Sprenger

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

All Works

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13 of 13 papers shown

Dijk, Marcory van, Sandra H. E. Sprenger, Paul Rombout, et al.. (2002). Distinct chromosomal aberrations in sinonasal mucosal melanoma as detected by comparative genomic hybridization. Genes Chromosomes and Cancer. 36(2). 151–158. 43 indexed citations

Branle, Fabrice, Florence Lefranc, Isabelle Camby, et al.. (2002). Evaluation of the efficiency of chemotherapy in in vivo orthotopic models of human glioma cells with and without 1p19q deletions and in C6 rat orthotopic allografts serving for the evaluation of surgery combined with chemotherapy. Cancer. 95(3). 641–655. 99 indexed citations

Jeuken, Judith W. M., Sandra H. E. Sprenger, Harry Vermeer, et al.. (2002). Chromosomal imbalances in primary oligodendroglial tumors and their recurrences: clues about malignant progression detected using comparative genomic hybridization. Journal of neurosurgery. 96(3). 559–564. 43 indexed citations

Gijtenbeek, Johanna M. M., Sandra H. E. Sprenger, Marc J. Eleveld, et al.. (2002). Analysis of von Hippel—Lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity. Journal of neurosurgery. 97(4). 977–982. 25 indexed citations

Jeuken, Judith W. M., Sandra H. E. Sprenger, & Pieter Wesseling. (2002). Comparative Genomic Hybridization: Practical Guidelines. Diagnostic Molecular Pathology. 11(4). 193–203. 24 indexed citations

Jeuken, Judith W. M., et al.. (2002). Correlation between localization, age, and chromosomal imbalances in ependymal tumours as detected by CGH. The Journal of Pathology. 197(2). 238–244. 45 indexed citations

Sprenger, Sandra H. E., Johanna M. M. Gijtenbeek, Pieter Wesseling, et al.. (2001). Characteristic Chromosomal Aberrations in Sporadic Cerebellar Hemangioblastomas Revealed by Comparative Genomic Hybridization. Journal of Neuro-Oncology. 52(3). 241–247. 24 indexed citations

Eleveld, Marc J., Daniëlle Bodmer, Gerard Merkx, et al.. (2001). Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15). Genes Chromosomes and Cancer. 31(1). 23–32. 29 indexed citations

Gilhuis, H. Jacobus, Hans J.J.A. Bernsen, Judith W. M. Jeuken, et al.. (2001). The Relationship Between Genetic Aberrations as Detected by Comparative Genomic Hybridization and Vascularization in Glioblastoma Xenografts. Journal of Neuro-Oncology. 51(2). 121–127. 6 indexed citations

10.

Jeuken, Judith W. M., Sandra H. E. Sprenger, Rudolf H. Boerman, et al.. (2001). Subtyping of oligo-astrocytic tumours by comparative genomic hybridization. The Journal of Pathology. 194(1). 81–87. 46 indexed citations

11.

Simons, Annet, Marga Schepens, Judith W. M. Jeuken, et al.. (2000). Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma. Cancer Genetics and Cytogenetics. 118(2). 89–98. 49 indexed citations

12.

Jeuken, Judith W. M., Sandra H. E. Sprenger, Pieter Wesseling, et al.. (2000). Genetic reflection of glioblastoma biopsy material in xenografts: characterization of 11 glioblastoma xenograft lines by comparative genomic hybridization. Journal of neurosurgery. 92(4). 652–658. 20 indexed citations

13.

Jeuken, Judith W. M., Sandra H. E. Sprenger, Pieter Wesseling, et al.. (1999). Identification of Subgroups of High-grade Oligodendroglial Tumors by Comparative Genomic Hybridization. Journal of Neuropathology & Experimental Neurology. 58(6). 606–612. 85 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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