Hartmut Peters

3.0k total citations
61 papers, 2.2k citations indexed

About

Hartmut Peters is a scholar working on Oceanography, Atmospheric Science and Global and Planetary Change. According to data from OpenAlex, Hartmut Peters has authored 61 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Oceanography, 28 papers in Atmospheric Science and 17 papers in Global and Planetary Change. Recurrent topics in Hartmut Peters's work include Oceanographic and Atmospheric Processes (32 papers), Tropical and Extratropical Cyclones Research (17 papers) and Climate variability and models (15 papers). Hartmut Peters is often cited by papers focused on Oceanographic and Atmospheric Processes (32 papers), Tropical and Extratropical Cyclones Research (17 papers) and Climate variability and models (15 papers). Hartmut Peters collaborates with scholars based in United States, Germany and Spain. Hartmut Peters's co-authors include William E. Johns, Helmut Z. Baumert, Michael C. Gregg, Tamay M. Özgökmen, Thomas B. Sanford, David M. Fratantoni, Amy S. Bower, Yeon S. Chang, Naomi Fukai and Valdenize Tiziani and has published in prestigious journals such as Nature Genetics, Journal of Geophysical Research Atmospheres and Geophysical Research Letters.

In The Last Decade

Hartmut Peters

61 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hartmut Peters United States 28 1.0k 800 540 464 381 61 2.2k
Hirohiko Nakamura Japan 27 841 0.8× 599 0.7× 444 0.8× 148 0.3× 108 0.3× 242 2.1k
Tor Knutsen Norway 32 584 0.6× 284 0.4× 797 1.5× 1.0k 2.2× 114 0.3× 97 3.3k
John A. Long Australia 43 86 0.1× 211 0.3× 212 0.4× 633 1.4× 57 0.1× 219 5.9k
Hiroshi Hotta Japan 24 129 0.1× 150 0.2× 33 0.1× 570 1.2× 286 0.8× 81 2.2k
P. M. Kelly United Kingdom 27 284 0.3× 1.5k 1.9× 1.5k 2.8× 189 0.4× 68 0.2× 62 2.8k
Matti Seppälä Finland 33 37 0.0× 1.6k 2.0× 150 0.3× 189 0.4× 124 0.3× 113 3.2k
Tim‐Rasmus Kiehl Canada 28 438 0.4× 2.5k 3.1× 2.5k 4.7× 280 0.6× 60 0.2× 62 4.6k
Martin Huber Germany 20 109 0.1× 696 0.9× 351 0.7× 256 0.6× 18 0.0× 79 2.3k
Elizabeth A. Burton United States 24 303 0.3× 411 0.5× 216 0.4× 361 0.8× 18 0.0× 46 2.5k
Yoshihisa Mori Japan 28 92 0.1× 122 0.2× 325 0.6× 676 1.5× 148 0.4× 63 2.3k

Countries citing papers authored by Hartmut Peters

Since Specialization
Citations

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

Fields of papers citing papers by Hartmut Peters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hartmut Peters

This figure shows the co-authorship network connecting the top 25 collaborators of Hartmut Peters. A scholar is included among the top collaborators of Hartmut Peters 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 Hartmut Peters. Hartmut Peters 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.
Pelegrí, Josep Lluís, Mikhail Emelianov, Miguel Bruno, et al.. (2017). Tracking the Mediterranean outflow in the Gulf of Cadiz. Progress In Oceanography. 157. 47–71. 16 indexed citations
2.
Hentschel, Julia, Dmitri Parkhomchuk, Ingo Kurth, et al.. (2016). Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool. Gene. 590(1). 1–4. 9 indexed citations
3.
Harder, Anja, Thomas Harder, Sigrid Tinschert, et al.. (2010). Monozygotic Twins With Neurofibromatosis Type 1 (NF1) Display Differences in Methylation ofNF1Gene Promoter Elements, 5' Untranslated region, Exon and Intron 1. Twin Research and Human Genetics. 13(6). 582–594. 20 indexed citations
4.
Ott, Claus‐Eric, Gundula Leschik, Louise Brueton, et al.. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. 31(8). E1587–E1593. 58 indexed citations
5.
Peters, Hartmut, Sandra Währisch, Thomas Harder, et al.. (2009). Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients. European Journal of Human Genetics. 18(1). 81–87. 20 indexed citations
6.
Hennewig, Ulrike, Markus Vogel, Thomas Meißner, et al.. (2008). Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant. Journal of Human Genetics. 53(6). 573–577. 33 indexed citations
7.
Brunetti‐Pierri, Nicola, Daniela del Gaudio, Hartmut Peters, et al.. (2008). Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation. American Journal of Medical Genetics Part A. 146A(21). 2804–2809. 16 indexed citations
8.
Beysen, Diane, Lara Moumné, Reiner A. Veitia, et al.. (2008). Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation. Human Molecular Genetics. 17(13). 2030–2038. 66 indexed citations
9.
Tzschach, Andreas, Christina Kelbova, Hartmut Peters, et al.. (2008). Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23). Ophthalmic Genetics. 29(1). 37–40. 6 indexed citations
10.
Bartels, Natalie Garcia, Luitgard M. Neumann, Anna Mleczko, et al.. (2007). Hay‐Wells syndrome in a child with mutation in the TP73L gene. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 5(10). 919–923. 2 indexed citations
11.
Peters, Hartmut & Mirko Orlić. (2005). Turbulent mixing in the springtime central Adriatic Sea. Geofizika. 22(1). 1–19. 5 indexed citations
12.
Hyckel, Peter, Alexander Berndt, Peter Schleier, et al.. (2005). Cherubism – new hypotheses on pathogenesis and therapeutic consequences. Journal of Cranio-Maxillofacial Surgery. 33(1). 61–68. 70 indexed citations
13.
Bower, Amy S., William E. Johns, David M. Fratantoni, & Hartmut Peters. (2005). Equilibration and Circulation of Red Sea Outflow Water in the Western Gulf of Aden*. Journal of Physical Oceanography. 35(11). 1963–1985. 41 indexed citations
14.
Ueki, Yasuyoshi, Valdenize Tiziani, Naomi Fukai, et al.. (2001). Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism. Nature Genetics. 28(2). 125–126. 259 indexed citations
15.
Fahsold, Raimund, Sven Hoffmeyer, Claudia Mischung, et al.. (2000). Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain. The American Journal of Human Genetics. 66(3). 790–818. 231 indexed citations
16.
17.
Tiziani, Valdenize, Ernst Reichenberger, Celso Luiz Buzzo, et al.. (1999). The Gene for Cherubism Maps to Chromosome 4p16. The American Journal of Human Genetics. 65(1). 158–166. 109 indexed citations
18.
Harder, Anja, Hartmut Peters, Sven Hoffmeyer, et al.. (1999). Two independent mutations in a family with neurofibromatosis type 1 (NF1). American Journal of Medical Genetics. 83(1). 6–12. 22 indexed citations
19.
Peters, Hartmut, et al.. (1999). A novel mutation L1425p in the GAP-region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE);. Human Mutation. 13(4). 337–337. 3 indexed citations
20.
Peters, Hartmut, et al.. (1999). Endocrinological and genetic studies in patients with Polycystic Ovary Syndrome (PCOS).. PubMed. 20(5). 323–327. 4 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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