Monika Cohen

3.3k citations
13 papers · 859 indexed · h-index 11
Topics
Genomic variations and chromosomal abnormalities (5 papers)Genetics and Neurodevelopmental Disorders (4 papers)Chromosomal and Genetic Variations (3 papers)

In The Last Decade

Monika Cohen

12 papers receiving 837 citations

Peers

Monika Cohen
Comparison fields: 5 of 70
  • Molecular Biology 551
  • Genetics 488
  • Cellular and Molecular Neuroscience 113
  • Pediatrics, Perinatology and Child Health 98
  • Plant Science 84
Replace Karen Buysse with:
Karen Buysse Belgium
Karen M. Lower Australia
Rasim Özgür Rosti United States
Marianna Baybis United States
A. Moncla France
Nathalie Van der Aa Belgium
Carmen Orellana Spain
Alexandra Afenjar France
Ute Grasshoff Germany
Marianne Till France
Monika Cohen relative to Karen Buysse Belgium Karen Buysse's profile →
Citations per field
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Citations per year

Countries citing papers authored by Monika Cohen

Since Specialization
Citations

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

Fields of papers citing papers by Monika Cohen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monika Cohen

This figure shows the co-authorship network connecting the top 25 collaborators of Monika Cohen. A scholar is included among the top collaborators of Monika Cohen 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 Monika Cohen. Monika Cohen 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
#WorkIndexed citations
1 2
2 40
3 73
4 28
5 215
6 18
7 41
8 100
9 47
10 41
11 178
12 4
13 72

About Monika Cohen

Monika Cohen is a scholar working on Genetics, Periodontics and Genetics, having authored 13 papers that have together received 859 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Genetics (488 citations), Molecular Biology (551 citations) and Developmental Neuroscience (30 citations). Monika Cohen has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Petra Muschke, Klaus Gerlach, Sibylle Jakubiczka, Hannelore Thiele, Ilse Wieland, Peter Wieacker, Ralf H. Adams, Thomy de Ravel, Juliane Hoyer and Alfredo Orrico. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

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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