Farkhondeh Behjati

2.3k citations
69 papers · 678 indexed · h-index 14
Topics
Genomic variations and chromosomal abnormalities (22 papers)Genetics and Neurodevelopmental Disorders (13 papers)Congenital heart defects research (8 papers)
Journals
SHILAP Revista de lepidopterologíaPLoS ONEThe American Journal of Human Genetics
Partner nations
IranGermanyNetherlands

In The Last Decade

Farkhondeh Behjati

61 papers receiving 662 citations

Peers

Farkhondeh Behjati
Comparison fields: 5 of 92
  • Molecular Biology 330
  • Genetics 271
  • Cancer Research 94
  • Oncology 66
  • Pediatrics, Perinatology and Child Health 58
Replace Meng‐Yin Tsai with:
Meng‐Yin Tsai Taiwan
Daniela Fietz Germany
Takashi Hirakawa Japan
Hector Macias United States
Paul G. Farnworth Australia
Francesco Antonica Italy
Hen Prizant United States
Dana Gaddy-Kurten United States
Maria M. Alves Netherlands
Frederick V. Schaefer United States
Farkhondeh Behjati relative to Meng‐Yin Tsai Taiwan Meng‐Yin Tsai's profile →
Citations per field
00.5×1.5×2.5×
Meng‐Yin Tsai · 1×
Citations per year

Countries citing papers authored by Farkhondeh Behjati

Since Specialization
Citations

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

Fields of papers citing papers by Farkhondeh Behjati

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Farkhondeh Behjati

This figure shows the co-authorship network connecting the top 25 collaborators of Farkhondeh Behjati. A scholar is included among the top collaborators of Farkhondeh Behjati 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 Farkhondeh Behjati. Farkhondeh Behjati 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 1
2 0
3 0
4 2
5 3
6 8
7 24
8 19
9 12
10 1
11 5
12 14
13 1
14 13
15 13
16 106
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Chromosomal anomalies in infertile azoospermic and oligospermic men
0
19
CHROMOSOMAL ABNORMALITIES IN A REFERRED POPULATION: A REPORT OF 383 IRANIAN CASES
3
20 10

About Farkhondeh Behjati

Farkhondeh Behjati is a scholar working on Genetics, Cancer Research and Hematology, having authored 69 papers that have together received 678 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Congenital heart defects research (8 papers). The work is most often cited by research in Genetics (271 citations), Cancer Research (94 citations) and Molecular Biology (330 citations). Farkhondeh Behjati has collaborated with scholars based in Iran, Germany and Netherlands. Frequent co-authors include Hossein Najmabadi, Kimia Kahrizi, Andreas Tzschach, Andreas W. Kuß, Masoud Garshasbi, Roxana Kariminejad, Hans Hilger Ropers, Valeh Hadavi, Saghar Ghasemi Firouzabadi and Ahad Muhammadnejad. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of 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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