Liena E. O. Elsayed

473 total citations
14 papers, 108 citations indexed

About

Liena E. O. Elsayed is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Liena E. O. Elsayed has authored 14 papers receiving a total of 108 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Neurology and 5 papers in Genetics. Recurrent topics in Liena E. O. Elsayed's work include Neurological diseases and metabolism (6 papers), Genomics and Rare Diseases (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Liena E. O. Elsayed is often cited by papers focused on Neurological diseases and metabolism (6 papers), Genomics and Rare Diseases (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Liena E. O. Elsayed collaborates with scholars based in Sudan, Saudi Arabia and France. Liena E. O. Elsayed's co-authors include Ammar Ahmed, Giovanni Stévanin, Mustafa A. Salih, Mahmoud Koko, Ahlam A. Hamed, Alexis Brice, Mutaz Amin, Eric Noé, Omer Mohamed Abdalla and Éric Leguern and has published in prestigious journals such as Frontiers in Neurology, Expert Review of Neurotherapeutics and BMC Neurology.

In The Last Decade

Liena E. O. Elsayed

12 papers receiving 107 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Liena E. O. Elsayed Sudan	6	53	40	31	28	22	14	108
Zoltán Grosz Hungary	8	57 1.1×	81 2.0×	44 1.4×	50 1.8×	18 0.8×	20	170
Andrés Ordóñez‐Ugalde Spain	6	26 0.5×	36 0.9×	33 1.1×	13 0.5×	39 1.8×	8	105
Matt Hurles United Kingdom	2	32 0.6×	51 1.3×	12 0.4×	10 0.4×	20 0.9×	3	107
Marion Gaussen France	3	52 1.0×	70 1.8×	35 1.1×	18 0.6×	12 0.5×	3	122
Marie‐France Rioux Canada	6	117 2.2×	140 3.5×	48 1.5×	32 1.1×	38 1.7×	8	270
Silvia Fenu Italy	5	60 1.1×	43 1.1×	37 1.2×	37 1.3×	16 0.7×	14	112
Monia Hammer United States	8	71 1.3×	111 2.8×	43 1.4×	16 0.6×	30 1.4×	12	213
Daniela Bernardo Italy	6	47 0.9×	72 1.8×	22 0.7×	31 1.1×	14 0.6×	13	146
Rosanna Trovato Italy	6	79 1.5×	146 3.6×	15 0.5×	33 1.2×	27 1.2×	20	201
Thomas Bourinaris United Kingdom	5	35 0.7×	23 0.6×	30 1.0×	16 0.6×	16 0.7×	10	86

Countries citing papers authored by Liena E. O. Elsayed

Since Specialization

Citations

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

Fields of papers citing papers by Liena E. O. Elsayed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Liena E. O. Elsayed. 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 Liena E. O. Elsayed. The network helps show where Liena E. O. Elsayed may publish in the future.

Co-authorship network of co-authors of Liena E. O. Elsayed

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

All Works

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14 of 14 papers shown

Elsayed, Liena E. O., et al.. (2024). Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype. Human Genomics. 18(1). 95–95.

Hamed, Ahlam A., Mahmoud Koko, Liena E. O. Elsayed, et al.. (2024). A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes. Neurogenetics. 25(4). 425–433.

Ahmed, Khabab Abbasher Hussien Mohamed, et al.. (2024). Awareness of consanguineous marriage burden and willingness towards premarital genetic testing in Sudan: a national cross-sectional study. Annals of Medicine and Surgery. 86(7). 3959–3971. 2 indexed citations

Tesson, Christelle, Liena E. O. Elsayed, Suzanne Lesage, et al.. (2023). PLA2G6‐associated late‐onset parkinsonism in a Sudanese family. Annals of Clinical and Translational Neurology. 10(6). 983–989. 2 indexed citations

Amin, Mutaz, Ahlam A. Hamed, Mohamed Mustafa, et al.. (2022). A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability. BMC Medical Genomics. 15(1). 236–236. 4 indexed citations

Chen, Zhefan Stephen, Ammar Ahmed, Mustafa A. Salih, et al.. (2021). A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report. BMC Neurology. 21(1). 78–78. 4 indexed citations

Baldassari, Sara, Guillaume Achaz, Stéphanie Baulac, et al.. (2021). Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy. Frontiers in Neurology. 12. 9 indexed citations

Elsayed, Liena E. O., et al.. (2021). Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview. Frontiers in Molecular Biosciences. 8. 690899–690899. 42 indexed citations

Elsayed, Liena E. O., Ahlam A. Hamed, Mustafa A. Salih, et al.. (2020). Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family. Frontiers in Neurology. 11. 569996–569996. 5 indexed citations

10.

Hamed, Ahlam A., Mahmoud Koko, Liena E. O. Elsayed, et al.. (2019). Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556. Neurogenetics. 20(2). 91–98. 14 indexed citations

11.

Elsayed, Liena E. O., et al.. (2019). Hereditary spastic paraplegias: time for an objective case definition and a new nosology for neurogenetic disorders to facilitate biomarker/therapeutic studies. Expert Review of Neurotherapeutics. 19(5). 409–415. 5 indexed citations

12.

Elsayed, Liena E. O., Mustafa A. Salih, Sarah El-Sadig, et al.. (2018). Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report. BMC Neurology. 18(1). 175–175. 11 indexed citations

13.

Elsayed, Liena E. O., Ahlam A. Hamed, Mustafa A. Salih, et al.. (2018). Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. BMC Medical Genetics. 19(1). 72–72. 8 indexed citations

14.

Amin, Mutaz, Liena E. O. Elsayed, & Ammar Ahmed. (2017). Clinical and Genetic Characteristics of Leukodystrophies in Africa. Journal of Neurosciences in Rural Practice. 8(S 01). S089–S093. 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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