Andreas Rump

32.6k total citations · 1 hit paper
57 papers, 2.2k citations indexed

About

Andreas Rump is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Andreas Rump has authored 57 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 29 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Andreas Rump's work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (6 papers) and BRCA gene mutations in cancer (6 papers). Andreas Rump is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (6 papers) and BRCA gene mutations in cancer (6 papers). Andreas Rump collaborates with scholars based in Germany, United States and Austria. Andreas Rump's co-authors include André Rosenthal, Evelin Schröck, M. Winkelmann, Walter Arnold, Werner Klipp, Alfred Pühler, Ursula B. Priefer, Ercole Rao, U. Heinrich and Gudrun Rappold and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Andreas Rump

56 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1997 701 citations Andreas Rump, M. Winkelmann et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andreas Rump Germany	21	1.3k	1.1k	246	236	165	57	2.2k
Tetsuo Kunieda Japan	25	1.3k 1.0×	806 0.8×	170 0.7×	184 0.8×	63 0.4×	138	2.4k
Ans M. M. van Pelt Netherlands	40	2.4k 1.8×	1.7k 1.6×	197 0.8×	170 0.7×	169 1.0×	117	5.0k
Sergei G. Tevosian United States	27	1.9k 1.4×	879 0.8×	207 0.8×	108 0.5×	86 0.5×	59	2.7k
Charles Hanson Sweden	26	1.0k 0.8×	969 0.9×	60 0.2×	138 0.6×	76 0.5×	71	2.2k
Pascal de Santa Barbara France	26	1.8k 1.4×	1.2k 1.1×	203 0.8×	56 0.2×	45 0.3×	60	2.7k
Hamid Gourabi Iran	30	1.3k 1.0×	674 0.6×	115 0.5×	129 0.5×	67 0.4×	139	2.6k
Ching‐Shwun Lin United States	25	1.1k 0.8×	666 0.6×	239 1.0×	274 1.2×	365 2.2×	56	2.5k
Robert S. Viger Canada	30	1.7k 1.3×	1.6k 1.5×	128 0.5×	88 0.4×	344 2.1×	60	2.8k
Young‐Wook Cho United States	21	2.3k 1.7×	573 0.5×	218 0.9×	113 0.5×	58 0.4×	52	2.9k
Jo K. Perry New Zealand	35	1.6k 1.2×	771 0.7×	570 2.3×	675 2.9×	740 4.5×	86	3.2k

Countries citing papers authored by Andreas Rump

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Rump

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Rump

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

All Works

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20 of 20 papers shown

Popp, Bernt, Melanie Brügger, Tobias Bartolomaeus, et al.. (2022). The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical Genetics. 103(2). 226–230. 2 indexed citations

Rump, Andreas, Maja von der Hagen, Karl Hackmann, et al.. (2020). Novel dominant-negative NR2F1 frameshift mutation and a phenotypic expansion of the Bosch-Boonstra-Schaaf optic atrophy syndrome. European Journal of Medical Genetics. 63(10). 104019–104019. 7 indexed citations

Rump, Andreas, et al.. (2018). PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome. European Journal of Medical Genetics. 62(12). 103587–103587. 7 indexed citations

Porrmann, Joseph, Andreas Rump, Karl Hackmann, et al.. (2018). Novel truncating PPM1D mutation in a patient with intellectual disability. European Journal of Medical Genetics. 62(1). 70–72. 6 indexed citations

Gieldon, Laura, Luisa Mackenroth, Anne‐Karin Kahlert, et al.. (2018). Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE. 13(8). e0201041–e0201041. 29 indexed citations

Porrmann, Joseph, Nataliya Di Donato, Anne‐Karin Kahlert, et al.. (2017). Novel PRPS1 gain‐of‐function mutation in a patient with congenital hyperuricemia and facial anomalies. American Journal of Medical Genetics Part A. 173(10). 2736–2742. 11 indexed citations

Gieldon, Laura, Luisa Mackenroth, Andreas Rump, et al.. (2017). Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability. American Journal of Medical Genetics Part A. 173(9). 2545–2550. 12 indexed citations

Becker, Kerstin, Luisa Mackenroth, Andreas Rump, et al.. (2017). Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study. Archives of Gynecology and Obstetrics. 295(5). 1227–1238. 16 indexed citations

Baker, O. K., Jun Fu, Barbara Klink, et al.. (2017). The contribution of homology arms to nuclease-assisted genome engineering. Nucleic Acids Research. 45(13). 8105–8115. 27 indexed citations

10.

Pistorius, Steffen, Barbara Klink, Jessica Pablik, et al.. (2016). An unusual case of Cowden syndrome associated with ganglioneuromatous polyposis. Hereditary Cancer in Clinical Practice. 14(1). 11–11. 6 indexed citations

11.

Hackmann, Karl, Anne‐Karin Kahlert, Luisa Mackenroth, et al.. (2016). Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH. Breast Cancer Research and Treatment. 159(3). 585–590. 12 indexed citations

12.

Abou‐El‐Ardat, Khalil, Michael Seifert, Kerstin Becker, et al.. (2016). Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomas. Neuro-Oncology. 19(4). 546–557. 78 indexed citations

13.

Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations

14.

Hackmann, Karl, Jens Schallner, Evelin Schröck, et al.. (2013). Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3. American Journal of Medical Genetics Part A. 161(12). 3144–3149. 13 indexed citations

15.

Hackmann, Karl, Maja von der Hagen, Barbara Klink, et al.. (2012). Partial deletion of GLRB and GRIA2 in a patient with intellectual disability. European Journal of Human Genetics. 21(1). 112–114. 19 indexed citations

16.

Donato, Nataliya Di, Karl Hackmann, Andreas Rump, et al.. (2012). Macrocephaly, obesity, mental (intellectual) disability, and ocular abnormalities: Alternative definition and further delineation of MOMO syndrome. American Journal of Medical Genetics Part A. 158A(11). 2857–2862. 6 indexed citations

17.

Kasper, Grit, Armin A. Weiser, Andreas Rump, et al.. (2005). Expression levels of the putative zinc transporter LIV‐1 are associated with a better outcome of breast cancer patients. International Journal of Cancer. 117(6). 961–973. 67 indexed citations

18.

Kasper, Grit, Stefan Taudien, Eike Staub, et al.. (2002). Different structural organization of the encephalopsin gene in man and mouse. Gene. 295(1). 27–32. 17 indexed citations

19.

Schiebel, K., Andreas Rump, André Rosenthal, et al.. (2000). Elevated DNA sequence diversity in the genomic region of the phosphatase PPP2R3L gene in the human pseudoautosomal region. Cytogenetic and Genome Research. 91(1-4). 224–230. 22 indexed citations

20.

Arnold, Walter, Andreas Rump, Werner Klipp, Ursula B. Priefer, & Alfred Pühler. (1988). Nucleotide sequence of a 24,206-base-pair DNA fragment carrying the entire nitrogen fixation gene cluster of Klebsiella pneumoniae. Journal of Molecular Biology. 203(3). 715–738. 208 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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