Robert Maiwald

1.3k total citations
13 papers, 460 citations indexed

About

Robert Maiwald is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Robert Maiwald has authored 13 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Robert Maiwald's work include Sexual Differentiation and Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Sperm and Testicular Function (2 papers). Robert Maiwald is often cited by papers focused on Sexual Differentiation and Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Sperm and Testicular Function (2 papers). Robert Maiwald collaborates with scholars based in Germany, United States and Poland. Robert Maiwald's co-authors include Jill Dixon, Saskia Seland, Lies H. Hoefsloot, Dorien J.M. Peters, A. Jeannette M. Hoogeboom, Christiane Zweier, Cornelia Daumer‐Haas, Arie van Haeringen, Claudia Ruivenkamp and Ana María Cobo and has published in prestigious journals such as Nature Genetics, Neurology and Human Molecular Genetics.

In The Last Decade

Robert Maiwald

13 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Maiwald Germany 8 253 214 45 39 39 13 460
Mahmoud Y. Issa Egypt 15 258 1.0× 156 0.7× 29 0.6× 56 1.4× 12 0.3× 45 482
Luigina Spaccini Italy 13 208 0.8× 159 0.7× 57 1.3× 15 0.4× 14 0.4× 47 455
Ho‐Ming Luk China 13 249 1.0× 267 1.2× 50 1.1× 26 0.7× 16 0.4× 67 471
Jane Juusola United States 13 218 0.9× 192 0.9× 21 0.5× 21 0.5× 11 0.3× 22 390
Bret L. Bostwick United States 9 225 0.9× 215 1.0× 25 0.6× 20 0.5× 6 0.2× 17 414
Mathilde Nizon France 13 239 0.9× 153 0.7× 28 0.6× 15 0.4× 6 0.2× 26 387
Rachel Sayuri Honjo Brazil 13 205 0.8× 174 0.8× 41 0.9× 25 0.6× 4 0.1× 60 460
Tawfeg Ben‐Omran Qatar 11 353 1.4× 225 1.1× 43 1.0× 42 1.1× 6 0.2× 24 584
Janice C. Palumbos United States 8 245 1.0× 161 0.8× 82 1.8× 67 1.7× 10 0.3× 13 391
Cristina Dias United Kingdom 11 172 0.7× 143 0.7× 20 0.4× 26 0.7× 17 0.4× 16 359

Countries citing papers authored by Robert Maiwald

Since Specialization
Citations

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

Fields of papers citing papers by Robert Maiwald

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Maiwald

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

All Works

13 of 13 papers shown
1.
Vardag, Sanam N. & Robert Maiwald. (2024). Optimising urban measurement networks for CO 2 flux estimation: a high-resolution observing system simulation experiment using GRAMM/GRAL. Geoscientific model development. 17(4). 1885–1902. 2 indexed citations
2.
Charzewska, Agnieszka, Robert Maiwald, Kimia Kahrizi, et al.. (2018). The power of the Mediator complex—Expanding the genetic architecture and phenotypic spectrum of MED12‐related disorders. Clinical Genetics. 94(5). 450–456. 17 indexed citations
3.
Tavian, Daniela, Sara Missaglia, E. Pennisi, et al.. (2012). Contribution of novel ATGL missense mutations to the clinical phenotype of NLSD-M: a strikingly low amount of lipase activity may preserve cardiac function. Human Molecular Genetics. 21(24). 5318–5328. 41 indexed citations
4.
Lehnen, H, et al.. (2011). Maternales Ehlers-Danlos Syndrom Typ II und fetale Duodenalatresie Grad II: Erstbeschreibung. Zeitschrift für Geburtshilfe und Neonatologie. 215(2). 83–85. 1 indexed citations
5.
Lehnen, H, et al.. (2011). Twin Pregnancies Conceived Spontaneously and by ART (Assisted Reproductive Technologies) – a Retrospective Analysis and Review. Geburtshilfe und Frauenheilkunde. 71(8). 669–676. 6 indexed citations
6.
Dauwerse, Johannes G., Jill Dixon, Saskia Seland, et al.. (2010). Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genetics. 43(1). 20–22. 243 indexed citations
7.
Henegariu, Octavian, P.N. Hirschmann, K. Kilian, et al.. (2009). Rapid screening of the Y chromosome in idiopathic sterile men, diagnostic for deletions in AZF, a genetic Y factor expressed during spermatogenesis. Andrologia. 26(2). 97–106. 12 indexed citations
8.
Lehnen, H, et al.. (2009). Severe Phenotype in a Girl with Partial Tetrasomy 7, Karyotype 46,XX,trp(7)(q35q36). Cytogenetic and Genome Research. 125(3). 248–252. 5 indexed citations
9.
Ramaekers, V., Steen Ingemann Hansen, Jan Holm, et al.. (2003). Reduced folate transport to the CNS in female Rett patients. Neurology. 61(4). 506–515. 77 indexed citations
10.
Müller, Franz, Ingrid Haußer, Daniel Berg, et al.. (2002). Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing. British Journal of Dermatology. 146(3). 495–499. 26 indexed citations
11.
Laccone, Franco, et al.. (1999). A fast polymerase chain reaction-mediated strategy for introducing repeat expansions into CAG-repeat containing genes. Human Mutation. 13(6). 497–502. 15 indexed citations
12.
Luche, Ralf M., Robert Maiwald, Elaine J. Carlson, & Charles J. Epstein. (1997). Novel mutations in an otherwise strictly conserved domain of CuZn superoxide dismutase. Molecular and Cellular Biochemistry. 168(1-2). 191–194. 6 indexed citations
13.
Maiwald, Robert, Ralf M. Luche, & C. J. Epstein. (1996). Isolation of a mouse homolog of the human DAZ (Deleted in Azoospermia) gene. Mammalian Genome. 7(8). 628–628. 9 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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