Aisha Al‐Khayat

421 total citations
7 papers, 168 citations indexed

About

Aisha Al‐Khayat is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Aisha Al‐Khayat has authored 7 papers receiving a total of 168 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Sensory Systems and 2 papers in Neurology. Recurrent topics in Aisha Al‐Khayat's work include Hearing, Cochlea, Tinnitus, Genetics (2 papers), Connexins and lens biology (2 papers) and Vestibular and auditory disorders (2 papers). Aisha Al‐Khayat is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (2 papers), Connexins and lens biology (2 papers) and Vestibular and auditory disorders (2 papers). Aisha Al‐Khayat collaborates with scholars based in Oman, United States and United Kingdom. Aisha Al‐Khayat's co-authors include Susanne A. Kraemer, Milan Maçek, Karen H. Friderici, Jeffrey R. Leipprandt, W. J. Kleijer, Mehmet Şımşek, Muralitharan Shanmugakonar, Jennifer N. Partlow, Barry A. Chioza and Saeed Al-Turki and has published in prestigious journals such as Neurology, Human Molecular Genetics and Human Mutation.

In The Last Decade

Aisha Al‐Khayat

7 papers receiving 164 citations

Peers

Aisha Al‐Khayat
Tae-Jun Kwon South Korea
Y L Lai China
George Milligan United Kingdom
Aisha Al‐Khayat
Citations per year, relative to Aisha Al‐Khayat Aisha Al‐Khayat (= 1×) peers Barbara Pawlik

Countries citing papers authored by Aisha Al‐Khayat

Since Specialization
Citations

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

Fields of papers citing papers by Aisha Al‐Khayat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aisha Al‐Khayat. 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 Aisha Al‐Khayat. The network helps show where Aisha Al‐Khayat may publish in the future.

Co-authorship network of co-authors of Aisha Al‐Khayat

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

All Works

7 of 7 papers shown
1.
Ahmed, Momin, Barry A. Chioza, Anna Rajab, et al.. (2015). Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 84(17). 1745–1750. 41 indexed citations
2.
Mahgoub, O., Hamza A. Babiker, I.T. Kadim, et al.. (2012). Disclosing the origin and diversity of Omani cattle. Animal Genetics. 44(3). 336–339. 11 indexed citations
3.
Wali, Yasser, et al.. (2012). Coexistence of sickle cell disease and severe congenital neutropenia: first impressions can be deceiving. European Journal Of Haematology. 89(3). 245–249. 9 indexed citations
4.
Al-Bahry, Saif N., et al.. (2004). Embryonic and larval staging of the Arabian Toad,Bufo arabicus(Amphibia: Bufonidae). Zoology in the Middle East. 32(1). 47–56. 5 indexed citations
5.
Şımşek, Mehmet, et al.. (2002). A PCR-RFLP Test for Simultaneous Detection of Two Single-Nucleotide Insertions in the Connexin-26 Gene Promoter. Genetic Testing. 6(3). 225–228. 4 indexed citations
6.
Şımşek, Mehmet, et al.. (2001). Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population. Human Mutation. 18(6). 545–546. 42 indexed citations
7.
Al‐Khayat, Aisha, Susanne A. Kraemer, Jeffrey R. Leipprandt, et al.. (1998). Human  -Mannosidase cDNA Characterization and First Identification of a Mutation Associated with Human  -Mannosidosis. Human Molecular Genetics. 7(1). 75–83. 56 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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