Mariam Al‐Mureikhi

1.3k total citations
18 papers, 591 citations indexed

About

Mariam Al‐Mureikhi is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Mariam Al‐Mureikhi has authored 18 papers receiving a total of 591 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Genetics. Recurrent topics in Mariam Al‐Mureikhi's work include Genomics and Rare Diseases (5 papers), Neurogenetic and Muscular Disorders Research (5 papers) and RNA modifications and cancer (4 papers). Mariam Al‐Mureikhi is often cited by papers focused on Genomics and Rare Diseases (5 papers), Neurogenetic and Muscular Disorders Research (5 papers) and RNA modifications and cancer (4 papers). Mariam Al‐Mureikhi collaborates with scholars based in Qatar, United States and Saudi Arabia. Mariam Al‐Mureikhi's co-authors include Rehab Ali, Noora Shahbeck, Tawfeg Ben‐Omran, Tawfeg Ben‐Omran, Ahmad S. Teebi, Mariam AlMulla, Laila Mahmoud, Nader Al‐Dewik, Shenela Lakhani and Patrik Vitazka and has published in prestigious journals such as The American Journal of Human Genetics, Gene Therapy and Human Genetics.

In The Last Decade

Mariam Al‐Mureikhi

18 papers receiving 586 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mariam Al‐Mureikhi Qatar 12 334 280 98 56 52 18 591
Nisha Patel Saudi Arabia 17 428 1.3× 267 1.0× 69 0.7× 52 0.9× 40 0.8× 39 727
Pelin Özlem Şimşek‐Kiper Türkiye 14 377 1.1× 326 1.2× 70 0.7× 48 0.9× 39 0.8× 99 662
Morad Khayat Israel 16 422 1.3× 162 0.6× 73 0.7× 46 0.8× 36 0.7× 50 664
Tawfeg Ben‐Omran Qatar 11 353 1.1× 225 0.8× 41 0.4× 43 0.8× 42 0.8× 24 584
Deborah Morrogh United Kingdom 9 247 0.7× 299 1.1× 83 0.8× 30 0.5× 26 0.5× 13 542
Adi Mory Israel 15 245 0.7× 147 0.5× 66 0.7× 43 0.8× 31 0.6× 40 592
Bryn D. Webb United States 13 588 1.8× 212 0.8× 59 0.6× 34 0.6× 43 0.8× 35 896
Elisa Giorgio Italy 16 413 1.2× 177 0.6× 60 0.6× 50 0.9× 24 0.5× 46 622
Gülen Eda Ütine Türkiye 14 367 1.1× 373 1.3× 54 0.6× 52 0.9× 40 0.8× 114 715
Marta Romani Italy 12 347 1.0× 314 1.1× 60 0.6× 66 1.2× 23 0.4× 17 600

Countries citing papers authored by Mariam Al‐Mureikhi

Since Specialization
Citations

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

Fields of papers citing papers by Mariam Al‐Mureikhi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariam Al‐Mureikhi

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

All Works

18 of 18 papers shown
1.
Ibrahim, Khalid, Mahmoud F. Elsaid, Mariam AlMulla, et al.. (2021). Gene therapy for spinal muscular atrophy: the Qatari experience. Gene Therapy. 28(10-11). 676–680. 32 indexed citations
2.
Maddirevula, Sateesh, Tawfeg Ben‐Omran, Mariam Al‐Mureikhi, et al.. (2020). Further delineation of HIDEA syndrome. American Journal of Medical Genetics Part A. 182(12). 2999–3006. 5 indexed citations
3.
Al‐Mureikhi, Mariam, Noora Shahbeck, Rehab Ali, et al.. (2020). A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. American Journal of Medical Genetics Part A. 182(11). 2570–2580. 8 indexed citations
4.
Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2019). Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. American Journal of Medical Genetics Part A. 179(6). 927–935. 32 indexed citations
5.
Cozma, Claudia, Marina Hovakimyan, Nawal Makhseed, et al.. (2019). Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome. Orphanet Journal of Rare Diseases. 14(1). 209–209. 7 indexed citations
6.
Eyaid, Wafaa, Kimberli J. Kamer, Rehab Ali, et al.. (2018). A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. JIMD Reports. 43. 79–83. 43 indexed citations
7.
Ben‐Omran, Tawfeg, Khushnooda Ramzan, Ruqaiah Altassan, et al.. (2018). Delineating the phenotypic spectrum of hyperphosphatasia with mental retardation syndrome 4 in 14 patients of Middle‐Eastern origin. American Journal of Medical Genetics Part A. 176(12). 2850–2857. 5 indexed citations
8.
Al‐Dewik, Nader, Mariam Al‐Mureikhi, Noora Shahbeck, et al.. (2018). Clinical genetics and genomic medicine in Qatar. Molecular Genetics & Genomic Medicine. 6(5). 702–712. 20 indexed citations
9.
Lakhani, Shenela, Ryan N. Doan, Mariam Al‐Mureikhi, et al.. (2017). Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy. European Journal of Medical Genetics. 60(5). 245–249. 21 indexed citations
10.
Maddirevula, Sateesh, Fatema Alzahrani, Shams Anazi, et al.. (2017). GWAS signals revisited using human knockouts. Genetics in Medicine. 20(1). 64–68. 3 indexed citations
11.
Marin‐Valencia, Isaac, Andreas Gerondopoulos, Maha S. Zaki, et al.. (2017). Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. The American Journal of Human Genetics. 101(3). 441–450. 43 indexed citations
12.
Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2015). High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders. Human Genetics. 134(9). 967–980. 140 indexed citations
13.
Zárate, Yuri A., Hazel Perry, Tawfeg Ben‐Omran, et al.. (2015). Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing. American Journal of Medical Genetics Part A. 167(5). 1026–1032. 37 indexed citations
14.
Ye, Yizhou, Megan T. Cho, Kyle Retterer, et al.. (2015). De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly. Molecular Case Studies. 1(1). a000455–a000455. 39 indexed citations
15.
Ben‐Omran, Tawfeg, Rehab Ali, Mariam Al‐Mureikhi, et al.. (2011). Phenotypic heterogeneity in Woodhouse–Sakati syndrome: Two new families with a mutation in the C2orf37 gene. American Journal of Medical Genetics Part A. 155(11). 2647–2653. 24 indexed citations
16.
Anastasio, Natascia, Tawfeg Ben‐Omran, Ahmad S. Teebi, et al.. (2010). Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome. The American Journal of Human Genetics. 87(4). 553–559. 45 indexed citations
17.
Ali, Rehab, et al.. (2010). Further delineation of the Van den Ende–Gupta syndrome. American Journal of Medical Genetics Part A. 152A(12). 3095–3100. 8 indexed citations
18.
Faiyaz‐Ul‐Haque, Muhammad, Syed Hassan Ejaz Zaidi, Mariam Al‐Ali, et al.. (2004). A novel missense mutation in the galactosyltransferase‐I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type. American Journal of Medical Genetics Part A. 128A(1). 39–45. 79 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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