Anoud Albader

652 total citations
4 papers, 29 citations indexed

About

Anoud Albader is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Anoud Albader has authored 4 papers receiving a total of 29 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Neurology. Recurrent topics in Anoud Albader's work include Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neuroblastoma Research and Treatments (1 paper). Anoud Albader is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neuroblastoma Research and Treatments (1 paper). Anoud Albader collaborates with scholars based in Saudi Arabia, Netherlands and France. Anoud Albader's co-authors include Dilek Çolak, Namik Kaya, Rawan Almass, Aziza Chedrawi, Stefan T. Arold, Mohammad A. Al–Muhaizea, Maha Al‐Rasheed, Peter Karachunski, Tahsin Stefan Barakat and Peter Bauer and has published in prestigious journals such as Acta Neuropathologica, Orphanet Journal of Rare Diseases and Neuromuscular Disorders.

In The Last Decade

Anoud Albader

3 papers receiving 29 citations

Peers

Anoud Albader
Peter Diakumis Australia
Clarissa Rocca United Kingdom
Steve Courel United States
Yamna Kriouile Morocco
Dyala Jaroudi Saudi Arabia
Marcos Madruga Spain
Moheb Ghobrial United States
Audrey Smith United Kingdom
Tanja Klein‐Rodewald Germany
Peter Diakumis Australia
Anoud Albader
Citations per year, relative to Anoud Albader Anoud Albader (= 1×) peers Peter Diakumis

Countries citing papers authored by Anoud Albader

Since Specialization
Citations

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

Fields of papers citing papers by Anoud Albader

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anoud Albader

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

All Works

4 of 4 papers shown
1.
Al–Muhaizea, Mohammad A., Anoud Albader, Rawan Almass, et al.. (2025). Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness. Orphanet Journal of Rare Diseases. 20(1). 415–415.
2.
Salih, Mustafa A., Muddathir H. Hamad, Marco Savarese, et al.. (2021). Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies. Genetic Testing and Molecular Biomarkers. 25(12). 757–764. 5 indexed citations
3.
Almass, Rawan, Anoud Albader, Peter Karachunski, et al.. (2020). Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy. Acta Neuropathologica. 139(4). 791–794. 15 indexed citations
4.
Al–Muhaizea, Mohammad A., Anoud Albader, Rawan Almass, et al.. (2020). Pyrostigmine therapy in a patient with VAMP1-related congenital myasthenic syndrome. Neuromuscular Disorders. 30(7). 611–615. 9 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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2026