Sahar Mansour

4.9k total citations
15 papers, 854 citations indexed

About

Sahar Mansour is a scholar working on Molecular Biology, Surgery and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Sahar Mansour has authored 15 papers receiving a total of 854 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 2 papers in Surgery and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Sahar Mansour's work include Mitochondrial Function and Pathology (2 papers), Pain Mechanisms and Treatments (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Sahar Mansour is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), Pain Mechanisms and Treatments (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Sahar Mansour collaborates with scholars based in United Kingdom, United States and France. Sahar Mansour's co-authors include Melita Irving, Frances Elmslie, Christine M Hall, George D. Yancopoulos, David M. Valenzuela, C. Pollitt, Robert B. Kimble, Michael Oldridge, Andrew O.M. Wilkie and Peter Propping and has published in prestigious journals such as Nature Genetics, Brain and The American Journal of Human Genetics.

In The Last Decade

Sahar Mansour

15 papers receiving 824 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sahar Mansour United Kingdom	11	575	288	81	65	63	15	854
Nisha Patel Saudi Arabia	17	428 0.7×	267 0.9×	53 0.7×	43 0.7×	51 0.8×	39	727
Rowida Almomani Jordan	16	522 0.9×	225 0.8×	100 1.2×	54 0.8×	166 2.6×	26	1.0k
Pauline Terhal Netherlands	18	574 1.0×	632 2.2×	51 0.6×	38 0.6×	33 0.5×	28	1.0k
Hiroko Koike Japan	17	547 1.0×	187 0.6×	68 0.8×	66 1.0×	52 0.8×	30	1.1k
Pelin Özlem Şimşek‐Kiper Türkiye	14	377 0.7×	326 1.1×	57 0.7×	68 1.0×	22 0.3×	99	662
Luitgard Graul‐Neumann Germany	19	539 0.9×	457 1.6×	97 1.2×	44 0.7×	37 0.6×	46	884
Hamad Alzaidan Saudi Arabia	14	283 0.5×	173 0.6×	67 0.8×	65 1.0×	55 0.9×	39	578
Silke Pauli Germany	16	438 0.8×	214 0.7×	55 0.7×	58 0.9×	39 0.6×	39	723
Trieu Nguyen United States	16	767 1.3×	201 0.7×	87 1.1×	80 1.2×	79 1.3×	24	1.1k
Boris Keren France	21	649 1.1×	515 1.8×	44 0.5×	61 0.9×	28 0.4×	70	1.1k

Countries citing papers authored by Sahar Mansour

Since Specialization

Citations

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

Fields of papers citing papers by Sahar Mansour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sahar Mansour

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

All Works

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15 of 15 papers shown

Wai, Htoo A., Anand Saggar, Tessa Homfray, et al.. (2022). Short amplicon reverse transcription‐polymerase chain reaction detects aberrant splicing in genes with low expression in blood missed by ribonucleic acid sequencing analysis for clinical diagnosis. Human Mutation. 43(7). 963–970. 7 indexed citations

King‐Robson, Josh, et al.. (2021). Ataxia-Pancytopenia Syndrome due to a de Novo SAMD9L Mutation. Neurology Genetics. 7(3). e580–e580. 6 indexed citations

Mansour, Sahar, et al.. (2021). SHORT Syndrome: Systematic Appraisal of the Medical and Dental Phenotype. The Cleft Palate-Craniofacial Journal. 59(7). 873–881. 2 indexed citations

Jones, Gabriela, Osric Navti, H. Mousa, et al.. (2017). Renal anomalies and lymphedema distichiasis syndrome. A rare association?. American Journal of Medical Genetics Part A. 173(8). 2251–2256. 4 indexed citations

Hull, Sarah, Aeesha NJ Malik, Gavin Arno, et al.. (2016). Expanding the Phenotype ofTRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal Dysfunction. JAMA Ophthalmology. 134(9). 1049–1049. 24 indexed citations

Dyment, David A., Amanda Smith, Diana Alcantara, et al.. (2013). Mutations in PIK3R1 Cause SHORT Syndrome. The American Journal of Human Genetics. 93(1). 158–166. 130 indexed citations

Dixit, Abhijit, Shane McKee, Sahar Mansour, et al.. (2012). 7q11.23 Microduplication: a recognizable phenotype. Clinical Genetics. 83(2). 155–161. 37 indexed citations

Simpson, Michael A., Melita Irving, Esra Asilmaz, et al.. (2011). Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss. Nature Genetics. 43(4). 303–305. 218 indexed citations

Tuppen, Helen, Vanessa Hogan, Langping He, et al.. (2010). The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families. Brain. 133(10). 2952–2963. 70 indexed citations

10.

Natkunarajah, J., Duncan Atherton, Frances Elmslie, Sahar Mansour, & Peter Mortimer. (2009). Treatment with carbamazepine and gabapentin of a patient with primary erythermalgia (erythromelalgia) identified to have a mutation in theSCN9Agene, encoding a voltage-gated sodium channel. Clinical and Experimental Dermatology. 34(8). e640–e642. 22 indexed citations

11.

Irving, Melita, Lyn S. Chitty, Sahar Mansour, & Christine M Hall. (2008). Chondrodysplasia punctata: a clinical diagnostic and radiological review. Clinical Dysmorphology. 17(4). 229–241. 60 indexed citations

12.

Clayton‐Smith, Jill, Sarah Walters, Emma Hobson, et al.. (2008). Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance. European Journal of Human Genetics. 17(4). 434–443. 64 indexed citations

13.

Drenth, Joost P.H., René H. M. te Morsche, Sahar Mansour, & Peter Mortimer. (2008). Primary Erythermalgia as a Sodium Channelopathy. Archives of Dermatology. 144(3). 320–4. 21 indexed citations

14.

Hérasse, Muriel, Zuzana Dobbie, Dieter Gläser, et al.. (2003). Severe hypophosphatasia: Characterization of fifteen novel mutations in the ALPL gene. Human Mutation. 22(1). 105–106. 26 indexed citations

15.

Oldridge, Michael, Ana María Fortuna, Monika Maringa, et al.. (2000). Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B. Nature Genetics. 24(3). 275–278. 163 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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