Mona Mohammad Almramhi

468 total citations
13 papers, 189 citations indexed

About

Mona Mohammad Almramhi is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Mona Mohammad Almramhi has authored 13 papers receiving a total of 189 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Mona Mohammad Almramhi's work include Genomics and Rare Diseases (2 papers), Skin and Cellular Biology Research (2 papers) and RNA regulation and disease (2 papers). Mona Mohammad Almramhi is often cited by papers focused on Genomics and Rare Diseases (2 papers), Skin and Cellular Biology Research (2 papers) and RNA regulation and disease (2 papers). Mona Mohammad Almramhi collaborates with scholars based in United Kingdom, Saudi Arabia and Pakistan. Mona Mohammad Almramhi's co-authors include Musharraf Jelani, Jumana Y. Al‐Aama, Saleem Ahmed, Jun Wang, Jamal Nasir, Nicholas Wood, Demis A. Kia, Yaser M. Alkhiary, Nirmal Vadgama and Kay Childs and has published in prestigious journals such as Neurology, Scientific Reports and Movement Disorders.

In The Last Decade

Mona Mohammad Almramhi

12 papers receiving 187 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mona Mohammad Almramhi United Kingdom	8	117	58	56	16	15	13	189
Neethukrishna Kausthubham India	7	112 1.0×	68 1.2×	39 0.7×	6 0.4×	14 0.9×	13	194
Ina Hainmann Germany	9	147 1.3×	18 0.3×	59 1.1×	13 0.8×	11 0.7×	11	248
Yannis Duffourd France	10	115 1.0×	132 2.3×	28 0.5×	7 0.4×	12 0.8×	25	221
Clemens Freiberg Germany	10	134 1.1×	124 2.1×	55 1.0×	8 0.5×	17 1.1×	15	287
Nuria García Segarra Switzerland	7	78 0.7×	45 0.8×	14 0.3×	13 0.8×	24 1.6×	10	148
Khalid Hundallah Saudi Arabia	7	88 0.8×	48 0.8×	15 0.3×	15 0.9×	15 1.0×	21	165
Carolin Wegbrod Germany	7	119 1.0×	44 0.8×	35 0.6×	5 0.3×	12 0.8×	7	184
Ramona Jühlen Germany	9	183 1.6×	52 0.9×	41 0.7×	7 0.4×	11 0.7×	17	261
Wenbai Zhou China	11	156 1.3×	50 0.9×	21 0.4×	10 0.6×	7 0.5×	17	299
Lauren K. Wasson United States	8	200 1.7×	39 0.7×	25 0.4×	6 0.4×	11 0.7×	13	280

Countries citing papers authored by Mona Mohammad Almramhi

Since Specialization

Citations

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

Fields of papers citing papers by Mona Mohammad Almramhi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mona Mohammad Almramhi. 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 Mona Mohammad Almramhi. The network helps show where Mona Mohammad Almramhi may publish in the future.

Co-authorship network of co-authors of Mona Mohammad Almramhi

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Almramhi, Mona Mohammad, Chris Finan, Amand F. Schmidt, et al.. (2023). Exploring the Role of Plasma Lipids and Statin Interventions on Multiple Sclerosis Risk and Severity. Neurology. 101(17). e1729–e1740. 2 indexed citations

Almramhi, Mona Mohammad, et al.. (2022). Prevalence and Risk Factors for Acute Kidney Injury Among Adults Undergoing Cardiac Interventions in King Abdulaziz University Hospital: A Retrospective Review. Cureus. 14(3). e23387–e23387.

Almramhi, Mona Mohammad, et al.. (2022). The role of body fat in multiple sclerosis susceptibility and severity: A Mendelian randomisation study. Multiple Sclerosis Journal. 28(11). 1673–1684. 7 indexed citations

Kia, Demis A., et al.. (2021). Mendelian Randomisation Finds No Causal Association between Urate and Parkinson's Disease Progression. Movement Disorders. 36(9). 2182–2187. 11 indexed citations

Kia, Demis A., et al.. (2020). Using Mendelian randomization to understand and develop treatments for neurodegenerative disease. Brain Communications. 2(1). fcaa031–fcaa031. 12 indexed citations

Ahmed, Saleem, Musharraf Jelani, Kay Childs, et al.. (2018). A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features. Scientific Reports. 8(1). 2053–2053. 26 indexed citations

Ahmed, Saleem, Mona Mohammad Almramhi, Taghreed Shuaib, et al.. (2016). The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family. Journal of the Neurological Sciences. 363. 240–244. 18 indexed citations

Jelani, Musharraf, Changsoo Kang, Mona Mohammad Almramhi, et al.. (2016). A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family. Archives of Oral Biology. 67. 28–33. 22 indexed citations

Jelani, Musharraf, et al.. (2015). Case of Sjögren–Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis. The Journal of Dermatology. 42(7). 706–709. 14 indexed citations

10.

Ahmed, Saleem, Musharraf Jelani, Mona Mohammad Almramhi, et al.. (2015). Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3. Journal of the Neurological Sciences. 353(1-2). 149–154. 37 indexed citations

11.

Alkhiary, Yaser M., et al.. (2015). Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon–Lefevre syndrome in a Saudi family. Saudi Journal of Biological Sciences. 23(5). 571–576. 6 indexed citations

12.

Jelani, Musharraf, et al.. (2015). Novel nonsense mutation in the PTRF gene underlies congenital generalized lipodystrophy in a consanguineous Saudi family. European Journal of Medical Genetics. 58(4). 216–221. 30 indexed citations

13.

Jelani, Musharraf, Mona Mohammad Almramhi, Saleem Ahmed, et al.. (2015). Identification of Two Homozygous Sequence Variants in the COL7A1 Gene Underlying Dystrophic Epidermolysis Bullosa by Whole‐Exome Analysis in a Consanguineous Family. Annals of Human Genetics. 79(5). 350–356. 4 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.

Explore authors with similar magnitude of impact