Dominik Seelow

13.1k total citations · 2 hit papers
50 papers, 2.6k citations indexed

About

Dominik Seelow is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Dominik Seelow has authored 50 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 29 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Dominik Seelow's work include Genomics and Rare Diseases (21 papers), Genomics and Phylogenetic Studies (12 papers) and Genomics and Chromatin Dynamics (10 papers). Dominik Seelow is often cited by papers focused on Genomics and Rare Diseases (21 papers), Genomics and Phylogenetic Studies (12 papers) and Genomics and Chromatin Dynamics (10 papers). Dominik Seelow collaborates with scholars based in Germany, United States and United Kingdom. Dominik Seelow's co-authors include Markus Schuelke, Peter N. Robinson, Sebastian Köhler, Sebastian Bauer, Stefan Mundlos, Denise Horn, Peter Nürnberg, Jana Marie Schwarz, Friedhelm Hildebrandt and Robin Steinhaus and has published in prestigious journals such as Nucleic Acids Research, Circulation and Nature Genetics.

In The Last Decade

Dominik Seelow

47 papers receiving 2.6k 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.

The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease

2008 622 citations Peter N. Robinson, Sebastian Köhler et al. The American Journal of Human Genetics profile →
MutationTaster2021

2021 167 citations Robin Steinhaus, Sebastian Proft et al. Nucleic Acids Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dominik Seelow Germany	19	1.8k	1.2k	301	217	149	50	2.6k
Damian Smedley United Kingdom	30	1.9k 1.1×	1.1k 1.0×	107 0.4×	375 1.7×	155 1.0×	85	2.8k
Ruth E. Swiderski United States	26	2.6k 1.4×	1.7k 1.4×	527 1.8×	170 0.8×	93 0.6×	34	3.9k
Ryan K. C. Yuen Canada	27	2.2k 1.2×	1.4k 1.2×	91 0.3×	395 1.8×	109 0.7×	49	3.7k
Akira Tanigami Japan	30	2.0k 1.1×	592 0.5×	367 1.2×	427 2.0×	174 1.2×	71	3.2k
Dilek Çolak Saudi Arabia	25	1.2k 0.6×	400 0.3×	229 0.8×	292 1.3×	39 0.3×	101	2.2k
Alexis Battle United States	27	2.0k 1.1×	1.2k 1.0×	71 0.2×	323 1.5×	86 0.6×	56	2.9k
Masoud Garshasbi Iran	24	1.5k 0.8×	729 0.6×	212 0.7×	354 1.6×	29 0.2×	127	2.4k
Daniel M. Jordan United States	14	1.8k 1.0×	1.4k 1.2×	150 0.5×	401 1.8×	27 0.2×	36	3.3k
Vasily Ramensky Russia	15	1.7k 0.9×	986 0.8×	101 0.3×	199 0.9×	26 0.2×	39	2.5k
Wenwu Cui United States	11	1.4k 0.8×	567 0.5×	108 0.4×	226 1.0×	40 0.3×	16	2.0k

Countries citing papers authored by Dominik Seelow

Since Specialization

Citations

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

Fields of papers citing papers by Dominik Seelow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dominik Seelow

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

Seelow, Dominik. (2024). The 22nd annual Nucleic Acids Research Web Server Issue 2024. Nucleic Acids Research. 52(W1). W1–W6.

Thamm, Michael, Michael Thamm, Jürgen Kratzsch, et al.. (2024). Normal Values for the fT3/fT4 Ratio: Centile Charts (0–29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay. International Journal of Molecular Sciences. 25(16). 8585–8585. 1 indexed citations

Holtgrewe, Manuel, Andranik Ivanov, Christèle Dubourg, et al.. (2024). Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy. Human Genetics. 143(5). 683–694. 2 indexed citations

Steinhaus, Robin, et al.. (2022). Deep phenotyping: symptom annotation made simple with SAMS. Nucleic Acids Research. 50(W1). W677–W681. 8 indexed citations

Steinhaus, Robin, Sebastian Proft, Markus Schuelke, et al.. (2021). MutationTaster2021. Nucleic Acids Research. 49(W1). W446–W451. 167 indexed citations breakdown →

Ehmke, Nadja, Barbara Plecko, Manuel Holtgrewe, et al.. (2021). Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive. Journal of Medical Genetics. 59(7). 662–668. 12 indexed citations

Boschann, Felix, Björn Fischer‐Zirnsak, Thomas F. Wienker, et al.. (2020). An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndrome. European Journal of Medical Genetics. 63(9). 103973–103973. 6 indexed citations

Schwarz, Jana Marie, et al.. (2019). RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants. Nucleic Acids Research. 47(W1). W106–W113. 17 indexed citations

Schuelke, Markus, Ellen Knierim, Nadja Ehmke, et al.. (2019). MutationDistiller: user-driven identification of pathogenic DNA variants. Nucleic Acids Research. 47(W1). W114–W120. 31 indexed citations

10.

Schwarz, Jana Marie, et al.. (2018). Phenotero: Annotate as you write. Clinical Genetics. 95(2). 287–292. 2 indexed citations

11.

Olry, Annie, Marc Hanauer, Valérie Serrière-Lanneau, et al.. (2018). Harmonising phenomics information for a better interoperability in the rare disease field. European Journal of Medical Genetics. 61(11). 706–714. 16 indexed citations

12.

Mueller, Noomi, Takayuki Sassa, Susanne Morales-Gonzalez, et al.. (2018). De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. Journal of Medical Genetics. 56(3). 164–175. 55 indexed citations

13.

Schwarz, Jana Marie, et al.. (2016). A systematic, large-scale comparison of transcription factor binding site models. BMC Genomics. 17(1). 388–388. 14 indexed citations

14.

Grüner, Barbara M., Stephanie Spranger, Adrian M. Stütz, et al.. (2013). Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype. Matrix Biology. 32(7-8). 387–392. 17 indexed citations

15.

Robinson, Peter N., Sebastian Köhler, Anika Oellrich, et al.. (2013). Improved exome prioritization of disease genes through cross-species phenotype comparison. Genome Research. 24(2). 340–348. 214 indexed citations

16.

Seelow, Dominik & Markus Schuelke. (2012). HomozygosityMapper2012--bridging the gap between homozygosity mapping and deep sequencing. Nucleic Acids Research. 40(W1). W516–W520. 54 indexed citations

17.

Knierim, Ellen, Barbara Lucke, Jana Marie Schwarz, Markus Schuelke, & Dominik Seelow. (2011). Systematic Comparison of Three Methods for Fragmentation of Long-Range PCR Products for Next Generation Sequencing. PLoS ONE. 6(11). e28240–e28240. 90 indexed citations

18.

Rajab, Anna, Volker Straub, Liza McCann, et al.. (2010). Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations. PLoS Genetics. 6(3). e1000874–e1000874. 181 indexed citations

19.

Attanasio, Massimo, N. Henriette Uhlenhaut, Vitor H. Sousa, et al.. (2007). Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis. Nature Genetics. 39(8). 1018–1024. 174 indexed citations

20.

Bergmann, Carsten, Jan Senderek, Dirk Anhuf, et al.. (2006). Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia. The American Journal of Human Genetics. 79(6). 1105–1109. 71 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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