Erfan Nur

3.2k citations
103 papers · 1.6k indexed · h-index 20
Topics
Hemoglobinopathies and Related Disorders (72 papers)Iron Metabolism and Disorders (23 papers)Erythrocyte Function and Pathophysiology (15 papers)

In The Last Decade

Erfan Nur

88 papers receiving 1.6k citations

Peers

Erfan Nur
Comparison fields: 5 of 106
  • Genetics 730
  • Hematology 649
  • Molecular Biology 310
  • Physiology 224
  • Pediatrics, Perinatology and Child Health 165
Replace Claudia Marsik with:
Claudia Marsik Austria
J Pinkhas Israel
Eman Abdel Rahman Ismail Egypt
Abraham Majluf‐Cruz Mexico
Eleni Gavriilaki Greece
Elizabeth A. Manci United States
Gian Carlo Avanzi Italy
Louis D. Wadsworth Canada
Daniele Longo United States
Claudio Sandoval United States
Erfan Nur relative to Claudia Marsik Austria Claudia Marsik's profile →
Citations per field
00.5×6.5×
Claudia Marsik · 1×
Citations per year

Countries citing papers authored by Erfan Nur

Since Specialization
Citations

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

Fields of papers citing papers by Erfan Nur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erfan Nur

This figure shows the co-authorship network connecting the top 25 collaborators of Erfan Nur. A scholar is included among the top collaborators of Erfan Nur 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 Erfan Nur. Erfan Nur 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
#WorkIndexed citations
1 0
2 0
3 1
4 1
5 1
6 5
7 4
8 2
9 1
10 0
11 1
12 2
13 0
14 8
15 5
16 10
17 8
18 4
19 22
20 61

About Erfan Nur

Erfan Nur is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 103 papers that have together received 1.6k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (72 papers), Iron Metabolism and Disorders (23 papers) and Erythrocyte Function and Pathophysiology (15 papers). The work is most often cited by research in Genetics (730 citations), Hematology (649 citations) and Internal Medicine (111 citations). Erfan Nur has collaborated with scholars based in Netherlands, United States and Switzerland. Frequent co-authors include Bart J. Biemond, Dees P. M. Brandjes, Sacha Zeerleder, John‐John B. Schnog, Hans‐Martin Otten, Kristof Van Avondt, Victor E. A. Gerdes, Alessandro Squizzato, Bregje van Zaane and Olaf M. Dekkers. Their work appears in journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Stroke.

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