Artur Darmanian

1.1k citations
15 papers · 539 indexed · h-index 11
Topics
Genomic variations and chromosomal abnormalities (7 papers)Prenatal Screening and Diagnostics (6 papers)Genetic Syndromes and Imprinting (4 papers)
Partner nations
AustraliaGermanyIndia

In The Last Decade

Artur Darmanian

15 papers receiving 493 citations

Peers

Artur Darmanian
Comparison fields: 5 of 54
  • Molecular Biology 315
  • Oncology 231
  • Genetics 195
  • Cancer Research 87
  • Pediatrics, Perinatology and Child Health 86
Replace Muhammad B. Ekram with:
Muhammad B. Ekram United States
Robert Stobezki United States
Mohsen Ahmadian United States
Nora Shannon United Kingdom
Betty K. Martin United States
Sou‐De Cheng Taiwan
E Emison United States
Dirk Reutzel Germany
Lakshmi Rambhatla United States
Katarzyna Klonowska Poland
Artur Darmanian relative to Muhammad B. Ekram United States Muhammad B. Ekram's profile →
Citations per field
00.5×1.5×2.4×
Muhammad B. Ekram · 1×
Citations per year

Countries citing papers authored by Artur Darmanian

Since Specialization
Citations

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

Fields of papers citing papers by Artur Darmanian

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Artur Darmanian

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

All Works

15 of 15 papers shown
#WorkIndexed citations
1 1
2 1
3 10
4 2
5 44
6 27
7 10
8 34
9 38
10 32
11 17
12 90
13 125
14 82
15 26

About Artur Darmanian

Artur Darmanian is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Oncology, having authored 15 papers that have together received 539 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Oncology (231 citations), Genetics (195 citations) and Cancer Research (87 citations). Artur Darmanian has collaborated with scholars based in Australia, Germany and India. Frequent co-authors include Helen Rizos, Richard Kefford, Graham J. Mann, Elizabeth A. Holland, Célia Bádenas, Josep Malvehy, Susana Puig, Montserrat Milà, Felicity Collins and Art Daniel. Their work appears in journals such as Journal of Biological Chemistry, Cancer Research and Oncogene.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026