Dagmar Weise

867 total citations
11 papers, 572 citations indexed

About

Dagmar Weise is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Dagmar Weise has authored 11 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Dagmar Weise's work include Congenital heart defects research (5 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (3 papers). Dagmar Weise is often cited by papers focused on Congenital heart defects research (5 papers), Genomics and Rare Diseases (3 papers) and RNA modifications and cancer (3 papers). Dagmar Weise collaborates with scholars based in Germany, Australia and Austria. Dagmar Weise's co-authors include Arpad von Moers, Annette Grüters, Roberto DiLauro, Dirk Schnabel, Frank K.H. van Landeghem, S. Schwarz, Heiko Krude, Antony Lafferty, Heike Biebermann and Holger Tönnies and has published in prestigious journals such as Journal of Clinical Investigation, Neurology and Clinical Neurophysiology.

In The Last Decade

Dagmar Weise

10 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dagmar Weise Germany 7 334 232 179 110 81 11 572
Amanda D. Taylor United Kingdom 12 288 0.9× 54 0.2× 170 0.9× 104 0.9× 50 0.6× 17 553
Paola Cambiaso Italy 13 205 0.6× 95 0.4× 300 1.7× 26 0.2× 71 0.9× 28 499
Heraldo Mendes Garmes Brazil 13 207 0.6× 186 0.8× 253 1.4× 25 0.2× 42 0.5× 39 635
Kensuke Takatsuki Japan 13 210 0.6× 81 0.3× 127 0.7× 94 0.9× 60 0.7× 32 506
Nicola M. Solomon Australia 7 293 0.9× 263 1.1× 105 0.6× 67 0.6× 73 0.9× 9 527
VK Han Canada 10 133 0.4× 87 0.4× 215 1.2× 32 0.3× 73 0.9× 11 385
A. Weber United Kingdom 13 255 0.8× 134 0.6× 381 2.1× 27 0.2× 177 2.2× 18 796
Mohamad Zubair Japan 16 660 2.0× 597 2.6× 235 1.3× 27 0.2× 134 1.7× 19 1.0k
Anna Edlund Sweden 11 217 0.6× 96 0.4× 78 0.4× 118 1.1× 278 3.4× 16 562
Anne Lienhardt-Roussie France 8 319 1.0× 261 1.1× 130 0.7× 15 0.1× 24 0.3× 17 569

Countries citing papers authored by Dagmar Weise

Since Specialization
Citations

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

Fields of papers citing papers by Dagmar Weise

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dagmar Weise

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

All Works

11 of 11 papers shown
1.
2.
Rosewich, Hendrik, Dagmar Weise, Andreas Ohlenbusch, Jutta Gärtner, & Knut Brockmann. (2014). Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome. Neurology. 83(9). 861–863. 34 indexed citations
3.
Korenkov, Michael, et al.. (2013). FTO and INSIG2 Genotyping Combined with Metabolic and Anthropometric Phenotyping of Morbidly Obese Patients. Molecular Syndromology. 4(6). 273–279. 4 indexed citations
4.
Shoukier, Moneef, Nina Klein, Bernd Auber, et al.. (2012). Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?. Clinical Genetics. 83(1). 53–65. 55 indexed citations
5.
Shoukier, Moneef, Iris Bartels, Bernd Auber, et al.. (2011). A 16q12 microdeletion in a boy with severe psychomotor delay, craniofacial dysmorphism, brain and limb malformations, and a heart defect. American Journal of Medical Genetics Part A. 158A(1). 229–235. 20 indexed citations
6.
Krude, Heiko, Heike Biebermann, Arpad von Moers, et al.. (2002). Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency. Journal of Clinical Investigation. 109(4). 475–480. 236 indexed citations
7.
Krude, Heiko, Heike Biebermann, Arpad von Moers, et al.. (2002). Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency. Journal of Clinical Investigation. 109(4). 475–480. 30 indexed citations
8.
Krude, Heiko, Heike Biebermann, Arpad von Moers, et al.. (2002). Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency. Journal of Clinical Investigation. 109(4). 475–480. 181 indexed citations
9.
Schumacher, Sabine, et al.. (2000). Single- and multiple-dose pharmacokinetics of repaglinide in patients with type 2 diabetes and renal impairment. Diabetes Research and Clinical Practice. 50. 72–73. 1 indexed citations
10.
Korenke, GC, Arpad von Moers, Dagmar Weise, et al.. (1999). 020 Epilepsy with seizures after fasting and retardation: The first familial cases of glucose transporter protein (GLUT-1) deficiency. European Journal of Paediatric Neurology. 3(6). A90–A91. 9 indexed citations
11.
Weise, Dagmar, et al.. (1957). Ein Skizzenbuch zur Chorfantasie Op. 80 und zu Anderen Werken. Medical Entomology and Zoology. 2 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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