Yalda Kia

634 total citations
24 papers, 579 citations indexed

About

Yalda Kia is a scholar working on Pharmacology, Organic Chemistry and Computational Theory and Mathematics. According to data from OpenAlex, Yalda Kia has authored 24 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pharmacology, 16 papers in Organic Chemistry and 12 papers in Computational Theory and Mathematics. Recurrent topics in Yalda Kia's work include Cholinesterase and Neurodegenerative Diseases (17 papers), Computational Drug Discovery Methods (12 papers) and Chemical synthesis and alkaloids (9 papers). Yalda Kia is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (17 papers), Computational Drug Discovery Methods (12 papers) and Chemical synthesis and alkaloids (9 papers). Yalda Kia collaborates with scholars based in Malaysia, Saudi Arabia and India. Yalda Kia's co-authors include Alireza Basiri, Vikneswaran Murugaiyah, Raju Suresh Kumar, Hasnah Osman, Subbu Perumal, Natarajan Arumugam, Abdulrahman I. Almansour, Habibah A. Wahab, Mehran Fadaeinasab and Ibrahim Abdul Razak and has published in prestigious journals such as Molecules, European Journal of Medicinal Chemistry and BioMed Research International.

In The Last Decade

Yalda Kia

23 papers receiving 573 citations

Peers

Yalda Kia
Yalda Kia
Citations per year, relative to Yalda Kia Yalda Kia (= 1×) peers Reyhaneh Sabourian

Countries citing papers authored by Yalda Kia

Since Specialization
Citations

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

Fields of papers citing papers by Yalda Kia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yalda Kia

