Davood Omrani

472 total citations
10 papers, 265 citations indexed

About

Davood Omrani is a scholar working on Surgery, Urology and Cognitive Neuroscience. According to data from OpenAlex, Davood Omrani has authored 10 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Surgery, 3 papers in Urology and 3 papers in Cognitive Neuroscience. Recurrent topics in Davood Omrani's work include Genetics and Neurodevelopmental Disorders (3 papers), Urological Disorders and Treatments (3 papers) and Autism Spectrum Disorder Research (3 papers). Davood Omrani is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Urological Disorders and Treatments (3 papers) and Autism Spectrum Disorder Research (3 papers). Davood Omrani collaborates with scholars based in Iran, Sweden and Qatar. Davood Omrani's co-authors include Kristina Lagerstedt‐Robinson, Louise Frisén, Ana Beleza‐Meireles, Agneta Nordenskjöld, Xiaolei Zhou, David J. Kelly, Simon C. Andrews, John R. Guest, Paul Golby and Fredrik Lundberg and has published in prestigious journals such as Journal of Bacteriology, European Journal of Human Genetics and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Davood Omrani

10 papers receiving 263 citations

Peers

Davood Omrani

MB

GENET

UROLO

SURGE

BIOCH

Farnoosh Jafarpour Iran

Yuan-Chao Sun China

Yi Ting Tsai United States

Wolfgang K�ster Germany

Hongsheng Men United States

Zihui Yan China

Mei Jin China

Junfeng He China

Kazushi Kunimatsu Japan

Farnoosh Jafarpour Iran

Davood Omrani

267 ×1.8

MB

93 ×0.9

GENET

17 ×0.2

UROLO

17 ×0.3

SURGE

10 ×0.5

BIOCH

Citations per year, relative to Davood Omrani Davood Omrani (= 1×) peers Farnoosh Jafarpour

Countries citing papers authored by Davood Omrani

Since Specialization

Citations

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

Fields of papers citing papers by Davood Omrani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davood Omrani

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

All Works

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10 of 10 papers shown

1.

Ghasemi, Mohammad‐Reza, Hossein Sadeghi, Reza Mirfakhraie, et al.. (2024). Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism. BMC Medical Genomics. 17(1). 196–196. 3 indexed citations

2.

Ghasemi, Mohammad‐Reza, et al.. (2022). Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case Series.. PubMed. 16(2). 117–128. 2 indexed citations

3.

Ghafouri‐Fard, Soudeh, et al.. (2019). P21-Associated ncRNA DNA Damage-Activated Expression in Bladder Cancer. Klinicka onkologie. 32(4). 277–280. 1 indexed citations

4.

Kazerouni, Faranak, et al.. (2017). Effect of Curcumin on Fatty Acid Synthase Expression and Enzyme Activity in Breast Cancer Cell Line SKBR3. International Journal of Cancer Management. 10(3). 16 indexed citations

5.

Omrani, Davood. (2009). Frequency of CCR5∆32 Variant in North-West of Iran. Journal of sciences, Islamic Republic of Iran. 20(2). 105–110. 5 indexed citations

6.

Beleza‐Meireles, Ana, Fredrik Lundberg, Kristina Lagerstedt‐Robinson, et al.. (2007). FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias. European Journal of Human Genetics. 15(4). 405–410. 62 indexed citations

7.

Zhou, Xiaolei, MaiBritt Giacobini, Britt‐Marie Anderlid, et al.. (2007). Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD). American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(3). 351–354. 29 indexed citations

8.

Nordenskjöld, Agneta, et al.. (2007). Polymorphisms of estrogen receptor beta gene are associated with hypospadias. Journal of Pediatric Urology. 3. S48–S48. 2 indexed citations

9.

Beleza‐Meireles, Ana, Davood Omrani, Ingrid Kockum, et al.. (2006). Polymorphisms of estrogen receptor β gene are associated with hypospadias. Journal of Endocrinological Investigation. 29(1). 5–10. 46 indexed citations

10.

Golby, Paul, et al.. (1999). Inactivation and Regulation of the Aerobic C ₄ -Dicarboxylate Transport ( dctA ) Gene of Escherichia coli. Journal of Bacteriology. 181(18). 5624–5635. 99 indexed citations

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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