Eman Alobeid

1.1k total citations
10 papers, 285 citations indexed

About

Eman Alobeid is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Eman Alobeid has authored 10 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Oncology. Recurrent topics in Eman Alobeid's work include RNA modifications and cancer (3 papers), RNA and protein synthesis mechanisms (3 papers) and RNA Research and Splicing (3 papers). Eman Alobeid is often cited by papers focused on RNA modifications and cancer (3 papers), RNA and protein synthesis mechanisms (3 papers) and RNA Research and Splicing (3 papers). Eman Alobeid collaborates with scholars based in Saudi Arabia, United States and Türkiye. Eman Alobeid's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Eric M. Phizicky, Nour Ewida, Eissa Faqeih, Lu Han, Tarfa Al‐Sheddi, Ghada M. H. Abdel‐Salam, Anas M. Alazami and Sateesh Maddirevula and has published in prestigious journals such as Hepatology, The American Journal of Human Genetics and Genome biology.

In The Last Decade

Eman Alobeid

9 papers receiving 285 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eman Alobeid Saudi Arabia 8 245 58 58 33 18 10 285
Nishant Singhal Germany 7 465 1.9× 56 1.0× 68 1.2× 18 0.5× 30 1.7× 12 511
Jennifer McDaid United Kingdom 8 271 1.1× 99 1.7× 29 0.5× 21 0.6× 22 1.2× 8 325
Amandine Bemmo Canada 6 244 1.0× 51 0.9× 53 0.9× 22 0.7× 11 0.6× 8 294
Yuzhong Jeff Meng United States 2 210 0.9× 33 0.6× 144 2.5× 18 0.5× 9 0.5× 2 284
Haiqing Xiong China 7 397 1.6× 29 0.5× 81 1.4× 22 0.7× 12 0.7× 12 418
Lindsey E. Montefiori United States 8 259 1.1× 67 1.2× 25 0.4× 10 0.3× 12 0.7× 12 329
H. Holster United States 2 312 1.3× 42 0.7× 44 0.8× 22 0.7× 13 0.7× 2 333
Barbara K. Fortini United States 9 117 0.5× 57 1.0× 49 0.8× 48 1.5× 13 0.7× 12 203
Gabrijela Dumbović United States 9 247 1.0× 42 0.7× 142 2.4× 13 0.4× 13 0.7× 17 308

Countries citing papers authored by Eman Alobeid

Since Specialization
Citations

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

Fields of papers citing papers by Eman Alobeid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eman Alobeid

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

All Works

10 of 10 papers shown
1.
Al–Muhaizea, Mohammad A., Anoud Albader, Rawan Almass, et al.. (2025). Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness. Orphanet Journal of Rare Diseases. 20(1). 415–415.
2.
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
3.
Patel, Nisha, Eman Alobeid, Tarfa Alshidi, et al.. (2020). Confirming the recessive inheritance of PERP‐related erythrokeratoderma. Clinical Genetics. 97(4). 661–665. 4 indexed citations
4.
Shaheen, Ranad, Sateesh Maddirevula, Ghada M. H. Abdel‐Salam, et al.. (2019). PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly. Human Genetics. 138(3). 231–239. 68 indexed citations
5.
Shamseldin, Hanan E., Nawal Makhseed, Niema Ibrahim, et al.. (2019). NUP214 deficiency causes severe encephalopathy and microcephaly in humans. Human Genetics. 138(3). 221–229. 14 indexed citations
6.
Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations
7.
Shaheen, Ranad, Saud Alsahli, Nour Ewida, et al.. (2019). Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans. Hepatology. 71(6). 2067–2079. 23 indexed citations
8.
Patel, Nisha, Hanan E. Shamseldin, Nadia Sakati, et al.. (2017). GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome. The American Journal of Human Genetics. 100(5). 831–836. 13 indexed citations
9.
Patel, Nisha, Arif O. Khan, Maher Al‐Saif, et al.. (2017). A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation. Genome biology. 18(1). 144–144. 17 indexed citations
10.
Shaheen, Ranad, Lu Han, Eissa Faqeih, et al.. (2016). A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognition. Human Genetics. 135(7). 707–713. 113 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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