Heidi Holtgreve-Grez

2.9k total citations
22 papers, 2.0k citations indexed

About

Heidi Holtgreve-Grez is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Heidi Holtgreve-Grez has authored 22 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Plant Science. Recurrent topics in Heidi Holtgreve-Grez's work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (6 papers) and Cancer Genomics and Diagnostics (6 papers). Heidi Holtgreve-Grez is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (6 papers) and Cancer Genomics and Diagnostics (6 papers). Heidi Holtgreve-Grez collaborates with scholars based in Germany, United States and United Kingdom. Heidi Holtgreve-Grez's co-authors include Anna Jauch, Jan Karlseder, Laure Crabbé, Evelin Schröck, Stanislas du Manoir, Agata Smogorzewska, Titia de Lange, Thomas Ried, Michael R. Speicher and Thomas Cremer and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Cell Biology.

In The Last Decade

Heidi Holtgreve-Grez

22 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heidi Holtgreve-Grez Germany 16 1.4k 547 403 377 307 22 2.0k
Akira Nabetani Japan 15 1.6k 1.1× 443 0.8× 894 2.2× 191 0.5× 164 0.5× 18 2.2k
Giuseppina Caretti Italy 27 2.4k 1.7× 286 0.5× 260 0.6× 555 1.5× 61 0.2× 42 2.8k
Kyoichi Isono Japan 29 2.2k 1.6× 357 0.7× 99 0.2× 170 0.5× 249 0.8× 58 2.6k
Hao Ding Canada 21 1.5k 1.1× 160 0.3× 443 1.1× 243 0.6× 84 0.3× 40 2.0k
Manuela Pellegrini Italy 24 1.4k 1.0× 541 1.0× 109 0.3× 225 0.6× 163 0.5× 56 2.1k
Yoshikazu Johmura Japan 20 1.3k 0.9× 266 0.5× 397 1.0× 180 0.5× 74 0.2× 47 1.9k
Victoriano Baladrón Spain 21 1.0k 0.8× 256 0.5× 241 0.6× 224 0.6× 86 0.3× 34 1.7k
Suzanne Szak United States 18 1.3k 1.0× 226 0.4× 100 0.2× 160 0.4× 728 2.4× 26 1.7k
Roberta Benetti Italy 20 1.6k 1.2× 130 0.2× 653 1.6× 531 1.4× 136 0.4× 26 2.1k
Piotr J. Balwierz Switzerland 18 1.6k 1.2× 210 0.4× 196 0.5× 617 1.6× 71 0.2× 22 2.2k

Countries citing papers authored by Heidi Holtgreve-Grez

Since Specialization
Citations

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

Fields of papers citing papers by Heidi Holtgreve-Grez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heidi Holtgreve-Grez. 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 Heidi Holtgreve-Grez. The network helps show where Heidi Holtgreve-Grez may publish in the future.

