Ilse Chudoba

1.2k total citations
36 papers, 858 citations indexed

About

Ilse Chudoba is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Ilse Chudoba has authored 36 papers receiving a total of 858 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Molecular Biology and 13 papers in Plant Science. Recurrent topics in Ilse Chudoba's work include Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (12 papers) and Prenatal Screening and Diagnostics (8 papers). Ilse Chudoba is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (12 papers) and Prenatal Screening and Diagnostics (8 papers). Ilse Chudoba collaborates with scholars based in Germany, United States and France. Ilse Chudoba's co-authors include Gabriele Senger, Johannes R. Lemke, U. Claussen, Andreas Plesch, T. Lörch, Christian Johannes, Christine J. Harrison, Hazel M. Robinson, Jonathan C. Strefford and Anthony V. Moorman and has published in prestigious journals such as Nature Communications, PLoS ONE and Oncogene.

In The Last Decade

Ilse Chudoba

36 papers receiving 823 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilse Chudoba Germany 16 436 410 222 171 156 36 858
Jack L. Spurbeck United States 17 330 0.8× 330 0.8× 164 0.7× 54 0.3× 112 0.7× 25 1.0k
Peter C. Verlander United States 14 695 1.6× 255 0.6× 82 0.4× 77 0.5× 45 0.3× 18 921
Jan Maahr Denmark 12 332 0.8× 498 1.2× 254 1.1× 44 0.3× 171 1.1× 19 798
Jacqueline R. Batanian United States 15 206 0.5× 186 0.5× 104 0.5× 92 0.5× 76 0.5× 56 568
Anne Marie Ottesen Denmark 11 371 0.9× 390 1.0× 70 0.3× 79 0.5× 71 0.5× 15 733
Kumi Nakazaki Japan 10 543 1.2× 315 0.8× 55 0.2× 58 0.3× 68 0.4× 34 996
Susi Scappaticci Italy 18 374 0.9× 262 0.6× 153 0.7× 65 0.4× 47 0.3× 47 784
Mary Ann Perle United States 15 298 0.7× 158 0.4× 39 0.2× 178 1.0× 89 0.6× 42 713
Marie‐Josée Le Bris France 18 420 1.0× 220 0.5× 97 0.4× 36 0.2× 140 0.9× 55 986
Mark A. Micale United States 14 259 0.6× 246 0.6× 81 0.4× 248 1.5× 65 0.4× 32 689

Countries citing papers authored by Ilse Chudoba

Since Specialization
Citations

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

Fields of papers citing papers by Ilse Chudoba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilse Chudoba

This figure shows the co-authorship network connecting the top 25 collaborators of Ilse Chudoba. A scholar is included among the top collaborators of Ilse Chudoba 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 Ilse Chudoba. Ilse Chudoba 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.
Krais, John J., Ilse Chudoba, Yifan Wang, et al.. (2023). Genetic separation of Brca1 functions reveal mutation-dependent Polθ vulnerabilities. Nature Communications. 14(1). 7714–7714. 12 indexed citations
2.
MacKinnon, Ruth N. & Ilse Chudoba. (2011). The Use of M-FISH and M-BAND to Define Chromosome Abnormalities. Methods in molecular biology. 730. 203–218. 8 indexed citations
3.
Robinson, Hazel M., Christine J. Harrison, Anthony V. Moorman, Ilse Chudoba, & Jonathan C. Strefford. (2007). Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage–fusion–bridge cycle. Genes Chromosomes and Cancer. 46(4). 318–326. 47 indexed citations
4.
Gazzo, Sophie, Ilse Chudoba, Alexandra Traverse‐Glehen, et al.. (2007). Detailed characterization of 7q deletions by multicolor banding (mBAND) in marginal zone cell lymphoma. Cancer Genetics and Cytogenetics. 175(2). 159–165. 4 indexed citations
5.
Leach, Natalia T., et al.. (2007). Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndrome. American Journal of Medical Genetics Part A. 143A(13). 1489–1493. 15 indexed citations
6.
7.
Kline, Antonie D., Constance A. Griffin, Mary Haddadin, et al.. (2004). A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies. American Journal of Medical Genetics Part A. 129A(2). 124–129. 4 indexed citations
8.
Chudoba, Ilse, et al.. (2004). mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations. Cytogenetic and Genome Research. 104(1-4). 390–393. 35 indexed citations
9.
Struski, Stéphanie, Martine Doco‐Fenzy, Michael Köehler, et al.. (2003). Cytogenetic Evolution of Human Ovarian Cell Lines Associated with Chemoresistance and Loss of Tumorigenicity. Analytical Cellular Pathology. 25(3). 115–122. 3 indexed citations
10.
11.
Brown, Jill M., et al.. (2002). Identification of a dup(5)(p15.3) by multicolor banding. Clinical Genetics. 61(4). 277–282. 4 indexed citations
12.
Martı́n-Subero, José I., Ilse Chudoba, Lana Harder, et al.. (2002). Multicolor-FICTION. American Journal Of Pathology. 161(2). 413–420. 61 indexed citations
13.
Lestou, Valia S., John X. OʼConnell, Joan Mathers, et al.. (2002). Cryptic t(X;18), ins(6;18), and SYT-SSX2 gene fusion in a case of intraneural monophasic synovial sarcoma. Cancer Genetics and Cytogenetics. 138(2). 153–156. 24 indexed citations
14.
Birnbacher, Robert, Ilse Chudoba, Hendrati Pirc‐Danoewinata, et al.. (2001). Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome. Annales de Génétique. 44(1). 13–18. 8 indexed citations
15.
Lemke, Johannes R., Ilse Chudoba, Gabriele Senger, et al.. (2001). Improved definition of chromosomal breakpoints using high-resolution multicolour banding. Human Genetics. 108(6). 478–483. 17 indexed citations
16.
Pirc‐Danoewinata, Hendrati, Hans G. Dauwerse, Margit König, et al.. (2000). CBFB/MYH11 fusion in a patient with AML-M4Eo and cytogenetically normal chromosomes 16. Genes Chromosomes and Cancer. 29(2). 186–191. 13 indexed citations
17.
18.
Chudoba, Ilse, Andreas Plesch, T. Lörch, et al.. (1999). High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenetic and Genome Research. 84(3-4). 156–160. 169 indexed citations
19.
Chudoba, Ilse, Eric Angevin, Marie‐José Terrier‐Lacombe, et al.. (1998). Overrepresentation of 7q31 and 17q in renal cell carcinomas. Genes Chromosomes and Cancer. 22(3). 171–178. 30 indexed citations
20.
Rüschoff, J., et al.. (1989). Investigations of chorionic villi after chorionic villus sampling (CVS). Human Genetics. 81(4). 329–334. 7 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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