Rawan Almass

500 total citations
14 papers, 102 citations indexed

About

Rawan Almass is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Rawan Almass has authored 14 papers receiving a total of 102 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Rawan Almass's work include Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Rawan Almass is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Rawan Almass collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Rawan Almass's co-authors include Namik Kaya, Dilek Çolak, Maysoon Alsagob, Mohammed Al‐Owain, Majid Alfadhel, Albandary AlBakheet, Mazhor Aldosary, Mohammad A. Al–Muhaizea, Ali Al‐Odaib and Robert W. Taylor and has published in prestigious journals such as Acta Neuropathologica, Cells and Frontiers in Psychiatry.

In The Last Decade

Rawan Almass

11 papers receiving 101 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rawan Almass Saudi Arabia	7	77	24	23	22	16	14	102
Maysoon Alsagob Saudi Arabia	6	62 0.8×	21 0.9×	5 0.2×	22 1.0×	15 0.9×	12	109
David Moore United Kingdom	4	107 1.4×	14 0.6×	27 1.2×	19 0.9×	11 0.7×	5	128
Resham Ejaz Canada	7	55 0.7×	42 1.8×	12 0.5×	19 0.9×	12 0.8×	16	132
Tom E. J. Theunissen Netherlands	7	163 2.1×	31 1.3×	21 0.9×	92 4.2×	8 0.5×	12	200
Lucia Laugwitz Germany	7	47 0.6×	12 0.5×	12 0.5×	17 0.8×	5 0.3×	15	97
Sila Hopton United Kingdom	8	219 2.8×	13 0.5×	14 0.6×	118 5.4×	25 1.6×	19	247
Selina Reich Germany	5	96 1.2×	24 1.0×	20 0.9×	17 0.8×	37 2.3×	8	127
Maria Concetta Cutrupi Italy	5	50 0.6×	44 1.8×	5 0.2×	8 0.4×	6 0.4×	7	124
Dmitriy Niyazov United States	7	140 1.8×	99 4.1×	7 0.3×	37 1.7×	11 0.7×	8	208
Zhanying Dong China	5	69 0.9×	30 1.3×	8 0.3×	3 0.1×	8 0.5×	7	113

Countries citing papers authored by Rawan Almass

Since Specialization

Citations

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

Fields of papers citing papers by Rawan Almass

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rawan Almass

This figure shows the co-authorship network connecting the top 25 collaborators of Rawan Almass. A scholar is included among the top collaborators of Rawan Almass 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 Rawan Almass. Rawan Almass 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

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.

Al‐Hassnan, Zuhair N., Mazhor Aldosary, Rawan Almass, et al.. (2024). A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4. Frontiers in Psychiatry. 15. 1428175–1428175.

Salih, Mustafa A., Albandary AlBakheet, Rawan Almass, et al.. (2024). Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings. Frontiers in Psychiatry. 15. 1501238–1501238. 2 indexed citations

AlBakheet, Albandary, Rawan Almass, Alya Qari, et al.. (2024). Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population. Clinical Dysmorphology. 33(2). 55–62. 1 indexed citations

Almass, Rawan, et al.. (2023). SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literature. Human Genome Variation. 10(1). 7–7. 3 indexed citations

Aldosary, Mazhor, Maysoon Alsagob, Stefan T. Arold, et al.. (2022). A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families. Cells. 11(19). 3154–3154.

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

Almass, Rawan, Hesham Aldhalaan, Maysoon Alsagob, et al.. (2021). Genetics of ataxia telangiectasia in a highly consanguineous population. Annals of Human Genetics. 86(1). 34–44. 4 indexed citations

Almass, Rawan, Anoud Albader, Peter Karachunski, et al.. (2020). Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy. Acta Neuropathologica. 139(4). 791–794. 15 indexed citations

10.

Al–Muhaizea, Mohammad A., Anoud Albader, Rawan Almass, et al.. (2020). Pyrostigmine therapy in a patient with VAMP1-related congenital myasthenic syndrome. Neuromuscular Disorders. 30(7). 611–615. 9 indexed citations

11.

Al‐Hassnan, Zuhair N., Rawan Almass, Albandary AlBakheet, et al.. (2018). Identification of novel genomic imbalances in Saudi patients with congenital heart disease. Molecular Cytogenetics. 11(1). 9–9. 8 indexed citations

12.

Alfadhel, Majid, Marwan Nashabat, Muhammad Talal Alrifai, et al.. (2017). Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases. European Journal of Paediatric Neurology. 22(1). 46–55. 22 indexed citations

13.

Al–Muhaizea, Mohammad A., Rawan Almass, Mazhor Aldosary, et al.. (2017). A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature. The Cerebellum. 17(3). 276–285. 16 indexed citations

14.

Alfares, Ahmed, Lamia Alsubaie, Mohammed Al‐Owain, et al.. (2017). A new association between CDK5RAP2 microcephaly and congenital cataracts. Annals of Human Genetics. 82(3). 165–170. 10 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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