Markus Stümm

5.5k total citations · 1 hit paper
78 papers, 3.5k citations indexed

About

Markus Stümm is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Markus Stümm has authored 78 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 38 papers in Pediatrics, Perinatology and Child Health and 32 papers in Molecular Biology. Recurrent topics in Markus Stümm's work include Prenatal Screening and Diagnostics (38 papers), Genomic variations and chromosomal abnormalities (30 papers) and DNA Repair Mechanisms (17 papers). Markus Stümm is often cited by papers focused on Prenatal Screening and Diagnostics (38 papers), Genomic variations and chromosomal abnormalities (30 papers) and DNA Repair Mechanisms (17 papers). Markus Stümm collaborates with scholars based in Germany, United States and Poland. Markus Stümm's co-authors include Raymonda Varon, Krystyńa Chrzańowska, Karen Cerosaletti, Patrick Concannon, Richard A. Gatti, Karl Sperling, André Reis, Kathrin Saar, E Seemanová and Peter Wieacker and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and The Journal of Cell Biology.

In The Last Decade

Markus Stümm

71 papers receiving 3.3k 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.

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

1998 811 citations Raymonda Varon, Christine Vissinga et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Markus Stümm Germany	24	2.5k	898	761	696	437	78	3.5k
Sat Dev Batish United States	26	2.5k 1.0×	1.3k 1.4×	618 0.8×	459 0.7×	246 0.6×	50	3.6k
Raymonda Varon Germany	30	2.9k 1.2×	813 0.9×	1.0k 1.3×	783 1.1×	333 0.8×	62	3.5k
Della Yee United States	25	3.4k 1.4×	864 1.0×	392 0.5×	518 0.7×	301 0.7×	36	4.4k
Arie van Haeringen Netherlands	26	1.9k 0.8×	1.3k 1.5×	324 0.4×	571 0.8×	194 0.4×	69	3.0k
Ruthild G. Weber Germany	33	2.0k 0.8×	859 1.0×	499 0.7×	477 0.7×	237 0.5×	72	3.7k
Detlev Schindler Germany	43	5.4k 2.2×	1.8k 2.1×	1.5k 2.0×	1.1k 1.6×	713 1.6×	164	6.6k
Eric Schoenmakers Belgium	34	2.5k 1.0×	2.1k 2.3×	705 0.9×	574 0.8×	219 0.5×	76	5.2k
Paul S. Knoepfler United States	43	4.5k 1.8×	726 0.8×	516 0.7×	677 1.0×	333 0.8×	88	5.8k
Hirofumi Ohashi Japan	36	3.1k 1.3×	2.5k 2.8×	243 0.3×	385 0.6×	356 0.8×	165	4.8k
Luciana Chessa Italy	28	2.1k 0.9×	371 0.4×	722 0.9×	693 1.0×	199 0.5×	75	2.7k

Countries citing papers authored by Markus Stümm

Since Specialization

Citations

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

Fields of papers citing papers by Markus Stümm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markus Stümm

This figure shows the co-authorship network connecting the top 25 collaborators of Markus Stümm. A scholar is included among the top collaborators of Markus Stümm 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 Markus Stümm. Markus Stümm 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

Stümm, Markus. (2016). Nichtinvasive pränatale Tests aus Sicht des Humangenetikers. Der Gynäkologe. 49(6). 429–436. 3 indexed citations

Stümm, Markus, et al.. (2014). Update der AG Reproduktionsgenetik der DGRM: Nicht-invasive Pränataltests aus mütterlichem Blut. 11(4). 186–188. 1 indexed citations

Stümm, Markus, Erich T. Boger, Christoph Gaissmaier, et al.. (2012). Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR. Osteoarthritis and Cartilage. 20(9). 1039–1045. 9 indexed citations

Becker, Rolf, et al.. (2012). ‘Normal’ nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspects. Prenatal Diagnosis. 32(6). 550–556. 22 indexed citations

Hagen, Anke, et al.. (2010). The Impact of First Trimester Screening and Early Fetal Anomaly Scan on Invasive Testing Rates in Women with Advanced Maternal Age. Ultraschall in der Medizin - European Journal of Ultrasound. 32(3). 302–306. 11 indexed citations

Lelij, Petra van der, Krystyńa Chrzańowska, Barbara C. Godthelp, et al.. (2010). Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1. The American Journal of Human Genetics. 86(2). 262–266. 169 indexed citations

Liehr, Thomas, Markus Stümm, R.‐D. Wegner, et al.. (2009). 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenetic and Genome Research. 124(1). 102–105. 27 indexed citations

Liehr, Thomas, Markus Stümm, Gordana Joksiċ, et al.. (2008). Pallister-Killian Syndrome: Rare Phenotypic Features and Variable Karyotypes. Balkan Journal of Medical Genetics. 11(2). 9 indexed citations

Stümm, Markus, et al.. (2006). Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics. Cytogenetic and Genome Research. 114(3-4). 296–301. 12 indexed citations

10.

Jakubiczka, Sibylle, Thomas Bettecken, Klaus Mohnike, et al.. (2006). Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC. European Journal of Pediatrics. 166(7). 743–745. 6 indexed citations

11.

Volleth, Marianne, Markus Stümm, Joachim Bürger, Petra Muschke, & P. Wieacker. (2004). Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14. Cytogenetic and Genome Research. 108(4). 283–286. 1 indexed citations

12.

Dörk, Thilo, et al.. (2003). Slow progression of ataxia‐telangiectasia with double missense and in frame splice mutations. American Journal of Medical Genetics Part A. 126A(3). 272–277. 29 indexed citations

13.

Röpke, Albrecht, Markus Stümm, & Peter Wieacker. (2002). Fluoreszenz-in-situ-Hybridisierung (FISH) an nichtkultivierten Amnionzellen zur Diagnostik häufiger Chromosomenstörungen. 18(5). 289–294. 1 indexed citations

14.

Struk, Berthold, Li Cai, Wan Ji, et al.. (2000). Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum. Journal of Molecular Medicine. 78(5). 282–286. 100 indexed citations

15.

Foray, Nicolas, Markus Stümm, Richard S. Maser, et al.. (2000). Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects.. PubMed. 60(17). 4881–8. 57 indexed citations

16.

Winter, Carsten, Susanne tom Dieck, Tobias M. Boeckers, et al.. (1999). The Presynaptic Cytomatrix Protein Bassoon: Sequence and Chromosomal Localization of the HumanBSNGene. Genomics. 57(3). 389–397. 22 indexed citations

17.

Bartsch, Oliver, et al.. (1999). FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy. European Journal of Human Genetics. 7(7). 748–756. 65 indexed citations

18.

Varon, Raymonda, Christine Vissinga, Matthias Platzer, et al.. (1998). Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome. Cell. 93(3). 467–476. 811 indexed citations breakdown →

19.

Saar, Kathrin, Krystyńa Chrzańowska, Markus Stümm, et al.. (1997). The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.. PubMed. 60(3). 605–10. 85 indexed citations

20.

Wegner, R.‐D., Evelin Schröck, M. Obladen, et al.. (1996). PARTIAL TRISOMY/MONOSOMY 6q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE. Prenatal Diagnosis. 16(8). 741–748. 13 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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