DD Farhud
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 10%
- Forensic and Genetic Research
- Genetic diversity and population structure
Papers in
-
- Connexins and lens biology 6
- Genetics 16
- Forensic and Genetic Research 4
- Dermatoglyphics and Human Traits 4
- Hemoglobinopathies and Related Disorders 3
- BRCA gene mutations in cancer 2
- Co-authors
- Morteza Hashemzadeh Chaleshtori (9 shared papers)Mahdis Kamali (3 shared papers)Leila Yazdanpanah (1 shared paper)Farideh Zaini (2 shared papers)Dominique Quinque (1 shared paper)Isabelle Dupanloup (1 shared paper)Ivan Nasidze (1 shared paper)Richard Cordaux (1 shared paper)
- Journals
- Annals of Human Genetics (1 paper)Skin Research and Technology (1 paper)Human Genetics (1 paper)Journal of Neuroimmunology (1 paper)SHILAP Revista de lepidopterología (29 papers)
- Partner nations
- IranUnited KingdomRussia
In The Last Decade
DD Farhud
45 papers receiving 458 citations
Peers
Comparison fields: 5 of 105
- Sensory Systems 102
- Genetics 192
- Endocrine and Autonomic Systems 43
- Neurology 43
- Archeology 37
Countries citing papers authored by DD Farhud
This map shows the geographic impact of DD Farhud'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 DD Farhud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites DD Farhud more than expected).
Fields of papers citing papers by DD Farhud
This network shows the impact of papers produced by DD Farhud. 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 DD Farhud. The network helps show where DD Farhud may publish in the future.
Co-authors
The 25 scholars most cited alongside DD Farhud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 110 | |
| 2 | 1986 | 39 | |
| 3 | Nutrigenomics and nutrigenetics. | 2010 | 34 |
| 4 | Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. | 2011 | 33 |
| 5 | Congratulation to Margaret Chan Familial and Sporadic GJB2-Related Deafness in Iran: Review of Gene Mutations | 2007 | 27 |
| 6 | GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY | 2008 | 27 |
| 7 | Aflatoxins in iran: nature, hazards and carcinogenicity. | 2011 | 27 |
| 8 | "Deafness –Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population" | 2002 | 19 |
| 9 | Economic Valuation of Air Pollution Health Impacts in the Tehran Area, Iran | 2008 | 19 |
| 10 | Aflatoxins in Iran: Nature, Hazards and Carcinogenicity | 2011 | 13 |
| 11 | 2003 | 12 | |
| 12 | 1982 | 12 | |
| 13 | 2009 | 11 | |
| 14 | Genetic doping and health damages. | 2011 | 11 |
| 15 | Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran | 2015 | 10 |
| 16 | Prevalence of Orofacial Complications in Iranian Patients with β -Thalassemia Major | 2007 | 9 |
| 17 | Gene and aging. | 2008 | 8 |
| 18 | 1999 | 8 | |
| 19 | First Report of New Oral Findings in a Case with Noonan Syndrome | 2008 | 6 |
| 20 | "Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations" | 2004 | 6 |
About DD Farhud
DD Farhud is a scholar working on Molecular Biology, Genetics, Sensory Systems, Pediatrics, Perinatology and Child Health and Genetics, having authored 48 papers that have together received 498 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Connexins and lens biology (6 papers), Forensic and Genetic Research (4 papers), Neuroscience of respiration and sleep (4 papers), Dermatoglyphics and Human Traits (4 papers), Hemoglobinopathies and Related Disorders (3 papers), BRCA gene mutations in cancer (2 papers) and Neonatal Health and Biochemistry (2 papers). The work is most often cited by research in Sensory Systems (102 citations), Genetics (192 citations), Endocrine and Autonomic Systems (43 citations), Neurology (43 citations) and Archeology (37 citations). DD Farhud has collaborated with scholars based in Iran, United Kingdom and Russia. Frequent co-authors include Morteza Hashemzadeh Chaleshtori, Mahdis Kamali, Leila Yazdanpanah, Farideh Zaini, Dominique Quinque, Isabelle Dupanloup, Ivan Nasidze, Richard Cordaux, Tamara Sarkisian and Oxana Yu. Naumova. Their work appears in journals such as Annals of Human Genetics, Skin Research and Technology, Human Genetics, Journal of Neuroimmunology and SHILAP Revista de lepidopterología.
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.