Farhad Hormozdiari

19.2k citations
56 papers · 3.1k indexed · 2 hit papers · h-index 27
  • Genetics top 0.5%
    • Genetic Associations and Epidemiology 27
    • Genetic Mapping and Diversity in Plants and Animals 21
    • Genomic variations and chromosomal abnormalities 11
    • Genetic and phenotypic traits in livestock 9
    • Genomics and Phylogenetic Studies 11
    • Gene expression and cancer classification 9
    • Bioinformatics and Genomic Networks 7
    • Genomics and Chromatin Dynamics 7

Farhad Hormozdiari

55 papers receiving 3.1k citations

Hit Papers

Colocalization of GWAS and eQTL Signals Detects Target Genes3802016202620192022100200300

Peers

Farhad Hormozdiari
Comparison fields: 5 of 132
  • Genetics 1.9k
  • Molecular Biology 1.8k
  • Cancer Research 276
  • Aging 17
  • Sensory Systems 30
Replace Sarah S. Murray with:
Sarah S. Murray United States
Manuel A. Rivas United States
Eric M. Sobel United States
Joannella Morales United States
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Claude Beazley United Kingdom
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Erin N. Smith United States
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Farhad Hormozdiari relative to Sarah S. Murray United States Sarah S. Murray's profile →
Citations per field
00.5×9.5×
Sarah S. Murray · 1×
Citations per year

Countries citing papers authored by Farhad Hormozdiari

Since Specialization
Citations

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

Fields of papers citing papers by Farhad Hormozdiari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Farhad Hormozdiari, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Farhad Hormozdiari Line = papers co-authored together Farhad Hormozdiari links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20250
2 202413
3 202325
4 202273
5 202137
6 20199
7 2018242
8 201893
9 201747
10 201623
11 201626
12 201648
13
Colocalization of GWAS and eQTL Signals Detects Target Genesbreakdown →
2016380
14
Chromosome conformation elucidates regulatory relationships in developing human brainbreakdown →
2016347
15 2014287
16 201428
17 20145
18 201443
19 201121
20 201112

About Farhad Hormozdiari

Farhad Hormozdiari is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 56 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (27 papers), Genetic Mapping and Diversity in Plants and Animals (21 papers), Genomic variations and chromosomal abnormalities (11 papers), Genomics and Phylogenetic Studies (11 papers), Genetic and phenotypic traits in livestock (9 papers), Gene expression and cancer classification (9 papers), Bioinformatics and Genomic Networks (7 papers) and Genomics and Chromatin Dynamics (7 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (1.8k citations) and Cancer Research (276 citations). Farhad Hormozdiari has collaborated with scholars based in United States, United Kingdom and South Korea. Frequent co-authors include Eleazar Eskin, Bogdan Paşaniuc, Alkes L. Price, Jong Wha J. Joo, Eun Yong Kang, Steven Gazal, Ayellet V. Segrè, Wen-Yun Yang, Emrah Kostem and Martijn van de Bunt. Their work appears in journals such as Nature, Nucleic Acids Research and Nature Communications.

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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