Fatma Al‐Jasmi

533 total citations
20 papers, 280 citations indexed

About

Fatma Al‐Jasmi is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Fatma Al‐Jasmi has authored 20 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Fatma Al‐Jasmi's work include Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (5 papers) and Lysosomal Storage Disorders Research (5 papers). Fatma Al‐Jasmi is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (5 papers) and Lysosomal Storage Disorders Research (5 papers). Fatma Al‐Jasmi collaborates with scholars based in United Arab Emirates, United States and Oman. Fatma Al‐Jasmi's co-authors include Jozef Hertecant, Abdul‐Kader Souid, Aisha Al‐Shamsi, Bassam R. Ali, Tracy Stockley, Jozef Hertecant, Lihadh Al‐Gazali, Salma Ben‐Salem, Joe T.R. Clarke and Kyong‐Soon Lee and has published in prestigious journals such as Frontiers in Pharmacology, Frontiers in Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

Fatma Al‐Jasmi

19 papers receiving 268 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fatma Al‐Jasmi United Arab Emirates 10 103 77 67 58 35 20 280
Marine Berquez Switzerland 8 116 1.1× 37 0.5× 52 0.8× 76 1.3× 68 1.9× 11 333
Han‐Wook Yoo South Korea 10 113 1.1× 59 0.8× 43 0.6× 79 1.4× 39 1.1× 16 253
Marta Camilot Italy 12 157 1.5× 80 1.0× 66 1.0× 18 0.3× 60 1.7× 29 385
Sun Hee Heo South Korea 10 138 1.3× 70 0.9× 18 0.3× 124 2.1× 12 0.3× 24 311
Fengxia Yao China 11 153 1.5× 94 1.2× 21 0.3× 26 0.4× 54 1.5× 31 270
Han Wook Yoo South Korea 10 116 1.1× 87 1.1× 73 1.1× 29 0.5× 47 1.3× 50 416
Çiğdem Seher Kasapkara Türkiye 9 167 1.6× 60 0.8× 103 1.5× 90 1.6× 21 0.6× 61 344
Zhengqing Qiu China 10 78 0.8× 96 1.2× 10 0.1× 95 1.6× 10 0.3× 40 273
Christine Hendrickson United States 10 251 2.4× 99 1.3× 246 3.7× 82 1.4× 54 1.5× 13 506
Patrícia Janeiro Portugal 8 117 1.1× 42 0.5× 89 1.3× 44 0.8× 31 0.9× 20 213

Countries citing papers authored by Fatma Al‐Jasmi

Since Specialization
Citations

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

Fields of papers citing papers by Fatma Al‐Jasmi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fatma Al‐Jasmi. 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 Fatma Al‐Jasmi. The network helps show where Fatma Al‐Jasmi may publish in the future.

Co-authorship network of co-authors of Fatma Al‐Jasmi

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

All Works

20 of 20 papers shown
1.
Ali, Amanat, et al.. (2024). Spectrum of genetic variants in bilateral sensorineural hearing loss. Frontiers in Genetics. 15. 1314535–1314535. 1 indexed citations
2.
Al‐Jasmi, Fatma, et al.. (2024). Exploring the efficacy and safety of Ambroxol in Gaucher disease: an overview of clinical studies. Frontiers in Pharmacology. 15. 1335058–1335058. 8 indexed citations
3.
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5.
Al‐Thihli, Khalid, et al.. (2023). Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families. Orphanet Journal of Rare Diseases. 18(1). 344–344. 1 indexed citations
6.
Ali, Amanat, et al.. (2022). A Type 3 Gaucher-Like Disease Due To Saposin C Deficiency in Two Emirati Families Caused by a Novel Splice Site Variant in the PSAP Gene. Journal of Molecular Neuroscience. 72(6). 1322–1333. 5 indexed citations
7.
Al‐Jasmi, Fatma, Srdjan Denic, & Abdul‐Kader Souid. (2020). A Curse of Knowledge in Diagnosis of Thalassemia. European Journal of Medical and Health Sciences. 2(2). 1 indexed citations
8.
Ghattas, Mohammad A., Aisha Al‐Shamsi, Taleb M. Almansoori, et al.. (2019). A Novel Homozygous Missense Variant in the NAGA Gene with Extreme Intrafamilial Phenotypic Heterogeneity. Journal of Molecular Neuroscience. 70(1). 45–55. 3 indexed citations
9.
Rodan, Lance H., Marissa Hauptman, Alissa M. D’Gama, et al.. (2018). Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies. Molecular Genetics and Metabolism. 124(2). 161–167. 35 indexed citations
10.
Meng, Linyan, Taraka Donti, Fan Xia, et al.. (2016). Homozygous variants in pyrroline‐5‐carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophy. American Journal of Medical Genetics Part A. 173(2). 460–470. 15 indexed citations
11.
Al‐Shamsi, Aisha, Jozef Hertecant, Abdul‐Kader Souid, & Fatma Al‐Jasmi. (2016). Whole exome sequencing diagnosis of inborn errors of metabolism and other disorders in United Arab Emirates. Orphanet Journal of Rare Diseases. 11(1). 94–94. 38 indexed citations
12.
Al‐Jasmi, Fatma, et al.. (2015). Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011–2014). JIMD Reports. 28. 127–135. 23 indexed citations
13.
Al‐Shamsi, Aisha, et al.. (2014). Mutation Spectrum and Birth Prevalence of Inborn Errors of Metabolism among Emiratis : A Study from Tawam Hospital Metabolic Center , United Arab Emirates. Sultan Qaboos University medical journal. 14(1). 42–49. 29 indexed citations
14.
Al‐Shamsi, Aisha, Salma Ben‐Salem, Jozef Hertecant, & Fatma Al‐Jasmi. (2014). Transaldolase deficiency caused by the homozygous p.R192C mutation of the TALDO1 gene in four Emirati patients with considerable phenotypic variability. European Journal of Pediatrics. 174(5). 661–668. 15 indexed citations
15.
16.
Akawi, Nadia, Fatma Al‐Jasmi, Aisha Al‐Shamsi, Bassam R. Ali, & Lihadh Al‐Gazali. (2013). LINS, a modulator of the WNT signaling pathway, is involved in human cognition. Orphanet Journal of Rare Diseases. 8(1). 87–87. 17 indexed citations
17.
Al‐Jasmi, Fatma, et al.. (2012). Prevalence and Novel Mutations of Lysosomal Storage Disorders in United Arab Emirates. JIMD Reports. 10. 1–9. 41 indexed citations
18.
Hertecant, Jozef, Salma Ben‐Salem, Fatma Al‐Jasmi, et al.. (2012). Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene. European Journal of Medical Genetics. 55(12). 671–676. 13 indexed citations
19.
Al‐Jasmi, Fatma, Harvey S. Penefsky, & Abdul‐Kader Souid. (2011). The phosphorescence oxygen analyzer as a screening tool for disorders with impaired lymphocyte bioenergetics. Molecular Genetics and Metabolism. 104(4). 529–536. 9 indexed citations
20.
Al‐Jasmi, Fatma, Mohamed Abdelhaleem, Tracy Stockley, Kyong‐Soon Lee, & Joe T.R. Clarke. (2008). Novel Mutation of the Perforin Gene and Maternal Uniparental Disomy 10 in a Patient With Familial Hemophagocytic Lymphohistiocytosis. Journal of Pediatric Hematology/Oncology. 30(8). 621–624. 23 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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