Mazhor Aldosary

961 total citations
17 papers, 454 citations indexed

About

Mazhor Aldosary is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Mazhor Aldosary has authored 17 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in Mazhor Aldosary's work include Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (8 papers) and RNA modifications and cancer (4 papers). Mazhor Aldosary is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (8 papers) and RNA modifications and cancer (4 papers). Mazhor Aldosary collaborates with scholars based in Saudi Arabia, United Kingdom and France. Mazhor Aldosary's co-authors include Robert W. Taylor, Emma L. Blakely, Robert McFarland, Charlotte L. Alston, John W. Yarham, Joanna L. Elson, Namik Kaya, Dilek Çolak, Helen Tuppen and Anas M. Alazami and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Mazhor Aldosary

14 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mazhor Aldosary Saudi Arabia 10 386 122 93 47 23 17 454
Mathilde Nizon France 13 239 0.6× 70 0.6× 153 1.6× 45 1.0× 41 1.8× 26 387
Alessia Nasca Italy 15 535 1.4× 256 2.1× 68 0.7× 55 1.2× 11 0.5× 27 605
Bader Alhaddad Germany 15 331 0.9× 89 0.7× 174 1.9× 69 1.5× 35 1.5× 29 516
Akihiko Miyauchi Japan 11 189 0.5× 85 0.7× 96 1.0× 45 1.0× 12 0.5× 24 326
Katarzyna Tońska Poland 14 400 1.0× 149 1.2× 44 0.5× 46 1.0× 11 0.5× 40 502
Elisa Rahikkala Finland 9 163 0.4× 61 0.5× 81 0.9× 37 0.8× 18 0.8× 38 269
Rocío Sánchez-Alcudia Spain 14 339 0.9× 118 1.0× 72 0.8× 40 0.9× 21 0.9× 18 418
Sietske H. Kevelam Netherlands 10 283 0.7× 86 0.7× 83 0.9× 32 0.7× 19 0.8× 11 473
Cristina Dias Portugal 11 172 0.4× 24 0.2× 143 1.5× 34 0.7× 23 1.0× 16 359
Emily Tuttle United States 7 211 0.5× 29 0.2× 113 1.2× 42 0.9× 19 0.8× 10 314

Countries citing papers authored by Mazhor Aldosary

Since Specialization
Citations

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

Fields of papers citing papers by Mazhor Aldosary

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mazhor Aldosary

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

All Works

17 of 17 papers shown
1.
Al‐Hassnan, Zuhair N., Mazhor Aldosary, Rawan Almass, et al.. (2024). A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4. Frontiers in Psychiatry. 15. 1428175–1428175.
2.
Altassan, Ruqaiah, Hindi Al‐Hindi, Hazem Ghebeh, et al.. (2023). Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy. American Journal of Medical Genetics Part A. 194(4). e63498–e63498.
3.
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.
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.
Aldosary, Mazhor, et al.. (2019). Involvement of mitochondrial dysfunction in pathogenesis of hemophagocytic lymphohistiocytosis. SHILAP Revista de lepidopterología. 2(1). 81–84. 1 indexed citations
7.
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
8.
Sulaiman, Raashda A., Marwan Shaheen, Hamad Alzaidan, et al.. (2016). Hemophagocytic lymphohistiocytosis: A rare cause of recurrent encephalopathy. Intractable & Rare Diseases Research. 5(3). 227–230. 9 indexed citations
9.
Dombi, Eszter, Alan Diot, Karl Morten, et al.. (2016). The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy. Neurology. 86(20). 1921–1923. 28 indexed citations
10.
Faqeih, Eissa, Mohammed Al‐Owain, Dilek Çolak, et al.. (2014). Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly. American Journal of Medical Genetics Part A. 164(6). 1565–1570. 12 indexed citations
11.
AlSayed, Moeenaldeen, Hamad Alzaidan, Albandary AlBakheet, et al.. (2013). Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay. The American Journal of Human Genetics. 93(4). 721–726. 69 indexed citations
12.
Tuppen, Helen, K Naess, Nancy G. Kennaway, et al.. (2012). Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. European Journal of Human Genetics. 20(8). 897–904. 11 indexed citations
13.
Alazami, Anas M., Muneera Alshammari, Mustafa A. Salih, et al.. (2012). Molecular characterization of Joubert syndrome in Saudi Arabia. Human Mutation. 33(10). 1423–1428. 45 indexed citations
14.
Yarham, John W., Mazhor Aldosary, Emma L. Blakely, et al.. (2011). A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations. Human Mutation. 32(11). 1319–1325. 136 indexed citations
15.
Tuppen, Helen, Vanessa Hogan, Langping He, et al.. (2010). The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families. Brain. 133(10). 2952–2963. 70 indexed citations
16.
Aldosary, Mazhor, Roger G. Whittaker, Robert McFarland, et al.. (2009). Neuromuscular disease presentation with three genetic defects involving two genomes. Neuromuscular Disorders. 19(12). 841–844. 6 indexed citations
17.
Tam, Emily, Annette Feigenbaum, Jane Addis, et al.. (2008). A Novel Mitochondrial DNA Mutation inCOX1Leads to Strokes, Seizures, and Lactic Acidosis. Neuropediatrics. 39(6). 328–334. 35 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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