Manuel Holtgrewe

4.9k total citations
37 papers, 927 citations indexed

About

Manuel Holtgrewe is a scholar working on Molecular Biology, Genetics and Information Systems and Management. According to data from OpenAlex, Manuel Holtgrewe has authored 37 papers receiving a total of 927 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Genetics and 5 papers in Information Systems and Management. Recurrent topics in Manuel Holtgrewe's work include Genomics and Phylogenetic Studies (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Manuel Holtgrewe is often cited by papers focused on Genomics and Phylogenetic Studies (9 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Manuel Holtgrewe collaborates with scholars based in Germany, United States and France. Manuel Holtgrewe's co-authors include Knut Reinert, David Weese, Marten Jäger, Sebastian Köhler, Julius O.B. Jacobsen, Peter N. Robinson, Melissa Haendel, Damian Smedley, Max Schubach and Dieter Beule and has published in prestigious journals such as Nucleic Acids Research, Bioinformatics and Scientific Reports.

In The Last Decade

Manuel Holtgrewe

37 papers receiving 907 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuel Holtgrewe Germany 15 598 344 158 105 77 37 927
Fuli Yu United States 22 694 1.2× 756 2.2× 56 0.4× 176 1.7× 97 1.3× 41 1.5k
Mohamed Abouelhoda Saudi Arabia 20 822 1.4× 388 1.1× 335 2.1× 98 0.9× 98 1.3× 72 1.6k
Maria Emília M. T. Walter Brazil 13 374 0.6× 153 0.4× 60 0.4× 73 0.7× 83 1.1× 78 789
Santiago Marco‐Sola Spain 12 578 1.0× 139 0.4× 216 1.4× 61 0.6× 166 2.2× 28 731
Son Nguyen Vietnam 12 482 0.8× 190 0.6× 70 0.4× 110 1.0× 252 3.3× 33 980
Yifei Chen China 9 678 1.1× 346 1.0× 158 1.0× 123 1.2× 38 0.5× 34 1.2k
Recep Çolak Canada 11 1.2k 2.1× 139 0.4× 56 0.4× 138 1.3× 48 0.6× 22 1.4k
Tobias Jakobi Germany 16 642 1.1× 91 0.3× 100 0.6× 172 1.6× 47 0.6× 25 833
Johan Rung United Kingdom 16 950 1.6× 218 0.6× 62 0.4× 154 1.5× 79 1.0× 26 1.3k
Giovanni Iacono Italy 17 479 0.8× 151 0.4× 40 0.3× 57 0.5× 29 0.4× 44 1.2k

Countries citing papers authored by Manuel Holtgrewe

Since Specialization
Citations

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

Fields of papers citing papers by Manuel Holtgrewe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuel Holtgrewe

This figure shows the co-authorship network connecting the top 25 collaborators of Manuel Holtgrewe. A scholar is included among the top collaborators of Manuel Holtgrewe 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 Manuel Holtgrewe. Manuel Holtgrewe 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.
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
2.
Nieminen, Mikko, et al.. (2022). SODAR: managing multiomics study data and metadata. GigaScience. 12. 3 indexed citations
3.
Weinhold, Leonie, Axel Schmidt, Manuel Holtgrewe, et al.. (2022). Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations. Human Genetics and Genomics Advances. 4(1). 100166–100166. 2 indexed citations
4.
Boschann, Felix, et al.. (2022). Xq27.1 palindrome mediated interchromosomal insertion likely causes familial congenital bilateral laryngeal abductor paralysis (Plott syndrome). Journal of Human Genetics. 67(7). 405–410. 3 indexed citations
5.
Neitzel, Heidemarie, Raymonda Varon, Peter Nürnberg, et al.. (2022). Transmission ratio distortion of mutations in the master regulator of centriole biogenesis PLK4. Human Genetics. 141(11). 1785–1794. 3 indexed citations
6.
Hülsemann, Wiebke, Manuel Holtgrewe, Denise Horn, et al.. (2021). GLI3 variants causing isolated polysyndactyly are not restricted to the protein's C‐terminal third. Clinical Genetics. 100(6). 758–765. 5 indexed citations
7.
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
8.
Coutelier, Marie, Manuel Holtgrewe, Marten Jäger, et al.. (2021). Combining callers improves the detection of copy number variants from whole-genome sequencing. European Journal of Human Genetics. 30(2). 178–186. 27 indexed citations
9.
Herczegfalvi, Ágnes, Heike Kölbel, Ulrike Schara, et al.. (2020). Expanding the clinical and molecular spectrum of ATP6V1A related metabolic cutis laxa. Journal of Inherited Metabolic Disease. 44(4). 972–986. 10 indexed citations
10.
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
11.
Robinson, Peter N., Vida Ravanmehr, Julius O.B. Jacobsen, et al.. (2020). Interpretable Clinical Genomics with a Likelihood Ratio Paradigm. The American Journal of Human Genetics. 107(3). 403–417. 51 indexed citations
12.
Obermayer, Benedikt, et al.. (2020). SCelVis: exploratory single cell data analysis on the desktop and in the cloud. PeerJ. 8. e8607–e8607. 5 indexed citations
13.
Kühnisch, Jirko, Manuel Holtgrewe, Anwar Baban, et al.. (2019). Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3. Clinical Genetics. 96(6). 549–559. 30 indexed citations
14.
Thiel, Anne, Ingo Kurth, Manuel Holtgrewe, et al.. (2019). Paroxysmal tonic upgaze: A heterogeneous clinical condition responsive to carbonic anhydrase inhibition. European Journal of Paediatric Neurology. 25. 181–186. 10 indexed citations
15.
Nieminen, Mikko, et al.. (2019). AltamISA: a Python API for ISA-Tab files. The Journal of Open Source Software. 4(40). 1610–1610. 2 indexed citations
16.
Blanc, Eric, et al.. (2019). Identification and ranking of recurrent neo-epitopes in cancer. BMC Medical Genomics. 12(1). 171–171. 2 indexed citations
17.
Holtgrewe, Manuel, Alexej Knaus, Jean Tori Pantel, et al.. (2018). Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation. Scientific Reports. 8(1). 14611–14611. 22 indexed citations
18.
Smedley, Damian, Julius O.B. Jacobsen, Marten Jäger, et al.. (2015). Next-generation diagnostics and disease-gene discovery with the Exomiser. Nature Protocols. 10(12). 2004–2015. 228 indexed citations
19.
Kehr, Birte, Kathrin Trappe, Manuel Holtgrewe, & Knut Reinert. (2014). Genome alignment with graph data structures: a comparison. BMC Bioinformatics. 15(1). 99–99. 20 indexed citations
20.
Holtgrewe, Manuel, Anne‐Katrin Emde, David Weese, & Knut Reinert. (2011). A novel and well-defined benchmarking method for second generation read mapping. BMC Bioinformatics. 12(1). 210–210. 54 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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