Maysoon Alsagob

538 total citations
12 papers, 109 citations indexed

About

Maysoon Alsagob is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Maysoon Alsagob has authored 12 papers receiving a total of 109 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Maysoon Alsagob's work include Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Maysoon Alsagob is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Maysoon Alsagob collaborates with scholars based in Saudi Arabia, United Kingdom and Finland. Maysoon Alsagob's co-authors include Namik Kaya, Dilek Çolak, Rawan Almass, Mazhor Aldosary, Ali Al‐Odaib, Albandary AlBakheet, Mohammad A. Al–Muhaizea, Robert W. Taylor, Roua A. Al‐Rijjal and Sezer Acar and has published in prestigious journals such as PLoS ONE, Journal of the Neurological Sciences and Cells.

In The Last Decade

Maysoon Alsagob

11 papers receiving 105 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Maysoon Alsagob Saudi Arabia 6 62 22 21 17 15 12 109
Anne Dieux‐Coëslier France 7 99 1.6× 25 1.1× 39 1.9× 25 1.5× 22 1.5× 12 156
Didem Ardıçlı Türkiye 8 50 0.8× 13 0.6× 35 1.7× 3 0.2× 14 0.9× 25 146
Carmela Preziuso Italy 5 144 2.3× 24 1.1× 16 0.8× 11 0.6× 8 0.5× 5 210
Katie B. Williams United States 7 70 1.1× 28 1.3× 60 2.9× 22 1.3× 6 0.4× 13 148
Chen-Jui Ho Taiwan 9 48 0.8× 7 0.3× 20 1.0× 5 0.3× 41 2.7× 16 160
Sirisak Chanprasert United States 8 158 2.5× 96 4.4× 33 1.6× 2 0.1× 11 0.7× 13 228
Alicia B. Byrne Australia 6 46 0.7× 9 0.4× 35 1.7× 7 0.4× 5 0.3× 8 91
Maria Concetta Cutrupi Italy 5 50 0.8× 8 0.4× 44 2.1× 1 0.1× 6 0.4× 7 124
Yah-Huei Wu-Chou Taiwan 8 63 1.0× 4 0.2× 65 3.1× 14 0.8× 26 1.7× 15 146
Matthew Spence Canada 6 124 2.0× 2 0.1× 13 0.6× 37 2.2× 11 0.7× 8 207

Countries citing papers authored by Maysoon Alsagob

Since Specialization
Citations

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

Fields of papers citing papers by Maysoon Alsagob

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maysoon Alsagob

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

All Works

12 of 12 papers shown
1.
2.
Aldosary, Mazhor, Maysoon Alsagob, Stefan T. Arold, et al.. (2022). A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families. Cells. 11(19). 3154–3154.
3.
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
4.
Aldosary, Mazhor, Rawan Almass, Maysoon Alsagob, et al.. (2021). SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion. JIMD Reports. 60(1). 75–87. 12 indexed citations
5.
Almass, Rawan, Hesham Aldhalaan, Maysoon Alsagob, et al.. (2021). Genetics of ataxia telangiectasia in a highly consanguineous population. Annals of Human Genetics. 86(1). 34–44. 4 indexed citations
6.
Alsagob, Maysoon, Mustafa A. Salih, Muddathir H. Hamad, et al.. (2019). First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient. Molecular Cytogenetics. 12(1). 21–21. 2 indexed citations
7.
Salih, Mustafa A., Muddathir H. Hamad, Maria Flavia Savarese, et al.. (2019). Delineating the phenotypes of early onset myopathy due to novel titin gene mutations. Journal of the Neurological Sciences. 405. 38–39. 1 indexed citations
8.
Acar, Sezer, Korcan Demir, Roua A. Al‐Rijjal, et al.. (2018). Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3. PLoS ONE. 13(3). e0193388–e0193388. 22 indexed citations
9.
Al‐Hassnan, Zuhair N., Rawan Almass, Albandary AlBakheet, et al.. (2018). Identification of novel genomic imbalances in Saudi patients with congenital heart disease. Molecular Cytogenetics. 11(1). 9–9. 8 indexed citations
10.
Alfadhel, Majid, Marwan Nashabat, Muhammad Talal Alrifai, et al.. (2017). Further delineation of the phenotypic spectrum of  ISCA2 defect: A report of ten new cases. European Journal of Paediatric Neurology. 22(1). 46–55. 22 indexed citations
11.
Al–Muhaizea, Mohammad A., Rawan Almass, Mazhor Aldosary, et al.. (2017). A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature. The Cerebellum. 17(3). 276–285. 16 indexed citations
12.
Alsagob, Maysoon, Dilek Çolak, & Namik Kaya. (2015). Genetics of autism spectrum disorder: an update on copy number variations leading to autism in the next generation sequencing era.. PubMed. 19(106). 367–79. 12 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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