This figure shows the co-authorship network connecting the top 25 collaborators of Yalda Kia. A scholar is included among the top collaborators of Yalda Kia 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 Yalda Kia. Yalda Kia 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
1.
Basiri, Alireza, Mohammed Oday Ezzat, Yalda Kia, et al.. (2017). Synthesis and cholinesterase inhibitory activity study of new piperidone grafted spiropyrrolidines. Bioorganic Chemistry. 75. 210–216. 21 indexed citations
2.
Osman, Hasnah, Mohammed Oday Ezzat, Alireza Basiri, et al.. (2016). Efficient Synthesis and Discovery of Schiff Bases as Potent Cholinesterase Inhibitors. Medicinal Chemistry. 12(6). 527–536. 11 indexed citations
3.
Khaw, Kooi Yeong, et al.. (2016). Design, synthesis and cholinesterase inhibitory evaluation study of fluorescent N-benzylpiperidine-4-one derivatives. Medicinal Chemistry Research. 25(8). 1705–1715. 5 indexed citations
4.
Fadaeinasab, Mehran, Alireza Basiri, Yalda Kia, et al.. (2015). New Indole Alkaloids from the Bark of Rauvolfia Reflexa and their Cholinesterase Inhibitory Activity. Cellular Physiology and Biochemistry. 37(5). 1997–2011. 37 indexed citations
5.
Almansour, Abdulrahman I., et al.. (2015). An Expedient Synthesis, Acetylcholinesterase Inhibitory Activity, and Molecular Modeling Study of Highly Functionalized Hexahydro-1,6-naphthyridines. BioMed Research International. 2015. 1–9. 14 indexed citations
6.
Kia, Yalda, Hasnah Osman, Raju Suresh Kumar, Alireza Basiri, & Vikneswaran Murugaiyah. (2014). Ionic liquid mediated synthesis of mono- and bis-spirooxindole-hexahydropyrrolidines as cholinesterase inhibitors and their molecular docking studies. Bioorganic & Medicinal Chemistry. 22(4). 1318–1328. 59 indexed citations
7.
Kia, Yalda, Hasnah Osman, Raju Suresh Kumar, Alireza Basiri, & Vikneswaran Murugaiyah. (2014). Synthesis and discovery of highly functionalized mono- and bis-spiro-pyrrolidines as potent cholinesterase enzyme inhibitors. Bioorganic & Medicinal Chemistry Letters. 24(7). 1815–1819. 50 indexed citations
8.
Osman, Hasnah, Alireza Basiri, Abdussalam Salhin, et al.. (2014). Ionic liquid mediated synthesis and molecular docking study of novel aromatic embedded Schiff bases as potent cholinesterase inhibitors. Bioorganic Chemistry. 57. 162–168. 12 indexed citations
9.
Kumar, Raju Suresh, Abdulrahman I. Almansour, Natarajan Arumugam, et al.. (2014). An Expedient Synthesis and Screening for Antiacetylcholinesterase Activity of Piperidine Embedded Novel Pentacyclic Cage Compounds. Medicinal Chemistry. 10(2). 228–236. 13 indexed citations
10.
Kia, Yalda, Hasnah Osman, Raju Suresh Kumar, et al.. (2014). An Efficient Ionic Liquid Mediated Synthesis, Cholinesterase Inhibitory Activity and Molecular Modeling Study of Novel Piperidone Embedded α ,β-Unsaturated Ketones. Medicinal Chemistry. 10(5). 512–520. 3 indexed citations
11.
Basiri, Alireza, Vikneswaran Murugaiyah, Hasnah Osman, et al.. (2013). Cholinesterase inhibitory activity versus aromatic core multiplicity: A facile green synthesis and molecular docking study of novel piperidone embedded thiazolopyrimidines. Bioorganic & Medicinal Chemistry. 22(2). 906–916. 22 indexed citations
12.
Kia, Yalda, Hasnah Osman, Raju Suresh Kumar, et al.. (2013). A facile chemo-, regio- and stereoselective synthesis and cholinesterase inhibitory activity of spirooxindole–pyrrolizine–piperidine hybrids. Bioorganic & Medicinal Chemistry Letters. 23(10). 2979–2983. 69 indexed citations
13.
Basiri, Alireza, Vikneswaran Murugaiyah, Hasnah Osman, et al.. (2013). An expedient, ionic liquid mediated multi-component synthesis of novel piperidone grafted cholinesterase enzymes inhibitors and their molecular modeling study. European Journal of Medicinal Chemistry. 67. 221–229. 41 indexed citations
14.
Kia, Yalda, Hasnah Osman, Raju Suresh Kumar, et al.. (2013). Synthesis and discovery of novel piperidone-grafted mono- and bis-spirooxindole-hexahydropyrrolizines as potent cholinesterase inhibitors. Bioorganic & Medicinal Chemistry. 21(7). 1696–1707. 92 indexed citations
15.
Basiri, Alireza, et al.. (2013). Microwave assisted synthesis, cholinesterase enzymes inhibitory activities and molecular docking studies of new pyridopyrimidine derivatives. Bioorganic & Medicinal Chemistry. 21(11). 3022–3031. 32 indexed citations
16.
Fadaeinasab, Mehran, A. Hamid A. Hadi, Yalda Kia, Alireza Basiri, & Vikneswaran Murugaiyah. (2013). Cholinesterase Enzymes Inhibitors from the Leaves of Rauvolfia Reflexa and Their Molecular Docking Study. Molecules. 18(4). 3779–3788. 24 indexed citations
17.
Kia, Yalda, Hasnah Osman, Vikneswaran Murugaiyah, Suhana Arshad, & Ibrahim Abdul Razak. (2012). (3E,5E)-3,5-Bis(naphthalen-1-ylmethylidene)piperidin-4-one. Acta Crystallographica Section E Structure Reports Online. 68(3). o802–o803. 1 indexed citations
18.
Kia, Yalda, Hasnah Osman, Vikneswaran Murugaiyah, Suhana Arshad, & Ibrahim Abdul Razak. (2012). (3E,5E)-3,5-Bis(4-methylbenzylidene)-1-[3-(piperidin-1-yl)propanoyl]piperidin-4-one. Acta Crystallographica Section E Structure Reports Online. 68(8). o2493–o2494.
19.
Kia, Yalda, Hasnah Osman, Vikneswaran Murugaiyah, Madhukar Hemamalini, & Hoong‐Kun Fun. (2011). (E)-2-(4-Methylbenzylidene)hydrazinecarboxamide. Acta Crystallographica Section E Structure Reports Online. 67(2). o242–o242. 3 indexed citations
20.
Habibi, Zohreh, et al.. (2008). EXTRACTION AND IDENTIFICATION OF β-STIGMASTEROL AND TWO FLAVONOIDS FROM THE AERIAL PARTS OF TANACETUM CANESCENS (DC.). Iranian Journal of Medicinal and Aromatic Plants Research. 24(240). 135–147. 1 indexed citations

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