Mohammed Mahnashi

477 total citations
5 papers, 24 citations indexed

About

Mohammed Mahnashi is a scholar working on Genetics, Rheumatology and Physiology. According to data from OpenAlex, Mohammed Mahnashi has authored 5 papers receiving a total of 24 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Rheumatology and 2 papers in Physiology. Recurrent topics in Mohammed Mahnashi's work include Carbohydrate Chemistry and Synthesis (1 paper), Glycogen Storage Diseases and Myoclonus (1 paper) and Genomics and Rare Diseases (1 paper). Mohammed Mahnashi is often cited by papers focused on Carbohydrate Chemistry and Synthesis (1 paper), Glycogen Storage Diseases and Myoclonus (1 paper) and Genomics and Rare Diseases (1 paper). Mohammed Mahnashi collaborates with scholars based in Saudi Arabia, Oman and Canada. Mohammed Mahnashi's co-authors include Fowzan S. Alkuraya, Moeenaldeen AlSayed, Wenkai Han, Kym M. Boycott, Almundher Al‐Maawali, Mais Hashem, Mohammed Al‐Owain, Hiroyuki Kuwahara, Mohamed H. Al‐Hamed and Xin Gao and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Cureus.

In The Last Decade

Mohammed Mahnashi

4 papers receiving 24 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mohammed Mahnashi Saudi Arabia	3	19	6	3	3	3	5	24
Daphne J. Smits Netherlands	3	12 0.6×	5 0.8×	5 1.7×	2 0.7×	6 2.0×	6	26
Shirin C C Saverimuttu United Kingdom	3	10 0.5×	7 1.2×		2 0.7×	3 1.0×	3	27
Fengyu Guo China	4	28 1.5×	12 2.0×	4 1.3×	3 1.0×		6	44
Deirdre Donnelly United Kingdom	3	27 1.4×	7 1.2×		2 0.7×	2 0.7×	4	38
Jaime Barea United States	2	6 0.3×	6 1.0×	2 0.7×	7 2.3×	2 0.7×	3	21
Hannah J. Perrin United States	2	18 0.9×	8 1.3×			3 1.0×	3	27
Giovanna Carpentieri Italy	4	13 0.7×	2 0.3×		3 1.0×	2 0.7×	4	14
Makiko Taira Japan	2	14 0.7×	11 1.8×			3 1.0×	4	18
Jeyanthy Rajkanna United Kingdom	4	15 0.8×	8 1.3×		2 0.7×		14	30
Charles Borromeo United States	4	11 0.6×	9 1.5×	2 0.7×			6	26

Countries citing papers authored by Mohammed Mahnashi

Since Specialization

Citations

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

Fields of papers citing papers by Mohammed Mahnashi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammed Mahnashi

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

All Works

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5 of 5 papers shown

1.

Mahnashi, Mohammed, et al.. (2024). Case report of congenital neutropenia type 4 with glucose‐6‐phosphatase catalytic subunit 3 (G6PC3) deficiency. SHILAP Revista de lepidopterología. 12(2). e8540–e8540. 1 indexed citations

2.

Mahnashi, Mohammed, et al.. (2021). Diagnosis and Management of Pompe Disease in Saudi Arabia. American Journal of Medicine and Medical Sciences. 11(5). 373–381. 2 indexed citations

3.

Mahnashi, Mohammed, et al.. (2021). Ellis-van Creveld Syndrome 2 With Novel Partial Exon 11 Deletion: A Case From Saudi Arabia. Cureus. 13(9). e17750–e17750.

4.

Alzahrani, Fatema, Hiroyuki Kuwahara, Mohammed Al‐Owain, et al.. (2020). Recessive, Deleterious Variants in SMG8 Expand the Role of Nonsense-Mediated Decay in Developmental Disorders in Humans. The American Journal of Human Genetics. 107(6). 1178–1185. 19 indexed citations

5.

Gari, Mamdooh, Farid Ahmed, Abdul Ali Peer‐Zada, et al.. (2012). JAK2 Mutations in Chronic Myeloproliferative Neoplasm; Towards the Application of Personalized Treatments for Saudi Patients. 2(2). 17–21. 2 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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