Co-authorship network of co-authors of Heidi Holtgreve-Grez

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi Holtgreve-Grez. A scholar is included among the top collaborators of Heidi Holtgreve-Grez 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 Heidi Holtgreve-Grez. Heidi Holtgreve-Grez 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.
Krunic, Damir, A. Jauch, Heidi Holtgreve-Grez, et al.. (2013). The telomere profile distinguishes two classes of genetically distinct cutaneous squamous cell carcinomas. Oncogene. 33(27). 3506–3518. 14 indexed citations
2.
Jauch, Anna, et al.. (2010). Telomere Disruption Results in Non-Random Formation of De Novo Dicentric Chromosomes Involving Acrocentric Human Chromosomes. PLoS Genetics. 6(8). e1001061–e1001061. 54 indexed citations
3.
Tuduri, Sandie, Laure Crabbé, Chiara Conti, et al.. (2009). Topoisomerase I suppresses genomic instability by preventing interference between replication and transcription. Nature Cell Biology. 11(11). 1315–1324. 417 indexed citations
4.
Crabbé, Laure, et al.. (2007). Telomere dysfunction as a cause of genomic instability in Werner syndrome. Proceedings of the National Academy of Sciences. 104(7). 2205–2210. 172 indexed citations
5.
Guo, Jianli, et al.. (2005). MULTICOLOR KARYOTYPE ANALYSES OF MOUSE EMBRYONIC STEM CELLS. In Vitro Cellular & Developmental Biology - Animal. 41(8). 278–278. 19 indexed citations
6.
Smogorzewska, Agata, Jan Karlseder, Heidi Holtgreve-Grez, Anna Jauch, & Titia de Lange. (2002). DNA Ligase IV-Dependent NHEJ of Deprotected Mammalian Telomeres in G1 and G2. Current Biology. 12(19). 1635–1644. 310 indexed citations
7.
8.
Popp, Susanne, Martin Granzow, Brigitte Schoell, et al.. (2001). Comparative genomic hybridization in childhood acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 124(2). 89–97. 14 indexed citations
9.
Granzow, Martin, Susanne Popp, Susanne N. Weber, et al.. (2001). Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics. Cancer Genetics and Cytogenetics. 130(1). 79–83. 14 indexed citations
10.
Granzow, Martin, Susanne Popp, Monika Keller, et al.. (2000). Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals. Human Genetics. 107(1). 51–57. 19 indexed citations
11.
Popp, Susanne, Petra Boukamp, Heidi Holtgreve-Grez, et al.. (2000). Genetic Characterization of a Human Skin Carcinoma Progression Model: from Primary Tumor to Metastasis. Journal of Investigative Dermatology. 115(6). 1095–1103. 42 indexed citations
12.
Gronwald, Jacek, Piotr Hadaczek, Stephan Störkel, et al.. (1999). Molecular Evidence for Derivation of Metastatic Cells from Minor Subclones of Primary Clear Renal Cell Carcinomas. Cancer Detection and Prevention. 23(6). 479–484. 6 indexed citations
13.
Gronwald, Jacek, Audrey Sylvia Baur, Heidi Holtgreve-Grez, et al.. (1999). Chromosomal abnormalities in renal cell neoplasms associated with acquired renal cystic disease. A series studied by comparative genomic hybridization and fluorescencein situ hybridization. The Journal of Pathology. 187(3). 308–312. 25 indexed citations
14.
15.
Dietzel, Steffen, Anna Jauch, Dirk Kienle, et al.. (1998). Separate and variably shaped chromosome arm domains are disclosed by chromosome arm painting in human cell nuclei. Chromosome Research. 6(1). 25–33. 75 indexed citations
16.
Gronwald, Jacek, Stefan Störkel, Heidi Holtgreve-Grez, et al.. (1997). Comparison of DNA gains and losses in primary renal clear cell carcinomas and metastatic sites: importance of 1q and 3p copy number changes in metastatic events.. PubMed. 57(3). 481–7. 82 indexed citations
17.
Ried, Thomas, Heidi Holtgreve-Grez, Stanislas du Manoir, et al.. (1995). Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas.. PubMed. 55(22). 5415–23. 200 indexed citations
18.
Levy, Finn Olav, Heidi Holtgreve-Grez, Kjetil Taskén, et al.. (1994). Assignment of the Gene Encoding the 5-HT1E Serotonin Receptor (S31) (Locus HTR1E)to Human Chromosome 6q14-q15. Genomics. 22(3). 637–640. 13 indexed citations
19.
Ried, Thomas, Iver Petersen, Heidi Holtgreve-Grez, et al.. (1994). Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization. Cancer Research. 11(5-6). 429–429. 182 indexed citations
20.
Schmale, Hartwig, et al.. (1990). Possible role for salivary gland protein in taste reception indicated by homology to lipophilic-ligand carrier proteins. Nature. 343(6256). 366–369. 127 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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